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Genetic vulnerability and adverse mental health outcomes following mild traumatic brain injury: a meta-analysis of CENTER-TBI and TRACK-TBI cohorts
Post-traumatic stress disorder (PTSD) and depression are common after mild traumatic brain injury (mTBI), but their biological drivers are uncertain. We therefore explored whether polygenic risk scores (PRS) derived for PTSD and major depressive disorder (MDD) are associated with the development of...
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Published in: | EClinicalMedicine 2024-12, Vol.78, p.102956, Article 102956 |
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creator | Levey, Daniel F. Sun, Xiaoying Menon, David K. Ackerlund, Cecilia Amrein, Krisztina Andreassen, Lasse Antoni, Anna Azzolini, Maria Luisa Bartels, Ronald Bellander, Bo-Michael Belli, Antonio Benali, Habib Beretta, Luigi Brazinova, Alexandra Brorsson, Camilla Caccioppola, Alessio Calvi, Maria Rosa Carbonara, Marco Dawes, Helen De Keyser, Véronique Dixit, Abhishek Donoghue, Emma Ercole, Ari Fabricius, Martin Feigin, Valery L. Gao, Guoyi Gruen, Russell L. Helseth, Eirik Hutchinson, Peter J. Jacobs, Bram Jiang, Ji-yao Jones, Kelly Kowark, Ana Lanyon, Linda Laureys, Steven Lecky, Fiona Lejeune, Aurelie Levi, Leon Maegele, Marc McMahon, Catherine Misset, Benoit Murray, Lynnette Negru, Ancuta Nelson, David Newcombe, Virginia Payen, Jean-François Persona, Paolo Piippo-Karjalainen, Anna Ples, Horia Helmrich, Isabel Retel Rosenthal, Guy Sandor, Janos Schäfer, Nadine Schoonman, Guus Singh, Ranjit D. Skandsen, Toril Sorinola, Abayomi Stewart, William Tenovuo, Olli Thomas, Matt Tibboel, Dick Trapani, Tony van der Jagt, Mathieu Van der Steen, Gregory van Dijck, Jeroen T.J.M. van Erp, Inge A. Van Hecke, Wim Vyvere, Thijs Vande Vega, Emmanuel Vik, Anne Vilcinis, Rimantas Volovici, Victor von Steinbüchel, Nicole Ylén, Peter Badjatia, Neeraj Boase, Kim Chesnut, Randall Corrigan, John Diaz-Arrastia, Ramon Ellenbogen, Richard Feeser, Venkata Ferguson, Adam R. Giacino, Joseph Gonzalez, Luis Grandhi, Ramesh Hemphill, Claude Hotz, Gillian Huie, Russell Levin, Harvey Madden, Christopher McAllister, Thomas Nelson, Lindsay Nolan, Amber Okonkwo, David Puccio, Ava Ben Rodgers, Richard Sander, Angelle Temkin, Nancy Toga, Arthur Vassar, Mary |
description | Post-traumatic stress disorder (PTSD) and depression are common after mild traumatic brain injury (mTBI), but their biological drivers are uncertain. We therefore explored whether polygenic risk scores (PRS) derived for PTSD and major depressive disorder (MDD) are associated with the development of cognate TBI-related phenotypes.
Meta-analyses were conducted using data from two multicenter, prospective observational cohort studies of patients with mTBI: the CENTER-TBI study (ClinicalTrials.gov ID NCT02210221) in Europe (December 2014–December 2017) and the TRACK-TBI study in the US (March 2014–July 2018). In both cohorts, the most common causes of injury were road traffic accidents and falls. Primary outcomes, specifically probable PTSD and depression, were defined at 6 months post-injury using scores ≥33 on the PTSD Checklist-5 and ≥15 on the Patient Health Questionnaire-9, respectively. We calculated PTSD-PRS and MDD-PRS for patients aged ≥17 years who had a Glasgow Coma Scale score of 13–15 upon hospital arrival and assessed their association with PTSD and depression following TBI. We also evaluated the transferability of the findings in a cohort of African Americans.
