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Departments of * Nephrology and
General Surgery, "Germans Trias i Pujol" Hospital, Department of Medicine, Universidad Autónoma de Barcelona, Barcelona, Spain
Address correspondence to: Dr. Ramón Romero, Department of Nephrology, "Germans Trias y Pujol" Hospital, Carretera de Canyet, s/n Badalona, 08916 Barcelona, Spain. Phone: +34-93-497-8898; Fax: +34-93-497-8852; E-mail: r.romero{at}uab.es
| Abstract |
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40 kg/m2) is a type of obesity that usually does not respond to medical treatment, with surgery being the current treatment of choice. Extreme obesity is associated with cardiovascular disease, type 2 diabetes, dyslipidemia, and hypertension. Recently, obesity has been related with high rate of renal lesions, but renal function and renal parameters in extreme obesity scarcely are documented. The objective of this study was to evaluate the effect of weight loss after bariatric surgery (BS) on BP, renal parameters, and renal function in 61 extremely obese (EO) patients after 24 mo of follow-up. A total of 61 EO adults (37 women) were studied prospectively before and 24 mo after surgery. Control subjects were 24 healthy, normal-weight adults (15 women). Anthropometric, BP, and renal parameters were determined. Presurgery weight, BMI, GFR, 24-h proteinuria, and 24-h albuminuria were higher in the EO patients than in control subjects (P < 0.001). All parameters improved at 12 mo after BS. However, during the second year of follow-up, only 24-h albuminuria (P = 0.006) and BMI (P = 0.014) continued to improve. At 24 mo after BS, obesity-related renal alterations considerably improved. This improvement was observed mainly in the first year after surgery, when the majority of weight loss occurred. However, 24-h albuminuria still improves during the second year of follow-up. It is possible that this decrease in 24-h albuminuria is not GFR related but rather is attributable to the persistence of the decrease in BMI and to the improvement of other weight-related metabolic factors. | Introduction |
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40 kg/m2) is a type of obesity that usually does not respond to medical treatment, with surgery being the current treatment of choice (1). Cardiovascular disease, diabetes, dyslipidemia, hypertension (24), and impaired renal parameters have been described as obesity-related comorbidities, although obesity-related renal lesions scarcely are documented (5,6). Both experimental and clinical data show that obesity produces glomerular hyperfiltration, although the physiopathologic mechanism still is unknown (7). Hyperlipidemia (8), hyperinsulinemia (9), and the implication of some adipocytokines such as leptin (10) may contribute to this state of hyperfiltration. Moreover, fat tissue may contribute to the increase of angiotensin II (AngII), which enhances tubular sodium reabsorption and activates tubuloglomerular feedback (11). These mechanisms lead to vasodilation of the afferent arterioles, with a consequent increase in renal blood flow, intraglomerular pressure, and GFR (7,12). Glomerular hyperfiltration favors the occurrence of microalbuminuria and proteinuria in obese patients with unknown renal disease (13) and, in addition, can increase the progression of preexisting renal disease (8,14,15). Reducing glomerular hyperfiltration, therefore, could prevent or delay the incidence of obesity-associated renal damage. Some studies have shown that both weight loss with hypocaloric diets and treatment with angiotensin-converting enzyme inhibitors (ACEI) and/or AngII type I receptor blockers are useful drugs for reducing obesity-related proteinuria (16,17). Bariatric surgery (BS) produces greater weight loss and is more effective in controlling hypertension, diabetes, dyslipidemia, and other cardiovascular risk factors (18,19). However, its effect on renal parameters (e.g., changes in GFR, albuminuria, and proteinuria) scarcely are described in the literature (12,1921), and, to our knowledge, there are no studies on the long-term evolution of these effects (2 yr follow-up). Therefore, the aim of this study was to evaluate the effect of weight loss after BS on BP, renal parameters, and renal function in 61 extremely obese (EO) patients after 24 mo of follow-up. | Materials and Methods |
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Twenty-one (35%) patients were smokers, and three (5%) had cardiovascular disease (two who had angina and had a normal coronary catheterism study and one who had undergone aortic-coronary bypass). None of the patients selected was being treated with insulin, oral antidiabetic drugs, or lipid-lowering drugs. Twenty-two patients were receiving treatment for hypertension (five with ACEI, four with AngII type I receptor blockers, three with diuretics, one with
blockers, and nine with ACEI in combination with other drugs). Medications were withdrawn 8 d before the analyses were performed. All patients in the study had normal levels of serum creatinine (normal values in our laboratory 44 to 106 µmol/L), and none had a history of renal disease.
Twenty-four healthy, normal-weight adults (nine men and 15 women) were included as a control group (mean BMI 23.52 ± 2.59 kg/m2; mean age 42.54 ± 11.39 yr). Only baseline studies were available for the control subjects.
