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Associations between body mass index and the risk of renal events in patients with type 2 diabetes

Nutrition & Diabetesvolume 8, Article number: 7 (2018) | Download Citation

Abstract

Background/objectives

We aimed to evaluate the relationship between BMI and the risk of renal disease in patients with type 2 diabetes in the Action in Diabetes and Vascular Disease: PreterAx and DiamicroN Modified-Release Controlled Evaluation (ADVANCE) study.

Subjects/methods

Participants were divided into six baseline BMI categories: <18.5 (underweight, n = 58); ≥18.5 to <25 (normal, n = 2894); ≥25 to <30 (overweight, n = 4340); ≥30 to <35 (obesity grade 1, n = 2265); ≥35 to <40 (obesity grade 2, n = 744); and ≥40 kg/m2 (obesity grade 3, n = 294); those underweight were excluded. The composite outcome “major renal event” was defined as development of new macroalbuminuria, doubling of creatinine, end stage renal disease, or renal death. These outcomes and development of new microalbuminuria were considered individually as secondary endpoints.

Results

During 5-years of follow-up, major renal events occurred in 487 (4.6%) patients. The risk increased with higher BMI. Multivariable-adjusted HRs (95% CIs), compared to normal weight, were: 0.91 (0.72–1.15) for overweight; 1.03 (0.77–1.37) for obesity grade 1; 1.42 (0.98–2.07) for grade 2; and 2.16 (1.34–3.48) for grade 3 (p for trend = 0.006). These findings were similar across subgroups by randomised interventions (intensive versus standard glucose control and perindopril-indapamide versus placebo). Every additional unit of BMI over 25 kg/m2 increased the risk of major renal events by 4 (1–6)%. Comparable results were observed with the risk of secondary endpoints.

Conclusions

Higher BMI is an independent predictor of major renal events in patients with type 2 diabetes. Our findings encourage weight loss to improve nephroprotection in these patients.

Introduction

Globally, obesity is common with alarming rates of increasing prevalence1,2. It is a key component of the metabolic syndrome, which is also characterised by hypertension, dyslipidaemia, and insulin resistance, and often leads to type 2 diabetes3. Diabetes is a leading cause of chronic kidney disease (CKD) and end-stage renal disease (ESRD)4. In the absence of diabetes, however, experimental and epidemiological studies have also provided accumulating evidence that obesity is an independent risk factor for CKD5,6, a risk mediated in part through intraglomerular hypertension and hyperfiltration7.

Most reported observational studies have found positive associations between being overweight or obese and kidney outcomes (which include development of CKD, rapid changes in kidney function or ESRD)8,9,10,11,12. However, few have been large enough to compare people with and without diabetes reliably9, and there remains some uncertainty in people with diabetes as to whether higher body mass index (BMI) increases risk of developing macroalbuminuria, and whether BMI–CKD associations are mediated through differences in renal risk factors affected by adiposity (e.g., glycemia and blood pressure).

In the present study, we aimed to evaluate the relationship between baseline BMI and major renal events among patients with type 2 diabetes in the Action in Diabetes and Vascular Disease: PreterAx and DiamicroN Modified-Release Controlled Evaluation (ADVANCE) trial (ClinicalTrials.gov number, NCT00145925). In order to investigate potential mechanisms for any associations, outcomes were analysed for the whole cohort and in subgroups for those randomised to different intensities of long-term glycaemic control and to use of placebo versus perindopril-indapamide, an ACE-inhibitor/diuretic combination drug that would be expected to reduce glomerular hyperfiltration.

Materials/subjects and methods

Study population

The ADVANCE study was a 2 × 2 factorial randomised controlled trial which tested the effects of intensive glucose control using a gliclazide-MR-based regimen, and routine blood pressure treatment using a fixed-dose combination of perindopril and indapamide, on the incidence of major macrovascular and microvascular events in patients with type 2 diabetes. The design and clinical characteristics of participants have been published previously13,14,15. Briefly, patients aged 55 years or older with diabetes diagnosed at 30 years or older with pre-existing cardiovascular disease or with at least one risk factor for cardiovascular disease were eligible. Participants were followed prospectively for clinical events and had blood pressure and urinary albumin to creatinine ratio (ACR) measured at local study clinics at 2-year, 4-year and final follow-up visits. The ADVANCE protocol was approved by the Institutional Ethics Committee of each participating centre and all participants provided written informed consent before their enrolment in the trial.

