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1.
J Am Acad Dermatol ; 52(2): 262-7, 2005 Feb.
Article in English | MEDLINE | ID: mdl-15692471

ABSTRACT

BACKGROUND: Methotrexate (MTX) is a folate analogue used in the treatment of moderate to severe psoriasis and rheumatoid arthritis (RA). It oppositely affects inflammation and hyperhomocysteinemia-two independent risk factors for vascular disease. To date, there are no published reports evaluating the impact of these potentially paradoxical action of MTX. OBJECTIVE: The purpose of this study was to evaluate the effect of MTX therapy on the incidence of vascular disease in patients with psoriasis and RA. METHODS: We conducted a retrospective cohort study in which we analyzed computerized records of 7,615 outpatients diagnosed with psoriasis and 6,707 with RA at the Veterans Integrated Service Network 8. RESULTS: Patients prescribed MTX therapy had a significantly reduced risk of vascular disease compared to those who were not prescribed MTX (psoriasis: RR = 0.73, 95% CI = 0.55-0.98; RA: 0.83, 0.71-0.96). This reduction was most evident for patients prescribed a low cumulative dose of MTX (psoriasis: RR = 0.50, 95% CI = 0.31-0.79; RA = 0.65, 0.52-0.80). Concomitant use of folic acid (FA) with MTX also reduced the incidence of vascular disease in patients prescribed MTX (psoriasis: RR = 0.56, 95% CI = 0.39-0.80; RA: 0.77, 0.38-1.56). CONCLUSIONS: MTX therapy reduced the incidence of vascular disease in veterans with psoriasis or RA. Low to moderate cumulative dose appears more beneficial than the higher dose. We hypothesize that this effect is caused by its anti-inflammatory properties. In addition, a combination of MTX and FA led to a further reduction in the incidence of vascular disease.


Subject(s)
Arthritis, Rheumatoid/drug therapy , Immunosuppressive Agents/therapeutic use , Methotrexate/therapeutic use , Psoriasis/drug therapy , Vascular Diseases/prevention & control , Aged , Arthritis, Rheumatoid/complications , Cohort Studies , Comorbidity , Databases, Factual , Drug Synergism , Drug Therapy, Combination , Female , Florida/epidemiology , Folic Acid/administration & dosage , Folic Acid/therapeutic use , Humans , Hyperhomocysteinemia/chemically induced , Hyperhomocysteinemia/prevention & control , Immunosuppressive Agents/administration & dosage , Immunosuppressive Agents/adverse effects , Incidence , Male , Medical Records Systems, Computerized , Methotrexate/administration & dosage , Methotrexate/adverse effects , Middle Aged , Psoriasis/complications , Retrospective Studies , Risk , Vascular Diseases/complications , Vascular Diseases/epidemiology , Veterans
2.
Int J Dermatol ; 42 Suppl 1: 29-35, 2003 Sep.
Article in English | MEDLINE | ID: mdl-14567368

ABSTRACT

UNLABELLED: BACKGROUND Tinea pedis (athlete's foot) is the most common fungal infection in the general population. Ciclopirox, a broad-spectrum hydroxypyridone antifungal, has proven efficacy against the organisms commonly implicated in tinea pedis; Trichophyton rubrum, T.mentagrophytes and Epidermophyton floccosum. OBJECTIVE: Two multicenter, double-blind, clinical studies compared the efficacy and safety of ciclopirox gel with that of its vehicle base in subjects with moderate interdigital tinea pedis with or without plantar involvement. METHODS: Three hundred and seventy-four subjects were enrolled and randomized to one of two treatment groups: ciclopirox gel 0.77%, or ciclopirox gel vehicle, applied twice daily for 28 days, with a final visit up to day 50. The primary efficacy variable was Treatment Success defined as combined mycological cure and clinical improvement >/= 75%. Secondary measures of effectiveness were Global Clinical Response, Sign and Symptom Severity Scores, Mycological Evaluation (KOH examination and final culture result), Mycological Cure (negative KOH and negative final culture results) and Treatment Cure (combined clinical and mycological cure). RESULTS: At endpoint (final post-baseline visit), 60% of the ciclopirox subjects achieved treatment success compared to 6% of the vehicle subjects. At the same time point, 66% of ciclopirox subjects compared with 19% of vehicle subjects were either cleared or had excellent improvement. Pooled data showed that 85% of ciclopirox subjects were mycologically cured, compared to only 16% of vehicle subjects at day 43, 2 weeks post-treatment. CONCLUSIONS: Ciclopirox gel 0.77% applied twice daily for 4 weeks is an effective treatment of moderate interdigital tinea pedis due to T. rubrum, T. mentagrophytes and E. floccosum and is associated with a low incidence of minor adverse effects.


Subject(s)
Antifungal Agents/administration & dosage , Pyridones/administration & dosage , Tinea Pedis/diagnosis , Tinea Pedis/drug therapy , Administration, Topical , Adolescent , Adult , Aged , Aged, 80 and over , Analysis of Variance , Ciclopirox , Dose-Response Relationship, Drug , Double-Blind Method , Drug Administration Schedule , Female , Follow-Up Studies , Gels/therapeutic use , Humans , Male , Middle Aged , Probability , Reference Values , Severity of Illness Index , Treatment Outcome
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