Albuminuria Testing in Hypertension and Diabetes: An Individual-Participant Data Meta-Analysis in a Global Consortium

Author:

Shin Jung-Im1,Chang Alex R.2,Grams Morgan E.1,Coresh Josef1ORCID,Ballew Shoshana H.1ORCID,Surapaneni Aditya1,Matsushita Kunihiro1,Bilo Henk J.G.3,Carrero Juan J.4ORCID,Chodick Gabriel5,Daratha Kenn B.6ORCID,Jassal Simerjot K.7,Nadkarni Girish N.8ORCID,Nelson Robert G.9,Nowak Christoph10ORCID,Stempniewicz Nikita11,Sumida Keiichi12,Traynor Jamie P.13ORCID,Woodward Mark114ORCID,Sang Yingying1,Gansevoort Ron T.15,Chalmers John,Tuttle Katherine,Alicic Radica,McPherson Sterling,Jones Cami,Singh Gurmukteshwar,Green Jamie,Kirchner H. Lester,Shalev Varda,Bottinger Erwin P.,Loos Ruth J.F.,Ellis Stephen B.,Cuddeback John,Ciemins Elizabeth,Carbonara Emily,Dunning Stephan,Knowler William C.,Looker Helen C.,Kieneker Lyane M.,Bakker Stephan J.L.,Hillege Hans L.,van der Harst Pim,Jassal Simerjot K.,Bergstrom Jacklyn,Ix Joachim,Kovesdy Csaba P.,Potukuchi Praveen,Trevisan Marco,Elinder Carl Gustaf,Wettermark Björn,Ärnlöv Johan,Mark Patrick B.,Thomson Peter C.,Geddes Colin C.,Landman Gijs W.D.,van Hateren Kornelis J.J.,Kleefstra Nanne,Gutierrez Orlando,Konta Tsuneo,Levey Andrew S.,Polkinghorne Kevan,Schäffner Elke,Chen Jingsha,Surapeneni Aditya

Affiliation:

1. From the Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD (J.-I.S., M.E.G., J.C., S.H.B., A.S., K.M., M.W., Y.S.)

2. Department of Nephrology and Kidney Health Research Institute, Geisinger Medical Center, Danville, Pennsylvania (A.R.C.)

3. Diabetes Centre, Isala, and Department of Internal Medicine (H.J.G.B.), University of Groningen, University Medical Center Groningen, the Netherlands

4. Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Huddinge, Sweden (J.J.C.)

5. Medical Division, Maccabi Healthcare Services, and Sackler Faculty of Medicine, Tel Aviv University, Israel (G.C.)

6. Providence St. Joseph Health on behalf of CURE-CKD Investigators, Spokane, WA (K.B.D.)

7. Division of General Internal Medicine, University of California, San Diego and VA San Diego Healthcare, California (S.K.J.)

8. Department of Medicine, Division of Nephrology, Icahn School of Medicine at Mount Sinai, New York (G.N.N.)

9. National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Phoenix, Arizona (R.G.N.)

10. Department of Neurobiology, Care Sciences and Society, Karolinska Institutet, Stockholm, Sweden (C.N.)

11. AMGA (American Medical Group Association), Alexandria, Virginia and OptumLabs Visiting Fellow, Eden Prairie, MN (N.S.)

12. Division of Nephrology, Department of Medicine, University of Tennessee Health Science Center, Memphis, TN (K.S.)

13. Glasgow Renal Transplant Unit, Queen Elizabeth University Hospital Glasgow Scotland, United Kingdom (J.P.T.)

14. George Institute for Global Health, Australia, and George Institute for Global Health, Imperial College, London, United Kingdom (M.W.).

15. Department of Nephrology (R.T.G.), University of Groningen, University Medical Center Groningen, the Netherlands

Abstract

Albuminuria is an under-recognized component of chronic kidney disease definition, staging, and prognosis. Guidelines, particularly for hypertension, conflict on recommendations for urine albumin-to-creatinine ratio (ACR) measurement. Separately among 1 344 594 adults with diabetes and 2 334 461 nondiabetic adults with hypertension from the chronic kidney disease Prognosis Consortium, we assessed ACR testing, estimated the prevalence and incidence of ACR ≥30 mg/g and developed risk models for ACR ≥30 mg/g. The ACR screening rate (cohort range) was 35.1% (12.3%–74.5%) in diabetes and 4.1% (1.3%–20.7%) in hypertension. Screening was largely unrelated to the predicted risk of prevalent albuminuria. The median prevalence of ACR ≥30 mg/g across cohorts was 32.1% in diabetes and 21.8% in hypertension. Higher systolic blood pressure was associated with a higher prevalence of albuminuria (odds ratio [95% CI] per 20 mm Hg in diabetes, 1.50 [1.42–1.60]; in hypertension, 1.36 [1.28–1.45]). The ratio of undetected (due to lack of screening) to detected ACR ≥30 mg/g was estimated at 1.8 in diabetes and 19.5 in hypertension. Among those with ACR <30 mg/g, the median 5-year incidence of ACR ≥30 mg/g across cohorts was 23.9% in diabetes and 21.7% in hypertension. Incident albuminuria was associated with initiation of renin-angiotensin-aldosterone system inhibitors (incidence-rate ratio [95% CI], diabetes 3.09 [2.71–3.53]; hypertension 2.87 [2.29–3.59]). In conclusion, despite similar risk of albuminuria to those with diabetes, ACR screening in patients with hypertension was low. Our findings suggest that regular albuminuria screening should be emphasized to enable early detection of chronic kidney disease and initiation of treatment with cardiovascular and renal benefits.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Internal Medicine

Reference26 articles.

1. Kdigo 2012 clinical practice guideline for the evaluation and management of chronic kidney disease.;Kidney Disease: Improving Global Outcomes (KDIGO) Blood Pressure Work Group;Kidney Intern Suppl,2013

2. Albuminuria and Risk of Cardiovascular Events, Death, and Heart Failure in Diabetic and Nondiabetic Individuals

3. Very Low Levels of Microalbuminuria Are Associated With Increased Risk of Coronary Heart Disease and Death Independently of Renal Function, Hypertension, and Diabetes

4. Association of estimated glomerular filtration rate and albuminuria with all-cause and cardiovascular mortality in general population cohorts: a collaborative meta-analysis.;Matsushita K;Lancet,2010

5. Lower estimated GFR and higher albuminuria are associated with adverse kidney outcomes. A collaborative meta-analysis of general and high-risk population cohorts

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