This is a systematic review and meta-analysis that synthesized data from 472,150 patients with rheumatoid arthritis to estimate the prevalence and risk factors for herpes zoster. The primary finding was a pooled proportion of herpes zoster of 6% (95% CI: 4%-8%), with a 95% prediction interval of 5% to 45% reflecting substantial heterogeneity.
The authors identified several factors significantly associated with increased herpes zoster risk. These included female gender (OR = 1.47; 95% CI: 1.15-1.89; P = 0.002), older age (OR = 1.12; 95% CI: 1.02-1.22; P = 0.012), and specific medication uses: corticosteroid dosage ≥7.5 mg/day (OR = 2.16; 95% CI: 1.85-2.53; P < 0.001), corticosteroid use (OR = 1.42; 95% CI: 1.19-1.69; P < 0.001), tumor necrosis factor inhibitors (OR = 1.94; 95% CI: 1.43-2.63; P < 0.001), methotrexate (OR = 1.68; 95% CI: 1.39-2.02; P < 0.001), and hydroxychloroquine (OR = 2.67; 95% CI: 1.24-5.74; P = 0.012).
Comorbidities also showed significant associations: pulmonary disease (OR = 1.42; 95% CI: 1.10-1.83; P = 0.007), hypertension (OR = 1.43; 95% CI: 1.15-1.77; P = 0.001), kidney disease (OR = 1.30; 95% CI: 1.04-1.62; P = 0.022), and heart disease (OR = 2.30; 95% CI: 1.17-4.52; P = 0.016).
The authors acknowledge limitations, including substantial heterogeneity as reflected by the wide prediction interval. They highlight the necessity for timely prevention and targeted strategies but do not report safety data, follow-up duration, or causality notes. Practice relevance is restrained, emphasizing the need for further research.
View Original Abstract ↓
The co-occurrence of herpes zoster (HZ) in patients with rheumatoid arthritis (RA) represents a significant public health concern, with notable implications for both physical and mental health. This meta-analysis aims to systematically evaluate the pooled proportion of HZ in RA patients and identify associated factors.
A comprehensive literature search was conducted across eight databases: PubMed, Web of Science, Embase, Cochrane Library, CNKI, VIP, WANFANG Data, and CBM. The review was conducted in accordance with PRISMA guidelines, and the quality of included studies was assessed using the Newcastle-Ottawa Scale (NOS). All statistical analyses were performed using Stata 17.0.
A total of 17 observational studies (seven case-control and ten cohort) comprising 472,150 patients were included in this meta-analysis, indicating a descriptive pooled proportion of herpes zoster of 6% (95% CI: 4%-8%). However, the 95% prediction interval was 5% to 45%, reflecting substantial heterogeneity. This estimate represents an average across diverse settings rather than a universally generalizable figure. Eleven potential factors were evaluated, and the results indicated that the following were significantly associated with HZ in RA patients: female gender (OR = 1.47, 95% CI, 1.15-1.89, P = 0.002), age (OR = 1.12, 95% CI, 1.02-1.22, P = 0.012), corticosteroid dosage ≥7.5 mg/day (OR = 2.16, 95% CI, 1.85-2.53, P < 0.001), corticosteroid use (OR = 1.42, 95% CI, 1.19-1.69, P < 0.001), use of tumor necrosis associated factor inhibitors (OR = 1.94, 95% CI, 1.43-2.63, P < 0.001), methotrexate use (OR = 1.68, 95% CI, 1.39-2.02, P < 0.001), hydroxychloroquine use (OR = 2.67, 95% CI, 1.24-5.74, P = 0.012), history of pulmonary disease (OR = 1.42, 95% CI, 1.10-1.83, P = 0.007), history of hypertension (OR = 1.43, 95% CI, 1.15-1.77, P = 0.001), history of kidney disease (OR = 1.30, 95% CI, 1.04-1.62, P = 0.022), and history of heart disease (OR = 2.30, 95% CI, 1.17-4.52, P = 0.016).
Our meta-analysis indicates that the observed 6% pooled proportion of HZ in patients with RA constitutes a significant burden compared to the general population, highlighting the necessity for timely prevention. Moreover, when assessing HZ risk, factors such as female gender, age, corticosteroid use and dosage ≥7.5 mg/day, use of tumor necrosis factor inhibitors, methotrexate, hydroxychloroquine, and a history of pulmonary disease, hypertension, kidney disease, or heart disease should be carefully considered. These findings highlight the need for further research into the associated factors and underlying biological mechanisms of HZ in RA patients and support the development of targeted prevention strategies that address modifiable risks.
https://www.crd.york.ac.uk/PROSPERO/view/, identifier CRD420251050627.