2008 JASN IMPACT FACTOR 7.505	HOME   AUTHOR INFO   EDITORIAL BOARD   SUBSCRIBE   FEEDBACK   ALERTS   HELP
advanced	CURRENT ISSUE	ARCHIVES	JASN Express	ONLINE SUBMISSION

This Article Abstract Full Text (PDF) Alert me when this article is cited Alert me if a correction is posted Citation Map Services Email this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Citing Articles Citing Articles via HighWire Citing Articles via Google Scholar Google Scholar Articles by SIFFERT, W. Articles by ROSSKOPF, D. Search for Related Content PubMed PubMed Citation Articles by SIFFERT, W. Articles by ROSSKOPF, D.

Worldwide Ethnic Distribution of the G Protein ß3 Subunit 825T Allele and Its Association with Obesity in Caucasian, Chinese, and Black African Individuals

WINFRIED SIFFERT^*, PETER FORSTER^**, KARL-HEINZ JÖCKEL, DAVID A. MVERE, BERND BRINKMANN^**, CHRISTOPH NABER^*, ROBERT CROOKES, ANTHON DU P. HEYNS, JÖRG T. EPPLEN^§§, JOY FRIDEY^||||, BARRY I. FREEDMAN^¶¶, NORBERT MÜLLER, DIETMAR STOLKE^¶, ARYA M. SHARMA^##, KHALAF AL MOUTAERY^***, HANS GROSSE-WILDE^§, BETTINA BUERBAUM^*, TANJA EHRLICH^*, HAKIMUDDIN RAZI AHMAD, BERNHARD HORSTHEMKE^||, ERNETTE D. DU TOIT, ANJA TIILIKAINEN^§§§, JUNBO GE^#, YULIN WANG^||||||, DONGLIANG YANG^¶¶¶, JOHANNES HÜSING and DIETER ROSSKOPF^*

^* Institute für Pharmakologie, Universitätsklinikum Essen, Essen, Germany
Institute für Medizinische Informatik, Biometrie und Epidemiologie, Universitätsklinikum Essen, Essen, Germany
Institute für Transfusionsmedizin
^§ Institute für Immunologie, Universitätsklinikum Essen, Essen, Germany
^|| Institute für Humangenetik, Universitätsklinikum Essen, Essen, Germany
^¶ Institute für Klinik für Neurochirurgie Universitätsklinikum Essen, Essen, Germany
^# Institute für Abteilung für Kardiologie, Universitätsklinikum Essen, Essen, Germany
^** Institut für Rechtsmedizin, Universität Münster, Münster, Germany
National Blood Transfusion Service Zimbabwe, Avondale, Harare, Zimbabwe
The South African Blood Transfusion Service, Johannesburg, South Africa
^§§ Molekulare Humangenetik, Ruhr-Universität, Bochum, Germany
^|||| Blood Bank of San Bernardino and Riverside Counties, San Bernardino, California
^¶¶ Section on Nephrology, Department of Medicine, Bowman Gray School of Medicine, Winston-Salem, North Carolina
^## Universitätsklinikum Benjamin Franklin, Abteilung für Endokrinologie und Nephrologie, Berlin, Germany
^*** Riyadh Armed Forces Hospital, Division of Neurosurgery, Riyadh, Saudi Arabia
The Aga Khan University, Department of Physiology and Pharmacology, Karachi, Pakistan
Laboratory for Tissue Immunology, Falmouth Building, Medical School, Cape Town, South Africa
^§§ Departement of Clinical Microbiology and Immunology, University of Oulu, Oulu, Finland
^|||| Department of Pediatrics, Shandong Provincial Hospital, Jinan, Shandong, People's Republic of China
^¶¶ Division of Clinical Immunology, Tongji Medical University, Wuhan, People's Republic of China.

Correspondence to Dr. Winfried Siffert, Institut für Pharmakologie, Universitätsklinikum, Hufelandstrasse 55, D-45122 Essen, Germany. Phone: +49 201 723 3470; Fax: +49 201 723 5968; E-mail: winfried.siffert{at}uni-essen.de

Abstract

Abstract. Recently, it was demonstrated that one allele (825T) of the gene encoding the G protein ß3 subunit (GNB3) is associated with hypertension in Germans. This study investigates a possible association with obesity in young male Germans, Chinese, and black South Africans with low, intermediate, and high 825T allele frequencies, respectively. In each of these three distinct cohorts, the 825T allele frequency was increased significantly in overweight (body mass index [BMI] 25 kg/m²) and obese individuals (BMI >27 kg/m²) compared to those with normal weight. The 825T allele frequencies in these three BMI groups were, respectively, 29.5, 39.3, and 47.7% in Germans, 46.8, 53.9, and 58.6% in Chinese, and 83.1, 87.7, and 90.9% in South Africans. In each of these three distinct groups, the 825T allele was significantly associated with obesity with odds ratios between 2 and 3. More urban than rural black Africans were overweight despite similar 825T allele frequencies in both populations, which underscores the role of both genetic and environmental factors. BP values in young male whites increased significantly with increasing BMI values but were independent of the C825T polymorphism, suggesting that hypertension associated with the 825T allele could be a consequence of obesity. Genotyping of 5254 individuals from 55 native population samples from Africa, the Americas, Europe, Asia, Australia, and New Guinea demonstrated highest 825T allele frequencies in black Africans (82%) and intermediate values in east Asians (47%). It is anticipated that high frequencies of the 825T allele in Africans and Asians may contribute to an obesity and hypertension epidemic if Westernization of lifestyles continues.

Currently available data suggest a worldwide continuous increase in obesity prevalence, which is recently also being observed in developing countries (1). This prompts some authors to predict an "obesity epidemic" (2) with an increased prevalence of hypertension, stroke, coronary artery disease, and type 2 diabetes mellitus, for which obesity is a major risk factor (3). A considerable part of obesity is due to environmental factors and lifestyle, but between 40 and 70% of the variation of body mass index (BMI) is estimated to be heritable (4).

We recently described a C825T polymorphism in the gene GNB3 encoding the ß3 subunit of heterotrimeric G proteins, which are key components of intracellular signal transduction in all cells of the body (5). The 825T allele is associated with the occurrence of a splice variant, termed Gß3-s, which, despite a deletion of 41 amino acids, is functionally active in a reconstituted system. The GNB3 825T allele is also associated with enhanced G protein activation, resulting in increased cell proliferation (6,7) and hypertension in Caucasians (5,8,9). The frequency of the 825T allele (fT) was markedly increased to 50% in young Canadian Oji-Cree Indians compared to 25 to 30% in Caucasians and, unexpectedly, the 825T allele was associated with lower rather than increased BP values (10). Nevertheless, fT was increased (57%) in subjects under antihypertensive therapy, although this was not statistically increased from control subjects potentially due to the small number of hypertensive individuals in this population. Similarly, fT amounted to 49% in Japanese, but no association of the 825T allele with hypertension was detected (11). Taken together, these findings suggested significant ethnic differences in 825T allele distributions and, possibly, inter-ethnic differences in associations with hypertension.

The present study was designed to investigate two main topics. First, we searched for a potential association between the 825T allele and obesity in individuals of different ethnicity and living habits in their native country. Second, we determined the worldwide ethnic distribution and the presumed ancestral state of the GNB3 825 polymorphism.

