Orlistat for the long-term treatment of obesity

被引:18
作者
Harp, JB [1 ]
机构
[1] Univ N Carolina, Dept Nutr, Chapel Hill, NC 27599 USA
来源
DRUGS OF TODAY | 1999年 / 35卷 / 02期
关键词
D O I
10.1358/dot.1999.35.2.527969
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Orlistat, a potent gastrointestinal lipase inhibitor, is a member of a new class of drugs designed for the long-term treatment of obesity. When given with a fat-containing meal, orlistat reduces dietary fat absorption by similar to 30%, which equates to a decrease in caloric absorption of similar to 200 kilocalories per day. A 2-year European study found a mean decrease in body weight of 10.2% (10.3 kg) in the orlistat group compared to 6.1% (6.1 kg) in the placebo group at 1 year. Additionally, 9.3% of the orlistat group versus 2.1% of the placebo group lost >20% of their initial weight. Serum lipids and diabetes control are also improved by orlistat. Related to orlistat's mechanism of action, side effects include oily spotting, flatulence and frequent loose stools, but not frank diarrhea or intestinal malabsorption. Vitamin D and beta-carotene levels decreased, but remained within the normal range. In summary, orlistat is the first example of a new class of antiobesity drugs that enhances weight loss and weight maintenance by interfering with dietary fat absorption. Orlistat has tolerable gastrointestinal side effects and no major drug toxicity. Orlistat is a viable adjunct to lifestyle interventions used in the long-term management Of obesity. (C) 1999 Prous Science. All rights reserved.
引用
收藏
页码:139 / 145
页数:7
相关论文
共 31 条
[1]   Effects of the lipase inhibitor orlistat on intake and preference for dietary fat in rats [J].
Ackroff, K ;
Sclafani, A .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 1996, 271 (01) :R48-R54
[2]   CALORIES, FAT AND CHOLESTEROL - INTAKE PATTERNS IN THE UNITED-STATES POPULATION BY RACE, SEX AND AGE [J].
BLOCK, G ;
ROSENBERGER, WF ;
PATTERSON, BH .
AMERICAN JOURNAL OF PUBLIC HEALTH, 1988, 78 (09) :1150-1155
[3]  
DRENT ML, LIPASE INHIBITION HO
[4]   Influence of orlistat on the regulation of gallbladder contraction in man - A randomized double-blind placebo-controlled crossover study [J].
Froehlich, F ;
Hartmann, D ;
Guezelhan, C ;
Gonvers, JJ ;
Jansen, JBMJ ;
Fried, M .
DIGESTIVE DISEASES AND SCIENCES, 1996, 41 (12) :2404-2408
[5]   NUTRITION AND SOMATOMEDIN .22. MOLECULAR REGULATION OF INSULIN-LIKE GROWTH FACTOR-I DURING FASTING AND REFEEDING IN RATS [J].
GOLDSTEIN, S ;
HARP, JB ;
PHILLIPS, LS .
JOURNAL OF MOLECULAR ENDOCRINOLOGY, 1991, 6 (01) :33-43
[6]  
GUERCIOHNI R, 1997, INT J OBESITY, V3, pS12
[7]  
GUZELHAN C, 1994, J INT MED RES, V22, P255
[8]   INHIBITION OF PANCREATIC LIPASE INVITRO BY THE COVALENT INHIBITOR TETRAHYDROLIPSTATIN [J].
HADVARY, P ;
LENGSFELD, H ;
WOLFER, H .
BIOCHEMICAL JOURNAL, 1988, 256 (02) :357-361
[9]   Lack of interaction between orlistat and oral contraceptives [J].
Hartmann, D ;
Guzelban, C ;
Zuiderwijk, PBM ;
Odink, J .
EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 1996, 50 (05) :421-424
[10]   EFFECT ON DIETARY-FAT ABSORPTION OF ORLISTAT, ADMINISTERED AT DIFFERENT TIMES RELATIVE TO MEAL INTAKE [J].
HARTMANN, D ;
HUSSAIN, Y ;
GUZELHAN, C ;
ODINK, J .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 1993, 36 (03) :266-270