Overall, 11.8% (219/1869) and 6.7% (124/1869) patients were classified as having probable PTSD and depression, respectively. The PTSD-PRS was significantly associated with higher adjusted odds of PTSD in both cohorts, with a pooled odds ratio (OR) of 1.55 [95% confidence interval (CI) 1.30–1.84, p |
doi_str_mv | 10.1016/j.eclinm.2024.102956 |
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Sun, Xiaoying ; Menon, David K. ; Ackerlund, Cecilia ; Amrein, Krisztina ; Andreassen, Lasse ; Antoni, Anna ; Azzolini, Maria Luisa ; Bartels, Ronald ; Bellander, Bo-Michael ; Belli, Antonio ; Benali, Habib ; Beretta, Luigi ; Brazinova, Alexandra ; Brorsson, Camilla ; Caccioppola, Alessio ; Calvi, Maria Rosa ; Carbonara, Marco ; Dawes, Helen ; De Keyser, Véronique ; Dixit, Abhishek ; Donoghue, Emma ; Ercole, Ari ; Fabricius, Martin ; Feigin, Valery L. ; Gao, Guoyi ; Gruen, Russell L. ; Helseth, Eirik ; Hutchinson, Peter J. ; Jacobs, Bram ; Jiang, Ji-yao ; Jones, Kelly ; Kowark, Ana ; Lanyon, Linda ; Laureys, Steven ; Lecky, Fiona ; Lejeune, Aurelie ; Levi, Leon ; Maegele, Marc ; McMahon, Catherine ; Misset, Benoit ; Murray, Lynnette ; Negru, Ancuta ; Nelson, David ; Newcombe, Virginia ; Payen, Jean-François ; Persona, Paolo ; Piippo-Karjalainen, Anna ; Ples, Horia ; Helmrich, Isabel Retel ; Rosenthal, Guy ; Sandor, Janos ; Schäfer, Nadine ; Schoonman, Guus ; Singh, Ranjit D. ; Skandsen, Toril ; Sorinola, Abayomi ; Stewart, William ; Tenovuo, Olli ; Thomas, Matt ; Tibboel, Dick ; Trapani, Tony ; van der Jagt, Mathieu ; Van der Steen, Gregory ; van Dijck, Jeroen T.J.M. ; van Erp, Inge A. ; Van Hecke, Wim ; Vyvere, Thijs Vande ; Vega, Emmanuel ; Vik, Anne ; Vilcinis, Rimantas ; Volovici, Victor ; von Steinbüchel, Nicole ; Ylén, Peter ; Badjatia, Neeraj ; Boase, Kim ; Chesnut, Randall ; Corrigan, John ; Diaz-Arrastia, Ramon ; Ellenbogen, Richard ; Feeser, Venkata ; Ferguson, Adam R. ; Giacino, Joseph ; Gonzalez, Luis ; Grandhi, Ramesh ; Hemphill, Claude ; Hotz, Gillian ; Huie, Russell ; Levin, Harvey ; Madden, Christopher ; McAllister, Thomas ; Nelson, Lindsay ; Nolan, Amber ; Okonkwo, David ; Puccio, Ava ; Ben Rodgers, Richard ; Sander, Angelle ; Temkin, Nancy ; Toga, Arthur ; Vassar, Mary</creator><creatorcontrib>Levey, Daniel F. ; Sun, Xiaoying ; Menon, David K. ; Ackerlund, Cecilia ; Amrein, Krisztina ; Andreassen, Lasse ; Antoni, Anna ; Azzolini, Maria Luisa ; Bartels, Ronald ; Bellander, Bo-Michael ; Belli, Antonio ; Benali, Habib ; Beretta, Luigi ; Brazinova, Alexandra ; Brorsson, Camilla ; Caccioppola, Alessio ; Calvi, Maria Rosa ; Carbonara, Marco ; Dawes, Helen ; De Keyser, Véronique ; Dixit, Abhishek ; Donoghue, Emma ; Ercole, Ari ; Fabricius, Martin ; Feigin, Valery L. ; Gao, Guoyi ; Gruen, Russell L. ; Helseth, Eirik ; Hutchinson, Peter J. ; Jacobs, Bram ; Jiang, Ji-yao ; Jones, Kelly ; Kowark, Ana ; Lanyon, Linda ; Laureys, Steven ; Lecky, Fiona ; Lejeune, Aurelie ; Levi, Leon ; Maegele, Marc ; McMahon, Catherine ; Misset, Benoit ; Murray, Lynnette ; Negru, Ancuta ; Nelson, David ; Newcombe, Virginia ; Payen, Jean-François ; Persona, Paolo ; Piippo-Karjalainen, Anna ; Ples, Horia ; Helmrich, Isabel Retel ; Rosenthal, Guy ; Sandor, Janos ; Schäfer, Nadine ; Schoonman, Guus ; Singh, Ranjit D. ; Skandsen, Toril ; Sorinola, Abayomi ; Stewart, William ; Tenovuo, Olli ; Thomas, Matt ; Tibboel, Dick ; Trapani, Tony ; van der Jagt, Mathieu ; Van der