Definition of BMI categories at baseline

Baseline BMI, computed as the weight in kilograms divided by the square of the height in metres, was categorised at baseline into six categories according to the World Health Organization classification16: underweight (<18.5), normal weight (≥18.5 to <25), overweight (≥25 to <30), and obesity grade 1 (≥30 to <35), grade 2 (≥35 to <40), and grade 3 (≥40 kg/m2).

Primary and secondary endpoints

As pre-specified in the ADVANCE protocol13, “major renal events” were defined as a composite of macroalbuminuria (defined as a urinary ACR > 300 mg/g), doubling of the serum creatinine level to at least 200 μmol/l, ESRD (defined as the need for renal-replacement therapy), or death due to renal disease. “New cases of microalbuminuria” (defined as 30 < ACR ≤ 300 mg/g), “Development of new macroalbuminuria”, and “doubling of creatinine, ESRD, or renal death”, were considered individually as secondary endpoints. The primary endpoints were reviewed by an independent End Point Adjudication Committee.

Statistical analyses

Clinical and biological characteristics of participants at baseline were presented both overall and according to BMI categories. Categorical variables were expressed as the number of patients with the corresponding percentage, and continuous variables as mean (SD), or as median (interquartile interval) for those with a skewed distribution. Patients with missing data regarding estimated glomerular filtration rate (eGFR) and ACR at baseline (n = 545) were excluded from the current study. Few (n = 58; 0.6 %) patients were underweight, and so these were also excluded from the main set of analyses, although included in a sensitivity analysis. Cox proportional hazards regression models were fitted to estimate hazard ratios (HRs), with associated 95% confidence intervals (CI), for major renal events by BMI categories, taking normal weight as the reference group. The primary model (model 1) adjusted for baseline age, sex, region of origin (Asia: Philippines, China, Malaysia, and India; established market economies: Australia, Canada, France, Germany, Ireland, Italy, Netherlands, New Zealand, United Kingdom; and Eastern Europe: Czech Republic, Estonia, Hungary, Lithuania, Poland, Russia, Slovakia), prior cardiovascular disease (defined as the presence at baseline of myocardial infarction, stroke, coronary artery bypass graft, percutaneous transluminal coronary angioplasty, hospital admission for unstable angina or transient ischaemic attack), eGFR (computed by the CKD–Epidemiology Collaboration equation)17, squared eGFR, urinary ACR, history of ever smoking and study allocation. In model 2 we additionally adjusted for baseline duration of diabetes, HbA1c, systolic blood pressure, total-cholestrol and HDL-cholesterol, and triglycerides. Since these are factors that BMI can be expected to affect causally, most results presented are from model 1. We also evaluated the association of BMI as a continuous variable with major renal events using piece-wise linear splines with knots at 18.5, 25, 30, 35, 40, and 45 kg/m2, and a reference value at 21 kg/m2. The hazard ratio for major renal events associated with each single additional unit of BMI above 25 kg/m2 was also estimated.

Sensitivity analyses were performed to test the association of BMI categories with the risk of major renal events: (i) in different groups of randomised study treatment (standard and intensive glucose control; placebo and perindopril-indapamide) considered separately; (ii) in different CKD stages (stage 1 [eGFR ≥ 90 mL/min/1.73 m2]; stage 2 [≥60 to <90], and stage 3 [<60]); (iii) after treating non-renal death as a competing risk using the Fine and Gray method18; (iv) in participants who did not change their BMI category during follow-up; (v) the association of BMI categories with the risk of new microalbuminuria in patients with normoalbuminuria at baseline; and (vi) after including patients with underweight, who were otherwise omitted.

Statistical analyses were performed using SAS software, version 9.3 (SAS Institute, www.sas.com) and Stata software version 13 (StataCorp., www.stata.com). A p-value < 0.05 was considered significant.

Results

Baseline characteristics by BMI categories

Among 10,537 participants investigated, 58% were men, and 38, 43, and 19% were from Asia, Established market economies, and Eastern Europe, respectively (Table 1). Their mean (SD) age and duration of diabetes were 66(6) and 8(6) years, respectively, and their mean HbA1c was 7.5 (1.5)%. Mean (SD) BMI at baseline was 28(5) kg/m2, and 2894 (27%), 4340 (41%), 2265 (22%), 744 (7%) and 294 (3%) patients, respectively, were in the normal weight, overweight and obesity grades 1, 2 and 3 categories. Mean eGFR was 75(17) mL/min/1.73 m2, and 2341 (22%), 5952 (57%) and 2244 (21%) were categorised as CKD stages 1, 2, and 3, respectively. Median urinary ACR was 15(7–40) mg/g, with 7312 (69%), 2824 (27%) and 401 (4%) in the normo-albuminuric, micro-albuminuric and macro-albuminuric ranges.

