Congruency of Genetic Predisposition to Lactase Persistence and Lactose Breath Test

被引:7
作者
Coluccia, Enza [1 ]
Iardino, Patrizia [2 ]
Pappalardo, Diego [1 ]
Brigida, Anna Lisa [1 ]
Formicola, Vincenzo [3 ]
De Felice, Bruna [4 ]
Guerra, Claudia [1 ]
Pucciarelli, Alessia [1 ]
Amato, Maria Rosaria [5 ]
Riegler, Gabriele [1 ]
De Magistris, Laura [1 ]
机构
[1] Univ Campania Luigi Vanvitelli, Dept Precis Med, I-81100 Caserta, Italy
[2] Univ Campania Luigi Vanvitelli, UOC Clin & Mol Pathol, I-81100 Caserta, Italy
[3] Med Diagnost Consultant, I-80053 Naples, Italy
[4] Univ Campania Luigi Vanvitelli, Dept Environm Biol & Pharmaceut Sci & Technol, I-81100 Caserta, Italy
[5] Univ Campania Luigi Vanvitelli, AOU, DAI Med Interna & Specialist, I-81100 Caserta, Italy
关键词
lactose; lactose intolerance; lactase; H-2; CH4 lactose breath test; lactase genetic test; gastrointestinal symptoms; ADULT-TYPE HYPOLACTASIA; INTOLERANCE; MALABSORPTION; DIAGNOSIS; DEFICIENCY; C/T-13910; ACCURACY; UPSTREAM; GENOTYPE; HISTORY;
D O I
10.3390/nu11061383
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
The physiological decline of lactase production in adulthood, in some individuals, is responsible for the so-called Lactose Intolerance. This clinical syndrome presents with gastrointestinal and non-gastrointestinal symptoms following the consumption of dairy containing food. Lactose intolerance can be evaluated by means of the Lactose Breath Test (phenotype) and/or genetic evaluation of lactase-gene polymorphism (genotype). A comparison of the two tests was carried out in a large number of symptomatic adult subjects, which are selected and not representative of the general population. Congruency was as high as 88.6%. Among lactase non-persistent (genotype C/C), 14 subjects showed a negative Lactose Breath Test (LBT), possibly due to young age. Among lactase-persistent (genotype C/T), four subjects showed a positive LBT, which helps to diagnose secondary lactose intolerance. Symptoms, both gastrointestinal and extra-gastrointestinal, were reported by 90% of patients during the breath test. Clinical use of both tests in the same patients could be taken into consideration as a sharp diagnostic tool. We suggest considering the use of the genetic test after LBT administration, when secondary hypolactasia is suspected, for completion of diagnostic procedures.
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