Steen, Gregory ; van Dijck, Jeroen T.J.M. ; van Erp, Inge A. ; Van Hecke, Wim ; Vyvere, Thijs Vande ; Vega, Emmanuel ; Vik, Anne ; Vilcinis, Rimantas ; Volovici, Victor ; von Steinbüchel, Nicole ; Ylén, Peter ; Badjatia, Neeraj ; Boase, Kim ; Chesnut, Randall ; Corrigan, John ; Diaz-Arrastia, Ramon ; Ellenbogen, Richard ; Feeser, Venkata ; Ferguson, Adam R. ; Giacino, Joseph ; Gonzalez, Luis ; Grandhi, Ramesh ; Hemphill, Claude ; Hotz, Gillian ; Huie, Russell ; Levin, Harvey ; Madden, Christopher ; McAllister, Thomas ; Nelson, Lindsay ; Nolan, Amber ; Okonkwo, David ; Puccio, Ava ; Ben Rodgers, Richard ; Sander, Angelle ; Temkin, Nancy ; Toga, Arthur ; Vassar, Mary ; The Genetic Associations In Neurotrauma (GAIN) Consortium (with contribution from the CENTER-TBI and TRACK-TBI studies) ; Genetic Associations In Neurotrauma (GAIN) Consortium (with contribution from the CENTER-TBI and TRACK-TBI studies)</creatorcontrib><description>Post-traumatic stress disorder (PTSD) and depression are common after mild traumatic brain injury (mTBI), but their biological drivers are uncertain. We therefore explored whether polygenic risk scores (PRS) derived for PTSD and major depressive disorder (MDD) are associated with the development of cognate TBI-related phenotypes.
Meta-analyses were conducted using data from two multicenter, prospective observational cohort studies of patients with mTBI: the CENTER-TBI study (ClinicalTrials.gov ID NCT02210221) in Europe (December 2014–December 2017) and the TRACK-TBI study in the US (March 2014–July 2018). In both cohorts, the most common causes of injury were road traffic accidents and falls. Primary outcomes, specifically probable PTSD and depression, were defined at 6 months post-injury using scores ≥33 on the PTSD Checklist-5 and ≥15 on the Patient Health Questionnaire-9, respectively. We calculated PTSD-PRS and MDD-PRS for patients aged ≥17 years who had a Glasgow Coma Scale score of 13–15 upon hospital arrival and assessed their association with PTSD and depression following TBI. We also evaluated the transferability of the findings in a cohort of African Americans.
Overall, 11.8% (219/1869) and 6.7% (124/1869) patients were classified as having probable PTSD and depression, respectively. The PTSD-PRS was significantly associated with higher adjusted odds of PTSD in both cohorts, with a pooled odds ratio (OR) of 1.55 [95% confidence interval (CI) 1.30–1.84, p < 0.001, I2 = 20.8%]. Although the MDD-PRS increased the risk of depression after TBI, it did not reach significance in the individual cohorts. However, in a combined analysis, the risk was significantly elevated with a pooled OR of 1.26 [95% CI 1.03–1.53, p = 0.02, I2 = 0%]. The addition of PRSs improved the proportion of outcome variance explained in the two study cohorts from 19.5% and 30.3% to 21.6% and 34.0% for PTSD; and from 11.0% and 22.5% to 12.8% and 22.6% for depression. Patients in the highest cognate PRS quintile had increased odds of 3.16 [95% CI 1.80–5.55] and 2.03 [95% CI 1.04–3.94] of developing PTSD or depression compared to the lowest quintile, respectively.
Associations of PRSs with PTSD and depression following TBI are not disorder-specific. However, the overlap between MDD-PRS and depression following TBI is less robust compared to PTSD-PRS and PTSD. PRSs could improve risk prediction, and permit enrichment for interventional trials.
