It does, however, make it difficult to compare the results direc

It does, however, make it difficult to compare the results directly to prior studies with either clinical

patients or typical lab-based control populations, but does represent an important characterization of the symptoms in the community-at-large that can begin to establish Web-normative scores. Our finding of symptom scores across a large range, in children and adolescents without a self-reported diagnosis of ADHD is important and novel for a Web-based community. Recent epidemiological reports from the Centers for Disease Control selleck bio suggest the community Inhibitors,research,lifescience,medical prevalence of a diagnosis of ADHD is over 8% (http://www.cdc.gov). Few studies, however, have looked broadly at symptoms that exist in the community. Inhibitors,research,lifescience,medical Our attention symptom finding supports reports that ADHD-related symptoms are dimensional (Lubke et al. 2009), and should be treated as quantitatively distributed traits in the population. Yet, similar to Lubke et al. (2009), we do find that cognitive test performance changes as function of symptom level, which may suggest different latent classes. These data may improve the ability to track the underlying genetic contribution Inhibitors,research,lifescience,medical of these symptoms. Our findings of high correlations

between parent and offspring scores on our cognitive control measures suggest high heritability of

these constructs, an important step in investigating genetic associations. Typically, www.selleckchem.com/products/Erlotinib-Hydrochloride.html examining heritability is difficult for new computerized measures, as recruiting and testing families in a large enough sample to measure heritability Inhibitors,research,lifescience,medical is not feasible. Further, with iterative development of new measures, it becomes more challenging for phenotypes to be adequately validated with respect to genetic studies. Studying a single parent and offspring allows us to compute narrow-sense heritability or what some have called Inhibitors,research,lifescience,medical biometric heritability (Lynch and Walsh 1998). These numbers provide a ceiling for additive genetic influences without taking into account shared environment or pure environment factors or epistasis. Drug_discovery Our calculations of narrow-sense heritability suggest high heritability but also unsurprisingly that these unmeasured sources of variance do play a role in working memory and response inhibition. They also suggest that some phenotypic indicators may not be useful in genetic association experiments going forward, as they display very low narrow-sense heritability (e.g., Working Memory load accuracy at low loads). These findings suggest our approach is feasible and extremely efficient for examining these questions, but larger pedigree-type data would be ideal for answering these questions.

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