Khan Aysha Habib, Jafri Lena, Siddiqui Areeba, Naureen Ghazala, Morris Howard, Moatter Tariq
Department of Pathology and Laboratory Medicine, Aga Khan University, Stadium Road, Karachi, Pakistan.
Department of Endocrine Bone Research Laboratory, University of South Australia, Adelaide, Australia.
J Coll Physicians Surg Pak. 2019 Aug;29(8):715-719. doi: 10.29271/jcpsp.2019.08.715.
To identify DBP gene rs4588 and rs7041 polymorphisms and associate with participants' serum 25(OH)D and BMD levels.
Cross-sectional descriptive study design.
Section of Chemical Pathology and Molecular Pathology, Department of Pathology and Laboratory Medicine, The Aga Khan University, Karachi, from July 2014 to September 2015.
Blood samples from 98 young adults, out of 101 samples collected, were genotyped for GC rs4588 and rs7041 polymorphisms by polymerase chain reaction-based restriction fragment length polymorphism assay. Questionnaires were administered to obtain information on demographics and anthropometric characteristics, BMD was assessed with heel ultrasound and 25(OH)D was measured using a Chemiluminescence immunoassay.
High prevalence of vitamin D deficiency was noted in the study population n=87 (86.1%) having median (IQR) 25(OH)D levels of 14.9 (20.9) ng/ml, in males and 12.1 (51.8) ng/ml in females. The C/C genotype of SNP rs4588 had the highest proportion n=50 (51%), whereas for rs7041 genotype G/T was most frequently observed n=53 (54%) in subjects. Highest 25(OH)D levels were observed within the homozygous genotypes C/C median 25(OH)D 14.0 (49.6) and G/G (median 25(OH)D 14.9 (37.1) ng/ml. Statistically significant relationship was noted between rs7041 genotype G/T and BMD (p 0.037).
Hypovitaminosis D was frequently found in young adults. Furthermore, G/T variant of rs7041 polymorphism was associated with lower 25(OH)D serum levels.
鉴定维生素D结合蛋白(DBP)基因rs4588和rs7041多态性,并将其与参与者的血清25(羟)维生素D[25(OH)D]水平和骨密度(BMD)相关联。
横断面描述性研究设计。
2014年7月至2015年9月,在卡拉奇阿迦汗大学病理与检验医学系化学病理学和分子病理学科室。
在收集的101份样本中,对98名年轻成年人的血液样本采用基于聚合酶链反应的限制性片段长度多态性分析方法进行GC rs4588和rs7041多态性基因分型。通过问卷调查获取人口统计学和人体测量学特征信息,采用足跟超声评估骨密度,使用化学发光免疫分析法测定25(OH)D。
研究人群中维生素D缺乏的患病率较高,n = 87(86.1%),男性25(OH)D水平中位数(四分位间距)为14.9(20.9)ng/ml,女性为12.1(51.8)ng/ml。SNP rs4588的C/C基因型比例最高,n = 50(51%),而对于rs7041,基因型G/T在受试者中最常观察到,n = 53(54%)。在纯合子基因型C/C(25(OH)D中位数14.0(49.6))和G/G(25(OH)D中位数14.9(37.1)ng/ml)中观察到最高的25(OH)D水平。rs7041基因型G/T与骨密度之间存在统计学显著关系(p = 0.037)。
在年轻成年人中经常发现维生素D缺乏。此外,rs7041多态性的G/T变异与较低的血清25(OH)D水平相关。