This study was supported by funding by an FP7 grant from the European Union, Hannelore Kohl Stiftung, Integra LifeSciences Corporation, NeuroTrauma Sciences, US National Institutes of Health, US Department of Defense, National Football League Advisory Board, US Department of Energy, and One Mind.</description><identifier>ISSN: 2589-5370</identifier><identifier>EISSN: 2589-5370</identifier><identifier>DOI: 10.1016/j.eclinm.2024.102956</identifier><identifier>PMID: 39720422</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Depression ; Mental health ; Polygenic risk score ; Post-traumatic stress disorder ; Traumatic brain injury</subject><ispartof>EClinicalMedicine, 2024-12, Vol.78, p.102956, Article 102956</ispartof><rights>2024 The Authors</rights><rights>2024 The Authors.</rights><rights>2024 The Authors 2024</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c297t-da31cde021b80954eea28c9d62f9f8a24d2be6c10b00e1081f323aaae3067e433</cites><orcidid>0000-0003-1612-1264 ; 0000-0002-1014-9138 ; 0000-0003-2090-8780</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11667043/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S2589537024005352$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,724,777,781,882,3536,27905,27906,45761,53772,53774</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39720422$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Levey, Daniel 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studies)</creatorcontrib><creatorcontrib>Genetic Associations In Neurotrauma (GAIN) Consortium (with contribution from the CENTER-TBI and TRACK-TBI studies)</creatorcontrib><title>Genetic vulnerability and adverse mental health outcomes following mild traumatic brain injury: a meta-analysis of CENTER-TBI and TRACK-TBI cohorts</title><title>EClinicalMedicine</title><addtitle>EClinicalMedicine</addtitle><description>Post-traumatic stress disorder (PTSD) and depression are common after mild traumatic brain injury (mTBI), but their biological drivers are uncertain. We therefore explored whether polygenic risk scores (PRS) derived for PTSD and major depressive disorder (MDD) are associated with the development of cognate TBI-related phenotypes.
Meta-analyses were conducted using data from two multicenter, prospective observational cohort studies of patients with mTBI: the CENTER-TBI study (ClinicalTrials.gov ID NCT02210221) in Europe (December 2014–December 2017) and the TRACK-TBI study in the US (March 2014–July 2018). In both cohorts, the most common causes of injury were road traffic accidents and falls. Primary outcomes, specifically probable PTSD and depression, were defined at 6 months post-injury using scores ≥33 on the PTSD Checklist-5 and ≥15 on the Patient Health Questionnaire-9, respectively. We calculated PTSD-PRS and MDD-PRS for patients aged ≥17 years who had a Glasgow Coma Scale score of 13–15 upon hospital arrival and assessed their association with PTSD and depression following TBI. We also evaluated the transferability of the findings in a cohort of African Americans.
Overall, 11.8% (219/1869) and 6.7% (124/1869) patients were classified as having probable PTSD and depression, respectively. The PTSD-PRS was significantly associated with higher adjusted odds of PTSD in both cohorts, with a pooled odds ratio (OR) of 1.55 [95% confidence interval (CI) 1.30–1.84, p < 0.001, I2 = 20.8%]. Although the MDD-PRS increased the risk of depression after TBI, it did not reach significance in the individual cohorts. However, in a combined analysis, the risk was significantly elevated with a pooled OR of 1.26 [95% CI 1.03–1.53, p = 0.02, I2 = 0%]. The addition of PRSs improved the proportion of outcome variance explained in the two study cohorts from 19.5% and 30.3% to 21.6% and 34.0% for PTSD; and from 11.0% and 22.5% to 12.8% and 22.6% for depression. Patients in the highest cognate PRS quintile had increased odds of 3.16 [95% CI 1.80–5.55] and 2.03 [95% CI 1.04–3.94] of developing PTSD or depression compared to the lowest quintile, respectively.
Associations of PRSs with PTSD and depression following TBI are not disorder-specific. However, the overlap between MDD-PRS and depression following TBI is less robust compared to PTSD-PRS and PTSD. PRSs could improve risk prediction, and permit enrichment for interventional trials.
