TY - JOUR
T1 - Epigenetic meta-analysis across three civilian cohorts identifies NRG1 and HGS as blood-based biomarkers for post-traumatic stress disorder
AU - Uddin, Monica
AU - Ratanatharathorn, Andrew
AU - Armstrong, Don
AU - Kuan, Pei Fen
AU - Aiello, Allison E.
AU - Bromet, Evelyn J.
AU - Galea, Sandro
AU - Koenen, Karestan C.
AU - Luft, Benjamin
AU - Ressler, Kerry J.
AU - Wildman, Derek E.
AU - Nievergelt, Caroline M.
AU - Smith, Alicia
N1 - Publisher Copyright:
© 2018 2018 Future Medicine Ltd.
PY - 2018/12
Y1 - 2018/12
N2 - Aim: Trauma exposure is a necessary, but not deterministic, contributor to post-traumatic stress disorder (PTSD). Epigenetic factors may distinguish between trauma-exposed individuals with versus without PTSD. Materials & methods: We conducted a meta-analysis of PTSD epigenome-wide association studies in trauma-exposed cohorts drawn from civilian contexts. Whole blood-derived DNA methylation levels were analyzed in 545 study participants, drawn from the three civilian cohorts participating in the PTSD working group of the Psychiatric Genomics Consortium. Results: Two CpG sites significantly associated with current PTSD in NRG1 (cg23637605) and in HGS (cg19577098). Conclusion: PTSD is associated with differential methylation, measured in blood, within HGS and NRG1 across three civilian cohorts.
AB - Aim: Trauma exposure is a necessary, but not deterministic, contributor to post-traumatic stress disorder (PTSD). Epigenetic factors may distinguish between trauma-exposed individuals with versus without PTSD. Materials & methods: We conducted a meta-analysis of PTSD epigenome-wide association studies in trauma-exposed cohorts drawn from civilian contexts. Whole blood-derived DNA methylation levels were analyzed in 545 study participants, drawn from the three civilian cohorts participating in the PTSD working group of the Psychiatric Genomics Consortium. Results: Two CpG sites significantly associated with current PTSD in NRG1 (cg23637605) and in HGS (cg19577098). Conclusion: PTSD is associated with differential methylation, measured in blood, within HGS and NRG1 across three civilian cohorts.
UR - https://www.scopus.com/pages/publications/85058077061
U2 - 10.2217/epi-2018-0049
DO - 10.2217/epi-2018-0049
M3 - Article
C2 - 30456986
AN - SCOPUS:85058077061
SN - 1750-1911
VL - 10
SP - 1585
EP - 1601
JO - Epigenomics
JF - Epigenomics
IS - 12
ER -