Our analyses were based on some underlying considerations: First, Na⁺/H⁺ exchanger activity, i.e., the intermediate phenotype leading to the detection of the C825T polymorphism (5,12), is elevated in obese hypertensive and normotensive subjects but not in lean individuals (13). Thus, hypertension associated with enhanced G protein activation as indicated by the 825T allele could develop secondary to obesity. Furthermore, intracellular signal transduction via pertussis toxin (PTX)-sensitive G proteins is of major importance in adipogenesis (14). Transgenic mice lacking the PTX-sensitive Gi2 subunit are lean and deficient in fat mass (15). On the other hand, increased expression of Gi2 or expression of constitutively active Gi2 subunits in fibroblasts results in lipid accumulation and adipogenic conversion of cells (16). Thus, we tested for an association of the GNB3 825T polymorphism and obesity in several ethnic groups.

Materials and Methods

This study was conducted in agreement with the Declaration of Helsinki, and informed consent was obtained from all enrolled individuals.

BMI Study
In addition to nutritional status and physical activity, BMI strongly depends on age, gender, social and ethnic background, as well as country of residence (17). Furthermore, existing disorders and medication can exert uncontrollable effects on body weight. Therefore, all measures were taken to render the involved study groups as similar as possible. In the present study, only men ages 18 to 30 were included. No attempt was made to specifically enrich the sample with underweight or overweight individuals. Thus, the enrolled cohorts roughly resemble cross-sectional samples of the respective gender and age groups of the respective countries. Body weight was determined in light clothing, and body height was measured without shoes, heels together, with back to the wall. Overweight was defined as BMI 25.0 kg/m² and obesity as >27.0 kg/m² (3).

German Cohort. We recruited 277 healthy male Caucasoid individuals ages 18 to 30 yr at the Department of Blood Transfusion Medicine, University Hospital of Essen. These individuals attend the blood bank usually every 3 mo for blood donation and are under close health surveillance to guarantee high-quality blood products. According to German law, blood donors must be free of any medication and acute or chronic infectious diseases, to mention but a few requirements. Thus, these individuals represent a cross-sectional sample of young healthy men of the German population. BP is measured regularly in these individuals at every visit in the sitting position after a rest of 10 min using standard sphygmomanometry.

Chinese Population Sample. Male healthy Chinese subjects ages 18 to 30 yr were recruited at the Jinan Technical College and the Tongji Medical University at Wuhan and the samples were combined.

African Populations. Black male, healthy individuals ages 18 to 30 yr were recruited by the National Blood Transfusion Service Zimbabwe (Harare; n = 450) and The South African Blood Transfusion Service (Johannesburg; n = 256).

Ethnic Distribution Study
DNA samples were obtained from previously established, anonymous human diversity collections or from newly recruited volunteers. No further information regarding health status is available. Thus, reported values are estimates of 825T allele frequencies in the different populations studied and cannot be used as reference values for disease-related studies. DNA samples from the West Pygmies were purchased from the Coriell Institute for Medical Research (Camden, NJ). DNA samples from nonhuman primates were prepared from mouth swabs and obtained from different zoos in Germany.

DNA Preparation and Genotyping
DNA was prepared and PCR-based genotyping was done as described previously (5). In the BMI studies, all genotyping was performed in a blinded manner, i.e., investigators were unaware of the individuals' data. PCR products of nonhuman primate DNA samples were directly sequenced using standard procedures.

Statistical Analyses
Allele frequencies were compared using Cochran-Mantel-Haenszel test for trend over the three genotypes. Other frequency comparisons were done using the ² test or the ² test for trend. Wherever continuous variables were compared, t test (in case of two groups) or one-way ANOVA (in case of more than two groups) was applied. When odds ratios (OR) adjusted for other terms (age or sample collective) were calculated, logistic regression was used. All confidence intervals are calculated at the 95% level.

Results

Characterization of Enrolled Individuals
Anthropometric data of the enrolled individuals are summarized in Table 1. 825T allele frequencies differed significantly between different ethnic groups and were lowest in Germans (31.9%), intermediate in Chinese (47.7%), and highest in Africans (81.4 to 84.1%). BMI values were significantly higher in Germans compared to all other ethnic groups (Figure 1). Remarkably, BMI was higher in urban compared to rural Zimbabweans. Using a definition for underweight of BMI <18.5 kg/m², a marked difference between Germany, a completely industrialized country with a largely uniform lifestyle, and the developing countries was observed. Conversely, the risk of being overweight (BMI 25.0 kg/m² versus <25.0 kg/m²) was increased in Germany compared to China, South Africa, and Harare (Figure 1 and Table 1). Interestingly, within Zimbabwe a significantly increased OR of 3.4 (1.8 to 6.7; P = 0.0002) for overweight was found upon comparison of the urban with the rural sample, which again shows the impact of lifestyle on BMI. Having confirmed this expected relationship between BMI and country of residence, we subsequently investigated the potential association between the 825T allele and BMI within the specified populations.

View larger version (77K): [in this window] [in a new window] [as a PowerPoint slide]   Figure 1. Distribution of body mass index (BMI) values in the different study groups. S. Africa, South Africa. For details, see the text and Table 1.

825T Allele, BMI, and BP in German Men
BMI was significantly different between genotypes (TT = 24.9 ± 2.3 kg/m²; TC = 23.6 ± 2.4 kg/m²; CC = 23.1 ± 2.5 kg/m²; P = 0.003) (Table 2). This difference was also seen when the TT and TC genotypes were combined (23.8 ± 2.4 kg/m²) and compared with the CC genotype (P = 0.01). BMI was correlated with weight but not height. Age was not significantly different between genotypes (TT = 26.4 ± 2.8; TC = 25.3 ± 3.5; CC = 25.7 ± 3.3 yr; P = 0.2). 825T allele frequency was 29.5, 39.3, and 47.7% in normal weight, overweight, and obesity, respectively (Table 2 and Figure 2). Genotype distribution of the overweight and obese group was significantly different from the group with normal weight (P < 0.05). For overweight (BMI 25 kg/m² versus <25 kg/m²), OR (TT/CC) was 2.5 (1.1 to 6.1; P = 0.03) and OR (TC/CC) was 1.5 (0.8 to 2.6; P = 0.2). OR (TT/CC) for BMI >27 kg/m² versus < 25 kg/m² was 5.0 (1.4 to 18.3; P = 0.0083) and OR (TC/CC) was 2.2 (0.8 to 6.3; P = 0.13). Systolic BP values were not significantly different between genotypes (TT: 129.6 ± 79.6 mmHg; TC: 129.3 ± 78.6 mmHg; CC: 130.4 ± 11.0 mmHg; P = 0.86), but significantly increased in the overweight and obese group compared to that with BMI <25 (P = 0.003) (Table 2). Systolic BP increased linearly by 0.5 mmHg per BMI unit (r² = 0.05; P = 0.0002). Likewise, diastolic BP values were independent of genotype (TT: 79.6 ± 6.1 mmHg; TC: 78.6 ± 8.4 mmHg; CC: 79.5 ± 7.9 mmHg; P = 0.78), but again significantly increased with BMI (P < 0.001) (Table 2) with a mean slope of 0.6 mmHg per BMI unit (r² = 0.09; P < 0.0001). Hence, the C825T polymorphism is apparently not directly associated with BP values in this group of young normotensive individuals, whereas BP values increase significantly with increased BMI values.

View larger version (52K): [in this window] [in a new window] [as a PowerPoint slide]   Figure 2. Genotype distribution according to BMI values in the German, Chinese, and South African sample. 1, BMI <25 kg/m2; 2, BMI 25 kg/m2; 3, BMI >27 kg/m2. Genotypes are given as % of total.

