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在自噬基因中,ATG16L1 而非 IRGM 与伊朗人的克罗恩病有关。

Among autophagy genes, ATG16L1 but not IRGM is associated with Crohn's disease in Iranians.

机构信息

Digestive Disease Research Center, Tehran University of Medical Sciences, Tehran, Iran; Molecular Medicine Department, Pasteur Institute of Iran, Tehran, Iran.

Molecular Medicine Department, Pasteur Institute of Iran, Tehran, Iran.

出版信息

Gene. 2018 Oct 30;675:176-184. doi: 10.1016/j.gene.2018.06.074. Epub 2018 Jun 28.

Abstract

BACKGROUND

The prevalence of inflammatory bowel diseases is uprising in countries like Iran. Genetic predisposing elements play prominent role in the pathogenesis of Crohn's disease. In this study we studied the role of autophagy genes like IRGM (Immunity related GTPase M) and ATG16L1 (Autophagy related 16 like 1) in the pathogenesis of Crohn's Disease in Iranian patients.

METHODS

One hundred thirty-eight patients and 99 normal controls were recruited in this study. Polymorphisms in -1644 and -308 upstream of IRGM gene were studied by PCR-sequencing and 20 kb CNVdel/insertion was studied by specific PCR. Rs10065171, rs4958847 in IRGM gene and rs2241880 in ATG16L1 were studied by Taqman genotyping assays.

RESULTS

None of the so-called predisposing alleles of IRGM gene predispose Iranians to Crohn's disease while the prevalence of some of them like CNV deletion was higher in normal controls. Surprisingly all the so-called predisposing alleles in IRGM were linked to each other (especially rs4958847 with rs10065172 and polymorphisms in -308 region with rs4958847). Patients harboring A allele in rs4958847 site showed higher ratio of fibrostenotic type of disease while in patients with C/T genotype in rs4958847, colonic involvement was seen more frequently. G allele in ATG16L1 was associated with Crohn's disease though it was not associated with any phenotypic manifestation.

CONCLUSION

In our study the association of ATG16L1 to Crohn's disease in Iranian patients was confirmed while it was shown that the studied polymorphisms in IRGM was not associated with Crohn's disease. Therefore in order to have a better picture about the genetics of Crohn's disease in Iranian patients, it is recommended to study other clinically effective polymorphisms in IRGM and ATG16L1 in addition to other genes which are responsible for the process of autophagy.

摘要

背景

在伊朗等国家,炎症性肠病的患病率正在上升。遗传易感因素在克罗恩病的发病机制中起着重要作用。在这项研究中,我们研究了自噬基因 IRGM(免疫相关 GTP 酶 M)和 ATG16L1(自噬相关 16 样 1)在伊朗患者克罗恩病发病机制中的作用。

方法

本研究纳入 138 例患者和 99 例正常对照。通过 PCR 测序研究了 IRGM 基因启动子-1644 和-308 位的多态性,通过特异性 PCR 研究了 20kb CNVdel/insertion。采用 Taqman 基因分型检测 IRGM 基因中的 rs10065171、rs4958847 和 ATG16L1 中的 rs2241880。

结果

IRGM 基因的所谓易感等位基因均不能使伊朗人易患克罗恩病,而某些等位基因如 CNV 缺失在正常对照中更为常见。令人惊讶的是,IRGM 中的所有所谓易感等位基因彼此相关(尤其是 rs4958847 与 rs10065172 和 -308 区域的多态性与 rs4958847)。携带 rs4958847 位点 A 等位基因的患者纤维化狭窄型疾病比例较高,而 rs4958847 为 C/T 基因型的患者结肠受累更为常见。ATG16L1 中的 G 等位基因与克罗恩病相关,尽管它与任何表型表现无关。

结论

在本研究中,证实了 ATG16L1 与伊朗患者克罗恩病的关联,同时表明研究中 IRGM 的多态性与克罗恩病无关。因此,为了更好地了解伊朗患者克罗恩病的遗传学,建议除了研究其他负责自噬过程的基因外,还研究 IRGM 和 ATG16L1 中其他具有临床意义的多态性。

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