This study was supported by funding by an FP7 grant from the European Union, Hannelore Kohl Stiftung, Integra LifeSciences Corporation, NeuroTrauma Sciences, US National Institutes of Health, US Department of Defense, National Football League Advisory Board, US Department of Energy, and One Mind.</description><subject>Depression</subject><subject>Mental health</subject><subject>Polygenic risk score</subject><subject>Post-traumatic stress disorder</subject><subject>Traumatic brain 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Jagt, Mathieu ; Van der Steen, Gregory ; van Dijck, Jeroen T.J.M. ; van Erp, Inge A. ; Van Hecke, Wim ; Vyvere, Thijs Vande ; Vega, Emmanuel ; Vik, Anne ; Vilcinis, Rimantas ; Volovici, Victor ; von Steinbüchel, Nicole ; Ylén, Peter ; Badjatia, Neeraj ; Boase, Kim ; Chesnut, Randall ; Corrigan, John ; Diaz-Arrastia, Ramon ; Ellenbogen, Richard ; Feeser, Venkata ; Ferguson, Adam R. ; Giacino, Joseph ; Gonzalez, Luis ; Grandhi, Ramesh ; Hemphill, Claude ; Hotz, Gillian ; Huie, Russell ; Levin, Harvey ; Madden, Christopher ; McAllister, Thomas ; Nelson, Lindsay ; Nolan, Amber ; Okonkwo, David ; Puccio, Ava ; Ben Rodgers, Richard ; Sander, Angelle ; Temkin, Nancy ; Toga, Arthur ; Vassar, 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- Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>EClinicalMedicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Levey, Daniel F.</au><au>Sun, Xiaoying</au><au>Menon, David K.</au><au>Ackerlund, Cecilia</au><au>Amrein, Krisztina</au><au>Andreassen, Lasse</au><au>Antoni, Anna</au><au>Azzolini, Maria Luisa</au><au>Bartels, Ronald</au><au>Bellander, Bo-Michael</au><au>Belli, Antonio</au><au>Benali, Habib</au><au>Beretta, Luigi</au><au>Brazinova, Alexandra</au><au>Brorsson, Camilla</au><au>Caccioppola, Alessio</au><au>Calvi, Maria Rosa</au><au>Carbonara, Marco</au><au>Dawes, Helen</au><au>De Keyser, Véronique</au><au>Dixit, Abhishek</au><au>Donoghue, Emma</au><au>Ercole, Ari</au><au>Fabricius, Martin</au><au>Feigin, Valery L.</au><au>Gao, Guoyi</au><au>Gruen, Russell L.</au><au>Helseth, Eirik</au><au>Hutchinson, Peter J.</au><au>Jacobs, Bram</au><au>Jiang, Ji-yao</au><au>Jones, Kelly</au><au>Kowark, Ana</au><au>Lanyon, Linda</au><au>Laureys, Steven</au><au>Lecky, Fiona</au><au>Lejeune, Aurelie</au><au>Levi, Leon</au><au>Maegele, Marc</au><au>McMahon, Catherine</au><au>Misset, Benoit</au><au>Murray, Lynnette</au><au>Negru, Ancuta</au><au>Nelson, David</au><au>Newcombe, Virginia</au><au>Payen, Jean-François</au><au>Persona, Paolo</au><au>Piippo-Karjalainen, Anna</au><au>Ples, Horia</au><au>Helmrich, Isabel Retel</au><au>Rosenthal, Guy</au><au>Sandor, Janos</au><au>Schäfer, Nadine</au><au>Schoonman, Guus</au><au>Singh, Ranjit D.</au><au>Skandsen, Toril</au><au>Sorinola, Abayomi</au><au>Stewart, William</au><au>Tenovuo, Olli</au><au>Thomas, Matt</au><au>Tibboel, Dick</au><au>Trapani, Tony</au><au>van der Jagt, Mathieu</au><au>Van der Steen, Gregory</au><au>van Dijck, Jeroen T.J.M.</au><au>van Erp, Inge A.</au><au>Van Hecke, Wim</au><au>Vyvere, Thijs Vande</au><au>Vega, Emmanuel</au><au>Vik, Anne</au><au>Vilcinis, Rimantas</au><au>Volovici, Victor</au><au>von Steinbüchel, Nicole</au><au>Ylén, Peter</au><au>Badjatia, Neeraj</au><au>Boase, Kim</au><au>Chesnut, Randall</au><au>Corrigan, John</au><au>Diaz-Arrastia, Ramon</au><au>Ellenbogen, Richard</au><au>Feeser, Venkata</au><au>Ferguson, Adam R.</au><au>Giacino, Joseph</au><au>Gonzalez, Luis</au><au>Grandhi, Ramesh</au><au>Hemphill, Claude</au><au>Hotz, Gillian</au><au>Huie, Russell</au><au>Levin, Harvey</au><au>Madden, Christopher</au><au>McAllister, Thomas</au><au>Nelson, Lindsay</au><au>Nolan, Amber</au><au>Okonkwo, David</au><au>Puccio, Ava</au><au>Ben Rodgers, Richard</au><au>Sander, Angelle</au><au>Temkin, Nancy</au><au>Toga, Arthur</au><au>Vassar, Mary</au><aucorp>The Genetic Associations In Neurotrauma (GAIN) Consortium (with contribution from the CENTER-TBI and TRACK-TBI studies)</aucorp><aucorp>Genetic Associations In Neurotrauma (GAIN) Consortium (with contribution from the CENTER-TBI and TRACK-TBI studies)</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Genetic vulnerability and adverse mental health outcomes following mild traumatic brain injury: a meta-analysis of CENTER-TBI and TRACK-TBI cohorts</atitle><jtitle>EClinicalMedicine</jtitle><addtitle>EClinicalMedicine</addtitle><date>2024-12-01</date><risdate>2024</risdate><volume>78</volume><spage>102956</spage><pages>102956-</pages><artnum>102956</artnum><issn>2589-5370</issn><eissn>2589-5370</eissn><abstract>Post-traumatic stress disorder (PTSD) and depression are common after mild traumatic brain injury (mTBI), but their biological drivers are uncertain. We therefore explored whether polygenic risk scores (PRS) derived for PTSD and major depressive disorder (MDD) are associated with the development of cognate TBI-related phenotypes.
