Evidence map›Paper›PMID 42087124›Full record

ArticleBMC psychiatry2026

Psychological heterogeneity and transitions of non-suicidal self-injury in adolescents: a two-wave longitudinal cohort study.

Xing Li, Qingqing Xiao, Yan Xiao, Lijuan Huang, Dandan Hou, Xuehua Huang

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Article in BMC psychiatry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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6 authors.

Xing Li *Department of Nephrology, Kidney Research Institute, West China Hospital, Sichuan University, Chengdu, Sichuan, China.
Qingqing Xiao *West China School of Nursing, Sichuan University, Chengdu, Sichuan, China.
Yan XiaoWest China School of Nursing, Sichuan University, Chengdu, Sichuan, China.
Lijuan HuangWest China School of Nursing, Sichuan University, Chengdu, Sichuan, China.
Dandan HouWest China School of Nursing, Sichuan University, Chengdu, Sichuan, China.
Xuehua HuangWest China School of Nursing, Sichuan University, Chengdu, Sichuan, China. huangxuehua10@163.com.

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6 · The paper itself

Abstract

backgroundNon-suicidal self-injury (NSSI) is common among adolescents and is associated with substantial psychological distress and elevated suicide risk. From an ecological-developmental perspective, adolescent NSSI may arise from interacting influences across individual vulnerabilities, developmental adversity, family relationships, and social resources. However, most previous studies have examined these factors using variable-centered approaches, which may overlook psychosocial heterogeneity within clinical populations. This study aimed to examine three-year transitions in NSSI among psychiatric adolescents and to investigate whether multidomain psychosocial profiles identified at baseline were associated with these transition outcomes.

methodsA two-wave longitudinal cohort study was conducted among 432 adolescent psychiatric inpatients (mean age = 14.6 years; 81.3% female) with a three-year follow-up interval. NSSI was assessed at baseline and follow-up, and transitions were categorized as stable no NSSI, new-onset NSSI, remission, or persistence. Latent profile analysis was used to identify psychosocial profiles based on multidomain indicators including emotional symptoms, trauma exposure, stressful life events, psychosocial resources, coping styles, and perceived parenting. Multinomial logistic regression models examined predictors of transition outcomes.

resultsNSSI prevalence declined from 22.9% at baseline to 14.1% at follow-up. Transition patterns included stable no NSSI (64.1%), remission (21.8%), new onset (13.0%), and persistence (1.2%). Latent profile analysis identified three psychosocial subgroups: a lower-risk/high-resource profile, an intermediate-risk profile, and a high-stress/low-support profile. Transition distributions differed significantly across profiles, with the lower-risk profile showing the highest remission proportion and the high-stress/low-support profile showing the lowest remission proportion. In multivariable models, low household economic status (RRR = 2.64), personal suicide history (RRR = 2.96), and lower paternal emotional warmth (RRR = 0.52) independently predicted current NSSI, whereas greater childhood trauma (RRR = 0.35) and stressful life events (RRR = 0.68) were associated with lower odds of remission.

conclusionsNSSI among adolescents receiving psychiatric care shows heterogeneous transition patterns and distinct psychosocial profiles. Multidomain psychosocial characteristics, including socioeconomic adversity, prior suicidality, trauma exposure, life stress, and paternal emotional warmth, appear to be important correlates of NSSI transitions. These findings highlight the value of incorporating multidomain psychosocial assessment into clinical risk evaluation and intervention planning. CLINICAL TRIAL NUMBER: Not applicable.

Indexed as

Self-Injurious BehaviorAdaptation, PsychologicalAdolescentFemaleHumansLongitudinal StudiesMaleParentingRisk FactorsAdolescentsLatent profile analysisLongitudinal studyNon-suicidal self-injuryPsychological heterogeneity

Identifiers

PMID42087124
PMCPMC13360038

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