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尼日利亚尼日尔三角洲地区染色体异常的患病率及诊断困境;产前诊断是否值得?

Prevalence and diagnostic dilemma of chromosomal abnormalities in the Niger Delta area of Nigeria; Is prenatal diagnosis worthwhile?

作者信息

Abbey Mkpe, West Boma Awoala, Amadi Simeon Chijioke, Oloyede Olufemi Adebari, Horsfall Faithwin, Nonye-Enyidah Esther Ijeoma, Okagua Kenneth Eghuan, Kwosah Ngozi Joseph, Kua Paul Ledee, Iwo-Amah Rose Sitonma, Ocheche Uduak Solomon, Ononuju Chidiebere Nwakanma, Briggs Nimi Ngo, Altraide Basil Omiebi, Sapira-Ordu Leesi, Inimgba Nestor

机构信息

Department of Obstetrics and gynaecology, Rivers State University Teaching Hospital, Port Harcourt, Nigeria.

Department of Paediatrics, Rivers State University Teaching Hospital, Port Harcourt, Nigeria.

出版信息

Niger Med J. 2025 Apr 3;66(1):60-69. doi: 10.71480/nmj.v66i1.561. eCollection 2025 Jan-Feb.

Abstract

BACKGROUND

Early detection of increasing numbers of cases of chromosomal abnormalities (aneuploides) at the Rivers State University Teaching Hospital (RSUTH) in the Niger Delta will enhance appropriate counseling of patients and early termination of the affected pregnancies. The study aimed to ascertain the prevalence of aneuploides at the RSUTH and to determine the necessity for early prenatal diagnosis in the Niger Delta.

METHODOLOGY

This was a prospective cross-sectional study carried out over a three-year period (01/01/2018 - 01/01/2021) at the RSUTH, Nigeria. Newborn babies delivered at 28 weeks and above were assessed at birth for the phenotypes of aneuploidy and associated birth defects. A convenient sampling method was used to recruit all the babies with chromosomal abnormalities and their mothers. Data including that of socio-demographic, obstetric characteristics, and the fetuses were taken and analyzed using Statistical Package for Social Sciences Version 23 (SPSS version 23). Quantitative variables were summarized using means and standard deviation while qualitative variables were expressed as frequencies and proportions.

RESULTS

The total number of babies that were delivered by the 5868 participants in the study was 6078, out of which 10 cases of aneuploides were identified - 3 cases of trisomy 18 and 7 cases of Trisomy 21. The prevalence of chromosomal abnormalities at birth at the RSUTH was 0.165% of the total births, 1:2000 and 1:654 for T18 and T21 respectively. 1:654 mothers had babies with chromosomal abnormalities, 1:2000 and 1:833 for T18 and T21 respectively.Conclusion: The prevalence of chromosomal abnormalities at birth at the RSUTH of 0.165% represented a gross underestimation because the diagnosis was based on the outward phenotypical appearance of the neonates and it was made not from babies delivered at 20 weeks and above as practiced in Europe and other countries, but from 28 weeks. Prenatal diagnosis was therefore highly recommended in the Niger Delta.

摘要

背景

在尼日尔三角洲的河流州立大学教学医院(RSUTH),早期发现越来越多的染色体异常(非整倍体)病例,将有助于对患者进行适当的咨询,并尽早终止受影响的妊娠。该研究旨在确定RSUTH医院非整倍体的患病率,并确定在尼日尔三角洲进行早期产前诊断的必要性。

方法

这是一项前瞻性横断面研究,在尼日利亚的RSUTH医院进行,为期三年(2018年1月1日至2021年1月1日)。对孕周28周及以上出生的新生儿在出生时进行非整倍体表型及相关出生缺陷的评估。采用方便抽样法招募所有染色体异常的婴儿及其母亲。收集包括社会人口统计学、产科特征和胎儿数据在内的数据,并使用社会科学统计软件包第23版(SPSS 23版)进行分析。定量变量用均值和标准差进行汇总,定性变量用频率和比例表示。

结果

该研究中5868名参与者分娩的婴儿总数为6078名,其中鉴定出10例非整倍体病例——3例18三体综合征和7例21三体综合征。RSUTH医院出生时染色体异常的患病率为总出生人数的0.165%,18三体综合征和21三体综合征分别为1:2000和1:654。1:654的母亲生育了染色体异常的婴儿,18三体综合征和21三体综合征分别为1:2000和1:833。

结论

RSUTH医院出生时染色体异常的患病率为0.165%,这是一个严重的低估,因为诊断是基于新生儿的外在表型,而且不是像欧洲和其他国家那样对孕周20周及以上出生的婴儿进行诊断,而是对孕周28周及以上出生的婴儿进行诊断。因此,强烈建议在尼日尔三角洲进行产前诊断。

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