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患有焦虑症的孕妇的生物学机制(快乐母亲-健康宝宝补充研究):一项纵向混合方法观察性研究的方案

Biological Mechanisms in Pregnant Women With Anxiety (Happy Mother-Healthy Baby Supplement Study): Protocol for a Longitudinal Mixed Methods Observational Study.

作者信息

Sherer Morgan L, Malik Abid, Osborne Lauren M, Rowther Armaan A, Zaidi Ahmed, Atif Najia, Rahman Atif, Kahloon Lubna E, Salman Muhammad, Yenokyan Gayane, Surkan Pamela J

机构信息

Johns Hopkins Center for Women's Reproductive Mental Health, Departments of Psychiatry & Behavioral Sciences and Gynecology & Obstetrics, Johns Hopkins School of Medicine, Baltimore, MD, United States.

Human Development Research Foundation, Gujar Khan, Pakistan.

出版信息

JMIR Res Protoc. 2023 Apr 11;12:e43193. doi: 10.2196/43193.

Abstract

BACKGROUND

Anxiety and depression are common in the perinatal period and negatively affect the health of the mother and baby. Our group has developed "Happy Mother-Healthy Baby" (HMHB), a cognitive behavioral therapy-based psychosocial intervention to address risk factors specific to anxiety during pregnancy in low- and middle-income countries (LMICs).

OBJECTIVE

The purpose of this study is to examine biological mechanisms that may be linked to perinatal anxiety in conjunction with a randomized controlled trial of HMHB in Pakistan.

METHODS

We are recruiting 120 pregnant women from the Holy Family Hospital, a public facility in Rawalpindi, Pakistan. Participants are assessed for at least mild anxiety symptoms using the Hospital Anxiety and Depression Scale (ie, a score ≥8 on the anxiety scale is necessary for inclusion in the anxiety groups and <8 for inclusion in the healthy control group). Women who meet the criteria for an anxiety group are randomized into either the HMHB intervention group or an enhanced usual care (EUC) control group. Participants receive HMHB or EUC throughout pregnancy and undergo blood draws at 4 time points (baseline, second trimester, third trimester, and 6 weeks post partum). We will assess peripheral cytokine concentrations using a multiplex assay and hormone concentrations using gas chromatography and mass spectrometry. The statistical analysis will use generalized linear models and mixed effects models to assess the relationships across time among anxiety, immune dysregulation, and hormone levels, and to assess whether these biological factors mediate the relationship between anxiety and birth and child development outcomes.

RESULTS

Recruitment started on October 20, 2020, and data collection was completed on August 31, 2022. The start date for recruitment for this biological supplement study was delayed by approximately half a year due to the COVID-19 pandemic. The trial was registered at ClinicalTrials.gov (NCT03880032) on September 22, 2020. The last blood samples were shipped to the United States on September 24, 2022, where they will be processed for analysis.

CONCLUSIONS

This study is an important addition to the HMHB randomized controlled trial of an intervention for antenatal anxiety. The intervention itself makes use of nonspecialist providers and, if effective, will represent an important new tool for the treatment of antenatal anxiety in LMICs. Our biological substudy is one of the first attempts to link biological mechanisms to antenatal anxiety in an LMIC in the context of a psychosocial intervention, and our findings have the potential to significantly advance our knowledge of the biological pathways of perinatal mental illness and treatment efficacy.

TRIAL REGISTRATION

ClinicalTrials.gov NCT03880032; https://clinicaltrials.gov/ct2/show/NCT03880032.

INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): DERR1-10.2196/43193.

摘要

背景

焦虑和抑郁在围产期很常见,会对母婴健康产生负面影响。我们的团队开发了“快乐母亲 - 健康宝宝”(HMHB),这是一种基于认知行为疗法的社会心理干预措施,旨在解决低收入和中等收入国家(LMICs)孕期焦虑的特定风险因素。

目的

本研究的目的是结合在巴基斯坦进行的HMHB随机对照试验,研究可能与围产期焦虑相关的生物学机制。

方法

我们正在从巴基斯坦拉瓦尔品第的一家公共机构圣家族医院招募120名孕妇。使用医院焦虑和抑郁量表评估参与者是否至少有轻度焦虑症状(即焦虑量表得分≥8分才能纳入焦虑组,<8分纳入健康对照组)。符合焦虑组标准的女性被随机分为HMHB干预组或强化常规护理(EUC)对照组。参与者在整个孕期接受HMHB或EUC,并在4个时间点(基线、孕中期、孕晚期和产后6周)进行采血。我们将使用多重检测法评估外周细胞因子浓度,使用气相色谱和质谱法评估激素浓度。统计分析将使用广义线性模型和混合效应模型来评估焦虑、免疫失调和激素水平随时间的关系,并评估这些生物学因素是否介导焦虑与出生及儿童发育结局之间的关系。

结果

招募工作于2020年10月20日开始,数据收集于2022年8月31日完成。由于COVID-19大流行,这项生物学补充研究的招募开始日期推迟了约半年。该试验于2020年9月22日在ClinicalTrials.gov(NCT03880032)注册。最后一批血样于2022年9月24日运往美国,将在那里进行分析处理。

结论

本研究是对HMHB产前焦虑干预随机对照试验的重要补充。该干预措施本身利用非专科医护人员,如果有效,将成为低收入和中等收入国家治疗产前焦虑的重要新工具。我们的生物学子研究是在社会心理干预背景下,将生物学机制与低收入和中等收入国家产前焦虑联系起来的首批尝试之一,我们的研究结果有可能显著推进我们对围产期精神疾病生物学途径和治疗效果的认识。

试验注册

ClinicalTrials.gov NCT03880032;https://clinicaltrials.gov/ct2/show/NCT03880032。

国际注册报告识别码(IRRID):DERR1-10.2196/43193。

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