Phenome-wide examination of comorbidity burden and multiple sclerosis disease severity

被引:15
|
作者
Zhang, Tingting [1 ]
Goodman, Matthew [2 ]
Zhu, Feng [3 ,4 ]
Healy, Brian [5 ]
Carruthers, Robert [3 ,4 ]
Chitnis, Tanuja [5 ]
Weiner, Howard [5 ]
Cai, Tianxi [2 ]
De Jager, Philip [5 ,6 ]
Tremlett, Helen [3 ,4 ]
Xia, Zongqi [5 ,7 ]
机构
[1] Brown Univ, Dept Hlth Serv Policy & Practice, Providence, RI 02912 USA
[2] Harvard TH Chan Sch Publ Hlth, Dept Biostat, Boston, MA USA
[3] Univ British Columbia, Dept Med Neurol, Vancouver, BC, Canada
[4] Univ British Columbia, Djavad Mowafaghian Ctr Brain Hlth, Vancouver, BC, Canada
[5] Brigham & Womens Hosp, Dept Neurol, 75 Francis St, Boston, MA 02115 USA
[6] Columbia Univ, Dept Neurol, New York, NY USA
[7] Univ Pittsburgh, Dept Neurol, Pittsburgh, PA 15260 USA
来源
基金
加拿大健康研究院;
关键词
D O I
10.1212/NXI.0000000000000864
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective We assessed the comorbidity burden associated with multiple sclerosis (MS) severity by performing a phenome-wide association study (PheWAS). Methods We conducted a PheWAS in 2 independent cohorts: a discovery (Boston, United States; 1993-2014) and extension cohort (British Columbia, Canada; 1991-2008). We included adults with MS, >= 1 Expanded Disability Status Scale (EDSS) score, and >= 1 International Classification of Diseases (ICD) code other than MS. We calculated the Multiple Sclerosis Severity Score (MSSS) using the EDSS. We mapped ICD codes into PheCodes (phenotypes), using a published system with each PheCode representing a unique medical condition. Association between the MSSS and the presence of each condition was assessed using logistic regression adjusted for covariates. Results The discovery and extension cohorts included 3,439 and 4,876 participants, respectively. After Bonferroni correction and covariate adjustments, a higher MSSS was associated with 37 coexisting conditions in the discovery cohort. Subsequently, 16 conditions, including genitourinary, infectious, metabolic, epilepsy, and movement disorders, met the reporting criteria, reaching the Bonferroni threshold of significance with the same direction of effect in the discovery and extension cohort. Notably, benign neoplasm of the skin was inversely associated with the MSSS. Conclusion The phenome-wide approach enabled a systematic interrogation of the comorbidity burden and highlighted clinically relevant medical conditions associated with MS severity (beyond MS-specific consequences) and defines a roadmap for comprehensive investigation of comorbidities in chronic neurologic diseases. Further prospective investigation of the bidirectional relationship between disability and comorbidities could inform the individualized patient management.
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页数:12
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