825T Allele and BMI in Chinese Men
Age was not significantly different between genotypes in the Chinese cohort (TT = 24.8 ± 4.5; TC = 24.6 ± 4.4; CC = 24.2 ± 4.3 yr). When compared by one-way ANOVA, BMI values were not significantly different between genotypes (TT = 22.0 ± 3.0 kg/m²; TC = 22.2 ± 2.7 kg/m²; CC = 21.8 ± 2.4 kg/m²; P = 0.2). However, when the values of TT and TC genotypes were combined (BMI = 22.1 ± 2.7 kg/m²), a statistically nonsignificant trend (P = 0.1) for increased BMI compared to CC genotype was noticed. 825T allele frequency was 46.8, 53.9, and 58.6% in normal weight, overweight, and obese individuals, respectively (Table 3 and Figure 2). OR (TT/CC) for overweight versus normal weight was 1.8 (1.0 to 3.1; P = 0.03) and OR (TC/CC) was 1.7 (1.0 to 2.7; P = 0.04). For BMI >27 kg/m² versus <25 kg/m², OR (TT/CC) was 2.7 (1.2 to 6.2; P = 0.01) and OR (TC/CC) was 1.8 (0.9 to 4.0; P = 0.09).

825T Allele and BMI in Black African Men
825T allele frequency and genotype distributions were similar in individuals from South Africa and Zimbabwe regardless of rural or urban origin (Table 4). The rural African sample had significantly lower age and body weight compared to the urban African sample (P < 0.01). The prevalence of overweight in rural Africans (5%) was significantly lower than in Africans from Harare (17.4%) and Johannesburg (20.9%). Using these latter figures, we calculate a crude OR for overweight (combined urban versus rural) of 3.8 (2.1 to 7.1; P < 0.0001), age-adjusted OR of 2.7 (1.4 to 5.3), indicating a strong effect of environmental influences on BMI. The risk for overweight associated with the 825T allele was difficult to estimate within the respective African samples due to the relative lack of individuals with the CC genotype. Only a common logistic model, therefore, was calculated for the samples pooled from the Johannesburg and Harare populations. Crude OR (TT/CC) for overweight in the combined urban Johannesburg and Harare samples was 3.8 (0.5 to 28.9; P = 0.16), and crude OR (TC/CC) is 3.1 (0.4 to 24.3; P = 0.25). Although these values did not reach statistical significance due to the low number of homozygous 825C allele carriers, this effect was qualitatively similar to that observed in Germans and Chinese. Age-adjusted OR (TC/TT) was 0.7 (0.3 to 1.7), and OR (CC/TT) was calculated at 0.6 (0.1 to 5.3). In the Johannesburg sample, 825T allele frequency increased to 90.9% in individuals with BMI >27 kg/m² (Table 4 and Figure 2). There was no correlation between age and genotype in the African samples.

Finally, the impact of the 825T allele on overweight in "lean" populations was estimated after combining the Chinese (Table 3) and African (Table 4) samples. After adjustment for age and sample collective, OR (TT/CC) was 1.8 (1.1 to 3.0; P < 0.02) and OR (TC/CC) was 1.6 (0.97 to 2.5; P = 0.06). Thus, the effect of the 825T allele on overweight was remarkably similar in "lean" and fully Westernized populations.

Ethnic Distribution of the GNB3 825T Allele
A total of 5254 DNA samples of unrelated individuals was analyzed. The ethnic distribution of the 825T allele is displayed in Table 5 and Figure 3. All populations with n > 40 were in Hardy-Weinberg equilibrium (HWE). This suggests that preferential selection of genotypes is not (or is no longer) detectable. The geographic frequency distribution of the 825T allele displays marked frequency intervals that correspond to the subdivision into major human ethnic groups, with black Africans (excluding the admixed American blacks, and the small Guinean sample) ranging from 74 to 91%, Mongoloids from 42 to 52%, and Caucasoid (except the Middle East) from 21 to 38%. In the Middle East and North Africa, the frequencies are transitional compared to Africans, ranging from 45 to 56%. The Amerindians have a wide frequency range (11 to 42%). Interestingly, the Khoisanoids and Pygmies, isolated descendants of the most ancient African populations (18,19), have lower values than other Africans, between 66 and 72%. Similarly, 825T allele frequencies were high in North Australian aborigines and individuals from Highland Papua New Guinea, but still lower than in Africans. In Table 5, the overall allele frequency of each major ethnic group (e.g., 82% for black Africans) is also given, averaging over subpopulation averages rather than over individuals, to avoid distortion due to variable sample sizes. To test whether the frequency differences between ethnic groups might be artifacts of inadequate sample sizes, the nine major ethnic groupings in Table 5 were submitted to 2 by 2 comparisons (20). Most pairwise differences were found to be statistically significant at the P < 0.05 level, except for comparisons involving the Pygmies and the Papuans, for whom the sample sizes are smallest. Motivated by the uniformity of 825T allele frequencies among Europeans (Germans approximately 30%) and black Africans (approximately 82%), we estimated the proportion of European admixture in U.S. blacks (72% 825T allele) at 21%, in good agreement with previous estimates of 15 to 20% (21).

View larger version (38K): [in this window] [in a new window] [as a PowerPoint slide]   Figure 3. Worldwide distribution of the GNB3 825T allele. The figures are 825T allele frequencies; the small South American samples are combined.

We also genotyped and sequenced DNA from unrelated animals of the species Pan troglodytes (common chimpanzee; n = 4), Pan paniscus (pygmy/Bonobo chimpanzee; n = 2), Gorilla gorilla (lowland gorilla; n = 3), Pongo pygmaeus (orangutan; n = 3), Cercopithecus aethiops (African green monkey; n = 1), Macaca mulatta (rhesus monkey; n = 3), and Sanguinus oedipus (cotton top tamarin; n = 1). All of these primates were typed homozygous carriers of the C825 allele in the GNB3, indicating the stability of this position for at least 30 million years, which in turn suggests that the C allele is the evolutionary ancestral allele in primates.

Discussion

825T Allele and BMI
The worldwide increasing prevalence of obesity prompts many researchers to determine modifiable and nonmodifiable (genetic) factors underlying this epidemic (22). We have investigated here whether the GNB3 825T allele, which predisposes for hypertension (5, 8, 9), potentially predisposes for obesity. This approach was prompted by the observation that enhanced signaling via PTX-sensitive G proteins enhances adipogenesis (16), whereas animals lacking the G protein Gi2 subunit are runted due to deficiency in fat mass (15). Thus, intracellular signal transduction via Gi2 could play a major role in the pathogenesis of obesity (14). Interestingly, the splice variant Gß3-s associated with the 825T allele can interact with Gi2 (5), and recent studies have confirmed that activation of heterotrimeric G proteins is enhanced in the presence of this splice variant (23). Thus, the 825T allele is not a nonfunctional genetic marker. Instead, it can be used for the prediction of enhanced intracellular signal transduction in humans. It should be noted, however, that linkage equilibrium with a yet unidentified alteration in GNB3 cannot be excluded. The complete coding region of the G protein ß3 subunit cDNA has been sequenced, and no changes apart from the C825T polymorphism have been identified (5). However, potential relevant mutations in introns of GNB3 cannot be excluded. The GNB3 locus located on chromosome 12p13 is flanked by the gene encoding CD4 and genes of unknown identity (24). Therefore,linkage disequilibrium of the GNB3 825T allele with polymorphisms in these genes cannot be excluded. However, this latter possibility appears rather unlikely since the 825T allele is closely associated with enhanced G protein signaling (5), and no sequences have been identified in the vicinity of 12p13 that encode for G protein subunits or regulators of G protein function.

