The prevalence and severity of intestinal disaccharidase deficiency in human immunodeficiency virus-infected subjects

被引:11
作者
Taylor, C
Hodgson, K
Sharpstone, D
Sigthorsson, G
Coutts, M
Sherwood, R
Menzies, I
Gazzard, B
Bjarnason, I
机构
[1] Chelsea & Westminster Hosp, Dept Sexually Transmitted Dis, London, England
[2] Chelsea & Westminster Hosp, Dept Gastroenterol, London, England
[3] St Thomas Med Sch, Dept Histopathol, Dept Genitourinary Med, London, England
[4] Guys Kings & Thomas Med Sch, Dept Med, London SE5 9PJ, England
基金
英国医学研究理事会;
关键词
acquired immunodeficiency syndrome; human immunodeficiency virus; intestinal absorption; intestinal function; intestinal infection; morphometry;
D O I
10.1080/003655200750023552
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Gasuointestinal symptoms are distressing features of human immunodeficiency virus (HN) infection, and management is often empirical, including withdrawal of dietary lactose. We assessed the prevalence and severity of intestinal disaccharidase deficiency in vitro and in vivo. Methods: Fifty-four HIV-seropositive patients (19 HIV well +/- mild diarrhoea, 7 acquired immunodeficiency syndrome (AIDS) well, and 28 AIDS with diarrhoea) were studied with a combined non-invasive absorption-permeability-disaccharidase test that enables quantitative assessment of the rate of intestinal hydrolysis of lactose, sucrose, and palatinose. Thirty patients had jejunal biopsy specimens suitable for histomorphometric assessment, and 36 had in vitro disaccharidase activity measurement. Results: Patients with HIV (with mild diarrhoea) and AIDS (with and without severe diarrhoea) had frequent but mild histomorphometric changes in jejunal specimens. This was associated with frequent (21%-100%) and often severe in vitro jejunal disaccharidase deficiency. In vivo hydrolysis of lactose, sucrose, and palatinose was impaired in 25%-75% of patients, apart from HIV well patients, who were normal. The prevalence of the in vivo lactase and sucrase deficiency was significantly (P < 0.006) lower than in vitro and severe in about 30%. Conclusions: Intestinal disaccharidase deficiency is common both in vitro and in vivo in HIV-seropositive patients but sufficiently severe to consider lactose withdrawal only in about a quarter of the patients with AIDS and diarrhoea.
引用
收藏
页码:599 / 606
页数:8
相关论文
共 30 条
[1]   REGULATORY MECHANISMS OF THE LACTASE ACTIVITY IN ADULT INTESTINE [J].
AURICCHIO, S .
GASTROENTEROLOGY, 1994, 106 (05) :1376-1378
[2]   Intestinal inflammation, ileal structure and function in HIV [J].
Bjarnason, I ;
Sharpstone, DR ;
Francis, N ;
Marker, A ;
Taylor, C ;
Barrett, M ;
Macpherson, A ;
Baldwin, C ;
Menzies, IS ;
Crane, RC ;
Smith, T ;
Pozniak, A ;
Gazzard, BG .
AIDS, 1996, 10 (12) :1385-1391
[3]   COMPARISON OF 4 MARKERS OF INTESTINAL PERMEABILITY IN CONTROL SUBJECTS AND PATIENTS WITH CELIAC-DISEASE [J].
BJARNASON, I ;
MAXTON, D ;
REYNOLDS, AP ;
CATT, S ;
PETERS, TJ ;
MENZIES, IS .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 1994, 29 (07) :630-639
[4]   INTESTINAL PERMEABILITY - AN OVERVIEW [J].
BJARNASON, I ;
MACPHERSON, A ;
HOLLANDER, D .
GASTROENTEROLOGY, 1995, 108 (05) :1566-1581
[5]   Evaluation of differential disaccharide excretion in urine for non-invasive investigation of altered intestinal disaccharidase activity caused by alpha-glucosidase inhibition, primary hypolactasia, and coeliac disease [J].
Bjarnason, I ;
Batt, R ;
Catt, S ;
Macpherson, A ;
Maxton, D ;
Menzies, IS .
GUT, 1996, 39 (03) :374-381
[6]   METRONIDAZOLE REDUCES INTESTINAL INFLAMMATION AND BLOOD-LOSS IN NONSTEROIDAL ANTIINFLAMMATORY DRUG-INDUCED ENTEROPATHY [J].
BJARNASON, I ;
HAYLLAR, J ;
SMETHURST, P ;
PRICE, A ;
GUMPEL, MJ .
GUT, 1992, 33 (09) :1204-1208
[7]   INVESTIGATION OF UPPER GASTROINTESTINAL SYMPTOMS IN PATIENTS WITH AIDS [J].
CONNOLLY, GM ;
FORBES, A ;
GLEESON, JA ;
GAZZARD, BG .
AIDS, 1989, 3 (07) :453-456
[8]  
FAIRCLOUGH PD, 1984, TXB GASTROENTEROLOGY, P361
[9]   PRACTICAL ADVICE FOR THE GASTROENTEROLOGIST DEALING WITH SYMPTOMATIC HIV DISEASE [J].
GAZZARD, BG .
GUT, 1990, 31 (07) :733-735
[10]  
HEPNER GW, 1974, GASTROENTEROLOGY, V63, P1250