Hypolactasia: a common enzyme deficiency leading to lactose malabsorption and intolerance

被引:0
作者
Lember, Margus [1 ,2 ]
机构
[1] Univ Tartu, Dept Internal Med, EE-51014 Tartu, Estonia
[2] Tartu Univ Hosp, EE-51014 Tartu, Estonia
来源
POLSKIE ARCHIWUM MEDYCYNY WEWNETRZNEJ-POLISH ARCHIVES OF INTERNAL MEDICINE | 2012年 / 122卷
关键词
clinical picture; epidemiology; hypolactasia; treatment; ADULT-TYPE HYPOLACTASIA; BONE-MINERAL DENSITY; LACTASE DEFICIENCY; MILK CONSUMPTION; TRANSIT-TIME; SMALL BOWEL; PREVALENCE; MALDIGESTERS; PERSISTENCE; TOLERANCE;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Adult-type hypolactasia (lactase nonpersistence or lactase deficiency) is the most common enzyme deficiency leading to lactose intolerance and primary lactose malabsorption. Clinical presentation of the condition includes symptoms resulting from bacterial fermentation of undigested lactose in the colon, which gives rise to gas bloat, increased motility, and loose stools. Diagnosis of the disease is based on clinical symptoms, biochemical, functional, histochemical and genetic tests. Treatment includes dietary restrictions, namely, use of low-lactose milk, in which lactose has been prehydrolyzed, or non-lactose milk.
引用
收藏
页码:60 / 64
页数:5
相关论文
共 42 条
  • [1] Prevalence and trends in adult-type hypolactasia in different age cohorts in Central Sweden diagnosed by genotyping for the adult-type hypolactasia-linked LCT-13910C>T mutation
    Almon, Ricardo
    Engfeldt, Peter
    Tysk, Curt
    Sjostrom, Michael
    Nilsson, Torbjorn K.
    [J]. SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 2007, 42 (02) : 165 - 170
  • [2] STRIP TEST IS RELIABLE IN COMMON PREVALENCES OF HYPOLACTASIA
    AROLA, H
    KOIVULA, T
    JOKELA, H
    JAUHIAINEN, M
    KEYRILAINEN, O
    UUSITALO, A
    ISOKOSKI, M
    [J]. SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 1987, 22 (04) : 509 - 512
  • [3] DIAGNOSIS OF HYPOLACTASIA AND LACTOSE-MALABSORPTION
    AROLA, H
    [J]. SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 1994, 29 : 26 - 35
  • [4] Genetic signatures of strong recent positive selection at the lactase gene
    Bersaglieri, T
    Sabeti, PC
    Patterson, N
    Vanderploeg, T
    Schaffner, SF
    Drake, JA
    Rhodes, M
    Reich, DE
    Hirschhorn, JN
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2004, 74 (06) : 1111 - 1120
  • [5] CHRISTOPHER NL, 1971, GASTROENTEROLOGY, V60, P845
  • [6] PREVALENCE OF PRIMARY ADULT LACTOSE-MALABSORPTION IN HUNGARY
    CZEIZEL, A
    FLATZ, G
    FLATZ, SD
    [J]. HUMAN GENETICS, 1983, 64 (04) : 398 - 401
  • [7] Molecularly defined lactose malabsorption, peak bone mass and bone turnover rate in young Finnish men
    Enattah, N
    Välimäki, VV
    Välimäki, MJ
    Löyttyniemi, E
    Sahi, T
    Järvelä, I
    [J]. CALCIFIED TISSUE INTERNATIONAL, 2004, 75 (06) : 488 - 493
  • [8] Identification of a variant associated with adult-type hypolactasia
    Enattah, NS
    Sahi, T
    Savilahti, E
    Terwilliger, JD
    Peltonen, L
    Järvelä, I
    [J]. NATURE GENETICS, 2002, 30 (02) : 233 - 237
  • [9] GILAT T, 1972, GASTROENTEROLOGY, V62, P1125
  • [10] Calcium supply, bone mineral density and genetically defined lactose maldigestion in a cohort of elderly men
    Gugatschka, M.
    Hoeller, A.
    Fahrleitner-Pammer, A.
    Dobnig, H.
    Pietschmann, P.
    Kudlacek, S.
    Obermayer-Pietsch, B.
    [J]. JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION, 2007, 30 (01) : 46 - 51