Suppr超能文献

通过LightCycler PCR对乳糖酶-根皮苷水解酶-13910多态性进行基因分型及其对乳糖不耐受诊断的意义

Genotyping of the lactase-phlorizin hydrolase -13910 polymorphism by LightCycler PCR and implications for the diagnosis of lactose intolerance.

作者信息

Bodlaj Gerd, Stöcher Markus, Hufnagl Peter, Hubmann Rainer, Biesenbach Georg, Stekel Herbert, Berg Jörg

机构信息

Institute of Laboratory Medicine, General Hospital Linz, Linz, Austria.

出版信息

Clin Chem. 2006 Jan;52(1):148-51. doi: 10.1373/clinchem.2005.057240.

Abstract

BACKGROUND

Hypolactasia and lactose intolerance are common conditions worldwide. Hypolactasia seems to be strongly correlated with genotype C/C of the genetic variant C-->T(-13910) upstream of the lactase phlorizin hydrolase (LPH) gene. We developed a rapid genotyping assay for LPH C-->T(-13910) and investigated the relationship of positive lactose breath hydrogen test (LBHT) results suggesting lactose intolerance with LPH C-->T(-13910) genotype.

METHODS

Using automated DNA purification on the MagNA Pure LC and real-time PCR on the LightCycler, we examined samples from 220 individuals to estimate genotype frequencies; we then determined LPH C-->T(-13910) genotype in samples from 54 Caucasian patients with a positive LBHT result and symptoms of lactose intolerance.

RESULTS

Genotyping of 220 individuals revealed frequencies of 21.4%, 41.8%, and 36.8% for genotypes C/C, C/T, and T/T. Of the patients with positive LBHT results, only 50% had the C/C genotype suggestive of primary adult hypolactasia in our study population. The other patients had various degrees of secondary hypolactasia or symptoms of lactose intolerance. Patients with C/C genotype had a mean (SD) peak H2 increase in the LBHT [108 (58) ppm] that was significantly higher than in patients with the C/T [65 (54) ppm] and T/T [44 (34) ppm] genotypes.

CONCLUSIONS

The new real-time PCR assay provides a rapid, labor-saving means for the genotyping of LPH C-->T(-13910). Use of the assay may assist in differentiating patients with primary hypolactasia from those with secondary hypolactasia and lactose intolerance, who may need further clinical examinations to diagnose their underlying primary diseases.

摘要

背景

低乳糖酶症和乳糖不耐受在全球范围内均为常见病症。低乳糖酶症似乎与乳糖酶-根皮苷水解酶(LPH)基因上游遗传变异C→T(-13910)的C/C基因型密切相关。我们开发了一种针对LPH C→T(-13910)的快速基因分型检测方法,并研究了提示乳糖不耐受的阳性乳糖呼气氢试验(LBHT)结果与LPH C→T(-13910)基因型之间的关系。

方法

我们使用MagNA Pure LC进行自动DNA纯化,并在LightCycler上进行实时PCR,检测了220名个体的样本以估计基因型频率;然后我们确定了54名LBHT结果为阳性且有乳糖不耐受症状的白种人患者样本中的LPH C→T(-13910)基因型。

结果

对220名个体进行基因分型显示,C/C、C/T和T/T基因型的频率分别为21.4%、41.8%和36.8%。在LBHT结果为阳性的患者中,在我们的研究人群中只有50%具有提示原发性成人低乳糖酶症的C/C基因型。其他患者有不同程度的继发性低乳糖酶症或乳糖不耐受症状。C/C基因型患者在LBHT中H2增加的平均(标准差)峰值为[108(58)ppm],显著高于C/T[65(5)ppm]和T/T[44(34)ppm]基因型的患者。

结论

新的实时PCR检测方法为LPH C→T(-13910)基因分型提供了一种快速、省力的手段。使用该检测方法可能有助于区分原发性低乳糖酶症患者与继发性低乳糖酶症和乳糖不耐受患者,后者可能需要进一步的临床检查以诊断其潜在的原发性疾病。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验