Exploratory analysis of osteoarthritis progression among medication users: data from the Osteoarthritis Initiative

被引:32
作者
Driban, Jeffrey B.
Lo, Grace H. [2 ,3 ]
Eaton, Charles B. [4 ,5 ,6 ]
Lapane, Kate L. [7 ]
Nevitt, Michael [8 ]
Harvey, William F. [1 ]
McCulloch, Charles E. [8 ]
McAlindon, Timothy E. [1 ]
机构
[1] Tufts Med Ctr, Div Rheumatol, 800 Washington St,Box 406, Boston, MA 02111 USA
[2] Michael E DeBakey VA Med Ctr, Houston Hlth Serv Res & Dev Ctr Excellence, Houston, TX USA
[3] Baylor Coll Med, Sect Immunol Allergy & Rheumatol, Houston, TX 77030 USA
[4] Brown Univ, Alpert Med Sch, Dept Family Med, Pawtucket, RI USA
[5] Brown Univ, Alpert Med Sch, Dept Epidemiol, Pawtucket, RI USA
[6] Mem Hosp Rhode Isl, Ctr Primary Care & Prevent, Pawtucket, RI USA
[7] Univ Massachusetts, Sch Med, Dept Quantitat Hlth Sci, Worcester, MA 01605 USA
[8] Univ Calif San Francisco, Dept Epidemiol & Biostat, San Francisco, CA 94143 USA
基金
美国国家卫生研究院;
关键词
knee; pain; radiographs; JOINT SPACE WIDTH; METABOLIC SYNDROME; PAIN; KNEE; ABNORMALITIES; ANGIOGENESIS; INFLAMMATION; MECHANISMS;
D O I
10.1177/1759720X16664323
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Background: We conducted an exploratory analysis of osteoarthritis progression among medication users in the Osteoarthritis Initiative to identify interventions or pathways that may be associated with disease modification and therefore of interest for future clinical trials. Methods: We used participants from the Osteoarthritis Initiative with annual medication inventory data between the baseline and 36-month follow-up visit (n = 2938). Consistent medication users were defined for each medication classification as a participant reporting at all four annual visits that they were regularly using an oral prescription medication at the time of the visit. The exploratory analysis focused on medication classes with 40 or more users. The primary outcome measures were medial tibiofemoral joint space width change and the Western Ontario and McMaster Universities Arthritis Index (WOMAC) knee pain score change (12-36-month visits). Within each knee, we explored eight comparisons between users and matched or unmatched nonusers (defined two ways). An effect size of each comparison was calculated. Medication classes had potential signals if (a) both knees had less progression among users compared with nonusers, or (b) there was less progression based on structure and symptoms in one knee. Results: We screened 28 medication classes. Six medication classes had signals for fewer structural changes and better knee pain changes: alpha-adrenergic blockers, antilipemic (excluding statins and fibric acid), anticoagulants, selective serotonin reuptake inhibitors, antihistamines, and antineoplastic agents. Four medication classes had signals for structural changes alone: anti-estrogen (median effect size = 0.28; range = -0.41-0.64), angiotensin-converting enzyme inhibitors (median effect size = 0.13; range = -0.08-0.28), beta-adrenergic blockers (median effect size = 0.09; range = 0.01-0.30), and thyroid agents (median effect size = 0.04; range = -0.05-0.14). Thiazide diuretics had evidence for symptom modification (median effect size = -0.12; range = -0.24-0.04). Conclusions: Users of neurovascular, antilipemic, or hormonal interventions may have less disease progression compared with nonusers.
引用
收藏
页码:207 / 219
页数:13
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