Charmanna Shuchi Odiyanda, Srinivas Anju, Prashant Akila, Jain Asmita, Kishor M, Shivashankar Kusuma K
Department of Biochemistry, JSS Medical College, JSS Academy of Higher Education and Research, Mysore, Karnataka, India.
Department of Clinical Psychology, JSS Medical College, JSS Academy of Higher Education and Research, Mysore, Karnataka, India.
Indian J Psychiatry. 2024 Oct;66(10):911-917. doi: 10.4103/indianjpsychiatry.indianjpsychiatry_461_24. Epub 2024 Oct 17.
Premenstrual dysphoric disorder (PMDD) is a condition that affects nearly 3-9% of the women in the reproductive age during the luteal phase of each menstrual cycle characterized by symptoms varying in severity and affecting the quality of life. Earlier research studies conducted have reported independent relationships between PvuII-ESR1-polymorphism and psychological traits in PMDD and risk for cognitive, behavioral, and affective symptoms. However, as the studies are few in number and the results are not consistent, there is a need for our study to link between the PvuII-ESR1gene and PMDD.
All nonpregnant women aged between 18 and 45 years and attending the OBG or Medicine or Psychiatry OPD for a routine health checkup were recruited into the study. The cross-sectional study recruited 35 samples each in the control and PMDD groups using a validated screening PMDD Assessment Scale Questionnaire (PMDDASQ). Mann-Whitney's U test and Chi-square test were used to calculate values for the continuous and categorical variables. Tetra-primer-amplification refractory mutation system-polymerase chain reaction was used to identify the PvuII-ESR1gene polymorphism after isolation of genomic DNA from the whole blood.
Data-Analysis Pak tool and Med-Calc software were used for data analysis. The PvuII-ESR1 genotype distribution was in Hardy-Weinberg equilibrium in both PMDD and controls. The PMDDASQ scoring showed a significance with ≤ 0.05. Pearson's Chi-Squared test performed for genotypes and alleles did not show any significant association with the phenotype.
PvuII-ESR1 SNP (T/C rs2234693) does not show any association with phenotype between the control and PMDD. However, PMDDAS questionnaire can be used to differentiate the women who are controls from PMDD.
经前烦躁障碍(PMDD)是一种影响近3%至9%育龄期女性的疾病,在每个月经周期的黄体期出现,症状严重程度各异,影响生活质量。早期开展的研究报告了PvuII - ESR1多态性与PMDD心理特征以及认知、行为和情感症状风险之间的独立关系。然而,由于研究数量较少且结果不一致,我们的研究有必要探讨PvuII - ESR1基因与PMDD之间的联系。
招募所有年龄在18至45岁之间、前往妇产科、内科或精神科门诊进行常规健康检查的非孕妇参与研究。横断面研究使用经过验证的筛查PMDD评估量表问卷(PMDDASQ),在对照组和PMDD组各招募35个样本。采用曼 - 惠特尼U检验和卡方检验计算连续变量和分类变量的值。从全血中分离基因组DNA后,使用四引物扩增阻滞突变系统 - 聚合酶链反应鉴定PvuII - ESR1基因多态性。
使用数据分析软件包工具和Med - Calc软件进行数据分析。PvuII - ESR1基因型分布在PMDD组和对照组中均处于哈迪 - 温伯格平衡。PMDDASQ评分具有显著性,P≤0.05。对基因型和等位基因进行的Pearson卡方检验未显示与表型有任何显著关联。
PvuII - ESR1单核苷酸多态性(T/C rs2234693)在对照组和PMDD组之间未显示与表型有任何关联。然而,PMDDAS问卷可用于区分对照组女性和PMDD患者。