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Data-Driven Patient Clustering and Differential Clinical Outcomes in the Brigham and Women's Rheumatoid Arthritis Sequential Study Registry
被引:10
|作者:
Curtis, Jeffrey R.
[1
]
Weinblatt, Michael
[2
]
Saag, Kenneth
[1
]
Bykerk, Vivian P.
[3
]
Furst, Daniel E.
[4
,5
,6
]
Fiore, Stefano
[7
]
St John, Gregory
[8
]
Kimura, Toshio
[9
]
Zheng, Shen
[7
]
Bingham, Clifton O., III
[10
]
Wright, Grace
Bergman, Martin
[11
]
Nola, Kamala
[12
]
Charles-Schoeman, Christina
[13
]
Shadick, Nancy
[2
]
机构:
[1] Univ Alabama Birmingham, Birmingham, W Midlands, England
[2] Brigham & Womens Hosp, 75 Francis St, Boston, MA 02115 USA
[3] Hosp Special Surg, 535 E 70th St, New York, NY 10021 USA
[4] Univ Calif Los Angeles, Los Angeles, CA USA
[5] Univ Washington, Seattle, WA 98195 USA
[6] Univ Florence, Florence, Italy
[7] Sanofi, Bridgewater, NJ USA
[8] Intercept Pharmaceut, New York, NY USA
[9] Regeneron Pharmaceut, Tarrytown, NY USA
[10] Johns Hopkins Univ, Baltimore, MD USA
[11] Drexel Univ, Coll Med, Philadelphia, PA 19104 USA
[12] Lipscomb Univ, Coll Pharm & Hlth Sci, Nashville, TN USA
[13] Univ Calif Los Angeles, Los Angeles, CA USA
关键词:
D O I:
10.1002/acr.24471
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Objective To use unbiased, data-driven, principal component (PC) and cluster analysis to identify patient phenotypes of rheumatoid arthritis (RA) that might exhibit distinct trajectories of disease progression, response to treatment, and risk for adverse events. Methods Patient demographic, socioeconomic, health, and disease characteristics recorded at entry into a large, single-center, prospective observational registry cohort, the Brigham and Women's Rheumatoid Arthritis Sequential Study (BRASS), were harmonized using PC analysis to reduce dimensionality and collinearity. The number of PCs was established by eigenvalue >1, cumulative variance, and interpretability. The resulting PCs were used to cluster patients using a K-means approach. Longitudinal clinical outcomes were compared between the clusters over 2 years. Results Analysis of 142 variables from 1,443 patients identified 41 PCs that accounted for 77% of the cumulative variance in the data set. Cluster analysis distinguished 5 patient clusters: 1) less RA disease activity/multimorbidity, shorter RA duration, lower incidence of comorbidities; 2) less RA disease activity/multimorbidity, longer RA duration, more infections, psychiatric comorbidities, health care utilization; 3) moderate RA disease activity/multimorbidity, more neurologic comorbidity; 4) more RA disease activity/multimorbidity, shorter RA duration, more metabolic comorbidity, higher body mass index; 5) more RA disease activity/multimorbidity, longer RA duration, more hepatic, orthopedic comorbidity and RA-related surgeries. The clusters exhibited differences in clinical outcomes over 2 years of follow-up. Conclusion Data-driven analysis of the BRASS registry identified 5 distinct phenotypes of RA. These results illustrate the potential of data-driven patient profiling as a tool to support personalized medicine in RA. Validation in an independent data set is ongoing.
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页码:471 / 480
页数:10
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