TY - JOUR
T1 - Systematic review
T2 - Placebo response in drug trials of fibromyalgia syndrome and painful peripheral diabetic neuropathy - Magnitude and patient-related predictors
AU - Häuser, Winfried
AU - Bartram-Wunn, Eva
AU - Bartram, Claas
AU - Reinecke, Henriette
AU - Tölle, Thomas
PY - 2011/8
Y1 - 2011/8
N2 - The magnitude of placebo response and its predictors in fibromyalgia syndrome (FMS) and painful peripheral diabetic neuropathy (DPN) had not been studied. We performed a systematic review by searching MEDLINE, CENTRAL, SCOPUS, and the databases of the U.S. National Institutes of Health and the Pharmaceutical Research and Manufacturers of America until July 2010. We included randomised controlled trials of any pharmacological therapy compared with pharmacological placebo in patients with FMS and painful DPN. Pain values were converted to a 0 to 100 scale. We computed the pooled weighted mean difference (WMD) between pain baseline and end of treatment scores in placebo and active drug groups using a random effects model. A total of 72 studies (9827 patients) in FMS and of 70 studies in DPN (10,297 patients) were included. The pooled WMD in the FMS-placebo group was 7.69 (95% confidence interval [CI] 6.10 to 9.29) and 17.11 (95% CI 16.41 to 17.90) in painful DPN. The pooled WMD in the FMS-active drug group was 13.96 (95% CI 11.93 to 15.99) and in painful DPN was 22.54 (95% CI 20.49 to 24.58). The correlation between WMD in the placebo and active drug group in FMS was r = 0.69 and painful DPN r = 0.47. Placebo accounted for 45% of the response in the drug groups in FMS and for 62% in painful DPN. The placebo response was higher in painful DPN than in FMS (P <.001). The placebo response was not associated with age, sex, and race, but with year of study initiation, pain baseline, and effect size in active drug groups in both diseases. Placebo achieved a substantial proportion of the benefits of drug trials in fibromyalgia syndrome and painful diabetic peripheral neuropathy. However, the effects of placebo on pain were small.
AB - The magnitude of placebo response and its predictors in fibromyalgia syndrome (FMS) and painful peripheral diabetic neuropathy (DPN) had not been studied. We performed a systematic review by searching MEDLINE, CENTRAL, SCOPUS, and the databases of the U.S. National Institutes of Health and the Pharmaceutical Research and Manufacturers of America until July 2010. We included randomised controlled trials of any pharmacological therapy compared with pharmacological placebo in patients with FMS and painful DPN. Pain values were converted to a 0 to 100 scale. We computed the pooled weighted mean difference (WMD) between pain baseline and end of treatment scores in placebo and active drug groups using a random effects model. A total of 72 studies (9827 patients) in FMS and of 70 studies in DPN (10,297 patients) were included. The pooled WMD in the FMS-placebo group was 7.69 (95% confidence interval [CI] 6.10 to 9.29) and 17.11 (95% CI 16.41 to 17.90) in painful DPN. The pooled WMD in the FMS-active drug group was 13.96 (95% CI 11.93 to 15.99) and in painful DPN was 22.54 (95% CI 20.49 to 24.58). The correlation between WMD in the placebo and active drug group in FMS was r = 0.69 and painful DPN r = 0.47. Placebo accounted for 45% of the response in the drug groups in FMS and for 62% in painful DPN. The placebo response was higher in painful DPN than in FMS (P <.001). The placebo response was not associated with age, sex, and race, but with year of study initiation, pain baseline, and effect size in active drug groups in both diseases. Placebo achieved a substantial proportion of the benefits of drug trials in fibromyalgia syndrome and painful diabetic peripheral neuropathy. However, the effects of placebo on pain were small.
KW - Fibromyalgia syndrome
KW - Meta-analysis
KW - Painful peripheral diabetic neuropathy
KW - Placebo
KW - Systematic review
UR - http://www.scopus.com/inward/record.url?scp=79957858434&partnerID=8YFLogxK
U2 - 10.1016/j.pain.2011.01.050
DO - 10.1016/j.pain.2011.01.050
M3 - Article
C2 - 21429668
AN - SCOPUS:79957858434
SN - 0304-3959
VL - 152
SP - 1709
EP - 1717
JO - Pain
JF - Pain
IS - 8
ER -