Table 1 Characteristics of participants by BMI categories

Compared to those with normal weight, patients with obesity were more frequently from established market economies, had a shorter duration of diabetes, and greater systolic blood pressure, and serum triglycerides concentration. They were more likely to use antihypertensive and lipid lowering treatments, and to have ever smoked.

Risk of major renal events during follow-up by BMI categories

Major renal events occurred in 487 (4.6%) participants during a median duration of follow-up of 5.0 (interquartile interval: 4.5–5.0) years. Patients who developed major renal events during follow-up, compared to those who did not, were more frequently men, had a longer duration of diabetes at baseline, higher systolic blood pressure, HbA1c, and urinary ACR levels, had a lower eGFR, and were more likely to use antihypertensive and lipid lowering drugs (Supplemental Table S1). Major renal events occurred in 144 (5.0%), 181 (4.2%), 96 (4.2%), 43 (5.8%), and 23 (7.8%) participants with normal weight, overweight, and obesity grades 1, 2 and 3, respectively (Table 2). The risk of major renal events increased gradually across increasing BMI categories, and the highest risk was observed in patients with severe obesity. Adjusted HRs (95% CIs) from model 1, compared to normal weight, were: overweight: 0.91 (0.72–1.15), obesity grade 1: 1.03 (0.77–1.37), grade 2: 1.42 (0.98–2.07), and grade 3: 2.16 (1.34–3.48, p for trend = 0.006). Very similar results were observed when additional adjustments, including mediating factors, were included (model 2)—as was the case for the remaining analyses (results not shown). The same pattern was seen when BMI was fitted as a continuous variable (Fig. 1). Above 25 kg/m2, the association of BMI with major renal events appeared to be log-linear, and each additional unit was associated with 4(1–6)% increased risk (p = 0.002).

Table 2 Major renal events during follow-up according to BMI categories at baseline
Fig. 1: Hazard ratios for a major renal event by BMI splines at baseline
Fig. 1

Multi-adjusted hazard ratios (solid line) and 95% confidence intervals (shaded region) for major renal events during follow-up according to baseline BMI as a continuous variable with a reference value at 21 kg/m2 (diamond). Analyses were adjusted for baseline age, sex, region of origin, prior cardiovascular disease, estimated glomerular filtration rate (and its square), urinary albumin to creatinine ratio, history of ever smoking, and study allocations

Risk of secondary endpoints during follow-up according to BMI categories at baseline

New cases of microalbuminuria, macroalbuminuria, and doubling of creatinine, ESRD or renal death occurred during follow-up in 2730 (25.9%), 389 (3.5%) and 162 (1.5%) participants, respectively. The risk of new microalbuminuria or macroalbuminuria increased gradually across increasing BMI categories (Table 3). The risk of doubling of creatinine, ESRD or renal death seems to be higher in patients with obesity stages 2 and 3, but the test for trend was non-significant. Each additional unit of BMI over 25 kg/m2 increased the risk of microalbuminuria (p = 0.0008), macroalbuminuria (p = 0.004), and doubling of creatinine, ESRD or renal death (p = 0.008) by 2(1–3), 4(1–6), and 5(1–10)%, respectively (using model 1).

Table 3 Secondary endpoints according to BMI categories at baseline

Sensitivity analyses

The associations of BMI categories with the risk of major renal events were compared in different groups of study treatments (Table 4, p for interaction between trend in BMI and glucose lowering control = 0.14 and p for interaction between trend in BMI and blood pressure treatment = 0.96), as well as in different baseline CKD stages (p for interaction = 0.14, Supplemental Table S2) and remained significant after treating non-renal death as a competing risk (p for trend = 0.01, Supplemental Table S3). During follow-up, 7103 (67%) participants maintained the same BMI categories as at baseline (Supplemental Table S4). When we considered only these participants, BMI categories remained significantly associated with major renal events (p for trend = 0.002, Supplemental Table S5). Similarly, the association of BMI categories with increasing risk of new microalbuminuria remained significant (p for trend = 0.02) in patients with normoalbuminuria at baseline (Supplemental Table S6). Finally, when we considered the entire cohort, underweight was associated with a higher risk of major renal events compared to normal weight (HR 2.17, 95% CI 1.01–4.67) (using model 1).

