scholarly journals Polygenic risk score for bipolar disorder associates with divergent thinking and brain structures in the prefrontal cortex

2021 ◽  
Author(s):  
Hikaru Takeuchi ◽  
Ryosuke Kimura ◽  
Hiroaki Tomita ◽  
Yasuyuki Taki ◽  
Yoshie Kikuchi ◽  
...  
2020 ◽  
Author(s):  
Nagahide Takahashi ◽  
Hanae Tainaka ◽  
Tomoko Nishimura ◽  
Taeko Harada ◽  
Akemi Okumura ◽  
...  

Abstract BackgroundPostpartum depression (PPD) is a common and highly heritabledisorder in the postnatal period of new mothers. The development of PPD is shown to affectneurodevelopment in children and recent evidence suggests thatthe trajectory of PPDisalso associated with children’s neurodevelopment and mental conditions. Thus, early identification and intervention for individuals at high risk of PPD are urgently needed.Additionally, it is not clear whether genetic factors affect thetrajectory of PPD. Therefore, using a polygenic risk score (PRS) approach, we investigated if PRS for depression (Depression-PRS) and bipolar disorder (Bipolar-PRS) are associated with the development and clinical course of PPD.Methods Usingrecent large genome-wide association studies(GWAS) of depression and bipolar disorder as discovery cohorts, we calculatedDepression-PRS and Bipolar-PRS in each individual. Then, we investigated the possible association between Depression-PRS and Bipolar-PRS with the development andtrajectory of PPD insubjects from the Hamamatsu Birth Cohort for mothers and children (n = 136). Depressive symptoms were assessed using the Edinburgh Postpartum Depression Scale. Gene-set enrichment analyses were used to identify pathways underlying these conditions. ResultsDepression-PRS was significantly higher in subjects with PPD than in those without PPD(t = -3.283, P = 0.002)and logistic analysis showed that Depression-PRS significantly increases therisk of developing PPD(OR [SE] = 2.274 [0.585], P = 0.002). Furthermore, Depression-PRS was positively associated with continuity of PPD (β [SE]=1.621 [0.672]; P = 0.032).Gene-set enrichment analyses revealed that pathways such as“response to hormone”(β[SE] -2.285[1.002], P < 0.001) and “epigenetic regulation”(β[SE] 2.831 [1.317], P < 0.001) were involved in the continuity of PPD. ConclusionThese preliminary findings indicate that the genetic component plays an important role not only in the development but also inthe continuity of PPD. A polygenic risk score approach could be useful to identify subjects at risk for PPD, especially for persistent PPD,who needcareful monitoring and intervention after delivery.


2019 ◽  
Vol 14 (4) ◽  
pp. 507-511 ◽  
Author(s):  
Carlo Maj ◽  
Sarah Tosato ◽  
Roberta Zanardini ◽  
Antonio Lasalvia ◽  
Angela Favaro ◽  
...  

Author(s):  
Boris Birmaher ◽  
Danella Hafeman ◽  
John Merranko ◽  
Alyson Zwicker ◽  
Benjamin Goldstein ◽  
...  

2020 ◽  
Vol 19 (8) ◽  
Author(s):  
Alex Ferrer ◽  
Javier Costas ◽  
Mònica Gratacos ◽  
Èrika Martínez‐Amorós ◽  
Javier Labad ◽  
...  

2020 ◽  
Vol 263 ◽  
pp. 555-557
Author(s):  
Søren D. Østergaard ◽  
John J. McGrath ◽  
Ole Mors ◽  
Preben B. Mortensen ◽  
Liselotte V. Petersen

2018 ◽  
Vol 8 (1) ◽  
Author(s):  
Matej Markota ◽  
Brandon J. Coombes ◽  
Beth R. Larrabee ◽  
Susan L. McElroy ◽  
David J. Bond ◽  
...  

2019 ◽  
Vol 29 ◽  
pp. S60-S61
Author(s):  
S.D. Ostergaard ◽  
J.J. McGrath ◽  
O. Mors ◽  
P.B. Mortensen ◽  
L.V. Petersen

Sign in / Sign up

Export Citation Format

Share Document