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...
Autores principales: | , , , , |
---|---|
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 |