Temporal patterns of self-injurious behavior correlate with stress hormone levels in the developmentally disabled

Abstract While the origins and developmental course of self-injurious behavior (SIB) remain relatively unknown, recent studies suggest a biological imbalance may potentiate or provoke the contagious recurrence of SIB patterns in individuals with severe developmental disabilities (DD). Evidence from...

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Veröffentlicht in:Psychiatry research 2008-01, Vol.157 (1), p.181-189
Hauptverfasser: Kemp, Aaron S, Fillmore, Paul T, Lenjavi, Mohammed R, Lyon, Melvin, Chicz-DeMet, Aleksandra, Touchette, Paul E, Sandman, Curt A
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Sprache:eng
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Zusammenfassung:Abstract While the origins and developmental course of self-injurious behavior (SIB) remain relatively unknown, recent studies suggest a biological imbalance may potentiate or provoke the contagious recurrence of SIB patterns in individuals with severe developmental disabilities (DD). Evidence from several laboratories indicates that functioning, relations, and processing of a stress-related molecule, proopiomelanocortin (POMC) may be perturbed among certain subgroups of individuals exhibiting SIB. The current investigation employed a unique time-pattern analysis program (THEME) to examine whether recurrent temporal patterns (T-patterns) of SIB were related to morning levels of two POMC-derived hormones: β-endorphin (βE) and adrenocorticotropic hormone (ACTH). THEME was used to quantify highly significant (non-random) T-patterns that included SIB within a dataset of in situ observational recordings spanning 8 days (∼ 40 h) in 25 subjects with DD. Pearson's product–moment analyses revealed highly significant correlations between the percentage of T-patterns containing SIB and basal levels of both βE and ACTH, which were not found with any other “control” T-patterns. These findings support the hypothesis that the recurrent temporal patterning of SIB represents a unique behavioral phenotype directly related to perturbed levels of POMC-derived stress hormones in certain individuals with severe DD.
ISSN:0165-1781
1872-7123
DOI:10.1016/j.psychres.2007.04.003