BACKGROUND: Circadian rhythms are largely dysregulated in Major Depressive Disorder (MDD). The present review provides a summary of the findings about the role of clock genes in the etiology of MDD. METHODS:A careful search of articles on Pubmed, PsycINFO, Isi Web of Knowledge was performed in order to obtain a comprehensive review about the topic. RESULTS:The studies reported contrasting results about the association of different single nucleotide polymorphisms (SNPs) in clock genes and MDD. The most consistent result reported the association between SNP rs2287161 of CRY1 and MDD development. LIMITATIONS: Most of the published papers on the topic show bias as a prevalence of Asian ethnicity or not blinded conditions of laboratory experiments with respect to subjects' conditions (healthy controls or MDD). CONCLUSION: Further epigenetic and genome-wide studies are necessary to have a more clear idea about the role of clock genes in the etiology of MDD.

The role of clock genes in the etiology of Major Depressive Disorder / M. Buoli, M. Serati, S. Grassi, L. Pergoli, L. Cantone, A. Altamura, V. Bollati. - In: JOURNAL OF AFFECTIVE DISORDERS. - ISSN 0165-0327. - 234:(2018 Jul), pp. 351-357. [10.1016/j.jad.2017.11.015]

The role of clock genes in the etiology of Major Depressive Disorder

M. Buoli
Primo
Writing – Original Draft Preparation
;
S. Grassi;L. Pergoli;L. Cantone;A. Altamura;V. Bollati
Ultimo
Writing – Review & Editing
2018

Abstract

BACKGROUND: Circadian rhythms are largely dysregulated in Major Depressive Disorder (MDD). The present review provides a summary of the findings about the role of clock genes in the etiology of MDD. METHODS:A careful search of articles on Pubmed, PsycINFO, Isi Web of Knowledge was performed in order to obtain a comprehensive review about the topic. RESULTS:The studies reported contrasting results about the association of different single nucleotide polymorphisms (SNPs) in clock genes and MDD. The most consistent result reported the association between SNP rs2287161 of CRY1 and MDD development. LIMITATIONS: Most of the published papers on the topic show bias as a prevalence of Asian ethnicity or not blinded conditions of laboratory experiments with respect to subjects' conditions (healthy controls or MDD). CONCLUSION: Further epigenetic and genome-wide studies are necessary to have a more clear idea about the role of clock genes in the etiology of MDD.
Settore MED/25 - Psichiatria
Settore MED/44 - Medicina del Lavoro
lug-2018
Article (author)
File in questo prodotto:
File Dimensione Formato  
clock genes.pdf

accesso aperto

Tipologia: Pre-print (manoscritto inviato all'editore)
Dimensione 737.57 kB
Formato Adobe PDF
737.57 kB Adobe PDF Visualizza/Apri
Pubblicazioni consigliate

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/570367
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 22
  • ???jsp.display-item.citation.isi??? 22
social impact