Department of Medical Genetics, Institute of Mother and Child, Warsaw, Poland.
Center for Exocrine Disorders, Department of Molecular and Cell Biology, Boston University, Henry M. Goldman School of Dental Medicine, Boston, MA, 02118, United States; Pediatric Nutritional Medicine & Else Kröner-Fresenius-Centre for Nutritional Medicine EKFZ, Technical University Munich TUM, Freising, Germany.
Pancreatology. 2022 Jun;22(5):564-571. doi: 10.1016/j.pan.2022.04.015. Epub 2022 May 1.
Non-alcoholic chronic pancreatitis (NACP) frequently develops in the setting of genetic susceptibility associated with alterations in genes that are highly expressed in the pancreas. However, the genetic basis of NACP remains unresolved in a significant number of patients warranting a search for further risk genes.
We analyzed CUZD1, which encodes the CUB and zona pellucida-like domains 1 protein that is found in high levels in pancreatic acinar cells. We sequenced the coding region in 1163 European patients and 2018 European controls. In addition, we analyzed 297 patients and 1070 controls from Japan. We analyzed secretion of wild-type and mutant CUZD1 from transfected cells using Western blotting.
In the European cohort, we detected 30 non-synonymous variants. Using different prediction tools (SIFT, CADD, PROVEAN, PredictSNP) or the combination of these tools, we found accumulation of predicted deleterious variants in patients (p-value range 0.002-0.013; OR range 3.1-5.2). No association was found in the Japanese cohort, in which 13 non-synonymous variants were detected. Functional studies revealed >50% reduced secretion of 7 variants, however, these variants were not significantly enriched in European CP patients.
Our data indicate that CUZD1 might be a novel susceptibility gene for NACP. How these variants predispose to pancreatitis remains to be elucidated.
非酒精性慢性胰腺炎(NACP)常发生于与胰腺高表达基因改变相关的遗传易感性背景下。然而,仍有相当数量的 NACP 患者的遗传基础尚未明确,需要进一步寻找风险基因。
我们分析了编码 CUB 和 zona pellucida-like 结构域 1 蛋白(在胰腺腺泡细胞中高表达)的 CUZD1 基因。我们对 1163 名欧洲患者和 2018 名欧洲对照者的编码区进行了测序。此外,我们还分析了来自日本的 297 名患者和 1070 名对照者。我们使用 Western blot 分析转染细胞中野生型和突变型 CUZD1 的分泌情况。
在欧洲队列中,我们检测到 30 个非同义变异。使用不同的预测工具(SIFT、CADD、PROVEAN、PredictSNP)或这些工具的组合,我们发现患者中预测有害变异的积累(p 值范围 0.002-0.013;OR 范围 3.1-5.2)。在日本队列中未发现关联,该队列中检测到 13 个非同义变异。功能研究显示,7 个变异的分泌减少超过 50%,然而,这些变异在欧洲 CP 患者中并未显著富集。
我们的数据表明,CUZD1 可能是 NACP 的一个新的易感基因。这些变异如何导致胰腺炎仍有待阐明。