Cargando…

Macrosomia is a risk factor for incident maternal chronic kidney disease

BACKGROUND: Gestational diabetes mellitus (GDM) and macrosomia are associated with several adverse outcomes including diabetes mellitus and cardiovascular diseases, however, the relationship between GDM/macrosomia with incident chronic kidney disease (CKD) is a matter of debate. The purpose of this...

Descripción completa

Detalles Bibliográficos
Autores principales: Vahidi, Mohammad, Asgari, Samaneh, Tohidi, Maryam, Azizi, Fereidoun, Hadaegh, Farzad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7968264/
https://www.ncbi.nlm.nih.gov/pubmed/33726706
http://dx.doi.org/10.1186/s12884-021-03695-8
_version_ 1783666028868272128
author Vahidi, Mohammad
Asgari, Samaneh
Tohidi, Maryam
Azizi, Fereidoun
Hadaegh, Farzad
author_facet Vahidi, Mohammad
Asgari, Samaneh
Tohidi, Maryam
Azizi, Fereidoun
Hadaegh, Farzad
author_sort Vahidi, Mohammad
collection PubMed
description BACKGROUND: Gestational diabetes mellitus (GDM) and macrosomia are associated with several adverse outcomes including diabetes mellitus and cardiovascular diseases, however, the relationship between GDM/macrosomia with incident chronic kidney disease (CKD) is a matter of debate. The purpose of this study was to examine the association between the history of macrosomia with or without GDM and incident maternal CKD. METHODS: The study population includes 2669 women aged 18–50 years without known diabetes mellitus and CKD from participants of the Tehran Lipid and Glucose Study. The study population was categorized into 3 groups; group 1: GDM/macrosomia and without diabetes mellitus (n = 204), group 2: newly diagnosed incident diabetes mellitus (NDM) in the presence or abcence of GDM/Macrosomia (n = 113), and, group 3: the reference group including women without prior history of GDM/macrosomia and free of NDM (n = 2352). CKD was defined as an estimated glomerular filtration rate (eGFR) < 60 ml/min/1.73 m(2). Multivariable Cox proportional hazard regression adjusted for baseline values of age, body mass index, waist circumference, parity numbers, smoking, educational level, gestational hypertension, eGFR, systolic and diastolic blood pressures (SBP and DBP, respectively), anti-hypertensive medication, and family history of diabetes mellitus was applied for data analyses. RESULTS: During a median follow-up of 11.9 years, 613 incident CKD cases were identified. The multivariable hazard ratio (HR) and 95% confidence interval (CI) on GDM/macrosomia group was [1.32 (1.02–1.72)]; the risk was more prominent among non-hypertensive women [1.41 (1.07–1.85); P for interaction: 0.046]. Moreover, the history of macrosomia alone also showed a significant risk [1.36 (1.04–1.78)]; however, history of GDM alone did not have a significant risk [0.92 (0.34–2.46)]. Age, current smoking, eGFR, and SBP remained as independent risk factors for incident CKD. CONCLUSIONS: A history of GDM/macrosomia or macrosomia alone, independent of subsequent diabetes mellitus was associated with significant risk for incident maternal CKD. Pregnancy may provide a unique situation to identify high-risk women at risk for CKD that could benefit from regular monitoring of kidney function and providing risk modifying strategies.
format Online
Article
Text
id pubmed-7968264
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-79682642021-03-22 Macrosomia is a risk factor for incident maternal chronic kidney disease Vahidi, Mohammad Asgari, Samaneh Tohidi, Maryam Azizi, Fereidoun Hadaegh, Farzad BMC Pregnancy Childbirth Research Article BACKGROUND: Gestational diabetes mellitus (GDM) and macrosomia are associated with several adverse outcomes including diabetes mellitus and cardiovascular diseases, however, the relationship between GDM/macrosomia with incident chronic kidney disease (CKD) is a matter of debate. The purpose of this study was to examine the association between the history of macrosomia with or without GDM and incident maternal CKD. METHODS: The study population includes 2669 women aged 18–50 years without known diabetes mellitus and CKD from participants of the Tehran Lipid and Glucose Study. The study population was categorized into 3 groups; group 1: GDM/macrosomia and without diabetes mellitus (n = 204), group 2: newly diagnosed incident diabetes mellitus (NDM) in the presence or abcence of GDM/Macrosomia (n = 113), and, group 3: the reference group including women without prior history of GDM/macrosomia and free of NDM (n = 2352). CKD was defined as an estimated glomerular filtration rate (eGFR) < 60 ml/min/1.73 m(2). Multivariable Cox proportional hazard regression adjusted for baseline values of age, body mass index, waist circumference, parity numbers, smoking, educational level, gestational hypertension, eGFR, systolic and diastolic blood pressures (SBP and DBP, respectively), anti-hypertensive medication, and family history of diabetes mellitus was applied for data analyses. RESULTS: During a median follow-up of 11.9 years, 613 incident CKD cases were identified. The multivariable hazard ratio (HR) and 95% confidence interval (CI) on GDM/macrosomia group was [1.32 (1.02–1.72)]; the risk was more prominent among non-hypertensive women [1.41 (1.07–1.85); P for interaction: 0.046]. Moreover, the history of macrosomia alone also showed a significant risk [1.36 (1.04–1.78)]; however, history of GDM alone did not have a significant risk [0.92 (0.34–2.46)]. Age, current smoking, eGFR, and SBP remained as independent risk factors for incident CKD. CONCLUSIONS: A history of GDM/macrosomia or macrosomia alone, independent of subsequent diabetes mellitus was associated with significant risk for incident maternal CKD. Pregnancy may provide a unique situation to identify high-risk women at risk for CKD that could benefit from regular monitoring of kidney function and providing risk modifying strategies. BioMed Central 2021-03-16 /pmc/articles/PMC7968264/ /pubmed/33726706 http://dx.doi.org/10.1186/s12884-021-03695-8 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Vahidi, Mohammad
Asgari, Samaneh
Tohidi, Maryam
Azizi, Fereidoun
Hadaegh, Farzad
Macrosomia is a risk factor for incident maternal chronic kidney disease
title Macrosomia is a risk factor for incident maternal chronic kidney disease
title_full Macrosomia is a risk factor for incident maternal chronic kidney disease
title_fullStr Macrosomia is a risk factor for incident maternal chronic kidney disease
title_full_unstemmed Macrosomia is a risk factor for incident maternal chronic kidney disease
title_short Macrosomia is a risk factor for incident maternal chronic kidney disease
title_sort macrosomia is a risk factor for incident maternal chronic kidney disease
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7968264/
https://www.ncbi.nlm.nih.gov/pubmed/33726706
http://dx.doi.org/10.1186/s12884-021-03695-8
work_keys_str_mv AT vahidimohammad macrosomiaisariskfactorforincidentmaternalchronickidneydisease
AT asgarisamaneh macrosomiaisariskfactorforincidentmaternalchronickidneydisease
AT tohidimaryam macrosomiaisariskfactorforincidentmaternalchronickidneydisease
AT azizifereidoun macrosomiaisariskfactorforincidentmaternalchronickidneydisease
AT hadaeghfarzad macrosomiaisariskfactorforincidentmaternalchronickidneydisease