医学
临床心理学
萧条(经济学)
妊娠期糖尿病
毒物控制
精神科
自杀未遂
伤害预防
自杀预防
怀孕
人为因素与人体工程学
职业安全与健康
内分泌系统
糖尿病
大麻
CTQ树
心理学
风险因素
胎龄
年轻人
作者
María Posada‐Ayala,Ping Wang,Gemma Barroso‐Garcia,Encarnación Donoso‐Navarro,Elena Hernández‐Álvarez,María Gil‐Ligero,Julián Romero,Silvia Rosado‐Garcia,Antonio José Sánchez‐López,Hilario Blasco‐Fontecilla
出处
期刊:
日期:2026-02-25
卷期号:2 (2): 155-166
被引量:1
摘要
ABSTRACT Background Differentiating between nonsuicidal self‐injury (NSSI) and suicide attempts (SA) in adolescents is crucial due to distinct underlying motivations, treatment needs, and potential outcomes associated with each behavior. This study explores biomarkers, specifically β ‐endorphin and endocannabinoids [anandamide (AEA), 2‐arachidonoylglycerol (2‐AG), N‐palmitoylethanolamide (PEA), and oleoylethanolamide (OEA)], in adolescents admitted for NSSI and/or SA. Objectives We aimed to explore potential differences in different variables among adolescents hospitalized for NSSI, SA, or both. Method This pilot study enrolled 68 adolescents admitted for NSSI and/or SA at Puerta de Hierro University Hospital. Excluding those with endocrine issues, participants underwent clinical assessments, blood collection, and serum analysis for ACTH, cortisol, and β ‐endorphin, with endocannabinoids measured via LC–MS. Clinical tools, such as the MINI Kid and CTQ and statistical analyses via SPSS and Stata aimed to elucidate behavioral and biological differences between NSSI and SA groups. Results No sociodemographic factor differentiated the groups. Gestational diabetes and depression during pregnancy were more frequent in the NSSI group ( p = 0.047 and p = 0.003, respectively). Abnormal presentation at birth was overrepresented in the SA group ( p = 0.001). Familial antecedents of either suicide or SB were more frequently reported in the NSSI + SA group ( p = 0.027 and p = 0.035, respectively). Blood PEA and β ‐endorphin were significantly elevated in the SA group ( p < 0.006 and 0.014, respectively). Discussion This study identified shared risk factors across NSSI and SA, with distinct variables for each group, including β ‐endorphin and PEA biomarker elevations linked to SA.
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