Maternal Hemoglobin A1c in the Third-Trimester May Underestimate Maternal Hyperglycemia and Its Impact on Offspring in Perinatal Demise Associated With Gestational Diabetes Mellitus: An Autopsy Case Series.

IF 1.3 4区 医学 Q3 PATHOLOGY
Pediatric and Developmental Pathology Pub Date : 2023-09-01 Epub Date: 2023-09-06 DOI:10.1177/10935266231194697
Elaine S Chan, Rati Chadha, Lawrence de Koning
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引用次数: 0

Abstract

Introduction: Gestational diabetes mellitus (GDM) is a common metabolic disorder linked to adverse pregnancy outcomes. Recent research indicates that HbA1c is reliable in detecting maternal glycemia during the first trimester but may underestimate glucose intolerance in the late second to third trimesters. Therefore, it is reasonable to hypothesize that mothers with GDM, despite apparently normal HbA1c levels in the third trimester, may give birth to infants displaying characteristic features often seen in infants of diabetic mothers with suboptimal glycemic control. This study aimed to describe a case series of autopsy cases involving stillborn or deceased neonates delivered in the third trimester to mothers diagnosed with GDM and having normal HbA1c levels at or around the time of delivery. The primary focus was on identifying and documenting the characteristic features commonly associated with "infants of diabetic mothers" with suboptimal glycemic control in this series of cases.

Materials and methods: We conducted a retrospective review of autopsy reports from our institution spanning 7.5 years. The study included cases that met the following criteria: (1) stillborn or infants who died in the early neonatal period, delivered in the third trimester; (2) mothers diagnosed with GDM; (3) normal maternal HbA1c levels of ≤6.1% at or around the time of delivery; (4) birthweight or femoral length exceeding the 90th percentile for gestational age; and (5) absence of genetic aberrations. We also examined these cases for other characteristic features associated with "infants of diabetic mothers."

Results: Ten autopsy cases met our inclusion criteria, including 9 stillbirths and 1 neonatal death. Gestational age at delivery ranged from 32 to 39 weeks (mean: 35.7 weeks). Femoral length exceeded the 90th percentile in all cases, and 6 cases had birthweights above the 90th percentile. Puffy facies were observed in 6 cases. Among the 9 cases with complete autopsies including internal examination, 6 exhibited excess adipose tissue, 4 had cardiomegaly, and 3 showed pancreatic islet hyperplasia. Hypoxic-ischemic encephalopathy was detected in 7 cases. No structural abnormalities were noted.

Discussion: Our findings demonstrated that fetuses and neonates born to mothers with apparently normal HbA1c levels in the third trimester could still display characteristic features commonly observed in infants of diabetic mothers with poor glycemic control, also known as "infants of diabetic mothers." This study underscores the potential of third-trimester maternal HbA1c measurements to underestimate maternal glycemia and its consequential impact on fetal development, as well as the subsequent manifestation of features of "infants of diabetic mothers."

妊娠晚期的母亲血红蛋白A1c可能低估了母亲高血糖及其对与妊娠糖尿病相关的围产期死亡的后代的影响:尸检病例系列
引言:妊娠期糖尿病(GDM)是一种常见的代谢紊乱,与不良妊娠结局有关。最近的研究表明,HbA1c在妊娠早期检测母亲血糖是可靠的,但可能低估了中晚期至晚期的葡萄糖不耐受。因此,可以合理地假设,尽管妊娠晚期HbA1c水平明显正常,但患有GDM的母亲可能会生下具有血糖控制不佳的糖尿病母亲婴儿常见特征的婴儿。本研究旨在描述一系列尸检病例,涉及在妊娠晚期分娩给被诊断为GDM且在分娩时或分娩前后HbA1c水平正常的母亲的死产或死亡新生儿。主要关注点是识别和记录这一系列病例中血糖控制不理想的“糖尿病母亲的婴儿”的常见特征。材料和方法:我们对我院7.5年的尸检报告进行了回顾性审查 年。该研究包括符合以下标准的病例:(1)死产或在新生儿早期死亡的婴儿,在妊娠晚期分娩;(2) 被诊断为GDM的母亲;(3) 分娩时或分娩前后的正常母体HbA1c水平≤6.1%;(4) 出生体重或股骨长度超过胎龄第90百分位;和(5)没有遗传畸变。我们还检查了这些病例与“糖尿病母亲的婴儿”相关的其他特征。结果:10例尸检病例符合我们的纳入标准,包括9例死产和1例新生儿死亡。分娩时的妊娠年龄从32岁到39岁不等 周(平均值:35.7 周)。在所有病例中,股骨长度都超过了第90个百分位,有6例的出生体重超过了第90%。观察到6例为蓬松相。在包括内部检查在内的9例完整尸检中,6例显示脂肪组织过多,4例心脏肥大,3例显示胰岛增生。缺氧缺血性脑病7例。未发现结构异常。讨论:我们的研究结果表明,在妊娠晚期,HbA1c水平明显正常的母亲所生的胎儿和新生儿仍然可以表现出血糖控制不佳的糖尿病母亲婴儿(也称为“糖尿病母亲的婴儿”)常见的特征。“这项研究强调了孕晚期母亲HbA1c测量低估母亲血糖及其对胎儿发育的影响的潜力,以及糖尿病母亲婴儿特征的后续表现。“
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来源期刊
CiteScore
3.70
自引率
5.30%
发文量
59
审稿时长
6-12 weeks
期刊介绍: The Journal covers the spectrum of disorders of early development (including embryology, placentology, and teratology), gestational and perinatal diseases, and all diseases of childhood. Studies may be in any field of experimental, anatomic, or clinical pathology, including molecular pathology. Case reports are published only if they provide new insights into disease mechanisms or new information.
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