Table 4 Major renal events during follow-up according to BMI categories at baseline, in each randomised group

Discussion

In the current investigation, we evaluated the effect of BMI at baseline on the 5-year risk of major renal events in patients with type 2 diabetes. Above 25 kg/m2, the risk of major renal events increased progressively through BMI categories: on average, each 1 unit higher BMI increased this risk by 4%. The increased risk of major renal events was independent of putative risk factors and was observed even after allowing for the competing risk of non-renal death. It was comparable in participants randomly assigned to either standard or intensive glucose control, and to placebo or perindopril-indapamide. Similar associations were also observed when we considered only participants who remained in the same BMI categories during follow-up.

Only a few prospective studies have examined the relationship between BMI and renal events separately among people who have already developed type 2 diabetes, and these have reported a range of findings9,19,20. One of the larger studies conducted in 5829 Chinese patients with type 2 diabetes (mean %HbA1 < 8) found an inverse association between BMI and CKD. However, these analyses adjusted for risk factors on the causal pathway between BMI and CKD, including blood pressure, albuminuria, diabetic characteristics, and other traits of metabolic syndrome (e.g. central obesity), and this adjustment may have distorted aetiological associations20. Our own larger study of 10,537 patients with type 2 diabetes provides clear evidence for an increased risk of major renal events with increasing BMI over 25 kg/m2, in Cox models including BMI both as a categorical and as a continuous variable. The highest risk was observed in patients with morbid obesity.

Despite little apparent cross-sectional association between baseline BMI and baseline urinary ACR in our study, there was a clear positive association between BMI and development of new cases of microalbuminuria and macroalbuminuria, and these hazards were similar in size to the trend toward association between BMI and doubling of creatinine, ESRD or death. Furthermore, each additional unit of BMI over 25 kg/m2 increased these endopints by 2, 4, and 5%, respectively. A key mechanism for obesity-associated albuminuria is intraglomerular hypertension, which increases renal blood flow and fractional urinary albumin clearance21,22,23,24. The consequent mechanical stress results in glomerular enlargement (hypertrophy) and an increased distance between the neighbouring podocytes, damaging a key cellular layer of the glomerular filtration barrier25 and perhaps causing podocyte death with focal segmental glomerulosclerosis26,27,28. Randomisation to perindopril + indapamide in ADVANCE reduced total renal events (major renal events plus new microalbuminuria) by 21% (relative risk 0.79, 0.73–0.85)15. However, in our subgroup analyses, we found BMI–major renal events associations were not modified by allocated to perindopril + indpamide, which is consistent with a hypothesis that general adiposity may affect renal risk by mechanisms in addition to the haemodynamic stress of glomerular hyperfiltration.

Hyperglycaemia has been suggested as a metabolic podocyte stressor25. An inverse association between high insulin sensitivity (estimated by euglycemic clamp) and impaired renal function in a community-based cohort has been reported29, and pre-diabetes has been associated with directly measured evidence of hyperfiltration independent of BMI7. However, our subgroup analyses suggested that the BMI–major renal events association was not significantly modified by glycaemic control allocation (average HbA1c difference 0.7%), despite the inverse relationship between HbA1c and weight30. Another mechanism by which adipose tissue may cause kidney disease is the visceral fat deposition in the renal sinus, which may compress the main renal artery and vein31,32,33, but measurements relevant to these mechanisms were not measured in this study.

Nevertheless, our findings are consistent with reports that weight loss may protect against the development of renal complications in overweight or obese individuals with type 2 diabetes. The Look AHEAD (Action for Health in Diabetes) trial showed that intensive lifestyle intervention, compared to standard education, resulted in 8% weight loss (on average 4 kg) and a consequent 31% reduction (hazard ratio 0.69 [0.55–0.87]) in “very-high-risk CKD” (based in KDIGO risk charts)34. Weight loss may also be one of the mechanisms by which sodium-glucose co-transporter 2 inhibitors or analogues of glucagon-like peptide 1 reduce renal risk35,36,37. Lastly, bariatric surgery has been associated with an improvement in renal function38,39,40. Regardless of the mechanism, higher risk with obesity suggests there may be greater absolute benefit from attention to all risk factors among patients with obesity and diabetes at risk for CKD progression.