Preoperative and postoperative (at 12 and 24 mo after bariatric surgery) blood samples were drawn between 8:00 and 9:00 a.m. after a minimum of 8 h of fasting. A 24-h urine sample also was collected from all patients. Plasma creatinine, urea, and urinary creatinine were determined using a routine clinical chemistry laboratory analyzer. Creatinine clearance was calculated as 24-h urine (ml) x urinary creatinine concentration x 1000/plasma creatinine concentration x 1440 min. Twenty-four-hour proteinuria was measured by a spectrophotometric method (Pyrogallol Red), and 24-h albuminuria was determined by nephelometry. Proteinuria values >0.15 g/24 h and albuminuria values
30 mg/24 h were considered pathologic. Microalbuminuria was defined as albumin levels in 24-h urine between 30 and 300 mg.
BMI was calculated as weight (kg)/height (m2). Waist circumference (cm) was measured with a soft tape measure in a horizontal plane around the abdomen at the level of the iliac crest. BP was measured using a standard mercury sphygmomanometer of appropriate cuff size. High casual systolic BP (SBP) and high casual diastolic BP (DBP) were defined as SBP
140 mmHg and DBP
90 mmHg in two different measurements. Glomerular hyperfiltration was considered when the creatinine clearance was >140 ml/min (26) and microhematuria when there were four or more red blood cells per high-power field in the urinary sediment, according to routine values of our laboratory.
Statistical Analyses
Data first were tested for normal distribution using the Kolmogorov-Smirnov test. Variables with normal distribution were expressed as mean ± SD. Nonparametric variables such as proteinuria and albuminuria were expressed as median (25th and 75th percentiles). The significance of differences between the control group and the obese patients was evaluated with unpaired t test or
2 test, as appropriate. Differences within the obese group before and after BS were evaluated with paired t test or the McNemar test, as appropriate. The t test was applied to the nonparametric data after log transformation.
All statistical analyses were made with the statistical software package SPSS (version 12.0; SPSS, Chicago, IL). Statistical significance was considered at P < 0.05.
| Results |
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| Discussion |
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Obesity is associated with glomerular hyperfiltration, which favors the occurrence of microalbuminuria and/or proteinuria in patients without known renal disease (7,27,28). Brochner et al. (20) demonstrated for the first time in the 1980s that GFR decreased in EO patients who had undergone intestinal bypass surgery. Only two studies support these results after 12 mo of follow-up (12,19), and there are no studies on GFR in patients who undergo BS and are followed over a longer period of time. In our study, an important percentage of EO patients had glomerular hyperfiltration before undergoing BS. This percentage decreased at 12 mo after BS in a similar way to patients in previous studies, including one from our group (12,19). However, this percentage of EO patients with high GFR did not improve significantly between 12 and 24 mo, even though there was a discrete weight loss during this time. That a few patients still had glomerular hyperfiltration at 24 mo after BS could be attributed to these patients still having type 1 obesity. The value of GFR was estimated using creatinine clearance as measured by 24-h urine sample, without correcting for body surface area, because the correction would underestimate considerably the real value of the GFR (29). For the same reason, we did not use other types of formulas to estimate the GFR (Cockcroft-Gault and Modification of Diet in Renal Disease), because these formulas are designed for patients with chronic renal failure and, if applied to our study population, also would underestimate the real value of GFR (30,31).
Almost half of the EO patients in our study presented with albuminuria and/or proteinuria before undergoing BS. This improved significantly at 12 mo after BS, although it did not disappear completely, which confirms previously published reports by other authors (12,19). During the second year of follow-up, albuminuria continued to decrease even though GFR did not decrease. Other weight-related factors, such as improvement of lipid alterations and hyperinsulinemia or decrease in plasma leptin levels, may contribute to the persistence of this improvement (our unpublished observations, 2005).
This is the first study to demonstrate that EO patients present with a greater percentage of microhematuria compared with the control group and that these alterations in urinary sediment improve within 12 mo of drastic weight loss. To evaluate these results further, we would have had to carry out subsequent histologic studies, which are difficult to justify for ethical reasons.
Although the cause-and-effect relationship of glomerular hyperfiltration in obesity is not fully understood, we do know that in these patients, there is an increase in the tubular reabsorption of sodium in the loop of Henle. As such, the macula densa receives less salt, which leads to vasodilatation of the afferent arterioles and a subsequent increase in GFR (3). This retention of sodium could be the physiopathologic mechanism of the arterial hypertension that is associated with obesity. This study shows that drastic weight loss and the subsequent decrease in glomerular filtration leads to a decrease in SBP and DBP, as shown in previous studies (12,18,19,21). SBP and DBP did not decrease more between the first and the second years, probably because of the lack of change in the GFR.
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