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妊娠期糖尿病的亚型与新生儿及儿童期代谢结局存在不同关联。

Subtypes of Gestational Diabetes Mellitus Are Differentially Associated With Newborn and Childhood Metabolic Outcomes.

作者信息

Osmulski Meredith E, Yu Yuanzhi, Kuang Alan, Josefson Jami L, Hivert Marie-France, Scholtens Denise M, Lowe William L

机构信息

Department of Medicine, Feinberg School of Medicine, Northwestern University, Chicago, IL.

Department of Preventive Medicine, Feinberg School of Medicine, Northwestern University, Chicago, IL.

出版信息

Diabetes Care. 2025 Mar 1;48(3):390-399. doi: 10.2337/dc24-1735.

DOI:10.2337/dc24-1735
PMID:39787502
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11870284/
Abstract

OBJECTIVE

Subtypes of gestational diabetes mellitus (GDM) based on insulin sensitivity and secretion have been described. We addressed the hypothesis that GDM subtypes are differentially associated with newborn and child anthropometric and glycemic outcomes.

RESEARCH DESIGN AND METHODS

Newborn and child (age 11-14 years) outcomes were examined in 7,970 and 4,160 mother-offspring dyads, respectively, who participated in the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) study and HAPO Follow-Up Study. GDM was classified as insulin-deficient GDM (insulin secretion <25th percentile with preserved insulin sensitivity), insulin-resistant GDM (insulin sensitivity <25th percentile with preserved insulin secretion), or mixed-defect GDM (both <25th percentile). Regression models for newborn and child outcomes included adjustment for field center, maternal BMI, and other pregnancy covariates. Child models also included adjustment for child age, sex, and family history of diabetes.

RESULTS

Compared with mothers with normal glucose tolerance, all three GDM subtypes were associated with birth weight and sum of skinfolds >90th percentile. Insulin-resistant and mixed-defect GDM were associated with higher risk of cord C-peptide levels >90th percentile. Insulin-resistant GDM was associated with higher risk of neonatal hypoglycemia. Insulin-resistant GDM was associated with higher risk of neonatal hypoglycemia and childhood obesity (odds ratio [OR] 1.53, 95% CI 1.127-2.08). The risk of childhood impaired glucose tolerance was higher with insulin-resistant GDM (OR 2.21, 95% CI 1.50-3.25) and mixed-defect GDM (OR 3.01, 95% CI 1.47-6.19).

CONCLUSIONS

GDM subtypes are differentially associated with newborn and childhood outcomes. Better characterizing individuals with GDM could help identify at-risk offspring to offer targeted, preventative interventions early in life.

摘要

目的

基于胰岛素敏感性和分泌情况对妊娠期糖尿病(GDM)的亚型进行了描述。我们探讨了GDM亚型与新生儿及儿童人体测量指标和血糖结局存在差异关联的这一假设。

研究设计与方法

分别在7970对母婴和4160对母婴中检查了新生儿及儿童(11 - 14岁)的结局,这些母婴参与了高血糖与不良妊娠结局(HAPO)研究及HAPO随访研究。GDM被分类为胰岛素缺乏型GDM(胰岛素分泌低于第25百分位数且胰岛素敏感性正常)、胰岛素抵抗型GDM(胰岛素敏感性低于第25百分位数且胰岛素分泌正常)或混合型缺陷GDM(两者均低于第25百分位数)。针对新生儿及儿童结局的回归模型对现场中心、母亲体重指数(BMI)及其他妊娠协变量进行了校正。儿童模型还对儿童年龄、性别及糖尿病家族史进行了校正。

结果

与糖耐量正常的母亲相比,所有三种GDM亚型均与出生体重及皮褶厚度总和高于第90百分位数相关。胰岛素抵抗型和混合型缺陷GDM与脐血C肽水平高于第90百分位数的风险更高相关。胰岛素抵抗型GDM与新生儿低血糖风险更高相关。胰岛素抵抗型GDM与新生儿低血糖和儿童期肥胖风险更高相关(优势比[OR]为1.53,95%置信区间[CI]为1.127 - 2.08)。胰岛素抵抗型GDM(OR为2.21,95% CI为1.50 - 3.25)和混合型缺陷GDM(OR为3.01,95% CI为1.47 - 6.19)的儿童糖耐量受损风险更高。

结论

GDM亚型与新生儿及儿童期结局存在差异关联。更好地对GDM个体进行特征描述有助于识别高危后代,以便在生命早期提供有针对性的预防性干预措施。

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本文引用的文献

1
Genetics of glucose homeostasis in pregnancy and postpartum.妊娠期及产后血糖稳态的遗传学。
Diabetologia. 2024 Dec;67(12):2726-2739. doi: 10.1007/s00125-024-06256-8. Epub 2024 Aug 24.
2
Maternal serum branched-chain amino acids in early pregnancy and offspring growth patterns from 1 year to 8 years of age.孕早期母体血清支链氨基酸与1至8岁后代的生长模式
Chin Med J (Engl). 2024 Aug 5;137(15):1876-1878. doi: 10.1097/CM9.0000000000002967. Epub 2024 Feb 26.
3
Metabolomic and genetic architecture of gestational diabetes subtypes.
妊娠期糖尿病亚型的代谢组学和遗传结构。
Diabetologia. 2024 May;67(5):895-907. doi: 10.1007/s00125-024-06110-x. Epub 2024 Feb 17.
4
Understanding risk and causal mechanisms for developing obesity in infants and young children: A National Institutes of Health workshop.了解婴儿和幼儿肥胖症发展的风险和因果机制:美国国立卫生研究院研讨会。
Obes Rev. 2024 Apr;25(4):e13690. doi: 10.1111/obr.13690. Epub 2024 Jan 11.
5
An unwelcome inheritance: childhood obesity after diabetes in pregnancy.不受欢迎的遗产:妊娠糖尿病后的儿童肥胖。
Diabetologia. 2023 Nov;66(11):1961-1970. doi: 10.1007/s00125-023-05965-w. Epub 2023 Jul 13.
6
Association of Maternal Metabolites and Metabolite Networks with Newborn Outcomes in a Multi-Ancestry Cohort.多血统队列中母体代谢物及代谢物网络与新生儿结局的关联
Metabolites. 2023 Mar 31;13(4):505. doi: 10.3390/metabo13040505.
7
Associations of maternal insulin sensitivity during pregnancy with childhood central adiposity in the Genetics of Glucose regulation in Gestation and Growth (Gen3G) cohort.妊娠期母体胰岛素敏感性与遗传与妊娠及生长中葡萄糖调节研究(Gen3G)队列中儿童中心性肥胖的相关性。
Pediatr Obes. 2023 Feb;18(2):e12982. doi: 10.1111/ijpo.12982. Epub 2022 Oct 11.
8
Trends and Characteristics in Gestational Diabetes: United States, 2016-2020.妊娠期糖尿病的趋势和特征:美国,2016-2020 年。
Natl Vital Stat Rep. 2022 Jul;71(3):1-15.
9
A Clinical Update on Gestational Diabetes Mellitus.妊娠期糖尿病的临床新进展。
Endocr Rev. 2022 Sep 26;43(5):763-793. doi: 10.1210/endrev/bnac003.
10
Physiological subtypes of gestational glucose intolerance and risk of adverse pregnancy outcomes.妊娠糖代谢异常的生理亚型与不良妊娠结局的风险。
Am J Obstet Gynecol. 2022 Feb;226(2):241.e1-241.e14. doi: 10.1016/j.ajog.2021.08.016. Epub 2021 Aug 19.