A key feature of major depressive disorder (MDD) is anhedonia, which is a predictor of response to antidepressant treatment. In order to shed light on its genetic underpinnings, we conducted a genome-wide association study (GWAS) followed by investigation of biological pathway enrichment using an anhedonia dimension for 759 patients with MDD in the GENDEP study. The GWAS identified 18 SNPs associated at genome-wide significance with the top one being an intronic SNP (rs9392549) in PRPF4B (pre-mRNA processing factor 4B) located on chromosome 6 (P = 2.07 × 10 −9 ) while gene-set enrichment analysis returned one gene ontology term, axon cargo transport (GO: 0008088) with a nominally significant P value (1.15 × 10 −5 ). Furthermore, our exploratory analysis yielded some interesting, albeit not statistically significant genetic correlation with Parkinson’s Disease and nucleus accumbens gray matter. In addition, polygenic risk scores (PRSs) generated from our association analysis were found to be able to predict treatment efficacy of the antidepressants in this study. In conclusion, we found some markers significantly associated with anhedonia, and some suggestive findings of related pathways and biological functions, which could be further investigated in other studies.

Genes associated with anhedonia: a new analysis in a large clinical trial (GENDEP) / H. Ren, C. Fabbri, R. Uher, M. Rietschel, O. Mors, N. Henigsberg, J. Hauser, A. Zobel, W. Maier, M.Z. Dernovsek, D. Souery, A. Cattaneo, G. Breen, I.W. Craig, A.E. Farmer, P. McGuffin, C.M. Lewis, K.J. Aitchison. - In: TRANSLATIONAL PSYCHIATRY. - ISSN 2158-3188. - 8:1(2018 Aug), pp. 150.1-150.11. [10.1038/s41398-018-0198-3]

Genes associated with anhedonia: a new analysis in a large clinical trial (GENDEP)

A. Cattaneo;
2018

Abstract

A key feature of major depressive disorder (MDD) is anhedonia, which is a predictor of response to antidepressant treatment. In order to shed light on its genetic underpinnings, we conducted a genome-wide association study (GWAS) followed by investigation of biological pathway enrichment using an anhedonia dimension for 759 patients with MDD in the GENDEP study. The GWAS identified 18 SNPs associated at genome-wide significance with the top one being an intronic SNP (rs9392549) in PRPF4B (pre-mRNA processing factor 4B) located on chromosome 6 (P = 2.07 × 10 −9 ) while gene-set enrichment analysis returned one gene ontology term, axon cargo transport (GO: 0008088) with a nominally significant P value (1.15 × 10 −5 ). Furthermore, our exploratory analysis yielded some interesting, albeit not statistically significant genetic correlation with Parkinson’s Disease and nucleus accumbens gray matter. In addition, polygenic risk scores (PRSs) generated from our association analysis were found to be able to predict treatment efficacy of the antidepressants in this study. In conclusion, we found some markers significantly associated with anhedonia, and some suggestive findings of related pathways and biological functions, which could be further investigated in other studies.
English
Adult; Depressive Disorder, Major; Female; Genetic Predisposition to Disease; Genome-Wide Association Study; Gray Matter; Humans; Male; Middle Aged; Multifactorial Inheritance; Nucleus Accumbens; Polymorphism, Single Nucleotide; Protein-Serine-Threonine Kinases; Regression Analysis; Ribonucleoprotein, U4-U6 Small Nuclear; Risk Assessment; Anhedonia
Settore BIO/14 - Farmacologia
Articolo
Esperti anonimi
Pubblicazione scientifica
ago-2018
Nature Publishing Group
8
1
150
1
11
11
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Periodico con rilevanza internazionale
scopus
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info:eu-repo/semantics/article
Genes associated with anhedonia: a new analysis in a large clinical trial (GENDEP) / H. Ren, C. Fabbri, R. Uher, M. Rietschel, O. Mors, N. Henigsberg, J. Hauser, A. Zobel, W. Maier, M.Z. Dernovsek, D. Souery, A. Cattaneo, G. Breen, I.W. Craig, A.E. Farmer, P. McGuffin, C.M. Lewis, K.J. Aitchison. - In: TRANSLATIONAL PSYCHIATRY. - ISSN 2158-3188. - 8:1(2018 Aug), pp. 150.1-150.11. [10.1038/s41398-018-0198-3]
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Prodotti della ricerca::01 - Articolo su periodico
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262
Article (author)
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H. Ren, C. Fabbri, R. Uher, M. Rietschel, O. Mors, N. Henigsberg, J. Hauser, A. Zobel, W. Maier, M.Z. Dernovsek, D. Souery, A. Cattaneo, G. Breen, I.W. Craig, A.E. Farmer, P. Mcguffin, C.M. Lewis, K.J. Aitchison
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/732377
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