Breakthrough – Co-Morbid Clusters in Autism

Comorbidity Clusters in Autism Spectrum Disorders: An Electronic Health Record Time-Series Analysis.

http://www.ncbi.nlm.nih.gov/pubmed/24323995

 

Center for Biomedical Informatics, Harvard Medical School, Boston, Massachusetts

Abstract

OBJECTIVE:

The distinct trajectories of patients with autism spectrum disorders (ASDs) have not been extensively studied, particularly regarding clinical manifestations beyond the neurobehavioral criteria from the Diagnostic and Statistical Manual of Mental Disorders. The objective of this study was to investigate the patterns of co-occurrence of medical comorbidities in ASDs.

METHODS:

International Classification of Diseases, Ninth Revision codes from patients aged at least 15 years and a diagnosis of ASD were obtained from electronic medical records. These codes were aggregated by using phenotype-wide association studies categories and processed into 1350-dimensional vectors describing the counts of the most common categories in 6-month blocks between the ages of 0 to 15. Hierarchical clustering was used to identify subgroups with distinct courses.

RESULTS:

Four subgroups were identified.

The first was characterized by seizures (n = 120, subgroup prevalence 77.5%).

The second (n = 197) was characterized by multisystem disorders including gastrointestinal disorders (prevalence 24.3%) and auditory disorders and infections (prevalence 87.8%),

and the third was characterized by psychiatric disorders (n = 212, prevalence 33.0%).

The last group (n = 4316) could not be further resolved.

The prevalence of psychiatric disorders was uncorrelated with seizure activity (P = .17), but a significant correlation existed between gastrointestinal disorders and seizures (P < .001).

The correlation results were replicated by using a second sample of 496 individuals from a different geographic region.

CONCLUSIONS:Three distinct patterns of medical trajectories were identified by unsupervised clustering of electronic health record diagnoses. These may point to distinct etiologies with different genetic and environmental contributions. Additional clinical and molecular characterizations will be required to further delineate these subgroups.

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Comment

It is certainly is another big breakthrough year in our understandings of Autism.

Further Readings of Interest

The co-morbidity burden of children and young adults with autism spectrum disorders.

http://www.ncbi.nlm.nih.gov/pubmed/22511918

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This entry was posted in Autism, co-morbid, Environment, Gut, Immune System, Inflammation, Mice, Neurology, Physiology, Treatment. Bookmark the permalink.

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