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MC2R基因的遗传多态性与婴儿痉挛症促肾上腺皮质激素治疗反应性相关。

Genetic polymorphisms of MC2R gene associated with responsiveness to adrenocorticotropic hormone therapy in infantile spasms.

作者信息

Liu Zhan-Li, He Bing, Fang Fang, Tang Cai-Yun, Zou Li-Ping

机构信息

Department of Neurology, Beijing Children's Hospital, Capital Medical University, Beijing 100045, China.

出版信息

Chin Med J (Engl). 2008 Sep 5;121(17):1627-32.

Abstract

BACKGROUND

Infantile spasms is a severe epileptic encephalopathy, which is refractory to conventional antiepileptic drugs. Adrenocorticotropic hormone (ACTH) has been the major therapy for infantile spasms; however, ACTH therapy is ineffective for some patients. The variations in the receptor genes can contribute to antiepileptic drug resistance. This study was to elucidate the possible associations between the variations of the MC2R gene and ACTH responsiveness in patients with infantile spasms.

METHODS

We screened for variations in the promoter and coding region of the MC2R gene in 91 Chinese patients with infantile spasms and 94 controls, using PCR and a direct sequencing method. The frequencies of the genotypes, alleles and reconstructed haplotypes were analyzed in the cases and controls. The association between ACTH responsiveness and genetic variations of the MC2R gene was also assessed.

RESULTS

Four single nucleotide polymorphisms (SNPs) were identified in the MC2R promoter, one of which was a novel specimen at position-2 from the transcription start site ATT, -2T > C. Three SNPs (rs1893220, rs2186944 and -2T > C) showed a significant difference between the cases and controls (P < 0.05 for all). The frequency of the common TCCT haplotype carrying four-SNP major alleles was significantly lower in the cases (39%) than in the controls (60%) (P = 0.00003). The homozygous carriers of the TCCT haplotype had a much lower relative risk than the non-carriers (RR = 0.42, 95% CI 0.26-0.70, P = 0.0001). ACTH responsiveness was strongly associated with the TCCT haplotype (P = 0.000082). Compared with non-carriers of the TCCT haplotype, the homozygous and heterozygous carriers were more responsive to ACTH therapy (P = 0.0002; P = 0.0003, respectively).

CONCLUSIONS

Our results indicated that the TCCT haplotype in the MC2R promoter is strongly associated with the responsiveness of the ACTH therapy performed on patients with infantile spasms. The polymorphisms of the MC2R promoter might be one important factor that influences the efficacy of ACTH therapy on infantile spasms.

摘要

背景

婴儿痉挛症是一种严重的癫痫性脑病,对传统抗癫痫药物难治。促肾上腺皮质激素(ACTH)一直是婴儿痉挛症的主要治疗方法;然而,ACTH治疗对一些患者无效。受体基因的变异可能导致抗癫痫药物耐药。本研究旨在阐明婴儿痉挛症患者中MC2R基因变异与ACTH反应性之间的可能关联。

方法

我们采用PCR和直接测序法,对91例中国婴儿痉挛症患者和94例对照者的MC2R基因启动子和编码区变异进行筛查。分析病例组和对照组中基因型、等位基因和重建单倍型的频率。还评估了ACTH反应性与MC2R基因遗传变异之间的关联。

结果

在MC2R启动子中鉴定出4个单核苷酸多态性(SNP),其中一个是位于转录起始位点ATT上游-2处的新样本,-2T>C。3个SNP(rs1893220、rs2186944和-2T>C)在病例组和对照组之间存在显著差异(均P<0.05)。携带4个SNP主要等位基因的常见TCCT单倍型频率在病例组(39%)显著低于对照组(60%)(P=0.00003)。TCCT单倍型的纯合携带者相对风险远低于非携带者(RR=0.42,95%CI 0.26-0.70,P=0.0001)。ACTH反应性与TCCT单倍型密切相关(P=0.000082)。与TCCT单倍型非携带者相比,纯合和杂合携带者对ACTH治疗反应更强(分别为P=0.0002;P=0.0003)。

结论

我们的结果表明,MC2R启动子中的TCCT单倍型与婴儿痉挛症患者接受的ACTH治疗反应性密切相关。MC2R启动子的多态性可能是影响ACTH治疗婴儿痉挛症疗效的一个重要因素。

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