Scholarlink

Background <p>Interventions to prevent type 1 diabetes (T1D), an immune-mediated disease requiring lifelong treatment, remain limited. We sought to identify novel therapeutic targets for T1D through Mendelian randomization and colocalization using immune cell-derived instruments.</p> Methods <p>We selected locally acting genetic variants from 14 transcriptomic studies to instrument expression of 8998 genes measured in immune cell types. Outcome associations were obtained from a T1D genome-wide association study that included 18,942 cases and 501,638 controls. Follow-up analyses included assessments of horizontal pleiotropy and novelty, as well as phenome-wide scans with colocalization (PheWAS-coloc) of instrumental variants.</p> Results <p>We prioritized 21 genes (<i>CLNK</i>, <i>EED</i>, <i>LZTFL1</i>, <i>MGAT4A</i>, <i>NAA38</i>, <i>NFKB1</i>, <i>PHACTR4</i>, <i>PHLPP2</i>, <i>PLEKHA1</i>, <i>P2RY12</i>, <i>REST</i>, <i>RGS14</i>, <i>SERPINB6</i>, <i>SESN3</i>, <i>SLC25A29</i>, <i>SPAG1</i>, <i>STIM2</i>, <i>THEMIS</i>, <i>TMEM80</i>, <i>VSIR</i>, <i>ZNF217</i>) that have not been identified in previous T1D genome-wide association studies. Notably, higher genetically predicted <i>VSIR</i> (encoding the immune checkpoint protein VISTA) was associated with decreased risk of T1D, providing human genetic support that complements existing animal-model evidence for VISTA’s protective role in autoimmune diseases. We also prioritized <i>P2RY12</i>, which is targeted by several approved drugs, revealing a possible repurposing opportunity. PheWAS-coloc analyses further linked <i>P2RY12</i> expression to Epstein-Barr virus EBNA-1 antibody levels, implicating a pathway relevant to autoimmunity.</p> Conclusions <p>Our findings provide novel avenues for drug development and repurposing to prevent or delay T1D onset.</p>

错误：搜索内容不能为空，请输入英文关键词
错误：关键词超出字数限制，请精简
高级检索

Immune cell-based transcriptomic Mendelian randomization and colocalization study on type 1 diabetes

  • 期刊论文

  • 出版模式：

    开放获取

  • 发表日期：

    2025年11月26日

查看全文
  • Julie Sklar,
  • David Stacey,
  • Grace Nickel,
  • Adam S. Butterworth,
  • Elias Allara,
  • Liam Gaziano

摘要

Background

Interventions to prevent type 1 diabetes (T1D), an immune-mediated disease requiring lifelong treatment, remain limited. We sought to identify novel therapeutic targets for T1D through Mendelian randomization and colocalization using immune cell-derived instruments.

Methods

We selected locally acting genetic variants from 14 transcriptomic studies to instrument expression of 8998 genes measured in immune cell types. Outcome associations were obtained from a T1D genome-wide association study that included 18,942 cases and 501,638 controls. Follow-up analyses included assessments of horizontal pleiotropy and novelty, as well as phenome-wide scans with colocalization (PheWAS-coloc) of instrumental variants.

Results

We prioritized 21 genes (CLNK, EED, LZTFL1, MGAT4A, NAA38, NFKB1, PHACTR4, PHLPP2, PLEKHA1, P2RY12, REST, RGS14, SERPINB6, SESN3, SLC25A29, SPAG1, STIM2, THEMIS, TMEM80, VSIR, ZNF217) that have not been identified in previous T1D genome-wide association studies. Notably, higher genetically predicted VSIR (encoding the immune checkpoint protein VISTA) was associated with decreased risk of T1D, providing human genetic support that complements existing animal-model evidence for VISTA’s protective role in autoimmune diseases. We also prioritized P2RY12, which is targeted by several approved drugs, revealing a possible repurposing opportunity. PheWAS-coloc analyses further linked P2RY12 expression to Epstein-Barr virus EBNA-1 antibody levels, implicating a pathway relevant to autoimmunity.

Conclusions

Our findings provide novel avenues for drug development and repurposing to prevent or delay T1D onset.