Department of Bromatology, Poznań University of Medical Sciences, Rokietnicka 3 Street, 60-806 Poznań, Poland.
Department of Biochemistry and Biotechnology, Poznań University of Life Sciences, Dojazd 11 Street, 60-647 Poznań, Poland.
Int J Mol Sci. 2023 Jun 15;24(12):10191. doi: 10.3390/ijms241210191.
Intolerance to dairy products resulting from the abnormal digestion of milk sugar (lactose) is a common cause of human gastrointestinal disorders. The aim of this study was to show that the -13910 C>T LCT gene polymorphism, together with genotypes of selected VDR gene polymorphisms and diet and nutritional status parameters, can impact the prevalence of vitamin D and calcium deficiency in young adults. This study was conducted on a group of 63 people, which comprised 21 individuals with primary adult lactase deficiency, and a control group of 42 individuals with no hypolactasia. The LCT and VDR gene genotypes were assessed using PCR restriction fragment length polymorphism (PCR-RFLP) analysis. A validated HPLC method was used to determine serum concentrations of 25(OH)D and 25(OH)D. Atomic absorption spectrometry was used to determine calcium levels. Their diets (self-reported 7-day estimated food record), estimated calcium intakes based on the ADOS-Ca questionnaire and basic anthropometric parameters were assessed. The CC genotype associated with hypolactasia was found in 33.3% of the subjects. The presence of the CC variant of the LCT gene polymorphism in the study group of young Polish adults was found to be associated with significantly lower milk (134.7 ± 66.7 g/d vs. 342.5 ± 176 g/d; = 0.012) and dairy product consumption (78.50 ± 36.2 g/d vs. 216.3 ± 102 g/d; = 0.008) compared with lactase persistence. At the same time, people with adult-type primary intolerance were found to have statistically significant lower serum levels of vitamin D and calcium ( < 0.05). There was a higher chance of vitamin D and calcium deficiency and a lower intake in the group exhibiting lactase non-persistence (OR > 1). The AA variant of the VDR gene's BsmI polymorphism present in people with hypolactasia may further contribute to an increased risk of vitamin D deficiency. Exclusion of lactose from the diet, combined with impaired vitamin D metabolism, may also lead to inhibited calcium absorption by the body. Further research should be carried out on a larger group of subjects to clarify the relationship between lactase activity and vitamin D and calcium levels in young adults.
乳糖不耐受是由于牛奶糖(乳糖)异常消化引起的,这是人类胃肠道疾病的常见原因。本研究旨在表明,-13910C>T LCT 基因多态性,以及选定的 VDR 基因多态性和饮食及营养状况参数的基因型,可能会影响年轻人维生素 D 和钙缺乏的患病率。该研究在 63 人组成的一组中进行,其中包括 21 名原发性成人乳糖酶缺乏症患者和 42 名无低乳糖血症的对照组。LCT 和 VDR 基因基因型通过 PCR 限制性片段长度多态性(PCR-RFLP)分析进行评估。采用经过验证的 HPLC 法测定血清 25(OH)D 和 25(OH)D 浓度。原子吸收光谱法用于测定钙水平。评估了他们的饮食(自我报告的 7 天估计食物记录)、根据 ADOS-Ca 问卷估计的钙摄入量和基本人体测量参数。在研究组中,发现与低乳糖相关的 CC 基因型在 33.3%的受试者中存在。在波兰年轻成年人研究组中,LCT 基因多态性的 CC 变体的存在与显著较低的牛奶(134.7 ± 66.7 g/d 与 342.5 ± 176 g/d; = 0.012)和乳制品消耗(78.50 ± 36.2 g/d 与 216.3 ± 102 g/d; = 0.008)相关。与此同时,患有成人型原发性不耐受症的人发现血清维生素 D 和钙水平存在统计学显著降低(<0.05)。在乳糖酶非持续性的组中,维生素 D 和钙缺乏的几率更高,摄入量更低(OR>1)。低乳糖血症患者中存在的 VDR 基因 BsmI 多态性的 AA 变体可能进一步增加维生素 D 缺乏的风险。饮食中去除乳糖,加上维生素 D 代谢受损,也可能导致身体吸收的钙减少。应在更大的研究对象组中进行进一步研究,以阐明乳糖酶活性与年轻人维生素 D 和钙水平之间的关系。