Epidermal growth factor enemas with oral mesalamine for mild-to-moderate left-sided ulcerative colitis or proctitis

被引:242
作者
Sinha, A
Nightingale, JMD [1 ]
West, KP
Berlanga-Acosta, J
Playford, RJ
机构
[1] Leicester Royal Infirm, Gastroenterol Ctr, Dept Gastroenterol, Leicester LE1 5WW, Leics, England
[2] Leicester Royal Infirm, Dept Pathol, Leicester LE1 5WW, Leics, England
[3] Ctr Genet Engn & Biotechnol, Havana, Cuba
[4] Univ London Imperial Coll Sci Technol & Med, Fac Med, Gastroenterol Sect, London, England
关键词
D O I
10.1056/NEJMoa013136
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Epidermal growth factor (EGF) is a potent mitogenic peptide produced by salivary glands. We examined whether EGF enemas are an effective treatment for active left-sided ulcerative colitis and ulceration limited to the rectum (proctitis). Methods: In a randomized, double-blind clinical trial conducted at Leicester Royal Infirmary, 12 patients with mild-to-moderate left-sided ulcerative colitis received daily enemas of 5 microg of EGF in 100 ml of an inert carrier and 12 received daily enemas with carrier alone for 14 days. All also began to receive 1.2 g of oral mesalamine per day or had their dose increased by 1.2 g per day. Patients were assessed clinically at 0, 2, 4, and 12 weeks and by sigmoidoscopy and biopsy at 0, 2, and 4 weeks. The primary end point was disease remission (defined by a St. Marks score of 4 or less without sigmoidoscopic evidence of inflammation) at two weeks. Secondary end points were clinically significant improvements in disease activity (defined by a decrease of more than 3 points in the St. Marks score or the ulcerative colitis disease-activity index) at two and four weeks. Analyses were performed according to the intention-to-treat principle. Results: After two weeks, 10 of the 12 patients given EGF enemas were in remission, as compared with 1 of 12 in the control group (83 percent vs. 8 percent, P<0.001). At the 2-week assessment, disease-activity scores, sigmoidoscopic score, and histologic scores were all significantly better in the EGF group than in the placebo group (P<0.01 for all comparisons), and this benefit was maintained at 4 weeks and at 12 weeks. Conclusions: This study provides preliminary data suggesting that EGF enemas are an effective treatment for active left-sided ulcerative colitis.
引用
收藏
页码:350 / 357
页数:8
相关论文
共 31 条
[1]  
ARAKI F, 1989, CHEM PHARM BULL, V37, P404
[2]   VARIATION BETWEEN OBSERVERS IN DESCRIBING MUCOSAL APPEARANCES IN PROCTOCOLITIS [J].
BARON, JH ;
CONNELL, AM ;
LENNARDJONES, JE .
BRITISH MEDICAL JOURNAL, 1964, 1 (5374) :89-+
[3]   HUMAN EPIDERMAL GROWTH-FACTOR PRECURSOR - CDNA SEQUENCE, EXPRESSION INVITRO AND GENE ORGANIZATION [J].
BELL, GI ;
FONG, NM ;
STEMPIEN, MM ;
WORMSTED, MA ;
CAPUT, D ;
KU, L ;
URDEA, MS ;
RALL, LB ;
SANCHEZPESCADOR, R .
NUCLEIC ACIDS RESEARCH, 1986, 14 (21) :8427-8446
[4]   Prophylactic use of epidermal growth factor reduces ischemia/reperfusion intestinal damage [J].
Berlanga, J ;
Prats, P ;
Remirez, D ;
Gonzalez, R ;
Lopez-Saura, P ;
Aguiar, J ;
Ojeda, M ;
Boyle, JJ ;
Fitzgerald, AJ ;
Playford, RJ .
AMERICAN JOURNAL OF PATHOLOGY, 2002, 161 (02) :373-379
[5]   ENHANCEMENT OF WOUND-HEALING BY TOPICAL TREATMENT WITH EPIDERMAL GROWTH-FACTOR [J].
BROWN, GL ;
NANNEY, LB ;
GRIFFEN, J ;
CRAMER, AB ;
YANCEY, JM ;
CURTSINGER, LJ ;
HOLTZIN, L ;
SCHULTZ, GS ;
JURKIEWICZ, MJ ;
LYNCH, JB .
NEW ENGLAND JOURNAL OF MEDICINE, 1989, 321 (02) :76-79
[6]   Potency and stability of C terminal truncated human epidermal growth factor [J].
Calnan, DP ;
Fagbemi, A ;
Berlanga-Acosta, J ;
Marchbank, T ;
Sizer, T ;
Lakhoo, K ;
Edwards, AD ;
Playford, RJ .
GUT, 2000, 47 (05) :622-627
[7]   COMBINED INTESTINAL TREFOIL FACTOR AND EPIDERMAL GROWTH-FACTOR IS PROPHYLACTIC AGAINST INDOMETHACIN-INDUCED GASTRIC DAMAGE IN THE RAT [J].
CHINERY, R ;
PLAYFORD, RJ .
CLINICAL SCIENCE, 1995, 88 (04) :401-403
[8]  
DRUMM B, 1988, LANCET, V1, P111
[9]   Ulcerative colitis [J].
Farrell, RJ ;
Peppercorn, MA .
LANCET, 2002, 359 (9303) :331-340
[10]   MEDICAL THERAPY OF ULCERATIVE-COLITIS [J].
HANAUER, SB .
LANCET, 1993, 342 (8868) :412-417