Comorbidity of Novel Gene Variants in Type 2 Diabetes and Depression.

Journal: International journal of molecular sciences

Volume: 23

Issue: 17

Year of Publication: 2022

Affiliated Institutions:  Institut National de la Santé et de la Recherche Médicale (INSERM), US-Orphanet, Paris, France. Laboratory of Statistical Genetics, Rockefeller University, New York, NY , USA. Department of Genetics, Rutgers University, Piscataway, NJ , USA. Department of Public Health Sciences, Penn State College of Medicine, Hershey, PA , USA. Mood and Anxiety Program, Department of Psychiatry, University of Maryland School of Medicine, Baltimore, MD , USA. Department of Psychiatry and Human Behavior, Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, PA , USA.

Abstract summary 

The corticotropin-releasing hormone receptor 2 () gene encodes CRHR2, contributing to the hypothalamic-pituitary-adrenal stress response and to hyperglycemia and insulin resistance. mice are hypersensitive to stress, and the locus has been linked to type 2 diabetes and depression. While variants confer risk for mood disorders, MDD, and type 2 diabetes, they have not been investigated in familial T2D and MDD. In 212 Italian families with type 2 diabetes and depression, we tested 17 single nucleotide polymorphisms (SNPs), using two-point parametric-linkage and linkage-disequilibrium (i.e., association) analysis (models: dominant-complete-penetrance-D1, dominant-incomplete-penetrance-D2, recessive-complete-penetrance-R1, recessive-incomplete-penetrance-R2). We detected novel linkage/linkage-disequilibrium/association to/with depression (3 SNPs/D1, 2 SNPs/D2, 3 SNPs/R1, 3 SNPs/R2) and type 2 diabetes (3 SNPs/D1, 2 SNPs/D2, 2 SNPs/R1, 1 SNP/R2). All detected risk variants are novel. Two depression-risk variants within one linkage-disequilibrium block replicate each other. Two independent novel SNPs were comorbid while the most significant conferred either depression- or type 2 diabetes-risk. Although the families were primarily ascertained for type 2 diabetes, depression-risk variants showed higher significance than type 2 diabetes-risk variants, implying has a stronger role in depression-risk than type 2 diabetes-risk. In silico analysis predicted variants' dysfunction. is for the first time linked to/in linkage-disequilibrium/association with depression-type 2 diabetes comorbidity and may underlie the shared genetic pathogenesis via pleiotropy.

Authors & Co-authors:  Amin Mutaz M Ott Jurg J Gordon Derek D Wu Rongling R Postolache Teodor T TT Vergare Michael M Gragnoli Claudia C

Study Outcome 

Source Link: Visit source

Statistics
Citations :  Smith S.M., Vale W.W. The role of the hypothalamic-pituitary-adrenal axis in neuroendocrine responses to stress. Dialogues Clin. Neurosci. 2006;8:383. doi: 10.31887/DCNS.2006.8.4/ssmith.
Authors :  7
Identifiers
Doi : 9819
SSN : 1422-0067
Study Population
Male,Female
Mesh Terms
Animals
Other Terms
association;corticotropin-releasing hormone receptor 2 (CRHR2);cortisol;hypothalamic–pituitary–adrenal (HPA);linkage;linkage disequilibrium (LD);major depressive disorder (MDD);stress;type 2 diabetes (T2D)
Study Design
Study Approach
Country of Study
Publication Country
Switzerland