To investigate the effect of the 825T allele on BMI and BP in ethnically and culturally diverse populations, we set up the population cohorts as homogeneously as possible by including only men in the age range of 18 to 30 yr. Although individuals were selected at random to resemble a healthy, quasi cross-sectional sample from the considered age groups, they obviously did not constitute a random sample of the respective populations. This makes selection effects a possible disadvantage of the study. However, whereas selection may act on phenotype, despite all cautionary measures taken, there is no rationale for over- or undersampling a certain genotype given the phenotype. Furthermore, the prevalences of underweight and overweight in the sample are in good accordance with what is known of these traits in the general populations. As an example, the prevalences of underweight (5.8%) and overweight (13.3%) in our Chinese sample are similar to those reported by others, which were 11.6 and 9.8%, respectively, with an increasing trend for obesity as a result of lifestyle changes (25, 26). Likewise, higher BMI in urban compared to rural areas of Zimbabwe has been documented (27).

We have used BMI as a measure of body fat mass, although we are aware of the fact that BMI is also influenced by muscle and bone mass. However, more sophisticated techniques for direct assessment of body fat, e.g., densitometry or bioelectrical impedance techniques, were not available in China and in Africa. On the other hand, most investigators agree that BMI values can be used to compare body composition across ethnic groups (28, 29). The BMI cutoff point of 25 kg/m² used here for defining overweight is commonly accepted. Obesity, on the other hand, is frequently defined as a BMI value of 30 kg/m², although others have used a cutoff value of >27 kg/m² in recent studies (30). Since most of our samples were taken from developing/transitional countries in which overt obesity is relatively rare in the studied age groups, we here defined obesity as a BMI > 27 kg/m².

A consistent and significant effect of the 825T allele on BMI is evident in three ethnically and culturally diverse populations. This effect was most pronounced in Germans, whose lifestyle is characterized by high-caloric, fat-enriched nutrition and low physical activity. A similar effect of the 825T allele on BMI was found in the Chinese cohort, despite the fact that nutrition is poor in fat but rich in rice and vegetables, thus being quite different from that of Germans. Interestingly, the OR (TT/CC) for overweight were comparable in the Chinese and the German samples. The precise risk for overweight associated with the 825T allele is difficult to estimate in the African samples due to the relative lack of individuals with the CC genotype. However, only one (= 4.8%) out of a total of 21 CC genotypes was found in the overweight group, suggesting a qualitatively similar effect. In general, we estimate the OR (TT/CC) for overweight to be approximately 2 to 3 for all populations studied, a rather impressive value for such a highly variable phenotype, and our finding of a consistent association across different ethnic groups makes a fortuitous association very unlikely.

On the basis of the available data, it is difficult to say whether the 825T allele exerts a codominant or a recessive influence on BMI, the latter being a weak phenotype and a quantitative trait strongly influenced by environmental factors. On the cellular level, one 825T allele suffices to generate Gß3-s via alternative splicing and to establish a phenotype of enhanced G protein reactivity (5). Anecdotal evidence suggests that G protein activation is further enhanced in cells from individuals with the TT genotype (W. Siffert, unpublished observations). Thus, the 825T allele appears to exert a codominant effect on G protein signaling on the cellular level, which may be explained by an increased expression of the splice variant Gß3-s in the presence of two affected alleles. Previous studies on hypertension suggested at least a gene-dose effect regarding BP with an increased risk for homozygous compared to heterozygous individuals (5). A similar trend was observed here, as heterozygous 825T allele had increased OR for overweight and obesity. This effect was statistically significant in the Chinese group. At present, we cautiously propose a codominant effect of the 825T allele on overweight, this hypothesis being, however, largely based on previously made observations on the cellular level (5). A definite answer to this pending question requires a different study setup, for example a case-control study specifically designed to compare genotype distribution in overtly obese (BMI >30 kg/m²) and normal weight individuals. Furthermore, studies are required to clarify the molecular mechanisms that may be responsible for the tendency to gain weight in individuals carrying an 825T allele. Although studies on transgenic animals and transfected cell lines suggest a major role of PTX-sensitive G proteins in adipogenesis (15, 16), such findings do not explain the associations made here. Additional studies on transgenic animals expressing Gß3-s are urgently required to establish a potential causal relationship between this splice variant, enhanced G protein activation, and obesity. In addition, characterization of signal transduction in adipocytes from homozygous 825T and C825 allele carriers is essential to determine whether obesity actually results from increased lipid accumulation.

The present study also demonstrates that obesity is not an inherited disease, but obviously requires the interaction of multiple susceptibility genes with environmental factors. This is illustrated by the large difference in overweight prevalence in the urban Harare and Johannesburg versus the rural Zimbabwe sample. The lifestyle of the rural sample is drastically different from the urban one with regard to two major aspects: The fat content of the diet is low and it consists mainly of maize meal and vegetables. Due to the lack of private cars and public transportation facilities, these individuals are accustomed to walking long distances. Thus, the level of physical activity can be considered high. In contrast, individuals from Johannesburg and Harare are largely Westernized with a high level of fat-rich nutrition and alcohol consumption. Thus, in the presence of an almost identical frequency of the 825T allele in the African rural and urban samples, only individuals exposed to an "unhealthy" Western lifestyle appear at risk for overweight. It is tempting to speculate that the 825T allele might be neutral as long as lifestyle resembles that of our hunter-gatherer ancestors but may become detrimental upon Westernization. Thus, presence of the 825T allele can only increase the risk for obesity in concert with certain behavorial or environmental factors, but clearly does not cause obesity by its sole presence. This would also be in accordance with the observation that the prevalence of overweight was highest in Germans despite lowest 825T allele frequency of the characterized samples. As an alternative hypothesis, one could propose that the genetic background of the different ethnic groups studied differs with regard to many other genes that induce or prevent obesity, thereby potentially enhancing or reducing the effect of the 825T allele in Chinese and black Africans. Although the genetic background of Caucasoid, Asian, and black populations is certainly different, we do not believe that this is a major argument to be considered here for two reasons. First, we found a consistent association of the 825T allele with BMI in individuals of different ethnic origin. Second, it is rather unlikely that urban and rural black individuals from Zimbabwe, all belonging to the Zimbabwean Shona tribe, differ substantially with regard to their genetic background. Nevertheless, overweight in the urban Zimbabwean sample was significantly more frequent compared to the rural sample. Hence, the gene effect is seen only when certain environmental factors come into play. Such a scenario is also compatible with the "thrifty genotype hypothesis" proposed by Neel (31). This hypothesis suggests that "ancestral," body fat-conserving genes may still be operative in modern man and may contribute to diabetes in conjunction with a sedentary lifestyle.

