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儿茶酚-O-甲基转移酶()rs4680 瓦尔 158 位蛋氨酸基因多态性与墨西哥有重度抑郁症的青少年自杀未遂的相关性研究。

Association study of Catechol-O-Methyltransferase () rs4680 Val158Met gene polymorphism and suicide attempt in Mexican adolescents with major depressive disorder.

机构信息

Departamento de Farmacogenética, Instituto Nacional de Psiquiatría "Ramón de la Fuente Muñiz", Mexico City, Mexico.

Hospital Psiquiátrico Infantil "Juan N. Navarro", Secretaría de Salud, Mexico City, Mexico.

出版信息

Nord J Psychiatry. 2022 Apr;76(3):202-206. doi: 10.1080/08039488.2021.1945682. Epub 2021 Aug 3.

Abstract

AIM

We analyzed the association between , , and genes and suicide attempt (SA) in Mexican adolescent patients with major depressive disorder (MDD).

METHODS

The sample included 197 adolescents (127 females and 70 males) with principal diagnosis of MDD. Among them, 63 patients had SA at least once and 134 had not SA. The mean age of patients with and without SA was 15±1.4 and 14±1.5years, respectively. We analyzed the genotype and allele distribution between patients with and without SA of (5HTTLPR/rs25531), (rs6275), (rs4680), and (uVNTR).

RESULTS

We did not find genotype or allele association between SA and (χ=0.67, =0.71; χ=0.07, =0.77, respectively), (χ=0.05, =0.97; χ=0.003, =0.95), and (females: χ=0.86, =0.64; χ=0, =1/males: χ=0.008, =0.92) genes. However, there were differences in genotype frequencies of /rs4680 between patients with SA and without SA (χ=11.17, =0.003). Also, we observed a high frequency of Met158 allele showing an increased risk of having presented at least one SA (χ=10.6, =0.001; OR=1.43; 95% CI, 1.17-1.74).

CONCLUSIONS

Our findings showed an association between low activity genotype and allele of Val158Met polymorphism of gene and SA in Mexican adolescents with MDD.

摘要

目的

我们分析了 、 、 和 基因与墨西哥青少年重性抑郁障碍(MDD)患者自杀未遂(SA)之间的关联。

方法

该样本包括 197 名青少年(127 名女性和 70 名男性),其主要诊断为 MDD。其中,63 名患者至少有一次 SA,134 名患者没有 SA。有 SA 和无 SA 的患者的平均年龄分别为 15±1.4 岁和 14±1.5 岁。我们分析了患者的基因型和等位基因分布,包括 (5HTTLPR/rs25531)、 (rs6275)、 (rs4680)和 (uVNTR)。

结果

我们没有发现 SA 与 (χ=0.67,=0.71;χ=0.07,=0.97,分别)、 (χ=0.05,=0.97;χ=0.003,=0.95)和 (女性:χ=0.86,=0.64;χ=0,=1/males:χ=0.008,=0.92)基因之间存在基因型或等位基因关联。然而,在有 SA 和无 SA 的患者中,/rs4680 的基因型频率存在差异(χ=11.17,=0.003)。此外,我们观察到 Met158 等位基因的高频率,表明有更高的出现至少一次 SA 的风险(χ=10.6,=0.001;OR=1.43;95% CI,1.17-1.74)。

结论

我们的研究结果表明,Val158Met 多态性 基因低活性基因型和等位基因与墨西哥青少年 MDD 患者的 SA 之间存在关联。

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