A case-control study to assess possible triggers and cofactors in chronic fatigue syndrome

被引:58
作者
MacDonald, KL
Osterholm, MT
LeDell, KH
White, KE
Schenck, CH
Chao, CC
Persing, DH
Johnson, RC
Barker, JM
Peterson, PK
机构
[1] UNIV MINNESOTA,SCH MED,DEPT PSYCHIAT,MINNEAPOLIS,MN 55455
[2] UNIV MINNESOTA,SCH MED,DEPT MED,MINNEAPOLIS,MN 55455
[3] UNIV MINNESOTA,SCH MED,DEPT MICROBIOL,MINNEAPOLIS,MN 55455
[4] HENNEPIN CTY MED CTR,DEPT PSYCHIAT,MINNEAPOLIS,MN
[5] HENNEPIN CTY MED CTR,DEPT MED,MINNEAPOLIS,MN
[6] MAYO CLIN & MAYO FDN,DIV EXPTL PATHOL,ROCHESTER,MN 55905
[7] MAYO CLIN & MAYO FDN,MOLEC MICROBIOL LAB,DIV CLIN MICROBIOL,DEPT LAB MED & PATHOL,ROCHESTER,MN 55905
[8] ASPEN MED GRP,ST PAUL,MN
关键词
D O I
10.1016/S0002-9343(96)00017-4
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
PURPOSE: To assess possible triggers and cofactors for chronic fatigue syndrome (CFS) and to compare levels of selected cytokines between cafes and an appropriately matched control group. PATIENTS AND METHODS: We conducted a case-control study of 47 cases of CFS obtained through a regional CFS research program maintained at a tertiary care medical center. One age-, gender-, and neighborhood-matched control was identified for each case through systematic community telephone sampling. Standardized questionnaires were administered to cases and controls. Sera were assayed for transforming growth factor-beta (TGF-beta), interleukin-1 beta, interleukin-6, tumor necrosis factor-alpha, and antibody to Borrelia burgdorferi and Babesia microti. RESULTS: Cases were more likely to have exercised regularly before illness onset than controls (67% versus 40%; matched odds ratio (MOR) = 3.4; 95% CI = 1.2 to 11.8; P = 0.02). Female cases were more likely to be nulliparous prior to onset of CFS than controls (51% versus 31%; MOR = 8.0; 95% CI = 1.03 to 170; P = 0.05). History of other major factors, including silicone-gel breast implants (one Female case and one female control), pre-morbid history of depression (15% of cases, 11% of controls) and history of allergies (66% of cases, 51% of controls) were similar for cases and controls. However, cases were more likely to have a diagnosis of depression subsequent to their diagnosis of CFS compared to a similar time frame for controls (MOR = undefined; 95% CI lower bound = 2.5; P < 0.001). Positive antibody titers to B burgdorferi (one case and one control) and B microti (zero cases and two controls) were also similar. CONCLUSIONS: Further investigation into the role of prior routine exercise as a cofactor for CFS is warranted. This study supports the concurrence of CFS and depression, although pre-morbid history of depression was similar for both groups.
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收藏
页码:548 / 554
页数:7
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