Francheska M Merced-Nieves, Marina Schechter, Elena Colicino, Allison Frost, Rosalind J Wright
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Mothers reported child wheeze at 4-month intervals to index wheezing episodes from age 6-30 months. We first assessed independent associations between ACE measures and wheeze frequency using Poisson regression. We then used weighted quantile sum (WQS) regression to derive an ACEs mixture index to estimate joint associations with wheeze frequency in the overall sample and stratified by maternal race and ethnicity adjusting for child sex, maternal asthma and education. There was a 2.05 increase (95% CI = 1.21, 3.49) in wheeze frequency with each quintile increase of the ACEs index in Black/Black Hispanics; the TESI (72%) contributed most strongly to the mixture. In non-Black Hispanics, there was a 1.33 (95% CI = 1.05, 1.67) increase in wheeze frequency with each ACEs quintile increase with EPDS (76%) contributing most strongly. Findings support the need to move the ACEs paradigm beyond a simple cumulative score when examining effects on early respiratory disease risk. 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引用次数: 0
摘要
识别有呼吸系统疾病风险的儿童需要了解早期风险因素。这项研究前瞻性地考察了特定类型的早期逆境如何影响儿童喘息,以及这些如何因种族和民族而变化。分析包括来自城市妊娠队列的N = 746对母子。母亲在婴儿6个月大时完成《终生应激源修正表》(LSC-R)、《爱丁堡产后抑郁量表》(EPDS)、《斯皮尔伯格状态-特质焦虑量表》(STAI)、《创伤后应激障碍平民版》(pclc - c)和《创伤事件筛查量表》(TESI)来评估不良童年经历(ace)。母亲每隔4个月报告一次孩子的喘息,以衡量6-30个月的喘息发作。我们首先使用泊松回归评估ACE测量和喘息频率之间的独立关联。然后,我们使用加权分位数和(WQS)回归得出ace混合指数,以估计总体样本中喘息频率的联合关联,并按母亲种族和民族分层,调整儿童性别,母亲哮喘和教育。黑人/西班牙裔黑人的ace指数每增加五分位数,喘息频率增加2.05 (95% CI = 1.21, 3.49);TESI(72%)对混合物的贡献最大。在非黑人西班牙裔人群中,每增加一个ace五分位数,喘息频率增加1.33 (95% CI = 1.05, 1.67),其中EPDS(76%)贡献最大。研究结果支持在检查对早期呼吸系统疾病风险的影响时,需要将ace模式超越简单的累积评分。研究结果还强调了早期生活经历的影响如何因种族身份而异。
Adverse childhood experiences (ACEs) and repeated wheezing from 6 to 30 months of age: exploring the role of race and ethnicity.
Identifying children at risk for respiratory disorders involves understanding early risk factors. This study prospectively examines how specific types of early adversity influence childhood wheeze and how these vary by race and ethnicity. Analyses included N = 746 mother-infant dyads from an urban pregnancy cohort. Mothers completed the Lifetime Stressor Checklist-Revised (LSC-R), Edinburgh Postnatal Depression Scale (EPDS), Spielberger State-Trait Anxiety Inventory (STAI), Posttraumatic stress disorder Checklist-Civilian version (PCL-C), and Traumatic Events Screening Inventory (TESI) when infants were 6 months old to assess adverse childhood experiences (ACEs). Mothers reported child wheeze at 4-month intervals to index wheezing episodes from age 6-30 months. We first assessed independent associations between ACE measures and wheeze frequency using Poisson regression. We then used weighted quantile sum (WQS) regression to derive an ACEs mixture index to estimate joint associations with wheeze frequency in the overall sample and stratified by maternal race and ethnicity adjusting for child sex, maternal asthma and education. There was a 2.05 increase (95% CI = 1.21, 3.49) in wheeze frequency with each quintile increase of the ACEs index in Black/Black Hispanics; the TESI (72%) contributed most strongly to the mixture. In non-Black Hispanics, there was a 1.33 (95% CI = 1.05, 1.67) increase in wheeze frequency with each ACEs quintile increase with EPDS (76%) contributing most strongly. Findings support the need to move the ACEs paradigm beyond a simple cumulative score when examining effects on early respiratory disease risk. Results also highlight how the impact of early life ACEs varies by ethnoracial identity.
期刊介绍:
The journal Stress aims to provide scientists involved in stress research with the possibility of reading a more integrated view of the field. Peer reviewed papers, invited reviews and short communications will deal with interdisciplinary aspects of stress in terms of: the mechanisms of stressful stimulation, including within and between individuals; the physiological and behavioural responses to stress, and their regulation, in both the short and long term; adaptive mechanisms, coping strategies and the pathological consequences of stress.
Stress will publish the latest developments in physiology, neurobiology, molecular biology, genetics research, immunology, and behavioural studies as they impact on the understanding of stress and its adverse consequences and their amelioration.
Specific approaches may include transgenic/knockout animals, developmental/programming studies, electrophysiology, histochemistry, neurochemistry, neuropharmacology, neuroanatomy, neuroimaging, endocrinology, autonomic physiology, immunology, chronic pain, ethological and other behavioural studies and clinical measures.