阿尔及利亚人群尿道下裂的潜在风险因素及与 DICER1 (rs3742330) A>G 变异的负相关:病例对照研究。

IF 1.6 4区 医学 Q4 DEVELOPMENTAL BIOLOGY Birth Defects Research Pub Date : 2024-05-27 DOI:10.1002/bdr2.2365
Laouar Rania, Chellat Djalila, Djoudi Brahim, Achou Rayene, Horchi Meroua, Touabti Souhem, Atrih Zoubir, Choutri Hichem, Boukri Asma, Satta Dalila, Sifi Karima
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引用次数: 0

摘要

背景:尿道下裂仍然是影响男性外生殖器的一种常见先天性畸形,其特点是病因不明,治疗方法复杂。本研究旨在调查尿道下裂的相关风险因素,并探讨其与 DICER1 rs3742330 变异的遗传联系:研究包括两组:105 名尿道下裂男童和 111 名健康男童作为匹配对照。对所有患者和对照组进行了详细的病史和体格检查。利用PCR-限制性片段长度多态性鉴定DICER1 rs3742330变异,分析基因型分布和等位基因频率。逻辑回归分析估计了尿道下裂的风险因素:尿道下裂患者的平均年龄为(4.56 ± 2.50)岁。尿道下裂最常见的类型是前尿道下裂,有 60 名患儿(57.14%)。宫内生长受限、高龄产妇和妊娠高血压被认为是尿道下裂的重要风险因素(分别为 p = .011、p = .016 和 p = .041)。在基因研究方面,病例组和对照组的 DICER1 rs3742330 变体的基因型和等位基因频率均无明显差异:结论:在阿尔及利亚人群中,DICER1 基因 rs3742330 变体与尿道下裂病例没有关联。然而,多变量逻辑回归分析发现,早产、低出生体重、宫内生长受限、高龄产妇、妊娠糖尿病和农村居民是尿道下裂最重要的独立预测因素。
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Potential risk factors for hypospadias and negative correlation with DICER1 (rs3742330) A>G variant in Algerian population: A case-control study

Background

Hypospadias continues to be a prevalent congenital anomaly affecting the male external genitalia, characterized by an unclear origin and complex treatment approaches. This study aimed to investigate the risk factors associated with hypospadias and explore its genetic link with the DICER1 rs3742330 variant.

Methods

The study involved two groups: 105 male children with hypospadias and 111 healthy male children as matched controls. Detailed history and physical examinations were conducted for all patients and controls. PCR-restriction fragment length polymorphism was utilized to identify the DICER1 rs3742330 variant, analyzing genotype distribution and allele frequency. Logistic regression analysis estimated the risk factors for hypospadias.

Results

The mean age in the hypospadias group was 4.56 ± 2.50 years. The most prevalent type of hypospadias observed was the anterior type in 60 children (57.14%). Intrauterine growth restriction, advanced maternal age, and gestational hypertension were identified as significant risk factors for hypospadias (p = .011, p = .016, and p = .041, respectively). Regarding the genetic study, no significant difference was found in both genotype and allele frequencies of the DICER1 rs3742330 variant between case and control groups.

Conclusions

The rs3742330 variant in the DICER1 gene showed no association with hypospadias cases in the Algerian population. However, multivariate logistic regression analysis identified preterm birth, low birth weight, intrauterine growth restriction, advanced maternal age, gestational diabetes, and rural residence as the most significant independent predictors for hypospadias.

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来源期刊
Birth Defects Research
Birth Defects Research Medicine-Embryology
CiteScore
3.60
自引率
9.50%
发文量
153
期刊介绍: The journal Birth Defects Research publishes original research and reviews in areas related to the etiology of adverse developmental and reproductive outcome. In particular the journal is devoted to the publication of original scientific research that contributes to the understanding of the biology of embryonic development and the prenatal causative factors and mechanisms leading to adverse pregnancy outcomes, namely structural and functional birth defects, pregnancy loss, postnatal functional defects in the human population, and to the identification of prenatal factors and biological mechanisms that reduce these risks. Adverse reproductive and developmental outcomes may have genetic, environmental, nutritional or epigenetic causes. Accordingly, the journal Birth Defects Research takes an integrated, multidisciplinary approach in its organization and publication strategy. The journal Birth Defects Research contains separate sections for clinical and molecular teratology, developmental and reproductive toxicology, and reviews in developmental biology to acknowledge and accommodate the integrative nature of research in this field. Each section has a dedicated editor who is a leader in his/her field and who has full editorial authority in his/her area.
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