The present investigation’s key strength was its comprehensive clinical and biological characterisation of participants, and 5 years of prospective follow-up including pre-specified renal outcomes confirmed by an independent adjudication committee13. However, it is possible that the number of major renal events may have been insufficiently large to identify important differences between the randomised groups. Also, ADVANCE did not collect detailed data on body fat distribution, so that important differences between body-mass composition between participants could not be assessed for its relevance to major renal events. Furthermore, creatinine determinations were not isotope dilution mass spectrometry (IDMS) traceable in the ADVANCE trial as all participants were enroled before the international recommendations for IDMS alignment41,42.

In conclusion, obesity at different stages was an independent predictor of major renal events in patients with type 2 diabetes. Our findings encourage comprehensive and motivated weight loss programmes for improving the prevention of the development and progression of kidney complications in patients with both type 2 diabetes and obesity.

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Acknowledgements

KM was supported by grants from the Société Francophone du Diabète (SFD) and the Association Diabète Risque Vasculaire (ADRV), and travel support from the Association pour le Développement de l’Enseignement et des Recherches auprès des universités, des centres de recherches et des entreprises d’Aquitaine (ADERA).

Author information

Affiliations

  1. The George Institute for Global Health, University of Sydney, Sydney, Australia

    • Kamel Mohammedi
    • , John Chalmers
    • , Qiang Li
    • , Anthony Rodgers
    • , Vlado Perkovic
    •  & Mark Woodward
  2. INSERM, UMRS 1138, Centre de Recherche des Cordeliers, Paris, France

    • Kamel Mohammedi
    •  & Michel Marre
  3. Department of Diabetology, Endocrinology and Nutrition, Assistance Publique Hôpitaux de Paris, Bichat Hospital, DHU FIRE, Paris, France

    • Kamel Mohammedi
    •  & Michel Marre
  4. Nuffield Department of Population Health, University of Oxford, Oxford, UK

    • William Herrington
  5. The University of Milan-Bicocca and Istituto Auxologico Italiano, Milan, Italy

    • Giuseppe Mancia
  6. Sorbonne Paris Cité, UFR de Médecine, University Paris Diderot, Paris, France

    • Michel Marre
  7. The International Centre for Circulatory Health, National Heart and Lung Institute, Imperial College, London, UK

    • Neil Poulter
  8. Institute of Cardiovascular Sciences, University College London (UCL) and NIHR UCL Hospitals Biomedical Research Centre, London, UK

    • Bryan Williams
  9. Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Johns Hopkins University, Baltimore, MD, USA

    • Josef Coresh
    •  & Mark Woodward
  10. The George Institute for Global Health, University of Oxford, Oxford, UK

    • Mark Woodward

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Contributions

K.M., M.W., and J.Ch. designed the study; K.M. wrote the manuscript with assistance from J.Ch., W.H. and M.W.; L.Q. reviewed the statistical analyses. G.M., M.M., N.P., A.R., B.W., V.P. and J.Co. contributed to discussion and reviewed the manuscript. M.W. and K.M. are the guarantors of this work and, as such, had full access to all the data in the study and take responsibility for the integrity of the data and the accuracy of the data analysis. All authors approved the current version of the manuscript.

Dr. Kamel Mohammedi reports personal fees from Novo-Nordisk, outside the submitted work; Prof. John Chalmers reports grants and personal fees from Servier, outside the submitted work; Prof. Giuseppe Mancia reports personal fees from Boehringer Ingelheim, personal fees from CVRx, personal fees from Daiichi Sankyo, personal fees from Medtronic, personal fees from Merck & Co., personal fees from Menarini, personal fees from Novartis, personal fees from Servier, outside the submitted work; Prof. Michel Marre reports grants and personal fees from Novo Nordisk, grants and personal fees from Sanofi, grants and personal fees from Eli Lilly, personal fees from Servier, grants and personal fees from Merck Sharp and Dohme, personal fees from Abbott, grants and personal fees from Novartis, personal fees from Astra Zeneca, outside the submitted work; Prof. Neil Poulter reports grants from the George Institute, grants from British Heart Foundation/Diabetes UK/The George Institute, during the conduct of the study; grants from The George Institute, grants from BHF/DUK/The George Institute, outside the submitted work; Prof. Bryan Williams reports personal fees from servier, outside the submitted work; and Prof. Mark Woodward reports personal fees from Amgen, outside the submitted work. No other potential conflict of interest relevant to this article was reported.

Corresponding author

Correspondence to John Chalmers.

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DOI

https://doi.org/10.1038/s41387-017-0012-y