Association of Maternal Diabetes Mellitus and Polymorphisms of the NKX2.5 Gene in Children with Congenital Heart Disease: A Single Centre-Based Case-Control Study
المؤلفون المشاركون
Zhu, Ping
Zhao, Mingyi
Yang, Yang
Diao, Jingyi
Huang, Peng
Li, Jinqi
Li, Yihuan
Luo, Liu
Zhang, Senmao
Chen, Letao
Wang, Tingting
Qin, Jiabi
المصدر
العدد
المجلد 2020، العدد 2020 (31 ديسمبر/كانون الأول 2020)، ص ص. 1-12، 12ص.
الناشر
Hindawi Publishing Corporation
تاريخ النشر
2020-09-26
دولة النشر
مصر
عدد الصفحات
12
التخصصات الرئيسية
الملخص EN
Background.
Congenital heart disease (CHD) is one of the most common birth defects among newborns, accounting for a large proportion of infant mortality worldwide.
However, the mechanisms remain largely undefinable.
This study aimed to investigate the association of CHD in offspring of mothers with diabetes mellitus (DM) and single nucleotide polymorphisms (SNPs) of NKX2.5.
Methods and Results.
A case-control study of 620 mothers of CHD patients and 620 mothers of healthy children admitted to Hunan Children’s Hospital from November 2017 to December 2019 was conducted.
We collected the mothers’ information by questionnaire and detected children’s NKX2.5 variants with a MassARRAY system.
The interaction coefficient (γ) was used to quantify the estimated gene-environment interactions.
Univariate and multivariate analyses both showed that the infants had a higher risk of CHD if their mothers had a history of DM, including gestational DM (GDM) during this pregnancy (adjusted odds ratio [aOR=4.98]), GDM in previous pregnancies (aOR=4.30), and pregestational DM (PGDM) in the 3 months before this pregnancy (aOR=6.78).
Polymorphisms of the NKX2.5 gene at rs11802669 (C/C vs.
T/T: aOR=4.97; C/T vs.
T/T: aOR=2.15) and rs2277923 (T/T vs.
C/C, aOR=1.74; T/C vs.
C/C, aOR=1.61) were significantly associated with the risk of CHD in offspring.
In addition, significant interactions between maternal DM and NKX2.5 genetic variants at rs11802669 (aOR=8.12) and rs2277923 (aOR=17.72) affecting the development of CHD were found.
Conclusions.
These results suggest that maternal DM, NKX2.5 genetic variants, and their interactions are significantly associated with the risk of CHD in offspring.
نمط استشهاد جمعية علماء النفس الأمريكية (APA)
Zhao, Mingyi& Diao, Jingyi& Huang, Peng& Li, Jinqi& Li, Yihuan& Yang, Yang…[et al.]. 2020. Association of Maternal Diabetes Mellitus and Polymorphisms of the NKX2.5 Gene in Children with Congenital Heart Disease: A Single Centre-Based Case-Control Study. Journal of Diabetes Research،Vol. 2020, no. 2020, pp.1-12.
https://search.emarefa.net/detail/BIM-1183073
نمط استشهاد الجمعية الأمريكية للغات الحديثة (MLA)
Zhao, Mingyi…[et al.]. Association of Maternal Diabetes Mellitus and Polymorphisms of the NKX2.5 Gene in Children with Congenital Heart Disease: A Single Centre-Based Case-Control Study. Journal of Diabetes Research No. 2020 (2020), pp.1-12.
https://search.emarefa.net/detail/BIM-1183073
نمط استشهاد الجمعية الطبية الأمريكية (AMA)
Zhao, Mingyi& Diao, Jingyi& Huang, Peng& Li, Jinqi& Li, Yihuan& Yang, Yang…[et al.]. Association of Maternal Diabetes Mellitus and Polymorphisms of the NKX2.5 Gene in Children with Congenital Heart Disease: A Single Centre-Based Case-Control Study. Journal of Diabetes Research. 2020. Vol. 2020, no. 2020, pp.1-12.
https://search.emarefa.net/detail/BIM-1183073
نوع البيانات
مقالات
لغة النص
الإنجليزية
الملاحظات
Includes bibliographical references
رقم السجل
BIM-1183073
قاعدة معامل التأثير والاستشهادات المرجعية العربي "ارسيف Arcif"
أضخم قاعدة بيانات عربية للاستشهادات المرجعية للمجلات العلمية المحكمة الصادرة في العالم العربي
تقوم هذه الخدمة بالتحقق من التشابه أو الانتحال في الأبحاث والمقالات العلمية والأطروحات الجامعية والكتب والأبحاث باللغة العربية، وتحديد درجة التشابه أو أصالة الأعمال البحثية وحماية ملكيتها الفكرية. تعرف اكثر