Literature DB >> 34202628

Genomics as a Clinical Decision Support Tool: Successful Proof of Concept for Improved ASD Outcomes.

Heather Way1, Grant Williams2, Sharon Hausman-Cohen2, Jordan Reeder2.   

Abstract

Considerable evidence is emerging that Autism Spectrum Disorder (ASD) is most often triggered by a range of different genetic variants that interact with environmental factors such as exposures to toxicants and changes to the food supply. Up to 80% of genetic variations that contribute to ASD found to date are neither extremely rare nor classified as pathogenic. Rather, they are less common single nucleotide polymorphisms (SNPs), found in 1-15% or more of the population, that by themselves are not disease-causing. These genomic variants contribute to ASD by interacting with each other, along with nutritional and environmental factors. Examples of pathways affected or triggered include those related to brain inflammation, mitochondrial dysfunction, neuronal connectivity, synapse formation, impaired detoxification, methylation, and neurotransmitter-related effects. This article presents information on four case study patients that are part of a larger ongoing pilot study. A genomic clinical decision support (CDS) tool that specifically focuses on variants and pathways that have been associated with neurodevelopmental disorders was used in this pilot study to help develop a targeted, personalized prevention and intervention strategy for each child. In addition to an individual's genetic makeup, each patient's personal history, diet, and environmental factors were considered. The CDS tool also looked at genomic SNPs associated with secondary comorbid ASD conditions including attention deficit hyperactivity disorder (ADHD), obsessive-compulsive disorder (OCD), anxiety, and pediatric autoimmune neuropsychiatric disorder associated with streptococcal infections/pediatric acute-onset neuropsychiatric syndrome (PANDAS/PANS). The interpreted genomics tool helped the treating clinician identify and develop personalized, genomically targeted treatment plans. Utilization of this treatment approach was associated with significant improvements in socialization and verbal skills, academic milestones and intelligence quotient (IQ), and overall increased ability to function in these children, as measured by autism treatment evaluation checklist (ATEC) scores and parent interviews.

Entities:  

Keywords:  ADHD; OCD; PANDAS; anxiety; autism spectrum disorder (ASD); clinical decision support tool; genomics; personalized treatment strategy; single nucleotide polymorphisms

Year:  2021        PMID: 34202628     DOI: 10.3390/jpm11070596

Source DB:  PubMed          Journal:  J Pers Med        ISSN: 2075-4426


  52 in total

1.  Exogenous melatonin inhibits neutrophil migration through suppression of ERK activation.

Authors:  Da-Long Ren; Ai-Ai Sun; Ya-Juan Li; Min Chen; Shu-Chao Ge; Bing Hu
Journal:  J Endocrinol       Date:  2015-08-24       Impact factor: 4.286

2.  Glutamate transporter gene SLC1A1 associated with obsessive-compulsive disorder.

Authors:  Paul Daniel Arnold; Tricia Sicard; Eliza Burroughs; Margaret A Richter; James L Kennedy
Journal:  Arch Gen Psychiatry       Date:  2006-07

3.  Prevalence of SHANK3 variants in patients with different subtypes of autism spectrum disorders.

Authors:  Luigi Boccuto; Maria Lauri; Sara M Sarasua; Cindy D Skinner; Daniela Buccella; Alka Dwivedi; Daniela Orteschi; Julianne S Collins; Marcella Zollino; Paola Visconti; Barb Dupont; Danilo Tiziano; Richard J Schroer; Giovanni Neri; Roger E Stevenson; Fiorella Gurrieri; Charles E Schwartz
Journal:  Eur J Hum Genet       Date:  2012-08-15       Impact factor: 4.246

Review 4.  The role of S-nitrosoglutathione reductase (GSNOR) in human disease and therapy.

Authors:  Scott D Barnett; Iain L O Buxton
Journal:  Crit Rev Biochem Mol Biol       Date:  2017-04-10       Impact factor: 8.250

5.  Genetic influences on ADHD symptom dimensions: Examination of a priori candidates, gene-based tests, genome-wide variation, and SNP heritability.

Authors:  L Cinnamon Bidwell; Joshua C Gray; Jessica Weafer; Abraham A Palmer; Harriet de Wit; James MacKillop
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2017-06       Impact factor: 3.568

Review 6.  Paraoxonase 1 (PON1) as a genetic determinant of susceptibility to organophosphate toxicity.

Authors:  Lucio G Costa; Gennaro Giordano; Toby B Cole; Judit Marsillach; Clement E Furlong
Journal:  Toxicology       Date:  2012-07-31       Impact factor: 4.221

7.  N-acetyl cysteine in the treatment of obsessive compulsive and related disorders: a systematic review.

Authors:  Georgina Oliver; Olivia Dean; David Camfield; Scott Blair-West; Chee Ng; Michael Berk; Jerome Sarris
Journal:  Clin Psychopharmacol Neurosci       Date:  2015-04-30       Impact factor: 2.582

Review 8.  Natural Product-Derived Treatments for Attention-Deficit/Hyperactivity Disorder: Safety, Efficacy, and Therapeutic Potential of Combination Therapy.

Authors:  James Ahn; Hyung Seok Ahn; Jae Hoon Cheong; Ike Dela Peña
Journal:  Neural Plast       Date:  2016-02-04       Impact factor: 3.599

9.  A kinome-wide RNAi screen identifies ERK2 as a druggable regulator of Shank3 stability.

Authors:  Li Wang; Carolyn J Adamski; Vitaliy V Bondar; Evelyn Craigen; John R Collette; Kaifang Pang; Kihoon Han; Antrix Jain; Sung Y Jung; Zhandong Liu; Richard N Sifers; J Lloyd Holder; Huda Y Zoghbi
Journal:  Mol Psychiatry       Date:  2019-01-29       Impact factor: 15.992

10.  The NQO1 polymorphism C609T (Pro187Ser) and cancer susceptibility: a comprehensive meta-analysis.

Authors:  B Lajin; A Alachkar
Journal:  Br J Cancer       Date:  2013-07-16       Impact factor: 7.640

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  3 in total

1.  Utilizing Genomically Targeted Molecular Data to Improve Patient-Specific Outcomes in Autism Spectrum Disorder.

Authors:  Sharon Hausman-Cohen; William LaValley; Heather Way; Emily Gutierrez; Jordan Reeder
Journal:  Int J Mol Sci       Date:  2022-02-16       Impact factor: 5.923

2.  A Personalized Approach to Evaluating and Treating Autism Spectrum Disorder.

Authors:  Richard E Frye; Shannon Rose; Richard G Boles; Daniel A Rossignol
Journal:  J Pers Med       Date:  2022-01-24

3.  Genomics as a Clinical Decision Support Tool for Identifying and Addressing Modifiable Causes of Cognitive Decline and Improving Outcomes: Proof of Concept Support for This Personalized Medicine Strategy.

Authors:  Sharon Hausman-Cohen; Carol Bilich; Sandeep Kapoor; Eduardo Maristany; Anne Stefani; Alexandra Wilcox
Journal:  Front Aging Neurosci       Date:  2022-04-18       Impact factor: 5.702

  3 in total

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