Reframing Psychiatry for Precision Medicine.

Elizabeth B Torres
Author Information
  1. Elizabeth B Torres: Department of Psychology, Rutgers University, New Brunswick, NJ 08854, USA.

Abstract

The art of observing and describing behaviors has driven diagnosis and informed basic science in psychiatry. In recent times, studies of mental illness are focused on understanding the brain's neurobiology but there is a paucity of information on the potential contributions from peripheral activity to mental health. In precision medicine, this common practice leaves a gap between bodily behaviors and genomics that we here propose to address with a new layer of inquiry that includes gene expression on tissues inclusive of brain, heart, muscle-skeletal and organs for vital bodily functions. We interrogate gene expression on human tissue as a function of disease-associated genes. By removing genes linked to disease from the typical human set, and recomputing gene expression on the tissues, we can compare the outcomes across mental illnesses, well-known neurological conditions, and non-neurological conditions. We find that major neuropsychiatric conditions that are behaviorally defined today (e.g., autism, schizophrenia, and depression) through DSM-observation criteria have strong convergence with well-known neurological conditions (e.g., ataxias and Parkinson's disease), but less overlap with non-neurological conditions. Surprisingly, tissues majorly involved in the central control, coordination, adaptation and learning of movements, emotion and memory are maximally affected in psychiatric diagnoses along with peripheral heart and muscle-skeletal tissues. Our results underscore the importance of considering both the brain-body connection and the contributions of the peripheral nervous systems to mental health.

Keywords

References

  1. Eur J Hum Genet. 2015 Oct;23(10):1334-40 [PMID: 25604858]
  2. Neurol Sci. 2001 Nov;22 Suppl 2:S88-92 [PMID: 11794486]
  3. Neuropsychologia. 2016 May;85:310-26 [PMID: 26951932]
  4. Sci Rep. 2016 Nov 21;6:37422 [PMID: 27869148]
  5. Nature. 2014 Jul 24;511(7510):421-7 [PMID: 25056061]
  6. Science. 2020 Sep 11;369(6509): [PMID: 32913073]
  7. Front Integr Neurosci. 2013 Jul 24;7:32 [PMID: 23898241]
  8. Handb Clin Neurol. 2018;155:143-174 [PMID: 29891056]
  9. Cold Spring Harb Perspect Med. 2012 Jan;2(1):a008888 [PMID: 22315721]
  10. Psychiatr Genet. 2020 Feb;30(1):1-9 [PMID: 31764709]
  11. Mov Disord. 2006 Apr;21(4):519-23 [PMID: 16250030]
  12. J Neurol Neurosurg Psychiatry. 2016 Jan;87(1):53-63 [PMID: 26157034]
  13. Curr Neurol Neurosci Rep. 2012 Jun;12(3):227-36 [PMID: 22527681]
  14. JAMA. 2001 Nov 14;286(18):2239-44 [PMID: 11710888]
  15. Sensors (Basel). 2020 Jan 20;20(2): [PMID: 31968701]
  16. Sci Rep. 2018 Jan 12;8(1):614 [PMID: 29330487]
  17. Front Integr Neurosci. 2020 Jun 17;14:23 [PMID: 32625069]
  18. Ann Neurol. 2002 Jan;51(1):14-8 [PMID: 11782979]
  19. Am J Med Genet B Neuropsychiatr Genet. 2017 Oct;174(7):757-764 [PMID: 28786528]
  20. Front Neurosci. 2015 Sep 01;9:296 [PMID: 26388713]
  21. Eur J Med Genet. 2015 Dec;58(12):704-14 [PMID: 26493318]
  22. Brain. 2009 Sep;132(Pt 9):2413-25 [PMID: 19389870]
  23. Genet Med. 2013 Sep;15(9):673-83 [PMID: 23538602]
  24. Orphanet J Rare Dis. 2013 Jan 18;8:14 [PMID: 23331413]
  25. Ann Neurol. 2002 Nov;52(5):549-55 [PMID: 12402251]
  26. Malays J Med Sci. 2004 Jul;11(2):3-11 [PMID: 22973121]
  27. J Vis Exp. 2019 Jul 24;(149): [PMID: 31403620]
  28. Sci Transl Med. 2015 Aug 12;7(300):300ps17 [PMID: 26268311]
  29. Sensors (Basel). 2018 Mar 29;18(4): [PMID: 29596342]
  30. Science. 2020 Sep 11;369(6509): [PMID: 32913075]
  31. Child Adolesc Psychiatr Clin N Am. 2020 Jan;29(1):157-170 [PMID: 31708045]

Grants

  1. NJDOH - CAUT17BSP024/The New Jersey Governor's Council for the Medical Research and Treatments of Autism
  2. Career Development Award/The Nancy Lurie Marks Family Foundation

Word Cloud

Created with Highcharts 10.0.0mentaltissuesconditionsgeneexpressionperipheraldiseaseneurologicalbehaviorscontributionshealthbodilyheartmuscle-skeletalhumangeneswell-knownnon-neurologicalegautismschizophreniadepressionnervoussystemsdisordersartobservingdescribingdrivendiagnosisinformedbasicsciencepsychiatryrecenttimesstudiesillnessfocusedunderstandingbrain'sneurobiologypaucityinformationpotentialactivityprecisionmedicinecommonpracticeleavesgapgenomicsproposeaddressnewlayerinquiryincludesinclusivebrainorgansvitalfunctionsinterrogatetissuefunctiondisease-associatedremovinglinkedtypicalsetrecomputingcancompareoutcomesacrossillnessesfindmajorneuropsychiatricbehaviorallydefinedtodayDSM-observationcriteriastrongconvergenceataxiasParkinson'slessoverlapSurprisinglymajorlyinvolvedcentralcontrolcoordinationadaptationlearningmovementsemotionmemorymaximallyaffectedpsychiatricdiagnosesalongresultsunderscoreimportanceconsideringbrain-bodyconnectionReframingPsychiatryPrecisionMedicineParkinson’sataxiafragileXmitochondria

Similar Articles

Cited By (8)