Adverse childhood experiences and the development of Down syndrome regression disorder

被引:2
|
作者
Wang, Sarah [1 ]
Patel, Lina [2 ]
Sannar, Elise A. [2 ]
Khoshnood, Mellad [1 ]
Boyd, Natalie K. [1 ]
Mendez, Lorena [1 ]
Spinazzi, Noemi A. [3 ]
Quinn, Eileen A. [4 ]
Rafii, Michael S. [5 ,6 ]
Santoro, Jonathan D. [1 ,5 ,7 ]
机构
[1] Childrens Hosp Los Angeles, Div Neurol, Los Angeles, CA USA
[2] Univ Colorado, Dept Psychiat, Aurora, CO USA
[3] Univ Calif San Francisco, Benioff Childrens Hosp, Dept Pediat, Oakland, CA USA
[4] Univ Toledo, Dept Pediat, Coll Med & Life Sci, Toledo, OH USA
[5] Univ Southern Calif, Dept Neurol, Keck Sch Med, Los Angeles, CA USA
[6] Univ Southern Calif, Alzheimers Translat Res Inst, San Diego, CA USA
[7] Childrens Hosp Los Angeles, Div Neurol, 4650 Sunset Blvd MS82, Los Angeles, CA 90027 USA
关键词
ACE; adverse childhood experiences; catatonia; down syndrome; neuroendocrine; regression; CHILDREN; STRESS;
D O I
10.1002/ajmg.a.63199
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Down syndrome regression disorder (DSRD) is a clinical symptom cluster of acute or subacute neurocognitive regression in otherwise health persons with Down syndrome. The objective of this study was to evaluate if adverse childhood experiences (ACEs) were more prevalent in children with DSRD than those with DS alone. A survey-based, cohort-based study was performed. Caregivers of individuals with DSRD with onset of symptoms between age 10 and 30 years and DS alone were administered the ACEs questionnaire via an online REDCap survey. A total of 159 responses were collected after excluding incomplete surveys and those not meeting criteria for DSRD. Individuals with DSRD were not more likely to experience ACEs (p = 0.18, 95% confidence interval [CI]: 0.43-1.17). In those with ACEs prior to the onset of symptoms, the median time prior was 7 months (interquartile range: 5-10). Individuals with DSRD were more likely to report three or more ACEs (52, 33%) compared to those with DS alone (39, 22%) (p = 0.02, 95% CI: 1.08-2.87). Exposure to ACEs were not predictive of response to particular therapeutic interventions although those with multiple ACEs 3 months prior to the onset of symptoms was associated with lower response rates to benzodiazepines and immunotherapy (p = 0.02, 95% CI: -3.64--1.13). This study provides preliminary data that individuals with DSRD experience ACEs at a similar rate to individuals with only DS alone, although three or more ACEs, often preceding the onset of symptoms, was more prevalent in individuals with DSRD.
引用
收藏
页码:1769 / 1782
页数:14
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