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早发性射精与多巴胺转运体基因(SLC6A3)遗传多态性的关系。

Relationship between premature ejaculation and genetic polymorphisms of the dopamine transporter gene (SLC6A3).

机构信息

Private Practice of Urology and Andrology, Tehran, Iran.

出版信息

BJU Int. 2011 Jul;108(2):292-6. doi: 10.1111/j.1464-410X.2010.09809.x. Epub 2010 Nov 2.

Abstract

OBJECTIVE

• To investigate the possible relationships between premature ejaculation (PE) polymorphisms in the dopamine transporter (DAT) gene (SLC6A3, DAT1), which has a polymorphic 40 base pair (40 bp) variable number of tandem repeats (VNTR) sequence in the 3'-untranslated region (3' VNTR).

PATIENTS AND METHODS

• Cohorts of 270 Iranian men with PE and 266 age-matched healthy Iranian subjects were genotyped for the DAT1-VNTR polymorphism.

RESULTS

• The 10-repeat allele frequencies were similar in the control (90.2%) and patient groups (88.5%) (P = 0.8). • A statistically significant association was observed between the presence of the nine-repeat allele and PE (chi-squared test = 4.346, odds ratio [OR] = 2.46, 95% confidence interval [CI] = 1.57-3.15, P = 0.026). • The frequencies of the 9/10 genotype were also significantly higher in the PE patients than in normal controls (chi-squared test = 4.466, OR = 2.47, 95% CI = 1.52-3.21, P = 0.028). The presence of the seven-repeat allele had a protective effect against PE (chi-squared test = 2.324, OR = 0.62, 95% CI = 0.47-0.89, P = 0.034).

CONCLUSIONS

• The findings of the present study suggest that DAT1-VNTR polymorphisms resulting in higher dopamine concentrations were associated with vulnerability to PE. • Further studies are needed to replicate these results and to evaluate the role of inconsistency in the DAT genes and how this affects the development of PE.

摘要

目的

研究多巴胺转运体(DAT)基因(SLC6A3,DAT1)中可能与早泄(PE)相关的多态性,该基因在 3'非翻译区(3'VNTR)有一个 40 个碱基对(40bp)的可变串联重复(VNTR)序列多态性。

患者和方法

对 270 名伊朗 PE 男性患者和 266 名年龄匹配的伊朗健康对照者进行 DAT1-VNTR 多态性基因分型。

结果

对照组(90.2%)和患者组(88.5%)中 10 重复等位基因频率相似(P=0.8)。在存在 9 重复等位基因与 PE 之间观察到统计学显著相关性(卡方检验=4.346,比值比[OR]=2.46,95%置信区间[CI]为 1.57-3.15,P=0.026)。PE 患者中 9/10 基因型的频率也显著高于正常对照组(卡方检验=4.466,OR=2.47,95%CI=1.52-3.21,P=0.028)。7 重复等位基因的存在对 PE 有保护作用(卡方检验=2.324,OR=0.62,95%CI=0.47-0.89,P=0.034)。

结论

本研究结果表明,导致多巴胺浓度升高的 DAT1-VNTR 多态性与易患 PE 相关。需要进一步研究来复制这些结果,并评估 DAT 基因不一致性的作用以及这如何影响 PE 的发展。

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