825T Allele and BP
Three independent case-control studies (5, 9, 32) and one association study in a WHO MONICA cohort (8) have confirmed an association of the GNB3 825T allele with hypertension in Caucasians. However, the mechanism by which enhanced G protein activation contributes to high BP has remained obscure. Based on theoretical considerations, increased vasoconstriction can be ruled out as most vasoactive hormones activate receptors coupled to PTX-insensitive G proteins. Homozygous and heterozygous 825T allele carriers do not respond with an exaggerated BP increase upon infusion of an 2-adrenergic receptor-activating compound (33). Thus, hypertension in 825T allele carriers appears to result from slow-acting mechanisms. The findings presented here for the German cohort apparently support this theoretical concept. Whereas BP was virtually independent of the C825T polymorphism, both systolic and diastolic BP were significantly dependent on BMI, and it is commonly known that overweight and obesity are main risk factors for hypertension. As a working hypothesis, therefore, we propose that the 825T allele may predominantly increase the risk for obesity, which, over years, could then precipitate in hypertension. A definite answer to this pending question requires additional studies specifically designed to address this problem.

Worldwide Distribution of the 825T Allele
The GNB3 825T allele frequencies reflect ethnic subdivisions (34, 35). The data, therefore, are compatible with (but they do not necessarily prove) a scenario in which the allele frequencies were subjected to random drift during racial differentiation. To investigate the alternative scenario of drift through selection, we have calculated the HWE for the larger samples (n > 40). As is seen in Table 5, there is no significant deviation from HWE, indicating that any recent selection on the genotypes is not detectable in our data. This does not exclude the possibility that selection is at work, but is not significantly affecting HWE. Also, significant selection may have acted during earlier times, but it seems unlikely that the selective forces would have desisted by today across all of the diverse ethnic groups and cultures that we tested for HWE. Furthermore, there are no correlations between 825T allele frequency and climate or lifestyle of the sampled populations, which include hunter-gatherers, nomadic pastoralists, sedentary agriculturalists, and industrialized Westerners. There remains the hypothesis that disease was involved in producing the current frequency distribution, which may be investigated when sufficient data on prehistoric diseases become available. It should be noted here that immune cell activation was found enhanced in Caucasoid 825T allele carriers as inferred from increased neutrophil chemotaxis (36). The 825T allele was absent in all of the primates we typed thus far, including the closest relatives of humans, the common chimp, pygmy chimp/Bonobo, lowland gorilla, and orangutan, suggesting that C is the ancestral state at nucleotide position 825, and that the mutation of C to T probably occurred since the human-chimpanzee split approximately 5 million years ago. A lower bound for the 825C to T mutation may be postulated on the basis of its present distribution in human populations: The hunter-gatherer West Pygmies and the Khoisan, who have been genetically isolated since an early African founder event about 100,000 years ago (18, 19), harbor both the 825C and 825T alleles at appreciable frequencies (Table 5). Accordingly, the C/T polymorphism would already have been present at the time of the subsequent major east African expansion 60,000 to 80,000 years ago, which probably populated Eurasia and repopulated most of Africa (18, 37, 38). Because agriculture did not commence until after climatic stabilization at the end of the Younger Dryas glacial phase 11,400 years ago (39), it is unlikely that agricultural lifestyle was involved in shaping the early 825C/T distribution.

Conclusions and Perspectives
Our findings may explain part of the significant ethnic differences regarding susceptibility to obesity and obesity-related disorders (40,41,42). For example, black Americans display a higher prevalence of obesity, hypertension, and type 2 diabetes mellitus compared to whites in the United States (43, 44). Black Americans still share much of their genetic makeup with their ancestors from West Africa, and many studies have been conducted to investigate the relationship between environmental factors, BMI, hypertension, and type 2 diabetes. The prevalence of hypertension and type 2 diabetes was consistently found to be low in African communities, but strongly increased across the Caribbean toward the United States (41, 44). Even within the African community, lifestyle changes (urbanization) contribute significantly to the prevalence of obesity and hypertension as illustrated by an increased prevalence of hypertension and obesity in urban Nigeria compared to rural farmers in the same country (41, 44,45,46). Compatible observations have been made in Australian aborigines who, upon adapting a "Western" lifestyle, show exceedingly high rates of obesity-related disorders, this process being apparently reversible if aborigines reverted temporarily to traditional hunter-gatherer diets and lifestyles (47). General lack of obesity may explain why the !Kung bushmen do not display an age-dependent BP rise (48) despite a high 825T allele frequency. We have shown here that black Americans as well as Australian aborigines display high frequencies of the 825T allele (Table 5). Assuming that the effect of the 825T allele on BMI described here for Germans, Chinese, and black Africans is similar in black Americans and Australian aborigines, we speculate that the high number of 825T allele carriers could be a major determinant for the observed difference in the prevalence of obesity and obesity-related disorders in specific ethnic groups living in countries with largely uniform lifestyle conditions. Finally, if Westernization of lifestyle continues at the present rate, the high prevalence of the 825T allele may be predictive of an obesity and hypertension epidemic in developing countries.

Acknowledgments

Acknowledgments

This study was supported by grants from the Fritz Thyssen-Stiftung (Germany) and from the Ministerium für Wissenschaft und Forschung Nordrhein-Westfalen (Germany). We thank H. Benkmann, A. Ishanov, E. Santos, P. v. Helden, J. ter Meulen, and the Musqueam Indian Band for human samples, and W. Schempp, U. Rümpler, and B. Uphoff for primate samples.

