TY - JOUR
T1 - Inflammatory bowel disease and risk of Parkinson's disease in Medicare beneficiaries
AU - Camacho-Soto, Alejandra
AU - Gross, Anat
AU - Searles Nielsen, Susan
AU - Dey, Neelendu
AU - Racette, Brad A.
N1 - Funding Information:
This work was supported by NIEHS K24ES017765-07 (BAR), Michael J. Fox Foundation (BAR, SSN), and American Parkinson Disease Association (BAR, SSN).
Funding Information:
Dr. Camacho-Soto received government research support from NCMRR ( K12HD00109719 ). Dr. Searles Nielsen reports government research support from the NIH ( R21 ES024120 [co-I], R01ES021488 [co-I], R01 ES025991 [co-I]) and research support from the Michael J. Fox Foundation . Dr. Racette reports research support from Teva (PI), U.S. World Meds (PI), Allergan (PI), and Vaccinex (PI); government research support from the NIH ( K24ES017765 [PI], R21ES17504 [PI], R01ES021488 [PI], R01ES021488-02S1 [PI], R01 ES025991 [PI], R01ES025991-02S1 [PI], R01ES026891 [PI]); research support from the Michael J. Fox Foundation ( 10289 ).
Funding Information:
Dr. Camacho-Soto received government research support from NCMRR (K12HD00109719). Dr. Searles Nielsen reports government research support from the NIH (R21 ES024120 [co-I], R01ES021488 [co-I], R01 ES025991 [co-I]) and research support from the Michael J. Fox Foundation. Dr. Racette reports research support from Teva (PI), U.S. World Meds (PI), Allergan (PI), and Vaccinex (PI); government research support from the NIH (K24ES017765 [PI], R21ES17504 [PI], R01ES021488 [PI], R01ES021488-02S1 [PI], R01 ES025991 [PI], R01ES025991-02S1[PI], R01ES026891 [PI]); research support from the Michael J. Fox Foundation (10289).
Publisher Copyright:
© 2018 Elsevier Ltd
PY - 2018/5
Y1 - 2018/5
N2 - Introduction: Gastrointestinal (GI) dysfunction precedes the motor symptoms of Parkinson's disease (PD) by several years. PD patients have abnormal aggregation of intestinal α-synuclein, the accumulation of which may be promoted by inflammation. The relationship between intestinal α-synuclein aggregates and central nervous system neuropathology is unknown. Recently, we observed a possible inverse association between inflammatory bowel disease (IBD) and PD as part of a predictive model of PD. Therefore, the objective of this study was to examine the relationship between PD risk and IBD and IBD-associated conditions and treatment. Methods: Using a case-control design, we identified 89,790 newly diagnosed PD cases and 118,095 population-based controls >65 years of age using comprehensive Medicare data from 2004-2009 including detailed claims data. We classified IBD using International Classification of Diseases version 9 (ICD-9) diagnosis codes. We used logistic regression to calculate odds ratios (ORs) and 95% confidence intervals (CIs) to evaluate the association between PD and IBD. Covariates included age, sex, race/ethnicity, smoking, Elixhauser comorbidities, and health care use. Results: PD was inversely associated with IBD overall (OR = 0.85, 95% CI 0.80–0.91) and with both Crohn's disease (OR = 0.83, 95% CI 0.74–0.93) and ulcerative colitis (OR = 0.88, 95% CI 0.82–0.96). Among beneficiaries with ≥2 ICD-9 codes for IBD, there was an inverse dose-response association between number of IBD ICD-9 codes, as a potential proxy for IBD severity, and PD (p-for-trend = 0.006). Conclusion: IBD is associated with a lower risk of developing PD.
AB - Introduction: Gastrointestinal (GI) dysfunction precedes the motor symptoms of Parkinson's disease (PD) by several years. PD patients have abnormal aggregation of intestinal α-synuclein, the accumulation of which may be promoted by inflammation. The relationship between intestinal α-synuclein aggregates and central nervous system neuropathology is unknown. Recently, we observed a possible inverse association between inflammatory bowel disease (IBD) and PD as part of a predictive model of PD. Therefore, the objective of this study was to examine the relationship between PD risk and IBD and IBD-associated conditions and treatment. Methods: Using a case-control design, we identified 89,790 newly diagnosed PD cases and 118,095 population-based controls >65 years of age using comprehensive Medicare data from 2004-2009 including detailed claims data. We classified IBD using International Classification of Diseases version 9 (ICD-9) diagnosis codes. We used logistic regression to calculate odds ratios (ORs) and 95% confidence intervals (CIs) to evaluate the association between PD and IBD. Covariates included age, sex, race/ethnicity, smoking, Elixhauser comorbidities, and health care use. Results: PD was inversely associated with IBD overall (OR = 0.85, 95% CI 0.80–0.91) and with both Crohn's disease (OR = 0.83, 95% CI 0.74–0.93) and ulcerative colitis (OR = 0.88, 95% CI 0.82–0.96). Among beneficiaries with ≥2 ICD-9 codes for IBD, there was an inverse dose-response association between number of IBD ICD-9 codes, as a potential proxy for IBD severity, and PD (p-for-trend = 0.006). Conclusion: IBD is associated with a lower risk of developing PD.
KW - Inflammatory bowel disease
KW - Medicare beneficiaries
KW - Parkinson's disease
KW - Prodromal period
UR - http://www.scopus.com/inward/record.url?scp=85042033339&partnerID=8YFLogxK
U2 - 10.1016/j.parkreldis.2018.02.008
DO - 10.1016/j.parkreldis.2018.02.008
M3 - Article
C2 - 29459115
AN - SCOPUS:85042033339
SN - 1353-8020
VL - 50
SP - 23
EP - 28
JO - Parkinsonism and Related Disorders
JF - Parkinsonism and Related Disorders
ER -