Meta-analyses were conducted using data from two multicenter, prospective observational cohort studies of patients with mTBI: the CENTER-TBI study (ClinicalTrials.gov ID NCT02210221) in Europe (December 2014–December 2017) and the TRACK-TBI study in the US (March 2014–July 2018). In both cohorts, the most common causes of injury were road traffic accidents and falls. Primary outcomes, specifically probable PTSD and depression, were defined at 6 months post-injury using scores ≥33 on the PTSD Checklist-5 and ≥15 on the Patient Health Questionnaire-9, respectively. We calculated PTSD-PRS and MDD-PRS for patients aged ≥17 years who had a Glasgow Coma Scale score of 13–15 upon hospital arrival and assessed their association with PTSD and depression following TBI. We also evaluated the transferability of the findings in a cohort of African Americans.
Overall, 11.8% (219/1869) and 6.7% (124/1869) patients were classified as having probable PTSD and depression, respectively. The PTSD-PRS was significantly associated with higher adjusted odds of PTSD in both cohorts, with a pooled odds ratio (OR) of 1.55 [95% confidence interval (CI) 1.30–1.84, p < 0.001, I2 = 20.8%]. Although the MDD-PRS increased the risk of depression after TBI, it did not reach significance in the individual cohorts. However, in a combined analysis, the risk was significantly elevated with a pooled OR of 1.26 [95% CI 1.03–1.53, p = 0.02, I2 = 0%]. The addition of PRSs improved the proportion of outcome variance explained in the two study cohorts from 19.5% and 30.3% to 21.6% and 34.0% for PTSD; and from 11.0% and 22.5% to 12.8% and 22.6% for depression. Patients in the highest cognate PRS quintile had increased odds of 3.16 [95% CI 1.80–5.55] and 2.03 [95% CI 1.04–3.94] of developing PTSD or depression compared to the lowest quintile, respectively.
Associations of PRSs with PTSD and depression following TBI are not disorder-specific. However, the overlap between MDD-PRS and depression following TBI is less robust compared to PTSD-PRS and PTSD. PRSs could improve risk prediction, and permit enrichment for interventional trials.
This study was supported by funding by an FP7 grant from the European Union, Hannelore Kohl Stiftung, Integra LifeSciences Corporation, NeuroTrauma Sciences, US National Institutes of Health, US Department of Defense, National Football League Advisory Board, US Department of Energy, and One Mind.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>39720422</pmid><doi>10.1016/j.eclinm.2024.102956</doi><orcidid>https://orcid.org/0000-0003-1612-1264</orcidid><orcidid>https://orcid.org/0000-0002-1014-9138</orcidid><orcidid>https://orcid.org/0000-0003-2090-8780</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2589-5370 |
ispartof | EClinicalMedicine, 2024-12, Vol.78, p.102956, Article 102956 |
issn | 2589-5370 2589-5370 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_11667043 |
source | Open Access: PubMed Central; ScienceDirect® |
subjects | Depression Mental health Polygenic risk score Post-traumatic stress disorder Traumatic brain injury |
title | Genetic vulnerability and adverse mental health outcomes following mild traumatic brain injury: a meta-analysis of CENTER-TBI and TRACK-TBI cohorts |
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