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Investigating Potential Biomarkers in Autism Spectrum Disorder.
Bridgemohan, Carolyn; Cochran, David M; Howe, Yamini J; Pawlowski, Katherine; Zimmerman, Andrew W; Anderson, George M; Choueiri, Roula; Sices, Laura; Miller, Karen J; Ultmann, Monica; Helt, Jessica; Forbes, Peter W; Farfel, Laura; Brewster, Stephanie J; Frazier, Jean A; Neumeyer, Ann M.
Afiliação
  • Bridgemohan C; Boston Children's Hospital, Boston, MA, United States.
  • Cochran DM; Harvard Medical School, Boston, MA, United States.
  • Howe YJ; University of Massachusetts Memorial Medical Center, Worcester, MA, United States.
  • Pawlowski K; University of Massachusetts Medical School, Worcester, MA, United States.
  • Zimmerman AW; Harvard Medical School, Boston, MA, United States.
  • Anderson GM; Lurie Center for Autism, Massachusetts General Hospital for Children, Lexington, MA, United States.
  • Choueiri R; Boston Children's Hospital, Boston, MA, United States.
  • Sices L; University of Massachusetts Memorial Medical Center, Worcester, MA, United States.
  • Miller KJ; University of Massachusetts Medical School, Worcester, MA, United States.
  • Ultmann M; Child Study Center, Yale University School of Medicine, New Haven, CT, United States.
  • Helt J; University of Massachusetts Memorial Medical Center, Worcester, MA, United States.
  • Forbes PW; University of Massachusetts Medical School, Worcester, MA, United States.
  • Farfel L; Boston University Medical Center, Boston, MA, United States.
  • Brewster SJ; Boston University School of Medicine, Boston, MA, United States.
  • Frazier JA; Center for Children with Special Needs, Floating Children's Hospital at Tufts Medical Center, Boston, MA, United States.
  • Neumeyer AM; Tufts University School of Medicine, Boston, MA, United States.
Front Integr Neurosci ; 13: 31, 2019.
Article em En | MEDLINE | ID: mdl-31427932
ABSTRACT

BACKGROUND:

Early identification and treatment of individuals with autism spectrum disorder (ASD) improves outcomes, but specific evidence needed to individualize treatment recommendations is lacking. Biomarkers that could be routinely measured within the clinical setting could potentially transform clinical care for patients with ASD. This demonstration project employed collection of biomarker data during regular autism specialty clinical visits and explored the relationship of biomarkers with clinical ASD symptoms.

METHODS:

Eighty-three children with ASD, aged 5-10 years, completed a multi-site feasibility study integrating the collection of biochemical (blood serotonin, urine melatonin sulfate excretion) and clinical (head circumference, dysmorphology exam, digit ratio, cognitive and behavioral function) biomarkers during routine ASD clinic visits. Parents completed a demographic survey and the Aberrant Behavior Checklist-Community. Cognitive function was determined by record review. Data analysis utilized Wilcoxon two-sample tests and Spearman correlations.

RESULTS:

Participants were 82% male, 63% White, 19% Hispanic, with a broad range of functioning. Group means indicated hyperserotonemia. In a single regression analysis adjusting for race and median household income, higher income was associated with higher levels of blood serotonin and urine melatonin sulfate excretion levels (p = 0.004 and p = 0.04, respectively). Melatonin correlated negatively with age (p = 0.048) and reported neurologic problems (p = 0.02). Dysmorphic status correlated with higher reported stereotyped behavior (p = 0.02) and inappropriate speech (p = 0.04).

CONCLUSION:

This demonstration project employed collection of multiple biomarkers, allowed for examination of associations between biochemical and clinical measures, and identified several findings that suggest direction for future studies. This clinical research model has promise for integrative biomarker research in individuals with complex, heterogeneous neurodevelopmental disorders such as ASD.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Guideline / Prognostic_studies Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Guideline / Prognostic_studies Idioma: En Ano de publicação: 2019 Tipo de documento: Article