TY - JOUR
T1 - Does gestational diabetes increase the risk of maternal kidney disease? A Swedish national cohort study
AU - Barrett, Peter M.
AU - McCarthy, Fergus P.
AU - Evans, Marie
AU - Kublickas, Marius
AU - Perry, Ivan J.
AU - Stenvinkel, Peter
AU - Kublickiene, Karolina
AU - Khashan, Ali S.
N1 - Publisher Copyright:
Copyright: © 2022 Barrett et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
PY - 2022/3
Y1 - 2022/3
N2 - Background Gestational diabetes (GDM) is associated with increased risk of type 2 diabetes (T2DM) and cardiovascular disease. It is uncertain whether GDM is independently associated with the risk of chronic kidney disease. The aim was to examine the association between GDM and maternal CKD and end-stage kidney disease (ESKD) and to determine whether this depends on progression to overt T2DM. Methods A population-based cohort study was designed using Swedish national registry data. Previous GDM diagnosis was the main exposure, and this was stratified according to whether women developed T2DM after pregnancy. Using Cox regression models, we estimated the risk of CKD (stages 3–5), ESKD and different CKD subtypes (tubulointerstitial, glomerular, hypertensive, diabetic, other). Findings There were 1,121,633 women included, of whom 15,595 (14%) were diagnosed with GDM. Overall, GDM-diagnosed women were at increased risk of CKD (aHR 181, 95% CI 154–214) and ESKD (aHR 452, 95% CI 275–744). Associations were strongest for diabetic CKD (aHR 881, 95% CI 636–1219) and hypertensive CKD (aHR 246, 95% CI 106–569). These associations were largely explained by post-pregnancy T2DM. Among women who had GDM + subsequent T2DM, strong associations were observed (CKD, aHR 2170, 95% CI 1717–2742; ESKD, aHR 11237, 95% CI 6122–20638). But among those with GDM only, associations were non-significant (CKD, aHR 111, 95% CI 089–138; ESKD, aHR 158, 95% CI 070–360 respectively). Conclusion Women who experience GDM and subsequent T2DM are at increased risk of developing CKD and ESKD. However, GDM-diagnosed women who never develop overt T2DM have similar risk of future CKD/ESKD to those with uncomplicated pregnancies.
AB - Background Gestational diabetes (GDM) is associated with increased risk of type 2 diabetes (T2DM) and cardiovascular disease. It is uncertain whether GDM is independently associated with the risk of chronic kidney disease. The aim was to examine the association between GDM and maternal CKD and end-stage kidney disease (ESKD) and to determine whether this depends on progression to overt T2DM. Methods A population-based cohort study was designed using Swedish national registry data. Previous GDM diagnosis was the main exposure, and this was stratified according to whether women developed T2DM after pregnancy. Using Cox regression models, we estimated the risk of CKD (stages 3–5), ESKD and different CKD subtypes (tubulointerstitial, glomerular, hypertensive, diabetic, other). Findings There were 1,121,633 women included, of whom 15,595 (14%) were diagnosed with GDM. Overall, GDM-diagnosed women were at increased risk of CKD (aHR 181, 95% CI 154–214) and ESKD (aHR 452, 95% CI 275–744). Associations were strongest for diabetic CKD (aHR 881, 95% CI 636–1219) and hypertensive CKD (aHR 246, 95% CI 106–569). These associations were largely explained by post-pregnancy T2DM. Among women who had GDM + subsequent T2DM, strong associations were observed (CKD, aHR 2170, 95% CI 1717–2742; ESKD, aHR 11237, 95% CI 6122–20638). But among those with GDM only, associations were non-significant (CKD, aHR 111, 95% CI 089–138; ESKD, aHR 158, 95% CI 070–360 respectively). Conclusion Women who experience GDM and subsequent T2DM are at increased risk of developing CKD and ESKD. However, GDM-diagnosed women who never develop overt T2DM have similar risk of future CKD/ESKD to those with uncomplicated pregnancies.
UR - https://www.scopus.com/pages/publications/85126081420
U2 - 10.1371/journal.pone.0264992
DO - 10.1371/journal.pone.0264992
M3 - Article
C2 - 35271650
AN - SCOPUS:85126081420
SN - 1932-6203
VL - 17
JO - PLOS ONE
JF - PLOS ONE
IS - 3 March
M1 - e0264992
ER -