Abstract

BackgroundPrevious cross-sectional studies demonstrated the close relationship between visceral obesity and the increased prevalence of proteinuria. But, little is known about the role of changes in visceral fat mass (∆VFM) over several years in the development of proteinuria. In this longitudinal cohort study with the general population, the changes in ∆VFM as well as baseline VFM on proteinuria development were evaluated.MethodsHealthy individuals (n = 2393) who participated in two health screening exams were analyzed. Subjects were divided into three groups based on gender-specific tertiles of baseline VFM and ∆VFM. Each patient was tested for proteinuria using a dipstick, and proteinuria was defined as 1+ or greater.ResultsThe mean age was 51.9±7.7 years, and the incidence of proteinuria was 3.9% (n = 93). During the 4 years, 52.5% of the subjects experienced a decline in ∆VFM. However, subjects who developed proteinuria exhibited a significant increase in ∆VFM. Even after adjustment for age, smoking, systolic and diastolic BP, serum creatinine, and hs-CRP levels, the highest tertiles for baseline VFM [men, odds ratio (OR) 3.43, 95% confidence interval (CI) 1.22–9.67; women, OR 2.01, 95% CI 1.05–4.15] and ∆VFM (men, OR 2.92, 95% CI 1.22–6.99; women, OR 3.16, 95% CI 1.56–6.39) were independent predictors of proteinuria development. Following adjustment of both parameters, subjects in the highest baseline VFM and ∆VFM tertiles exhibited the greatest risk of proteinuria development, which suggested the additive harmful effects of the two factors.ConclusionsBaseline VFM and greater increase in ∆VFM were both important risk factors for developing proteinuria in the general population. Appropriate education and interventions to prevent accumulation of VFM should be the major focus of preemptive strategies.

Highlights

  • As the prevalence of obesity continues to increase, the theory that obesity is a chronic, inflammatory, and contagious disease has become widely accepted

  • Even after adjustment for age, smoking, systolic and diastolic blood pressure (BP), serum creatinine, and high-sensitivity C-reactive protein (hs-CRP) levels, the highest tertiles for baseline VFM [men, odds ratio (OR) 3.43, 95% confidence interval (CI) 1.22– 9.67; women, OR 2.01, 95% CI 1.05–4.15] and ΔVFM were independent predictors of proteinuria development

  • Following adjustment of both parameters, subjects in the highest baseline VFM and ΔVFM tertiles exhibited the greatest risk of proteinuria development, which suggested the additive harmful effects of the two factors

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Summary

Introduction

As the prevalence of obesity continues to increase, the theory that obesity is a chronic, inflammatory, and contagious disease has become widely accepted. Numerous studies have demonstrated the close relationship between obesity and various conditions with high morbidity and mortality, such as coronary heart disease, ischemic stroke, type 2 diabetes, cancer, and osteoarthritis. Obesity is recognized as an independent risk factor for the development of chronic kidney disease (CKD)[1,2]. Previous cross-sectional studies demonstrated the close relationship between visceral obesity and the increased prevalence of proteinuria. Little is known about the role of changes in visceral fat mass (ΔVFM) over several years in the development of proteinuria. In this longitudinal cohort study with the general population, the changes in ΔVFM as well as baseline VFM on proteinuria development were evaluated

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Conclusion

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