Footnotes

American Society of Nephrology

References

1. Björntorp P: Obesity.Lancet 350:423 -426, 1997[Medline]
2. Taubes G: As obesity rates rise, experts struggle to explain why.Science 280:1367 -1368, 1998[Free Full Text]
3. Bray GA: Obesity: A time bomb to be defused. Lancet352 : 160-161,1998[Medline]
4. Comuzzie AG, Allison DB: The search for human obesity genes.Science 280:1374 -1377, 1998[Abstract/Free Full Text]
5. Siffert W, Rosskopf D, Siffert G, Busch S, Moritz A, Erbel R, Sharma AM, Ritz E, Wichmann HE, Jakobs KH, Horsthemke B: Association of a human G-protein ß3 subunit variant with hypertension. Nat Genet 18: 45-48,1998[Medline]
6. Pietruck F, Moritz A, Montemurro M, Sell A, Busch S, Rosskopf D, Virchow S, Esche H, Brockmeyer N, Jakobs KH, Siffert W: Selectively enhanced cellular signalling by G_i proteins in essential hypertension: G_i2, G_i3, G_ß1 and G_ß2 are not mutated. Circ Res79 : 974-983,1996[Abstract/Free Full Text]
7. Siffert W, Rosskopf D, Moritz A, Wieland T, Kaldenberg-Stasch S, Kettler N, Hartung K, Beckmann S, Jakobs KH: Enhanced G protein activation in immortalized lymphoblasts from patients with essential hypertension. J Clin Invest 96:759 -766, 1995
8. Schunkert H, Hense HW, Döring A, Riegger GAJ, Siffert W: Association between a polymorphism in the G protein ß3 subunit gene and lower renin and elevated diastolic blood pressure.Hypertension 32:510 -513, 1998[Abstract/Free Full Text]
9. Benjafield AV, Jeyasingam CL, Nyholt DR, Griffiths LR, Morris BJ: G-protein ß3 subunit gene (GNB3) variant in causation of essential hypertension. Hypertension 32:1094 -1097, 1998[Abstract/Free Full Text]
10. Hegele RA, Harris SB, Hanley AJ, Cao H, Zinman B: G protein ß3 subunit gene variant and blood pressure variation in Canadian Oji-Cree.Hypertension 32:688 -692, 1998[Abstract/Free Full Text]
11. Kato N, Sugiyama T, Morita H, Kurihara H, Yamori Y, Yazaki Y: G protein ß3 subunit variant and essential hypertension in Japanese.Hypertension 32:935 -938, 1998[Abstract/Free Full Text]
12. Siffert W: G proteins and hypertension: An alternative candidate gene approach. Kidney Int 53:1466 -1470, 1998[Medline]
13. Delva P, Pastori C, Provoli E, Degan M, Arosio E, Montesi G, Steele A, Lechi A: Erythrocyte Na⁺-H⁺ exchange activity in essential hypertensive and obese patients: Role of excess body weight.J Hypertens 11:823 -830, 1993[Medline]
14. Wang HY, Malbon CC: The G_s/G_i2 axis controls adipogenesis independently of adenylylcyclase. Int J Obes 20[Suppl 3]:S26 -S31, 1996
15. Moxham CM, Hod Y, Malbon CC: Induction of G_i2-specific antisense RNA in vivo inhibits neonatal growth.Science 260:991 -995, 1993[Abstract/Free Full Text]
16. Su HL, Malbon CC, Wang HY: Increased expression of Gi 2 in mouse embryo stem cells promotes terminal differentiation to adipocytes.Am J Physiol 265:C1729 -C1735, 1993[Abstract/Free Full Text]
17. Berrios X, Koponen T, Huiguang T, Khaltaev N, Puska P, Nissinen A: Distribution and prevalence of major risk factors of noncommunicable diseases in selected countries: The WHO Inter-Health Programme. Bull WHO75 : 99-108,1997[Medline]
18. Watson E, Forster P, Richards MB, Bandelt HJ: Mitochondrial footprints of human expansions in Africa. Am J Hum Genet61 : 691-704,1997[Medline]
19. Bandelt HJ, Forster P: The myth of bumpy hunterer-gatherer mismatch distributions. Am J Hum Genet 61:980 -983, 1997[Medline]
20. Sachs L: Angewandte Statistik, Berlin, Springer,1978 , p 269
21. Hummel K: Serotype frequencies in different human populations; racial composition of individuals; statistical evaluation and frequency mix.Adv Forensic Haemogenet 1:491 -496, 1986
22. Popkin BM, Doak CM: The obesity epidemic is a worldwide phenomenon.Nutr Rev 56:106 -114, 1998[Medline]
23. Busch S, Geerdes J, Rosskopf D, Siffert W: Functional characterisation of a novel splice variant of the human G protein subunit Gß3 [Abstract]. Naunyn-Schmiedeberg's Arch Pharmacol358 : R647,1998
24. Ansari-Lari MA, Muzny DM, Lu J, Lu F, Lilley CE, Spanos S, Malley T, Gibbs RA: A gene-rich cluster between the CD4 and triosephosphate isomerase genes at human chromosome 12p13. Genome Res6 : 314-326,1996[Abstract/Free Full Text]
25. Paeratakul S, Popkin BM, Keyou G, Adair LS, Stevens J: Changes in diet and physical activity affect the body mass index of Chinese adults.Int J Obes Relat Metab Disord 22:424 -431, 1998[Medline]
26. Ge K, Weisell R, Guo X, Cheng L, Ma H, Zhai F, Popkin BM: The body mass index of Chinese adults in the 1980s. Eur J Clin Nutr48 [Suppl 3]: S148-S154,1994
27. Allain TJ, Wilson AO, Gomo ZA, Adamchak DJ, Matenga JA: Diet and nutritional status in elderly Zimbabweans. Age Ageing26 : 463-470,1997[Abstract/Free Full Text]
28. Gallagher D, Visser M, Sepulveda D, Pierson RN, Harris T, Heymsfield SB: How useful is body mass index for comparison of body fatness across age, sex, and ethnic groups? Am J Epidemiol143 : 228-239,1996[Abstract/Free Full Text]
29. Wang J, Deurenberg P: The validity of predicted body composition in Chinese adults from anthropometry and bioelectrical impedance in comparison with densitometry. Br J Nutr 76:175 -182, 1996[Medline]
30. Considine RV, Sinha MK, Heiman ML, Kriauciunas A, Stephens TW, Nyce MR, Ohannesian JP, Marco CC, McKee LJ, Bauer TL: Serum immunoreactive-leptin concentrations in normal-weight and obese humans. N Engl J Med334 : 292-295,1996[Abstract/Free Full Text]
31. Neel JV: Diabetes mellitus: A thrifty genotype rendered detrimental by progress? Am J Hum Genet 14:353 -362, 1962[Medline]
32. Beige J, Hohenbleicher H, Distler A, Sharma AM: G-protein ß3 subunit C825T variant and ambulatory blood pressure in essential hypertension.Hypertension 33:1049 -1051, 1999[Abstract/Free Full Text]
33. Schäfers RF, Nürnberger J, Siffert W, Wenzel RR, Philipp T, Michel MC: Haemodynamic characterisation of healthy subjects carrying the 825T allele of the G protein ß3 subunit [Abstract].Naunyn-Schmiedeberg's Arch Pharmacol358 : R650,1998
34. Cavalli-Sforza LL, Menozzi P, Piazza A: The History and Geography of Human Genes, Princeton, NJ, Princeton University Press,1994
35. Forster P, Harding R, Torroni A, Bandelt HJ: Origin and evolution of native American mtDNA Variation: A reappraisal. Am J Hum Genet 59: 935-945,1996[Medline]
36. Virchow S, Ansorge N, Rübben H, Siffert G, Siffert W: Enhanced fMLP-stimulated chemotaxis in human neutrophils from individuals carrying the G protein ß3 subunit 825 T-allele.FEBS Lett 436:155 -158, 1998[Medline]
37. Richards MB, Corte-Real H, Forster P, Macaulay V, Wilkinson-Herbots H, Demaine A, Papiha S, Hedges R, Bandelt HJ, Sykes BC: Palaeolithic and neolithic lineages in the European mitochondrial gene pool. Am J Hum Genet 59: 185-203,1996[Medline]
38. Forster P, Kayser M, Meyer E, Roewer L, Pfeiffer H, Benkmann H, Brinkmann B: Phylogenetic resolution of complex mutational features at Y-STR DYS390 in aboriginal Australians and Papuans. Mol Biol Evol15 : 1108-1114,1998[Abstract]
39. Björck S, Kromer B, Johnsen S, Bennike O, Hammarlund D, Lemdahl G, Possnert G, Rasmussen TL, Wohlfahrt B, Hammer CU, Spurk M: Synchronised terrestrial-atmospheric deglacial records around the north Atlantic. Science 274:1155 -1160, 1996[Abstract/Free Full Text]
40. Kaufman JS, Asuzu MC, Mufunda J, Forrester T, Wilks R, Luke A, Long AE, Cooper RS: Relationship between blood pressure and body mass index in lean populations. Hypertension 30:1511 -1516, 1997[Abstract/Free Full Text]
41. Kaufman JS, Durazo-Arvizu RA, Rotimi CN, McGee DL, Cooper RS: Obesity and hypertension prevalence in populations of African origin. The Investigators of the International Collaborative Study on Hypertension in Blacks. Epidemiology 7:398 -405, 1996[Medline]
42. Jones DW: Hypertension in East Asia. Am J Hypertens8 [Suppl]: 111S-114S,1995
43. Burt VL, Whelton P, Roccella EJ, Brown C, Cutler JA, Higgins M, Horan MJ, Labarthe D: Prevalence of hypertension in the US adult population: Results from the Third National Health and Nutrition Examination Survey, 1988-1991. Hypertension 25:305 -313, 1995[Abstract/Free Full Text]
44. Cooper RS, Rotimi CN, Kaufman JS, Owoaje EE, Fraser H, Forrester T, Wilks R, Riste LK, Cruickshank JK: Prevalence of NIDDM among populations of the African diaspora. Diabetes Care 20:343 -348, 1997[Abstract]
45. Kaufman JS, Owoaje EE, James SA, Rotimi CN, Cooper RS: Determinants of hypertension in West Africa: Contribution of anthropometric and dietary factors to urban-rural and socioeconomic gradients. Am J Epidemiol 143:1203 -1218, 1996[Abstract/Free Full Text]
46. Cooper R, Rotimi C, Ataman S, McGee D, Osotimehin B, Kadiri S, Muna W, Kingue S, Fraser H, Forrester T, Bennett F, Wilks R: The prevalence of hypertension in seven populations of West African origin. Am J Public Health 87: 160-168,1997[Abstract/Free Full Text]
47. O'Dea K: Cardiovascular disease risk factors in Australian aborigines. Clin Exp Pharmacol Physiol18 : 85-88,1991[Medline]
48. Truswell AS, Kennelly BM, Hansen JD, Lee RB: Blood pressures of Kung bushmen in Northern Botswana. Am Heart J84 : 5-12,1972[Medline]

