Sulfasalazine and pentoxifylline in psoriasis: A possible safe alternative

被引:22
作者
El-Mofty, Medhat [1 ]
El-Darouti, Mohamed [1 ]
Rasheed, Hoda [1 ]
Bassiouny, Dalia Ahmed [1 ]
Abdel-Halim, Mona [1 ]
Zaki, Naglaa Sameh [1 ]
El-Hanafy, Ghada [1 ]
El-Hadidi, Heba [1 ]
Azzam, Omar [1 ]
El-Ramly, Amany [1 ]
Fawzy, Marwa [1 ]
机构
[1] Cairo Univ, Kasr El Aini Univ Hosp, Dept Dermatol, Cairo, Egypt
关键词
NECROSIS-FACTOR-ALPHA; TNF-ALPHA; IN-VIVO; DISEASE; THERAPY; CELLS; RELEASE; ABSORPTION; IL-1-BETA; DRUGS;
D O I
10.3109/09546630903460260
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100227 [皮肤病学];
摘要
Background: Conventional therapy of extensive psoriasis is effective but has complications. Biologics are safer but expensive. Objective: To assess the efficacy of sulfasalazine and pentoxifylline, which have TNF antagonizing and anti-proliferative action in the treatment of psoriasis. Methods: In this randomized controlled trial, 32 patients with extensive psoriasis were divided into four groups: group A received sulfasalazine; group B received pentoxifylline; group C received both drugs; and group D received methotrexate. The Psoriasis Area and Severity Index (PASI) score was done at weeks 0, 2, 4, 6 and 8. Results: A significant reduction in PASI score occurred in groups C and D (p = 0.043 and 0.018, respectively). A significantly higher percentage of PASI score reduction occurred in group D compared with groups A, B and C (p = 0.006, 0.003 and 0.030, respectively). An excellent response occurred in one patient (14.3%) in group D. A very good response occurred in two patients (22.2%) in group C, and in five patients (71.4%) in group D. A moderate response occurred in three patients (37.5%) in group A, one patient (12.5%) in group B, and one patient (14.3%) in group D. Conclusion: Although incomparable to methotrexate, combined sulfasalazine and pentoxifylline produced a good response in cases of extensive psoriasis. Multicentre studies are needed to validate these results.
引用
收藏
页码:31 / 37
页数:7
相关论文
共 31 条
[1]
Ashcroft DM, 1999, BRIT J DERMATOL, V141, P185
[2]
Baumgartner TedA., 1998, CONDUCTING READING R, Vsecond
[3]
EFFECT OF PENTOXIFYLLINE ON THE PHAGOCYTIC-ACTIVITY, CAMP LEVELS, AND SUPEROXIDE ANION PRODUCTION BY MONOCYTES AND POLYMORPHONUCLEAR CELLS [J].
BESSLER, H ;
GILGAL, R ;
DJALDETTI, M ;
ZAHAVI, I .
JOURNAL OF LEUKOCYTE BIOLOGY, 1986, 40 (06) :747-754
[4]
Bissonnette EY, 1996, J IMMUNOL, V156, P218
[5]
Pentoxifylline inhibits human T-cell adhesion to dermal endothelial cells [J].
Bruynzeel, I ;
vanderRaaij, LMH ;
Willemze, R ;
Stoof, TJ .
ARCHIVES OF DERMATOLOGICAL RESEARCH, 1997, 289 (04) :189-193
[6]
LACK OF EFFECT OF CLONIDINE AND PENTOXIFYLLINE IN SHORT-TERM THERAPY OF DIABETIC PERIPHERAL NEUROPATHY [J].
COHEN, KL ;
LUCIBELLO, FE ;
CHOMIAK, M .
DIABETES CARE, 1990, 13 (10) :1074-1077
[7]
Interaction between azathioprine and aminosalicylates:: an in vivo study in patients with Crohn's disease [J].
Dewit, O ;
Vanheuverzwyn, R ;
Desager, JP ;
Horsmans, Y .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2002, 16 (01) :79-85
[8]
The use of sulfasalazine and pentoxifylline (low-cost antitumour necrosis factor drugs) as adjuvant therapy for the treatment of pemphigus vulgaris: a comparative study [J].
El-Darouti, M. ;
Marzouk, S. ;
Hay, R. Abdel ;
El Tawdy, A. ;
Fawzy, M. ;
Leheta, T. ;
Gammaz, H. ;
Al Gendy, N. .
BRITISH JOURNAL OF DERMATOLOGY, 2009, 161 (02) :313-319
[9]
FRANKLIN JL, 1973, GASTROENTEROLOGY, V64, P517
[10]
Gilhar A, 1996, ACTA DERM-VENEREOL, V76, P437