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Prevalence of cervical HPV infection in women with systemic lupus erythematosus: A systematic review and meta-analysis
Authors:Mario García-Carrasco  Claudia Mendoza-Pinto  Adriana Rojas-Villarraga  Nicolás Molano-González  Verónica Vallejo-Ruiz  Pamela Munguía-Realpozo  Aurelio López Colombo  Ricard Cervera
Affiliation:1. Systemic Autoimmune Diseases Research Unit, Hospital de Especialidades, UMAE CMNMAC - CIBIOR, Instituto Mexicano del Seguro Social, Puebla, Puebla, Mexico;2. Department of Immunology and Rheumatology, Medicine School, Benemérita Universidad Autónoma de Puebla, Puebla, Puebla, Mexico;3. Fundación Universitaria de Ciencias de la Salud –FUCS, Bogotá, Colombia;4. Center for Autoimmune Diseases Research (CREA), School of Medicine and Health Sciences, Universidad del Rosario, Bogotá, Colombia;5. Centro de Investigación Biomédica de Oriente, Instituto Mexicano del Seguro Social, Km. 4.5 Carretera Federal Atlixco-Metepec, Atlixco, C.P. 74360, Puebla, Mexico;6. Puebla Research Coordination, Highly Specialized Medical Unit, Speciality Hospital of Puebla, Instituto Mexicano del Seguro Social, Puebla, Mexico;7. Department of Autoimmune Diseases, Hospital Clinic, Barcelona, Catalonia, Spain
Abstract:

Objective

The objectives of this systematic review and meta-regression were: 1) to compare the prevalence of cervical HPV infection between SLE patients and healthy controls and 2) to evaluate the relationship between cervical HPV infection and traditional and SLE-related risk factors for cervical HPV infection in these patients.

Methods

We conducted a systematic literature review (PubMed, Cochrane Library, Embase, Virtual Health Library and SciELO databases) following PRISMA guidelines and using meta-regression to investigate the pooled prevalence of cervical HPV infection in adult women with SLE. The articles included were independently evaluated by two investigators who extracted information on study characteristics, defined outcomes, risk of bias and summarized strength of evidence [Quality of evidence using the Oxford Centre for evidence-based medicine (EBM) Levels of Evidence]. Using meta-regression, we further analyzed whether factors such as multiple sexual partners and immunosuppressive therapy were associated with HPV prevalence. We evaluated the quality of evidence included using the Oxford Centre for EBM levels of evidence. Pooled odds ratios (ORs) and 95% confidence intervals (CI) were calculated for studies providing data on HPV prevalence in women with SLE and in healthy controls.

Results

A total of 687 articles were identified; 9 full-text articles examining the prevalence of cervical HPV infection in SLE women were included, comprising 751 SLE women. Eight studies employed PCR using general primers. The HPV prevalence varied from 3.1% to 80.7%. In the random effects meta-analysis, the pooled prevalence of cervical HPV infection in SLE vs. controls was 34.15% (95% CI: 19.6%–52.5%) vs. 15.3% (95% CI 0.79–27.8%), OR?=?2.87 (95% CI: 2.20–3.76) p?2?=?95.4%). When only SLE women were evaluated, meta-regression showed no significant differences between patients with and without a background of multiple sexual partners and any immunosuppressive therapy. In addition, the prevalence of cervical HPV infection did not significantly differ between SLE patients on azathioprine or cyclophosphamide.

Conclusions

This meta-analysis suggests that the prevalence of cervical HPV infection is higher in SLE women than in healthy controls. However, multiple sexual partners and any immunosuppressive therapy or specific immunosuppressive treatment (azathioprine and cyclophosphamide) were not associated with the prevalence of cervical HPV infection.
Keywords:Systemic lupus erythematosus  Human papillomavirus infection  Meta-regressions  CI.UB  confidence interval upper bound  EBM  evidence-based medicine  GCT  glucocorticoid  HGSIL  high-grade squamous intraepithelial lesions  HPV  human papillomavirus  HR  high-risk  IC  interval confidence  INTRCPT  intercept  MSP  multiple sexual partners  PCR  polymerase chain reaction  PRISMA  Preferred Reporting Items for Systematic Reviews and Meta-Analyses  SLE  systemic lupus erythematosus
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