This article has been cited by other articles:

				E. Zintzaras and N. Zdoukopoulos A Field Synopsis and Meta-Analysis of Genetic Association Studies in Peripheral Arterial Disease: The CUMAGAS-PAD Database Am. J. Epidemiol., July 1, 2009; 170(1): 1 - 11. [Abstract] [Full Text] [PDF]

				U. H. Frey, M. Adamzik, E. Kottenberg-Assenmacher, H. Jakob, I. Manthey, M. Broecker-Preuss, L. Bergmann, G. Heusch, W. Siffert, J. Peters, et al. A novel functional haplotype in the human GNAS gene alters G{alpha}s expression, responsiveness to {beta}-adrenoceptor stimulation, and peri-operative cardiac performance Eur. Heart J., June 1, 2009; 30(11): 1402 - 1410. [Abstract] [Full Text] [PDF]

				G. F. Lehnerdt, P. Franz, A. Bankfalvi, S. Grehl, A. Kelava, H. Nuckel, S. Lang, K. W. Schmid, W. Siffert, and H. S. Bachmann The regulatory BCL2 promoter polymorphism (-938C>A) is associated with relapse and survival of patients with oropharyngeal squamous cell carcinoma Ann. Onc., June 1, 2009; 20(6): 1094 - 1099. [Abstract] [Full Text] [PDF]

				N. Eynon, J. Oliveira, Y. Meckel, M. Sagiv, C. Yamin, M. Sagiv, R. Amir, and J. A. Duarte The guanine nucleotide binding protein \#946; polypeptide 3 gene C825T polymorphism is associated with elite endurance athletes Exp Physiol, March 1, 2009; 94(3): 344 - 349. [Abstract] [Full Text] [PDF]

				M. Lelonek, T. Pietrucha, M. Matyjaszczyk, and J. H. Goch A novel approach to syncopal patients: association analysis of polymorphisms in G-protein genes and tilt outcome Europace, January 1, 2009; 11(1): 89 - 93. [Abstract] [Full Text] [PDF]

				G. F. Lehnerdt, P. Franz, A. Bankfalvi, S. Grehl, K. Jahnke, S. Lang, K. W. Schmid, W. Siffert, and U. H. Frey Association Study of the G-Protein {beta}3 Subunit C825T Polymorphism with Disease Progression an Overall Survival in Patients with Head and Neck Squamous Cell Carcinoma Cancer Epidemiol. Biomarkers Prev., November 1, 2008; 17(11): 3203 - 3207. [Abstract] [Full Text] [PDF]

				L. Wang, C. Fang, A. Zhang, J. Du, L. Yu, J. Ma, G. Feng, Q. Xing, and L. He The --1019 C/G polymorphism of the 5-HT1A receptor gene is associated with negative symptom response to risperidone treatment in schizophrenia patients J Psychopharmacol, November 1, 2008; 22(8): 904 - 909. [Abstract] [PDF]

				U. H. Frey, W. Lieb, J. Erdmann, D. Savidou, G. Heusch, K. Leineweber, H. Jakob, H.-W. Hense, H. Lowel, N. H. Brockmeyer, et al. Characterization of the GNAQ promoter and association of increased Gq expression with cardiac hypertrophy in humans Eur. Heart J., April 1, 2008; 29(7): 888 - 897. [Abstract] [Full Text] [PDF]

				G. F. Lehnerdt, P. Franz, A. Zaqoul, K. J. Schmitz, S. Grehl, S. Lang, K. W. Schmid, W. Siffert, K. Jahnke, and U. H. Frey Overall and Relapse-Free Survival in Oropharyngeal and Hypopharyngeal Squamous Cell Carcinoma Are Associated with Genotypes of T393C Polymorphism of the GNAS1 Gene Clin. Cancer Res., March 15, 2008; 14(6): 1753 - 1758. [Abstract] [Full Text] [PDF]

				M. Adamzik, U. Frey, S. Sixt, L. Knemeyer, M. Beiderlinden, J. Peters, and W. Siffert ACE I/D but not AGT (-6)A/G polymorphism is a risk factor for mortality in ARDS Eur. Respir. J., March 1, 2007; 29(3): 482 - 488. [Abstract] [Full Text] [PDF]

				S. Hahn, U. H Frey, W. Siffert, S. Tan, K. Mann, and O. E Janssen The CC genotype of the GNAS T393C polymorphism is associated with obesity and insulin resistance in women with polycystic ovary syndrome. Eur. J. Endocrinol., November 1, 2006; 155(5): 763 - 770. [Abstract] [Full Text] [PDF]

				H. Tummala, M. Ali, P. Getty, P. M. Hocking, D. W. Burt, C. F. Inglehearn, and D. H. Lester Mutation in the Guanine Nucleotide-Binding Protein {beta}-3 Causes Retinal Degeneration and Embryonic Mortality in Chickens Invest. Ophthalmol. Vis. Sci., November 1, 2006; 47(11): 4714 - 4718. [Abstract] [Full Text] [PDF]

				U. H. Frey, H. Nuckel, L. Sellmann, D. Siemer, R. Kuppers, J. Durig, U. Duhrsen, and W. Siffert The GNAS1 T393C Polymorphism Is Associated with Disease Progression and Survival in Chronic Lymphocytic Leukemia. Clin. Cancer Res., October 1, 2006; 12(19): 5686 - 5692. [Abstract] [Full Text] [PDF]

				U. H. Frey, G. Lummen, T. Jager, K.-H. Jockel, K. W. Schmid, H. Rubben, N. Muller, W. Siffert, and A. Eisenhardt The GNAS1 T393C Polymorphism Predicts Survival in Patients with Clear Cell Renal Cell Carcinoma Clin. Cancer Res., February 1, 2006; 12(3): 759 - 763. [Abstract] [Full Text] [PDF]

				R. T. Stone, E. Casas, T. P. L. Smith, J. W. Keele, G. Harhay, G. L. Bennett, M. Koohmaraie, T. L. Wheeler, S. D. Shackelford, and W. M. Snelling Identification of genetic markers for fat deposition and meat tenderness on bovine chromosome 5: Development of a low-density single nucleotide polymorphism map J Anim Sci, October 1, 2005; 83(10): 2280 - 2288. [Abstract] [Full Text] [PDF]

