Evidence map›Paper›PMID 25670954›Full record

ArticlePsychiatry investigation2015

CRY1 Variations Impacts on the Depressive Relapse Rate in a Sample of Bipolar Patients.

Antonio Drago, Barbara Monti, Diana De Ronchi, Alessandro Serretti

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Article in Psychiatry investigation, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Antonio DragoI.R.C.C.S. "San Giovanni di Dio", Fatebenefratelli, Brescia, Italy.
Barbara MontiDepartment of Pharmacy and Biotechnologies, University of Bologna, Bologna, Italy.
Diana De RonchiDepartment of Biomedical and Neuromotor Sciences - DIBINEM -, University of Bologna, Bologna, Italy.
Alessandro SerrettiDepartment of Biomedical and Neuromotor Sciences - DIBINEM -, University of Bologna, Bologna, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveA relevant part of the social and personal burden caused by Bipolar Disorder (BD) is related to depressive phases. Authors investigated the genetic impact of a set of variations located in CRY1, a gene involved in the control of the circadian rhythms, towards depressive episodes in a sample of bipolar patients from the STEP-BD sample. As a secondary analysis, CYR1 variations were analyzed as predictors of sleep disruption.

methods654 bipolar patients were included in the analysis. Data were available genome-wide. The part of the genome coding for the CRY1 was imputed and pruned according to standards in the field. 7 SNPs were available for the analysis. A correction for multitesting was applied and we had sufficient power (0.80) to detect a small-medium effect size (0.22) between two allelic frequencies each one represented by at least 300 subjects.

resultsIntronic rs10861688 was associated with the number of depressive events corrected for the times patients were assessed during the period of observation. In particular, AA subjects (n=21) had 4.46±3.15 events, AG (n=141) had 3.08±3.17 and GG (n=342) 2.65±2.97 (p=0.0048, beta=-0.22). No other significant associations were reported.

conclusionWe bring further evidence that genes involved in the regulation of circadian rhythms may be relevant to depressive bipolar phases. Independent confirmation analyses are mandatory.

Indexed as

Bipolar disorderCRY1Depressive episodeGeneSNP

Identifiers

PMID25670954
PMCPMC4310909

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