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遗传因素对泰国-缅甸边境地区新生儿高胆红素血症高发病率的影响。

Contribution of genetic factors to high rates of neonatal hyperbilirubinaemia on the Thailand-Myanmar border.

作者信息

Bancone Germana, Gornsawun Gornpan, Peerawaranun Pimnara, Penpitchaporn Penporn, Paw Moo Kho, Poe Day Day, Win December, Cicelia Naw, Mukaka Mavuto, Archasuksan Laypaw, Thielemans Laurence, Nosten Francois, White Nicholas J, McGready Rose, Carrara Verena I

机构信息

Shoklo Malaria Research Unit, Mahidol-Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol University, Mae Sot, Thailand.

Centre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.

出版信息

PLOS Glob Public Health. 2022 Jun 17;2(6):e0000475. doi: 10.1371/journal.pgph.0000475. eCollection 2022.

Abstract

Very high unconjugated bilirubin plasma concentrations in neonates (neonatal hyperbilirubinaemia; NH) may cause neurologic damage (kernicterus). Both increased red blood cell turn-over and immaturity of hepatic glucuronidation contribute to neonatal hyperbilirubinaemia. The incidence of NH requiring phototherapy during the first week of life on the Thailand-Myanmar border is high (approximately 25%). On the Thailand-Myanmar border we investigated the contribution of genetic risk factors to high bilirubin levels in the first month of life in 1596 neonates enrolled in a prospective observational birth cohort study. Lower gestational age (<38 weeks), mutations in the genes encoding glucose-6-phosphate dehydrogenase (G6PD) and uridine 5'-diphospho-glucuronosyltransferase (UGT) 1A1 were identified as the main independent risk factors for NH in the first week, and for prolonged jaundice in the first month of life. Population attributable risks (PAR%) were 61.7% for lower gestational age, 22.9% for hemi or homozygous and 9.9% for heterozygous G6PD deficiency respectively, and 6.3% for UGT1A16 homozygosity. In neonates with an estimated gestational age ≥ 38 weeks, G6PD mutations contributed PARs of 38.1% and 23.6% for "early" (≤ 48 hours) and "late" (49-168 hours) NH respectively. For late NH, the PAR for UGT1A16 homozygosity was 7.7%. Maternal excess weight was also a significant risk factor for "early" NH while maternal mutations on the beta-globin gene, prolonged rupture of membranes, large haematomas and neonatal sepsis were risk factors for "late" NH. For prolonged jaundice during the first month of life, G6PD mutations and UGT1A1*6 mutation, together with lower gestational age at birth and presence of haematoma were significant risk factors. In this population, genetic factors contribute considerably to the high risk of NH. Diagnostic tools to identify G6PD deficiency at birth would facilitate early recognition of high risk cases.

摘要

新生儿体内极高的非结合胆红素血浆浓度(新生儿高胆红素血症;NH)可能会导致神经损伤(核黄疸)。红细胞周转率增加和肝脏葡萄糖醛酸化不成熟均会导致新生儿高胆红素血症。在泰国 - 缅甸边境,出生后第一周需要光疗的NH发病率很高(约25%)。在泰国 - 缅甸边境,我们对参与一项前瞻性观察性出生队列研究的1596名新生儿出生后第一个月内高胆红素水平的遗传风险因素贡献进行了调查。较低的胎龄(<38周)、编码葡萄糖 - 6 - 磷酸脱氢酶(G6PD)和尿苷5'-二磷酸葡萄糖醛酸基转移酶(UGT)1A1的基因突变被确定为出生后第一周NH以及出生后第一个月内持续性黄疸的主要独立风险因素。人群归因风险(PAR%)分别为:较低胎龄61.7%,半合子或纯合子G6PD缺乏22.9%,杂合子G6PD缺乏9.9%,UGT1A16纯合子6.3%。在估计胎龄≥38周的新生儿中,G6PD突变对“早期”(≤48小时)和“晚期”(49 - 168小时)NH的PAR分别为38.1%和23.6%。对于晚期NH,UGT1A16纯合子的PAR为7.7%。母亲超重也是“早期”NH的一个重要风险因素,而母亲β - 珠蛋白基因突变、胎膜早破、巨大血肿和新生儿败血症是“晚期”NH的风险因素。对于出生后第一个月内的持续性黄疸,G6PD突变和UGT1A1*6突变,以及较低的出生胎龄和血肿的存在是重要风险因素。在这一人群中,遗传因素对NH的高风险有很大影响。出生时识别G6PD缺乏的诊断工具将有助于早期识别高危病例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ce1/10021142/796f2e6b7e1e/pgph.0000475.g001.jpg

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