TY - JOUR
T1 - “Soldiers heart”
T2 - A genetic basis for elevated cardiovascular disease risk associated with post-traumatic stress disorder
AU - Pollard, Harvey B.
AU - Shivakumar, Chittari
AU - Starr, Joshua
AU - Eidelman, Ofer
AU - Jacobowitz, David M.
AU - Dalgard, Clifton L.
AU - Srivastava, Meera
AU - Wilkerson, Matthew D.
AU - Stein, Murray B.
AU - Ursano, Robert J.
N1 - Publisher Copyright:
© 2016 Pollard, Shivakumar, Starr, Eidelman, Jacobowitz, Dalgard, Srivastava, Wilkerson, Stein and Ursano.
PY - 2016/9/23
Y1 - 2016/9/23
N2 - “Soldier’s Heart,” is an American Civil War term linking post-traumatic stress disorder (PTSD) with increased propensity for cardiovascular disease (CVD). We have hypothesized that there might be a quantifiable genetic basis for this linkage. To test this hypothesis we identified a comprehensive set of candidate risk genes for PTSD, and tested whether any were also independent risk genes for CVD. A functional analysis algorithm was used to identify associated signaling networks. We identified 106 PTSD studies that report one or more polymorphic variants in 87 candidate genes in 83,463 subjects and controls. The top upstream drivers for these PTSD risk genes are predicted to be the glucocorticoid receptor (NR3C1) and Tumor Necrosis Factor alpha (TNFA). We find that 37 of the PTSD candidate risk genes are also candidate independent risk genes for CVD. The association between PTSD and CVD is significant by Fisher’s Exact Test (P = 3 × 10−-54). We also find 15 PTSD risk genes that are independently associated with Type 2 Diabetes Mellitus (T2DM; also significant by Fisher’s Exact Test (P = 1.8 × 10− -16). Our findings offer quantitative evidence for a genetic link between post-traumatic stress and cardiovascular disease, Computationally, the common mechanism for this linkage between PTSD and CVD is innate immunity and NFκB-mediated inflammation.
AB - “Soldier’s Heart,” is an American Civil War term linking post-traumatic stress disorder (PTSD) with increased propensity for cardiovascular disease (CVD). We have hypothesized that there might be a quantifiable genetic basis for this linkage. To test this hypothesis we identified a comprehensive set of candidate risk genes for PTSD, and tested whether any were also independent risk genes for CVD. A functional analysis algorithm was used to identify associated signaling networks. We identified 106 PTSD studies that report one or more polymorphic variants in 87 candidate genes in 83,463 subjects and controls. The top upstream drivers for these PTSD risk genes are predicted to be the glucocorticoid receptor (NR3C1) and Tumor Necrosis Factor alpha (TNFA). We find that 37 of the PTSD candidate risk genes are also candidate independent risk genes for CVD. The association between PTSD and CVD is significant by Fisher’s Exact Test (P = 3 × 10−-54). We also find 15 PTSD risk genes that are independently associated with Type 2 Diabetes Mellitus (T2DM; also significant by Fisher’s Exact Test (P = 1.8 × 10− -16). Our findings offer quantitative evidence for a genetic link between post-traumatic stress and cardiovascular disease, Computationally, the common mechanism for this linkage between PTSD and CVD is innate immunity and NFκB-mediated inflammation.
KW - Candidate gene
KW - Cardiovascular disease
KW - Post traumatic stress disorder
KW - Type 2 diabetes mellitus
UR - http://www.scopus.com/inward/record.url?scp=84989903975&partnerID=8YFLogxK
U2 - 10.3389/fnmol.2016.00087
DO - 10.3389/fnmol.2016.00087
M3 - Article
AN - SCOPUS:84989903975
SN - 1662-5099
VL - 9
JO - Frontiers in Molecular Neuroscience
JF - Frontiers in Molecular Neuroscience
IS - SEP2016
M1 - 87
ER -