Lifespan Brain Institute, Penn Medicine and Children's Hospital of Philadelphia, The Department of Psychiatry, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA; The Department of Child and Adolescent Psychiatry and Behavioral Sciences, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Lifespan Brain Institute, Penn Medicine and Children's Hospital of Philadelphia, The Department of Psychiatry, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA; The Department of Child and Adolescent Psychiatry and Behavioral Sciences, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
J Psychiatr Res. 2021 Jun;138:319-325. doi: 10.1016/j.jpsychires.2021.03.058. Epub 2021 Apr 13.
The presentation of neurogenetic disorders such as 22q11.2 Deletion Syndrome (22q11.2DS) includes broad neuropsychiatric phenotypes that impact functioning and require assessment and treatment. Like in non-syndromal neuropsychiatric disorders, there is heterogeneity in symptom severity and illness course. The study of risk and resilience in the general population has benefited from measurement tools that parse heterogeneity and guide treatment. Suitability of such tools in neurogenetic disorders has not been examined and is essential to establish as prerequisite for examining whether similar processes modulate psychopathology in these populations.
We applied the Risk & Resilience Battery assessing intrapersonal, interpersonal, and environmental domains, to 80 patients with 22q11.2DS, 30 from Philadelphia, USA and 50 from Tel-Aviv, Israel. We also evaluated global functioning and obtained self-reports of anxiety and depression. We examined the Risk & Resilience Battery reliability for each factor and used partial correlations to examine relations between the Risk & Resilience Battery factors and clinical measures.
Across samples, items within each risk and resilience factor showed good to excellent internal consistency. Higher scores on peer victimization, emotion dysregulation, and hostile close relationships were related to reports of anxiety and depression. Higher levels of self-reliance related to lower anxiety while greater security in close relationships related to lower depression.
The Risk & Resilience Battery can be applied to 22q11.2DS samples and advance Gene X Environment research and interventions.
神经遗传疾病,如 22q11.2 缺失综合征(22q11.2DS),其临床表现包括广泛的神经精神表型,影响功能,需要评估和治疗。与非综合征性神经精神障碍一样,症状严重程度和疾病进程存在异质性。在普通人群中,对风险和韧性的研究受益于能够解析异质性并指导治疗的测量工具。这些工具在神经遗传疾病中的适用性尚未得到检验,这对于研究这些人群中是否存在类似的过程来调节精神病理学至关重要。
我们应用了风险与韧性量表(Risk & Resilience Battery),评估个体内部、人际和环境领域,共对 80 名 22q11.2DS 患者进行了评估,其中 30 名来自美国费城,50 名来自以色列特拉维夫。我们还评估了总体功能,并获得了焦虑和抑郁的自我报告。我们检查了每个因素的风险与韧性量表的可靠性,并使用偏相关来检查风险与韧性量表因素与临床测量之间的关系。
在两个样本中,每个风险和韧性因素内的项目均表现出良好到极好的内部一致性。同伴侵害、情绪失调和敌对亲密关系得分较高与焦虑和抑郁报告有关。较高的自力更生水平与较低的焦虑相关,而较亲密的关系的安全感与较低的抑郁相关。
风险与韧性量表可应用于 22q11.2DS 样本,推进基因与环境研究和干预措施。