Nonsynonymous Variation in NKPD1 Increases Depressive Symptoms in European Populations

Najaf Amin, Nadezhda M. Belonogova, Olivera Jovanova, Rutger W.W. Brouwer, Jeroen G.J. van Rooij, Mirjam C.G.N. van den Hout, Gulnara R. Svishcheva, Robert Kraaij, Irina V. Zorkoltseva, Anatoly V. Kirichenko, Albert Hofman, André G. Uitterlinden, Wilfred F.J. van IJcken, Henning Tiemeier, Tatiana I. Axenovich, Cornelia M. van Duijn

Результат исследования: Научные публикации в периодических изданияхстатья

12 Цитирования (Scopus)

Аннотация

Background Despite high heritability, little success was achieved in mapping genetic determinants of depression-related traits by means of genome-wide association studies. Methods To identify genes associated with depressive symptomology, we performed a gene-based association analysis of nonsynonymous variation captured using exome-sequencing and exome-chip genotyping in a genetically isolated population from the Netherlands (n = 1999). Finally, we reproduced our significant findings in an independent population-based cohort (n = 1604). Results We detected significant association of depressive symptoms with a gene NKPD1 (p = 3.7 × 10−08). Nonsynonymous variants in the gene explained 0.9% of sex- and age-adjusted variance of depressive symptoms in the discovery study, which is translated into 3.8% of the total estimated heritability (h2 = 0.24). Significant association of depressive symptoms with NKPD1 was also observed (n = 1604; p = 1.5 × 10−03) in the independent replication sample despite little overlap with the discovery cohort in the set of nonsynonymous genetic variants observed in the NKPD1 gene. Meta-analysis of the discovery and replication studies improved the association signal (p = 1.0 × 10−09). Conclusions Our study suggests that nonsynonymous variation in the gene NKPD1 affects depressive symptoms in the general population. NKPD1 is predicted to be involved in the de novo synthesis of sphingolipids, which have been implicated in the pathogenesis of depression.

Язык оригиналаанглийский
Страницы (с-по)702-707
Число страниц6
ЖурналBiological Psychiatry
Том81
Номер выпуска8
DOI
СостояниеОпубликовано - 15 апр 2017

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