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乳糖酶缺乏症间接诊断方法的比较。

Comparison of indirect diagnostic methods for hypolactasia.

作者信息

Arola H, Koivula T, Jokela H, Jauhiainen M, Keyriläinen O, Ahola T, Uusitalo A, Isokoski M

机构信息

Dept. of Public Health, University of Tampere, Finland.

出版信息

Scand J Gastroenterol. 1988 Apr;23(3):351-7. doi: 10.3109/00365528809093878.

DOI:10.3109/00365528809093878
PMID:3133752
Abstract

The aim of this study was to continue our previously published work and to compare the different indirect diagnostic methods for hypolactasia with the lactase to sucrase ratio obtained by jejunal biopsy. The following tests were performed in 63 adult patients: the breath hydrogen test, the lactose tolerance test with ethanol (serum galactose measurement after oral lactose load with ethanol), the urinary lactose tolerance test (urinary galactose measurement after oral lactose load with ethanol), and the strip test (like the former but using a special test strip for urinary galactose). Specificities of all these tests were good (96-98%). The 3-h breath hydrogen test was less sensitive (69%) than the other methods (81-94%). The strip test is recommended for the general practitioner for the diagnosis of this common cause of abdominal complaints.

摘要

本研究的目的是延续我们之前发表的工作,并将不同的乳糖酶缺乏间接诊断方法与通过空肠活检获得的乳糖酶与蔗糖酶比值进行比较。对63名成年患者进行了以下测试:呼气氢试验、乙醇乳糖耐量试验(口服乳糖负荷加乙醇后测定血清半乳糖)、尿乳糖耐量试验(口服乳糖负荷加乙醇后测定尿半乳糖)以及试纸条试验(与前者类似,但使用用于尿半乳糖的特殊试纸条)。所有这些测试的特异性都很好(96 - 98%)。3小时呼气氢试验的敏感性(69%)低于其他方法(81 - 94%)。建议全科医生使用试纸条试验来诊断这种常见的腹部不适病因。

相似文献

1
Comparison of indirect diagnostic methods for hypolactasia.乳糖酶缺乏症间接诊断方法的比较。
Scand J Gastroenterol. 1988 Apr;23(3):351-7. doi: 10.3109/00365528809093878.
2
Strip test is reliable in common prevalences of hypolactasia.在常见的乳糖酶缺乏患病率情况下,试纸检测是可靠的。
Scand J Gastroenterol. 1987 May;22(4):509-12. doi: 10.3109/00365528708991499.
3
Concordance of indirect methods for the detection of lactose malabsorption in diabetic and nondiabetic subjects.糖尿病患者和非糖尿病患者乳糖吸收不良间接检测方法的一致性
Digestion. 1991;48(2):81-8. doi: 10.1159/000200677.
4
Diagnosis of hypolactasia and lactose malabsorption.低乳糖酶症和乳糖吸收不良的诊断
Scand J Gastroenterol Suppl. 1994;202:26-35. doi: 10.3109/00365529409091742.
5
Breath hydrogen as a diagnostic method for hypolactasia.呼出气氢气作为乳糖不耐受的诊断方法。
Lancet. 1975 May 24;1(7917):1155-7. doi: 10.1016/s0140-6736(75)93135-9.
6
The strip test for hypolactasia also works without ethanol.乳糖不耐受的简易检验在没有乙醇的情况下也可行。
Scand J Gastroenterol. 1988 Sep;23(7):851-5. doi: 10.3109/00365528809090772.
7
Comparison of a portable breath hydrogen analyser (Micro H2) with a Quintron MicroLyzer in measuring lactose maldigestion, and the evaluation of a Micro H2 for diagnosing hypolactasia.便携式呼气氢分析仪(Micro H2)与Quintron MicroLyzer在测量乳糖消化不良方面的比较,以及对Micro H2用于诊断低乳糖酶症的评估。
Scand J Clin Lab Invest. 1998 May;58(3):217-24. doi: 10.1080/00365519850186607.
8
Lactase deficiency--a comparative study of diagnostic methods.乳糖酶缺乏症——诊断方法的比较研究
Am J Clin Nutr. 1977 Oct;30(10):1597-602. doi: 10.1093/ajcn/30.10.1597.
9
Diagnosis of adult-type hypolactasia/lactase persistence: genotyping of single nucleotide polymorphism (SNP C/T-13910) is not consistent with breath test in Colombian Caribbean population.成人型低乳糖酶症/乳糖酶持续性的诊断:单核苷酸多态性(SNP C/T - 13910)基因分型与哥伦比亚加勒比人群的呼气试验结果不一致。
Arq Gastroenterol. 2012 Jan-Mar;49(1):5-8. doi: 10.1590/s0004-28032012000100002.
10
13CO2 breath test using naturally 13C-enriched lactose for detection of lactase deficiency in patients with gastrointestinal symptoms.使用天然富含13C的乳糖进行13CO2呼气试验以检测有胃肠道症状患者的乳糖酶缺乏症。
J Lab Clin Med. 1988 Aug;112(2):193-200.

引用本文的文献

1
Lactose Breath Test: Possible Strategies to Optimize Test Performance, Accuracy, and Clinical Impact.乳糖呼气试验:优化试验性能、准确性和临床影响的可能策略。
Nutrients. 2024 Oct 17;16(20):3516. doi: 10.3390/nu16203516.
2
The European lactase persistence genotype determines the lactase persistence state and correlates with gastrointestinal symptoms in the Hispanic and Amerindian Chilean population: a case-control and population-based study.欧洲乳糖持续存在基因型决定乳糖持续存在状态,并与智利西班牙裔和美洲印第安人群的胃肠道症状相关:一项病例对照和基于人群的研究。
BMJ Open. 2011 Jul 29;1(1):e000125. doi: 10.1136/bmjopen-2011-000125.
3
The T allele of a single-nucleotide polymorphism 13.9 kb upstream of the lactase gene (LCT) (C-13.9kbT) does not predict or cause the lactase-persistence phenotype in Africans.
乳糖酶基因(LCT)上游13.9千碱基处单核苷酸多态性(C-13.9kbT)的T等位基因并不能预测或导致非洲人的乳糖酶持久性表型。
Am J Hum Genet. 2004 Jun;74(6):1102-10. doi: 10.1086/421050. Epub 2004 Apr 20.
4
Applicability of short hydrogen breath test for screening of lactose malabsorption.短时间氢呼气试验在乳糖吸收不良筛查中的适用性。
Dig Dis Sci. 2003 Jul;48(7):1333-8. doi: 10.1023/a:1024163327183.
5
Treatment of lactose intolerance with exogenous beta-D-galactosidase in pellet form.用丸剂形式的外源性β-D-半乳糖苷酶治疗乳糖不耐受症。
Eur J Drug Metab Pharmacokinet. 1998 Apr-Jun;23(2):350-5. doi: 10.1007/BF03189363.