کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
5528842 1548553 2017 4 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
What is the impact of gestational diabetes mellitus on frequency of structural chromosome aberrations in pregnant women and their offspring?
ترجمه فارسی عنوان
تاثیر دیابت بارداری بر فراوانی ابروهای کروموزوم ساختاری در زنان باردار و فرزندانشان چیست؟
کلمات کلیدی
بارداری، دیابت بارداری، نوزادان، خون بند ناف، اختلالات کروموزوم ساختاری،
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی تحقیقات سرطان
چکیده انگلیسی


- Structural CA was increased but did not reach statistical significance.
- Structural CA in GDM mothers did not correlate with babies' aberrations.
- Structural CA in GDM mothers did not correlate with HbA1C level.

Gestational diabetes mellitus (GDM) is defined as carbohydrate intolerance which results in hyperglycemia first diagnosed during pregnancy. It is associated with an increased levels of oxidative stress due to overproduction of reactive oxygen species (ROS). Overproduction of ROS induces protein oxidation, lipid peroxidation and different types of DNA damage. The objective of this study was to determine the frequencies of structural chromosome aberrations (CA) in peripheral blood of pregnant women (mothers) with GDM and in cord blood of their newborns. Peripheral blood lymphocytes were collected from 35 GDM mothers and cord blood lymphocytes from their 35 newborns. The control group included 30 pregnant mothers without diabetes mellitus (DM) and their 30 newborns. CA were evaluated with in vitro chromosome aberration assays. We observed a moderate increase of the mean numbers of structural CA between GDM mothers and their newborns, GDM mothers and mothers without DM, GDM mothers' offspring and the offspring of mothers without DM, mothers without DM and their newborns, but this effect did not reach statistical significance (p > 0.1).

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Mutation Research/Genetic Toxicology and Environmental Mutagenesis - Volume 818, June 2017, Pages 27-30
نویسندگان
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