LEP -2548G/A启动子与基线体重的关系,LEPR Gln223Arg和Lys656Asn变异与接受利培酮治疗的阿拉伯儿童和青少年BMI z评分变化的关系

Molecular Neuropsychiatry Pub Date : 2018-10-01 Epub Date: 2018-10-05 DOI:10.1159/000490463
Noor B Almandil, Rohit J Lodhi, Hongyan Ren, Frank M C Besag, David Rossolatos, Ruth Ohlsen, Caitlin Slomp, Diego L Lapetina, Giona Plazzotta, Macey L Murray, Abdulsalam A Al-Sulaiman, Paul Gringras, Ian C K Wong, Katherine J Aitchison
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引用次数: 5

摘要

基线数据(antipsychotics-naïve)年龄、体重和身高,以及随后3个随访时间点(313.6天)的变化(95% CI 303.5-323.7),来自沙特阿拉伯一家儿科神经病学诊所的181名接受利哌酮治疗的儿童和青少年(平均年龄12.58岁,SD 4.99,范围2.17-17.7)。由于亚样本中基因型分布的差异,报告了阿拉伯白人人群的结果(n = 144)。计算年龄和性别规范的体重指数(BMI)标准化z分数(BMI z) (LMSgrowth program)。基线体重和BMI z进行线性回归,BMI z的变化采用随机效应有序逻辑回归进行评估。分析了以下单核苷酸多态性(snp): LEP启动子中的rs7799039, LEPR中的rs1805094(以前的rs8179183), rs1137100和rs1137101,以及HTR2C中的rs1414334。我们发现rs7799309与基线体重之间存在名义上的显著关联,调整了身高、年龄、性别和诊断(a /G, p = 0.035, β = -3.62 vs. G/G)。rs1137101 (G/G, p = 0.018,比值比[OR] = 4.13 vs. A/A)和rs1805094 C等位基因携带者(p = 0.019, OR = 0.51)与BMI z类别的变化有名义上的显著相关性。我们的数据支持并重复了先前这些变异的相关关联(包括使用利培酮时体重增加),同时这是阿拉伯种族患者中此类关联的首次报告。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Associations between the LEP -2548G/A Promoter and Baseline Weight and between LEPR Gln223Arg and Lys656Asn Variants and Change in BMI z Scores in Arab Children and Adolescents Treated with Risperidone.

Data on baseline (antipsychotics-naïve) age, weight, and height, and change in these at 3 subsequent follow-up time points up to 313.6 days (95% CI 303.5-323.7) were collected from 181 risperidone-treated children and adolescents (mean age 12.58 years, SD 4.99, range 2.17-17.7) attending a pediatric neurology clinic in Saudi Arabia. Owing to differences in genotypic distributions in the subsamples, results are reported for the white Arab population (n = 144). Age- and gender-normed body mass index (BMI)-standardized z scores (BMI z) were calculated (LMSgrowth program). Linear regression was performed for baseline weight and BMI z, while change in BMI z was assessed using random effects ordered logistic regression. The following single nucleotide polymorphisms (SNPs) were analyzed: rs7799039 in the LEP promoter, rs1805094 (previously rs8179183), rs1137100 and rs1137101 in the LEPR, and rs1414334 in HTR2C. We found a nominally significant association between rs7799309 and baseline weight, adjusting for height, age, gender, and diagnosis (A/G, p = 0.035, β = -3.62 vs. G/G). The rs1137101 (G/G, p = 0.018, odds ratio [OR] = 4.13 vs. A/A) and rs1805094 C allele carriers (p = 0.019, OR = 0.51) showed nominally significant associations with change in BMI z categories. Our data support and replicate previous relevant associations for these variants (including with weight gain when on risperidone), whilst being the first report of such associations in patients of Arab ethnicity.

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