Literature DB >> 27045100

Genetics as a molecular window into recovery, its treatment, and stress responses after stroke.

Vanessa Juth1, E Alison Holman1, Michelle K Chan1, Steven C Cramer2.   

Abstract

Stroke remains a major source of adult disability in the USA and worldwide. Most patients show some recovery during the weeks to months following a stroke, but this is generally incomplete. An emerging branch of therapeutics targets the processes underlying this behavioral recovery from stroke toward the goal of reducing long-term disability. A key factor hampering these efforts is the very large degree of variability between stroke survivors. Available data suggest that genetic differences could explain an important fraction of the differences between subjects. The current review considers this from several angles, including genetic differences in relation to drugs that promote recovery. Genetic factors related to physiological and psychological stress responses may also be critically important to understanding recovery after stroke and its treatment. The studies reviewed provide insights into recovery and suggest directions for further research to improve clinical decision-making in this setting. Genetic differences between patients might be used to help clinical trials select specific patient subgroups, on a biological basis, in order to sharpen the precision with which new treatments are evaluated. Pharmacogenomic factors might also provide insights into inter-subject differences in treatment side effects for pharmacological prescriptions, and behavioral interventions, and others. These efforts must be conducted with the strictest ethical standards given the highly sensitive nature of genetic data. Understanding the effect of selected genetic measures could improve a clinician's ability to predict the risk and efficacy of a restorative therapy and to make maximally informed decisions, and in so doing, facilitate individual patient care.
Copyright © 2016 American Federation for Medical Research.

Entities:  

Keywords:  Stroke

Mesh:

Year:  2016        PMID: 27045100      PMCID: PMC4942179          DOI: 10.1136/jim-2016-000126

Source DB:  PubMed          Journal:  J Investig Med        ISSN: 1081-5589            Impact factor:   2.895


  102 in total

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Journal:  Circulation       Date:  2010-02-23       Impact factor: 29.690

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Journal:  Stroke       Date:  2011-07       Impact factor: 7.914

7.  Epidemiological, clinical, and neuropathological study of apolipoprotein E genotype in Alzheimer's disease.

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10.  Elevated brain cannabinoid CB1 receptor availability in post-traumatic stress disorder: a positron emission tomography study.

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Journal:  Mol Psychiatry       Date:  2013-05-14       Impact factor: 15.992

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  1 in total

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Journal:  BMJ Open       Date:  2019-05-22       Impact factor: 2.692

  1 in total

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