Tan Ene-Choo, Chua Tze-Ern, Lee Theresa M Y, Tan Hui-San, Ting Joe L Y, Chen Helen Y
KK Research Centre, KK Women's and Children's Hospital, 100 Bukit Timah Road, Singapore, 229899, Singapore.
Paediatrics Academic Clinical Programme, SingHealth Duke-NUS Graduate Medical School, 8 College Road, Singapore, 169857, Singapore.
BMC Pregnancy Childbirth. 2015 Oct 30;15:283. doi: 10.1186/s12884-015-0720-z.
Depression during pregnancy or after childbirth is the most frequent perinatal illness affecting women of reproductive age. It could result in unfavourable outcomes for both women and their newborns. The incidence of perinatal depression is higher for those with family history of depression and other mental illness, suggesting the contribution of genetic factors. There is postulation that disruption or fluctuation of reproductive hormones could play a part in women who are sensitive to such changes.
This is a case-control study comparing the frequencies of candidate gene variants in patients with perinatal depression with controls. Patients of Chinese descent (N = 725) were recruited from the outpatient clinics of the hospital between 2010 and 2013. Controls were patients who came for postnatal consultations at the obstetrics clinics and scored ≤ 7 on the Edinburgh Postnatal Depression Scale (EPDS) at the postnatal screening programme of the hospital. Cases with confirmed diagnosis of clinical (major) depression related to pregnancy/postpartum were recruited from the hospital's outpatient clinic. Genomic DNA was extracted from saliva samples and genotyped for the polymorphisms of interest. Differences between groups were assessed by chi-square analysis.
CRHR1 rs242939 and rs1876828 were not polymorphic in the study population. There was no statistically significant association of perinatal depression for CRHR1 rs242941 and GR rs41423247 (BclI). When all subjects were grouped based on family history of mental illness, there was a statistically significant association of CRHR1 rs242941 with family history regardless of depression status (P = 0.043). There was also a statistically significant difference for GR rs41423247 and regularity of menstrual periods (P < 0.000). Although not statistically significant, women with perinatal depression showed a trend towards higher frequency of self-reported menstrual irregularity.
No evidence was found for the association of any of the genetic markers with perinatal depression in this study cohort. Instead, the possible genetic links were found in women with positive family history of mental illness and menstrual irregularity, suggesting these could be identifying risk markers for women.
孕期或产后抑郁是影响育龄女性最常见的围产期疾病。它可能会给女性及其新生儿带来不良后果。有抑郁和其他精神疾病家族史的人群围产期抑郁发病率更高,提示遗传因素的作用。有一种假设认为,生殖激素的紊乱或波动可能在对这种变化敏感的女性中起作用。
这是一项病例对照研究,比较围产期抑郁患者与对照组中候选基因变异的频率。2010年至2013年间,从医院门诊招募了华裔患者(N = 725)。对照组为在产科门诊进行产后咨询且在医院产后筛查项目中爱丁堡产后抑郁量表(EPDS)得分≤7分的患者。确诊为与妊娠/产后相关的临床(重度)抑郁的病例从医院门诊招募。从唾液样本中提取基因组DNA,并对感兴趣的多态性进行基因分型。通过卡方分析评估组间差异。
CRHR1 rs242939和rs1876828在研究人群中无多态性。CRHR1 rs242941和GR rs41423247(BclI)与围产期抑郁无统计学显著关联。当所有受试者根据精神疾病家族史分组时,无论抑郁状态如何,CRHR1 rs242941与家族史有统计学显著关联(P = 0.043)。GR rs41423247与月经周期规律也有统计学显著差异(P < 0.000)。尽管无统计学显著差异,但围产期抑郁女性自我报告月经不规律的频率有升高趋势。
在该研究队列中,未发现任何遗传标记与围产期抑郁相关的证据。相反,在有精神疾病家族史和月经不规律的女性中发现了可能的遗传联系,提示这些可能是女性的风险识别标记。