AUTHOR=Li Yang , Miao Yahu , Feng Qing , Zhu Weixi , Chen Yijing , Kang Qingqing , Wang Zhen , Lu Fangting , Zhang Qiu 

TITLE=Mitochondrial dysfunction and onset of type 2 diabetes along with its complications: a multi-omics Mendelian randomization and colocalization study

JOURNAL=Frontiers in Endocrinology

VOLUME=15

YEAR=2024

URL=https://www.frontiersin.org/journals/endocrinology/articles/10.3389/fendo.2024.1401531

DOI=10.3389/fendo.2024.1401531

ISSN=1664-2392

ABSTRACT=<sec><title>Background</title><p>Mitochondrial dysfunction plays a crucial role in Type 2 Diabetes Mellitus (T2DM) and its complications. However, the genetic pathophysiology remains under investigation. Through multi-omics Mendelian Randomization (MR) and colocalization analyses, we identified mitochondrial-related genes causally linked with T2DM and its complications.</p></sec><sec><title>Methods</title><p>Summary-level quantitative trait loci data at methylation, RNA, and protein levels were retrieved from European cohort studies. GWAS summary statistics for T2DM and its complications were collected from the DIAGRAM and FinnGen consortiums, respectively. Summary-data-based MR was utilized to estimate the causal effects. The heterogeneity in dependent instrument test assessed horizontal pleiotropy, while colocalization analysis determined whether genes and diseases share the same causal variant. Enrichment analysis, drug target analysis, and phenome-wide MR were conducted to further explore the biological functions, potential drugs, and causal associations with other diseases.</p></sec><sec><title>Results</title><p>Integrating evidence from multi-omics, we identified 18 causal mitochondrial-related genes. Enrichment analysis revealed they were not only related to nutrient metabolisms but also to the processes like mitophagy, autophagy, and apoptosis. Among these genes, Tu translation elongation factor mitochondrial (<italic>TUFM</italic>), 3-hydroxyisobutyryl-CoA hydrolase (<italic>HIBCH</italic>), and iron-sulfur cluster assembly 2 (<italic>ISCA2</italic>) were identified as Tier 1 genes, showing causal links with T2DM and strong colocalization evidence. <italic>TUFM</italic> and <italic>ISCA2</italic> were causally associated with an increased risk of T2DM, while <italic>HIBCH</italic> showed an inverse causal relationship. The causal associations and colocalization effects for <italic>TUFM</italic> and <italic>HIBCH</italic> were validated in specific tissues. <italic>TUFM</italic> was also found to be a risk factor for microvascular complications in T2DM patients including retinopathy, nephropathy, and neuropathy. Furthermore, drug target analysis and phenome-wide MR underscored their significance as potential therapeutic targets.</p></sec><sec><title>Conclusions</title><p>This study identified 18 mitochondrial-related genes causally associated with T2DM at multi-omics levels, enhancing the understanding of mitochondrial dysfunction in T2DM and its complications. <italic>TUFM</italic>, <italic>HIBCH</italic>, and <italic>ISCA2</italic> emerge as potential therapeutic targets for T2DM and its complications.</p></sec>