				M. Bamshad Genetic Influences on Health: Does Race Matter? JAMA, August 24, 2005; 294(8): 937 - 946. [Abstract] [Full Text] [PDF]

				U. H. Frey, H. Alakus, J. Wohlschlaeger, K. J. Schmitz, G. Winde, H. G. van Calker, K.-H. Jockel, W. Siffert, and K. W. Schmid GNAS1 T393C Polymorphism and Survival in Patients with Sporadic Colorectal Cancer Clin. Cancer Res., July 15, 2005; 11(14): 5071 - 5077. [Abstract] [Full Text] [PDF]

				E J Parra, C J Hoggart, C Bonilla, S Dios, J M Norris, J A Marshall, R F Hamman, R E Ferrell, P M McKeigue, and M D Shriver Relation of type 2 diabetes to individual admixture and candidate gene polymorphisms in the Hispanic American population of San Luis Valley, Colorado J. Med. Genet., November 1, 2004; 41(11): e116 - e116. [Full Text] [PDF]

				K. E. North, K. M. Rose, I. B. Borecki, A. Oberman, S. C. Hunt, M. B. Miller, J. Blangero, L. Almasy, and J. S. Pankow Evidence for a Gene on Chromosome 13 Influencing Postural Systolic Blood Pressure Change and Body Mass Index Hypertension, April 1, 2004; 43(4): 780 - 784. [Abstract] [Full Text] [PDF]

				M. Sartori, A. Semplicini, W. Siffert, P. Mormino, A. Mazzer, F. Pegoraro, L. Mos, M. Winnicki, and P. Palatini G-Protein {beta}3-Subunit Gene 825T Allele and Hypertension: A Longitudinal Study in Young Grade I Hypertensives Hypertension, November 1, 2003; 42(5): 909 - 914. [Abstract] [Full Text] [PDF]

				W. Siffert Effects of the G protein {beta}3-subunit gene C825T polymorphism: should hypotheses regarding the molecular mechanisms underlying enhanced G protein activation be revised? Focus on "A splice variant of the G protein {beta}3-subunit implicated in disease states does not modulate ion channels" Physiol Genomics, April 16, 2003; 13(2): 81 - 84. [Full Text] [PDF]

				V. Ruiz-Velasco and S. R. Ikeda A splice variant of the G protein {beta}3-subunit implicated in disease states does not modulate ion channels Physiol Genomics, April 16, 2003; 13(2): 85 - 95. [Abstract] [Full Text] [PDF]

				T. C. Wascher, B. Paulweber, L. Malaimare, A. Stadlmayr, B. Iglseder, I. Schmoelzer, and W. Renner Associations of a Human G Protein {beta}3 Subunit Dimorphism With Insulin Resistance and Carotid Atherosclerosis Stroke, March 1, 2003; 34(3): 605 - 609. [Abstract] [Full Text] [PDF]

				J. M. Fernandez-Real, G. Penarroja, C. Richart, A. Castro, J. Vendrell, M. Broch, A. Lopez-Bermejo, and W. Ricart G Protein {beta}3 Gene Variant, Vascular Function, and Insulin Sensitivity in Type 2 Diabetes Hypertension, January 1, 2003; 41(1): 124 - 129. [Abstract] [Full Text] [PDF]

				H.-W. Chang, C.-Y. Yen, S.-Y. Liu, G. Singer, and I.-M. Shih Genotype Analysis Using Human Hair Shaft Cancer Epidemiol. Biomarkers Prev., September 1, 2002; 11(9): 925 - 929. [Abstract] [Full Text] [PDF]

				M. Ryden, G. Faulds, J. Hoffstedt, A. Wennlund, and P. Arner Effect of the (C825T) G{beta}3 Polymorphism on Adrenoceptor-Mediated Lipolysis in Human Fat Cells Diabetes, May 1, 2002; 51(5): 1601 - 1608. [Abstract] [Full Text] [PDF]

				D. Dobrev, E. Wettwer, A. Kortner, M. Knaut, S. Schuler, and U. Ravens Human inward rectifier potassium channels in chronic and postoperative atrial fibrillation Cardiovasc Res, May 1, 2002; 54(2): 397 - 404. [Abstract] [Full Text] [PDF]

				G. Heusch, R. Erbel, and W. Siffert Genetic determinants of coronary vasomotor tone in humans Am J Physiol Heart Circ Physiol, October 1, 2001; 281(4): H1465 - H1468. [Full Text] [PDF]

				A Meirhaeghe, C Bauters, N Helbecque, M Hamon, E McFadden, J.-M Lablanche, M Bertrand, and P Amouyel The human G-protein {beta}3 subunit C825T polymorphism is associated with coronary artery vasoconstriction Eur. Heart J., May 2, 2001; 22(10): 845 - 848. [Abstract] [PDF]

				A. C. Morrison, P. A. Doris, A. R. Folsom, F. J. Nieto, E. Boerwinkle, and R. A. Hegele G-Protein {beta}3 Subunit and {{alpha}}-Adducin Polymorphisms and Risk of Subclinical and Clinical Stroke Editorial Comment : Candidate Genes for Stroke: If Elected, Will They Serve? Stroke, April 1, 2001; 32(4): 822 - 829. [Abstract] [Full Text] [PDF]

				C. Hengstenberg, H. Schunkert, B. Mayer, A. Doring, H. Lowel, H.-W. Hense, M. Fischer, G. A.J Riegger, and S. R Holmer Association between a polymorphism in the G protein {beta}3 subunit gene (GNB3) with arterial hypertension but not with myocardial infarction Cardiovasc Res, March 1, 2001; 49(4): 820 - 827. [Abstract] [Full Text] [PDF]

				S. T. Turner, G. L. Schwartz, A. B. Chapman, and E. Boerwinkle C825T Polymorphism of the G Protein {beta}3-Subunit and Antihypertensive Response to a Thiazide Diuretic Hypertension, February 1, 2001; 37(2): 739 - 743. [Abstract] [Full Text] [PDF]

				C. K. Naber, J. Husing, U. Wolfhard, R. Erbel, and W. Siffert Interaction of the ACE D Allele and the GNB3 825T Allele in Myocardial Infarction Hypertension, December 1, 2000; 36(6): 986 - 989. [Abstract] [Full Text] [PDF]

				W. Siffert G protein {beta}3 subunit 825T allele, hypertension, obesity, and diabetic nephropathy Nephrol. Dial. Transplant., September 1, 2000; 15(9): 1298 - 1306. [Abstract] [Full Text] [PDF]

				D. Rosskopf, S. Busch, I. Manthey, and W. Siffert G Protein {beta}3 Gene : Structure, Promoter, and Additional Polymorphisms Hypertension, July 1, 2000; 36(1): 33 - 41. [Abstract] [Full Text] [PDF]

				T. Rankinen, T. Rice, A. S. Leon, J. S. Skinner, J. H. Wilmore, D. C. Rao, and C. Bouchard G protein {beta}3 polymorphism and hemodynamic and body composition phenotypes in the HERITAGE Family Study Physiol Genomics, February 28, 2002; 8(2): 151 - 157. [Abstract] [Full Text] [PDF]

This Article Abstract Full Text (PDF) Alert me when this article is cited Alert me if a correction is posted Citation Map Services Email this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Citing Articles Citing Articles via HighWire Citing Articles via Google Scholar Google Scholar Articles by SIFFERT, W. Articles by ROSSKOPF, D. Search for Related Content PubMed PubMed Citation Articles by SIFFERT, W. Articles by ROSSKOPF, D.