Lifelong Association of Disorders Related to Military Trauma with Subsequent Parkinson's Disease.


Journal

Movement disorders : official journal of the Movement Disorder Society
ISSN: 1531-8257
Titre abrégé: Mov Disord
Pays: United States
ID NLM: 8610688

Informations de publication

Date de publication:
08 2023
Historique:
revised: 08 05 2023
received: 02 03 2023
accepted: 10 05 2023
medline: 23 10 2023
pubmed: 13 6 2023
entrez: 13 6 2023
Statut: ppublish

Résumé

Trauma-related disorders such as traumatic brain injury (TBI) and posttraumatic stress disorder (PTSD) are emerging as risk factors for Parkinson's disease (PD), but their association with development of PD and independence from comorbid disorders remains unknown. To examine TBI and PTSD related to early trauma in military veterans using a case-control study. PD was identified by International Classification of Diseases (ICD) code, recurrent PD-specific prescriptions, and availability of 5+ years of earlier records. Validation was performed by chart review by a movement disorder-trained neurologist. Control subjects were matched 4:1 by age, duration of preceding health care, race, ethnicity, birth year, and sex. TBI and PTSD were identified by ICD code and onset based on active duty. Association and interaction were measured for TBI and PTSD with PD going back 60 years. Interaction was measured for comorbid disorders. A total of 71,933 cases and 287,732 controls were identified. TBI and PTSD increased odds of subsequent PD at all preceding 5-year intervals back to year -60 (odds ratio range: 1.5 [1.4, 1.7] to 2.1 [2.0, 2.1]). TBI and PTSD showed synergism (synergy index range: 1.14 [1.09, 1.29] to 1.28 [1.09, 1.51]) and additive association (odds ratio range: 2.2 [1.6, 2.8] to 2.7 [2.5, 2.8]). Chronic pain and migraine showed greatest synergy with PTSD and TBI. Effect sizes for trauma-related disorders were comparable with established prodromal disorders. TBI and PTSD are associated with later PD and are synergistic with chronic pain and migraine. These findings provide evidence for TBI and PTSD as risk factors preceding PD by decades and could aid in prognostic calculation and earlier intervention. © 2023 International Parkinson and Movement Disorder Society. This article has been contributed to by U.S. Government employees and their work is in the public domain in the USA.

Sections du résumé

BACKGROUND
Trauma-related disorders such as traumatic brain injury (TBI) and posttraumatic stress disorder (PTSD) are emerging as risk factors for Parkinson's disease (PD), but their association with development of PD and independence from comorbid disorders remains unknown.
OBJECTIVE
To examine TBI and PTSD related to early trauma in military veterans using a case-control study.
METHODS
PD was identified by International Classification of Diseases (ICD) code, recurrent PD-specific prescriptions, and availability of 5+ years of earlier records. Validation was performed by chart review by a movement disorder-trained neurologist. Control subjects were matched 4:1 by age, duration of preceding health care, race, ethnicity, birth year, and sex. TBI and PTSD were identified by ICD code and onset based on active duty. Association and interaction were measured for TBI and PTSD with PD going back 60 years. Interaction was measured for comorbid disorders.
RESULTS
A total of 71,933 cases and 287,732 controls were identified. TBI and PTSD increased odds of subsequent PD at all preceding 5-year intervals back to year -60 (odds ratio range: 1.5 [1.4, 1.7] to 2.1 [2.0, 2.1]). TBI and PTSD showed synergism (synergy index range: 1.14 [1.09, 1.29] to 1.28 [1.09, 1.51]) and additive association (odds ratio range: 2.2 [1.6, 2.8] to 2.7 [2.5, 2.8]). Chronic pain and migraine showed greatest synergy with PTSD and TBI. Effect sizes for trauma-related disorders were comparable with established prodromal disorders.
CONCLUSIONS
TBI and PTSD are associated with later PD and are synergistic with chronic pain and migraine. These findings provide evidence for TBI and PTSD as risk factors preceding PD by decades and could aid in prognostic calculation and earlier intervention. © 2023 International Parkinson and Movement Disorder Society. This article has been contributed to by U.S. Government employees and their work is in the public domain in the USA.

Identifiants

pubmed: 37309872
doi: 10.1002/mds.29457
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

1483-1492

Subventions

Organisme : BLRD VA
ID : IK2 BX005760
Pays : United States
Organisme : CSRD VA
ID : IK2 CX002539
Pays : United States

Informations de copyright

© 2023 International Parkinson and Movement Disorder Society. This article has been contributed to by U.S. Government employees and their work is in the public domain in the USA.

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Auteurs

Gregory D Scott (GD)

Department of Pathology, Oregon Health and Science University, Portland, Oregon, USA.
Department of Pathology and Laboratory Services, VA Portland Medical Center, Portland, Oregon, USA.

Lee E Neilson (LE)

Department of Neurology, Oregon Health and Science University, Portland, Oregon, USA.
Department of Neurology, VA Portland Medical Center, Portland, Oregon, USA.

Randy Woltjer (R)

Department of Pathology, Oregon Health and Science University, Portland, Oregon, USA.

Joseph F Quinn (JF)

Department of Neurology, Oregon Health and Science University, Portland, Oregon, USA.
Department of Neurology, VA Portland Medical Center, Portland, Oregon, USA.

Miranda M Lim (MM)

Department of Neurology, Oregon Health and Science University, Portland, Oregon, USA.
Department of Neurology, VA Portland Medical Center, Portland, Oregon, USA.
VA VISN20 Northwest Mental Illness Research Education and Clinical Center, Portland, Oregon, USA.
Department of Behavioral Neuroscience, Oregon Health and Science University, Portland, Oregon, USA.

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