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Then, C.* ; Ritzel, K.* ; Herder, C.* ; Then, H.* ; Sujana, C. ; Heier, M. ; Meisinger, C. ; Peters, A. ; Koenig, W.* ; Rathmann, W.* ; Roden, M.* ; Maalmi, H.* ; Stumvoll, M.* ; Meitinger, T.* ; Bidlingmaier, M.* ; Seissler, J.* ; Thorand, B. ; Reincke, M.*

Association of renin and aldosterone with glucose metabolism in a Western European population: The KORA F4/FF4 study.

BMJ Open Diab. Res. Care 10:e002558 (2022)
Verlagsversion Forschungsdaten DOI PMC
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Creative Commons Lizenzvertrag
INTRODUCTION: Primary aldosteronism is associated with impaired glucose tolerance. Whether plasma aldosterone and/or renin concentrations are associated with type 2 diabetes and continuous measures of glucose metabolism in the general population is still under debate. RESEARCH DESIGN AND METHODS: The analyses included 2931 participants of the KORA F4 study at baseline and 2010 participants of the KORA FF4 study after a median follow-up of 6.5 years. The associations of active plasma renin and aldosterone concentrations with type 2 diabetes and continuous measures of glucose metabolism were assessed using logistic and linear regression models. Results were adjusted for sex, age, body mass index (BMI), estimated glomerular filtration rate, potassium, use of ACE inhibitors, angiotensin receptor blockers, beta blockers, diuretics and calcium channel blockers. RESULTS: Cross-sectionally, renin was associated with type 2 diabetes (OR per SD: 1.25, 95% CI 1.10 to 1.43, p<0.001), fasting glucose, 2-hour glucose, insulin, proinsulin, HOMA-B (homeostasis model assessment of beta cell function) and HOMA-IR (homeostasis model assessment of insulin resistance) (all p values <0.001). Aldosterone was not associated with type 2 diabetes (OR: 1.04, 95% CI 0.91 to 1.19; p=0.547) but with insulin, proinsulin and HOMA-IR (all p values <0.001). The aldosterone-renin ratio was inversely associated with type 2 diabetes and several measures of glucose metabolism. Longitudinally, neither renin (OR: 1.12, 95% CI 0.92 to 1.36) nor aldosterone (OR: 0.91, 95% CI 0.74 to 1.11) were associated with incident type 2 diabetes. Renin was inversely associated with changes of insulin concentrations. CONCLUSIONS: In the KORA F4/FF4 study, renin and aldosterone were not associated with incident type 2 diabetes and largely unrelated to changes of measures of glucose metabolism. Cross-sectionally, aldosterone was associated with surrogate parameters of insulin resistance. However, these associations were not independent of renin.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Adipokines ; General Population ; Insulin Resistance ; Type 2 Diabetes; Decreases Insulin-secretion; Endothelial Dysfunction; Plasma-aldosterone; Diabetes-mellitus; Risk-factors; Sensitivity; Resistance; Hypertension; Adiponectin; Mechanisms
Sprache englisch
Veröffentlichungsjahr 2022
HGF-Berichtsjahr 2022
ISSN (print) / ISBN 2052-4897
e-ISSN 2052-4897
Zeitschrift BMJ Open Diabetes Research & Care
Quellenangaben Band: 10, Heft: 1, Seiten: , Artikelnummer: e002558 Supplement: ,
Verlag BMJ Publishing Group
Verlagsort London
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Epidemiology (EPI)
Independent Research Group Clinical Epidemiology (KEPI)
POF Topic(s) 30202 - Environmental Health
Forschungsfeld(er) Genetics and Epidemiology
PSP-Element(e) G-504000-002
G-504090-001
G-504000-006
G-502900-001
G-504000-010
Förderungen DFG (CRC/TRR 205 'The Adrenal Gland')
Clinical Cooperation Group Diabetes, Ludwig-Maximilians-University Munchen
German Diabetes Center
Federal Ministry of Health (Berlin, Germany)
e Ministry of Culture and Science of the state North Rhine Westphalia (Dusseldorf, Germany)
Helmholtz Zentrum Munchen German Research Center for Environmental Health - German Federal Ministry of Education and Research (BMBF)
State of Bavaria
German Federal Ministry of Education and Research (BMBF)
Deutsche Diabetes Gesellschaft (DDG)
German Research Foundation
Else Kroner-Fresenius Stiftung
Else-Kroner Hyperaldosteronismus -German Conn Registry)
European Research Council under the European Union's Horizon 2020 Research and Innovation Programme
Virtual Diabetes Institute (Helmholtz Zentrum Munchen)
DOI 10.1136/bmjdrc-2021-002558
WOS ID WOS:000748915300003
Scopus ID 85123905258
PubMed ID 35086943
Erfassungsdatum 2022-05-16
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