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DOI: 10.1055/s-2003-44306
Treatment of Pouchitis with Dehydroepiandrosterone (DHEA) - a Case Report
Behandlung der Pouchitis mit Dehydroepiandrosteron (DHEA) - ein FallberichtPublication History
Publication Date:
01 December 2003 (online)

Zusammenfassung
Hintergrund: Dehydroepiandrosteron (DHEA) inhibiert die Aktivierung von „nuclear factor kappa B” über den „peroxisome proliferator-activated receptor α”. Eine Aktivierung von „nuclear factor kappa B” ist in aktiv entzündeter Darmschleimhaut bei der Colitis ulcerosa nachweisbar. Die Pouchitis ist eine Komplikation nach Proktokolektomie aufgrund einer Colitis ulcerosa und stellt nach wie vor eine therapeutische Herausforderung dar.
Fall: Wir berichten über die Behandlung einer 35-jährigen Patientin mit Pouchitis mittels DHEA 200 mg/d über acht Wochen. Die Patientin wurde über weitere acht Wochen nachbeobachtet.
Die Stuhlfrequenz fiel von 15-18/d auf 8/d und die initiale Schleimbeimengung verschwand. Die Stuhlkonsistenz besserte sich von flüssig/weich zu weich/fest. Vorher vorhandene Bauchschmerzen verschwanden. Die endoskopisch-makroskopischen Entzündungszeichen besserten sich. Acht Wochen nach Beendigung der DHEA-Einnahme litt die Patientin erneut an 12 bis 18 weichen bis flüssigen Stühlen pro Tag und leichten Bauchschmerzen.
Schlussfolgerung: Die therapeutischen Effekte von DHEA bei der Pouchitis verdienen eine weitere, systematische Überprüfung.
Abstract
Background: Dehydroepiandrosterone (DHEA) inhibits activation of nuclear factor kappa B (NF-κB), which is known to be activated in inflammatory lesions of ulcerative colitis, via PPARα. In a pilot trial DHEA was effective for the treatment of active ulcerative colitis. Pouchitis is a common complication after proctocolectomy for ulcerative colitis and still a therapeutical challenge.
Case: DHEA 200 mg/d was tested in chronic active pouchitis in a 35-year-old female patient. DHEA was given for eight weeks, and follow up for further eight weeks was performed. The number of stools dropped from 15-18/d to 8/d, the addition of mucus, which was observed initially, was absent during treatment. The consistence of stools improved from liquid/soft to soft/solid. Abdominal pain resolved and endoscopical signs of inflammation improved. Eight weeks after termination of treatment with DHEA, the patient again suffered from 12 to 18 soft to liquid stools per day and mild abdominal pain.
Conclusion: Therapeutic effects of DHEA in pouchitis should be evaluated systematically.
Schlüsselwörter
Pouchitis - Dehydroepiandrosteron - Colitis ulcerosa
Key words
Pouchitis - Dehydroepiandrosterone - ulcerative colitis
References
- 1 Gionchetti P, Amadini C, Rizzello F. et al . Review article: treatment of mild to moderate ulcerative colitis and pouchitis. Aliment Pharmacol Ther. 2002; 16 13-19 (Suppl 4)
- 2 Straub R H, Vogl D, Gross V. et al . Association of humoral markers of inflammation and dehydroepiandrosterone sulfate or cortisol serum levels in patients with chronic inflammatory bowel disease. Am J Gastroenterol. 1998; 93 2197-2202
- 3 Straub R H, Lehle K, Herfarth H. et al . Dehydroepiandrosterone in relation to other adrenal hormones during an acute inflammatory stressful disease state compared with chronic inflammatory disease: role of interleukin-6 and tumour necrosis factor. Eur J Endocrinol. 2002; 146 365-374
- 4 Poynter M E, Daynes R A. Peroxisome proliferator-activated receptor alpha activation modulates cellular redox status, represses nuclear factor-kappaB signaling, and reduces inflammatory cytokine production in aging. J Biol Chem. 1998; 273 32 833-32 841
- 5 Cheng G F, Tseng J. Regulation of murine interleukin-10 production by dehydroepiandrosterone. J Interferon Cytokine Res. 2000; 20 471-478
- 6 Andus T, Klebl F, Rogler G. et al . Patients with refractory Crohn’s disease and ulcerative colitis respond to dehydroepiandrosterone in a pilot study. Aliment Pharmacol Ther. 2003; 17 409-414
- 7 Meagher A P, Farouk R, Dozois R R. et al . J ileal pouch-anal anastomosis for chronic ulcerative colitis: Complications and long-term outcome in 1310 patients. Br J Surg. 1998; 85 800-803
- 8 Sandborn W J, McLeod R, Jewell D P. Medical therapy for induction and maintenance of remission in pouchitis: a systematic review. Inflamm Bowel Dis. 1999; 5 33-39
- 9 Shen B, Achkar J P, Lashner B A. et al . A randomized clinical trial of ciprofloxacin and metronidazole to treat acute pouchitis. Inflamm Bowel Dis. 2001; 7 301-305
- 10 Mimura T, Rizzello F, Helwig U. et al . Four-week open-label trial of metronidazole and ciprofloxacin for the treatment of recurrent or refractory pouchitis. Aliment Pharmacol Ther. 2002; 16 909-917
- 11 Sambuelli A, Boerr L, Negreira S. et al . Budesonide enema in pouchitis - a double-blind, double-dummy, controlled trial. Aliment Pharmacol Ther. 2002; 16 27-34
- 12 Miglioli M, Barbara L, Di Febo G. et al . Topical administration of 5-aminosalicylic acid: a therapeutic proposal for the treatment of pouchitis. N Engl J Med. 1989; 320 257
- 13 Kuzela L, Kascak M, Vavrecka A. Induction and maintenance of remission with non-pathogenic Escherichia coli in patients with pouchitis. Am J Gastroenterol. 2001; 96 3218-3219
- 14 Chang D M, Lan J L, Lin H Y. et al . Dehydroepiandrosterone treatment of women with mild-to-moderate systemic lupus erythematosus: a multicenter randomised, double-blind, placebo-controlled trial. Arthritis Rheum. 2002; 46 2924-2927
- 15 Petri M A, Lahita R G, van Vollenhoven R F. et al . Effects of prasterone on corticosteroid requirements of women with systemic lupus erythematosus: a double-blind, randomised, placebo-controlled trial. Arthritis Rheum. 2002; 46 1820-1829
- 16 Allolio B, Arlt W. DHEA treatment: myth or reality?. Trends Endocrinol Metab. 2002; 13 288-294
- 17 Dyner T S, Lang W, Geaga J. et al . An open-label dose-escalation trial of oral dehydroepiandrosterone tolerance and pharmacokinetics in patients with HIV disease. J Acquir Immune Defic Syndr. 1993; 6 459-465
- 18 Kroboth P D, Salek F S, Pittenger A L. et al . DHEA and DHEA-S. a review. J Clin Pharmacol. 1999; 39 327-348
Dr. med. Frank Klebl
Klinik und Poliklinik für Innere Medizin I, Klinikum der Universität Regensburg
93042 Regensburg
Germany
Email: frank.klebl@klinik.uni-regensburg.de