尼日利亚南南孕妇对孕前基因型筛查的认识和接受情况

Ngozi Roy Maduka, Paul O. Okubor
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摘要

镰状细胞病(SCD)是一种世界性的遗传性遗传病。尼日利亚被认为是该疾病的中心,每年出生的SCD婴儿数量很高。一旦两对杂合夫妇结合,生出SCD婴儿的风险仍然很高;因此,在结婚和受孕前了解自己的基因型是非常必要的。目前,只有教堂坚持在结婚前进行基因检测。结果是一对杂合子夫妇之间的婚姻,极有可能生下SCD婴儿。这项横断面研究调查了430连续同意产前门诊客户提出预约在中心医院,阿格博尔,三角洲州,尼日利亚。这些妇女完成了一份调查问卷,问卷内容包括社会人口学属性、对SCD及其基因型的认识、对伴侣基因型的认识、信息来源以及改善孕前基因型筛查的方法。年龄在25-34岁之间的人占研究人口的68.1%,其中大多数(95.1%)信仰基督教。已婚妇女占90.1%。只有55.1%的参与者在受孕前知道自己的基因型。高等教育程度、是否为基督徒、婚姻状况、婚姻类型显著影响患者对自身基因型的认知。他们中的大多数人从健康专业人员那里听说过基因型筛查(30.5%),而他们中许多人进行基因型筛查的最常见原因是为了入学(13.3%),为了知识(12.1%)和结婚(24.7%)。建议的有助于增加基因型筛查的一些方法包括社区会议、短信和WhatsApp消息、电视和广播消息。尽管尼日利亚仍然是世界上SCD的中心,但孕前基因型筛查的使用率仍然很低。政府、卫生工作者、教会和婚姻顾问以及社区在提高对孕前基因型筛查的认识和接受方面可发挥重要作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Awareness and uptake of pre-conceptional genotype screening among pregnant women in South-South Nigeria
Sickle Cell Disease (SCD) is an inheritable genetic disease occurring worldwide. Nigeria is regarded as the epicenter of the disease, with a high number of SCD babies born annually. The risk of having an SCD baby remains high once there is a union between two heterozygous couple; therefore, it is imperative for intending couples to know their genotypes before marriage and conception. Currently, it is only the churches that insist on genotype before marriage. The result subsequently is a marriage between a heterozygous couple with a high possibility of the birth of an SCD baby. This cross-sectional study surveyed 430 consecutive consenting antenatal clinic clients presenting for booking in Central Hospital, Agbor, Delta State, Nigeria. The women completed a questionnaire with sections on sociodemographic attributes, awareness of their SCD and their genotype, awareness of their partner’s genotype, source of information, and ways to improve uptake of preconception genotype screening. The age range 25-34 years constituted 68.1% of the study population, with the majority of them (95.1%) of the Christian faith. Married women form 90.1% of the participants. Only 55.1% of the participants were aware of their genotype before conception. Higher education, being a Christian, marital status, and the type of marriage significantly affected patients’ awareness of their genotype. The majority of them heard about genotype screening from a health professional (30.5%), while the commonest reasons why many of them did genotype screening were for school admission 13.3%, for knowledge’s sake (12.1%) and as a requirement for marriage (24.7%). Some of the ways suggested to help increase the uptake of genotype screening include community meetings, text and WhatsApp messages, television and radio messages. Despite the fact that Nigeria remains the epicenter of SCD in the world, the uptake of preconception genotype screening is still low. The government, health workers, churches and marriage counselors, and the community have a major role to play in increasing the awareness and uptake of preconception genotype screening.
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