Cutaneous papillomavirus infection in patients with rheumatoid arthritis or systemic lupus erythematosus. A case-control study
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作者:
Martinez-Martinez, M. U.
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机构:Hosp Cent Dr Ignacio Morones Prieto, Reg Unit Rheumatol & Osteoporosis, San Luis Potosi 78240, Mexico
Martinez-Martinez, M. U.
Baranda-Candido, L.
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机构:Hosp Cent Dr Ignacio Morones Prieto, Reg Unit Rheumatol & Osteoporosis, San Luis Potosi 78240, Mexico
Baranda-Candido, L.
Abud-Mendoza, C.
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Hosp Cent Dr Ignacio Morones Prieto, Reg Unit Rheumatol & Osteoporosis, San Luis Potosi 78240, MexicoHosp Cent Dr Ignacio Morones Prieto, Reg Unit Rheumatol & Osteoporosis, San Luis Potosi 78240, Mexico
Abud-Mendoza, C.
[1
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机构:
[1] Hosp Cent Dr Ignacio Morones Prieto, Reg Unit Rheumatol & Osteoporosis, San Luis Potosi 78240, Mexico
Previous studies informed an increased prevalence of cutaneous papillomavirus (cHPV) infection in patients with systemic lupus erythematosus (SLE). The main objective of our study was to evaluate factors associated with cHPV infection in patients with either rheumatoid arthritis (RA) or SLE, and to determine whether SLE itself is an independent risk factor for cHPV infection. We included 670 patients (in consecutive selection) in this cross-sectional study (550 with RA and 120 with SLE). All patients were evaluated by a dermatologist; patients with cHPV infection were selected as cases (63) and the other 607 patients were selected as controls. The prevalence of cHPV infection was increased 2.8-fold in SLE patients (20%) compared with RA patients (7.1%). When comparing cases with controls, bivariate analysis showed statistically significant differences for: age, having SLE, and treatment with mycophenolate mofetil (MMF). When all of the potential risk factors identified using bivariate analysis (age, having SLE, and MMF) were included into a multivariate model, independent risk factors for cHPV infection were: having SLE (odds ratio: 2.16, 95% confidence interval: 1.04-4.48) and MMF therapy (odds ratio: 2.91, 95% confidence interval: 1.18-7.14).
机构:
Sorbonne Univ, AP HP, Inst E3M, Grp Hosp Pitie Salpetriere,Ctr Natl Reference Lupu, Paris, FranceSorbonne Univ, AP HP, Inst E3M, Grp Hosp Pitie Salpetriere,Ctr Natl Reference Lupu, Paris, France
Papo, M.
Haroche, J.
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Sorbonne Univ, AP HP, Inst E3M, Grp Hosp Pitie Salpetriere,Ctr Natl Reference Lupu, Paris, FranceSorbonne Univ, AP HP, Inst E3M, Grp Hosp Pitie Salpetriere,Ctr Natl Reference Lupu, Paris, France
Haroche, J.
Sene, D.
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Univ Paris Cite, Hop Lariboisiere, AP HP, Dept Med Interne, Paris, FranceSorbonne Univ, AP HP, Inst E3M, Grp Hosp Pitie Salpetriere,Ctr Natl Reference Lupu, Paris, France
Sene, D.
Galicier, L.
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Hop St Louis, AP HP, Dept Immunol Clin, Paris, FranceSorbonne Univ, AP HP, Inst E3M, Grp Hosp Pitie Salpetriere,Ctr Natl Reference Lupu, Paris, France
Galicier, L.
Remy, P.
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Hop Henri Mondor, AP HP, Serv Nephrol, Paris, FranceSorbonne Univ, AP HP, Inst E3M, Grp Hosp Pitie Salpetriere,Ctr Natl Reference Lupu, Paris, France
Remy, P.
Misslin, C.
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Ctr Hosp Ouest Guyanais, Serv Medecine, St Laurent Du Maroni, FranceSorbonne Univ, AP HP, Inst E3M, Grp Hosp Pitie Salpetriere,Ctr Natl Reference Lupu, Paris, France
Misslin, C.
Amoura, Z.
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Sorbonne Univ, AP HP, Inst E3M, Grp Hosp Pitie Salpetriere,Ctr Natl Reference Lupu, Paris, France
Grp Hosp Pitie Salpetriere, AP HP, Ctr Natl Reference Lupus Syndrome Anticorps Antiph, Serv Med Interne 2,Inst E3M,Inserm UMRS,Ctr Immuno, Paris, FranceSorbonne Univ, AP HP, Inst E3M, Grp Hosp Pitie Salpetriere,Ctr Natl Reference Lupu, Paris, France
Amoura, Z.
Mathian, A.
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Grp Hosp Pitie Salpetriere, AP HP, Ctr Natl Reference Lupus Syndrome Anticorps Antiph, Serv Med Interne 2,Inst E3M,Inserm UMRS,Ctr Immuno, Paris, FranceSorbonne Univ, AP HP, Inst E3M, Grp Hosp Pitie Salpetriere,Ctr Natl Reference Lupu, Paris, France