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Preliminary studies on apparent mendelian psychotic disorders in consanguineous families

BACKGROUND: Psychiatric disorders are characterized by alteration in emotions, mood and behavior. Genetics is known to play a significant role in the development of psychiatric disorders. Genome-wide association studies have identified several loci associated with psychiatric illnesses. We hypothesi...

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Autores principales: Kanwal, Ambreen, Sheikh, Sohail A., Iftikhar, Amina, Naz, Sadaf, Pardo, José V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9667425/
https://www.ncbi.nlm.nih.gov/pubmed/36384485
http://dx.doi.org/10.1186/s12888-022-04304-4
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author Kanwal, Ambreen
Sheikh, Sohail A.
Iftikhar, Amina
Naz, Sadaf
Pardo, José V.
author_facet Kanwal, Ambreen
Sheikh, Sohail A.
Iftikhar, Amina
Naz, Sadaf
Pardo, José V.
author_sort Kanwal, Ambreen
collection PubMed
description BACKGROUND: Psychiatric disorders are characterized by alteration in emotions, mood and behavior. Genetics is known to play a significant role in the development of psychiatric disorders. Genome-wide association studies have identified several loci associated with psychiatric illnesses. We hypothesize the existence of rare variants following Mendelian recessive mode of inheritance. These variants can be identified in families with multiple affected individuals born to unaffected consanguineous parents. METHODS: We visited psychiatric outpatient departments of multiple hospitals in Lahore, Pakistan. We focused on psychosis, as it can occur in several DSM disorders such as schizophrenia, dementia and bipolar disorder. After clinical diagnosis by an American trained psychiatrist, detailed clinical assessments using Diagnostic Interview for Genetic Studies (DIGS), Diagnostic Interview for Psychosis and Affective Disorders (DI-PAD), Positive and Negative Syndrome Scale (PANSS), Hamilton Depression and Anxiety Rating Scale (HAM-D; HAM-A) were administered to all willing affected and unaffected participants. RESULTS: We identified eight pedigrees with two or more psychotic individuals in each family. Clinical diagnoses determined by their psychiatrists included ten individuals with schizophrenia; four individuals with psychosis and bipolar disorder; and two patients with “unspecified psychosis.” The rating instruments rigorously confirmed the diagnosis of psychosis in the affected patients from the six families as well as the absence of psychotic disorders in unaffected individuals from the six families. We obtained DNA samples from willing members of all eight families for future genetic analyses. CONCLUSION: Our research highlights an alternative approach to discovery of rare recessively inherited genetic variants causing psychiatric disorders that have remained unidentified to date. These findings could illuminate underlying biological mechanisms leading toward development of targeted therapies in future.
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spelling pubmed-96674252022-11-16 Preliminary studies on apparent mendelian psychotic disorders in consanguineous families Kanwal, Ambreen Sheikh, Sohail A. Iftikhar, Amina Naz, Sadaf Pardo, José V. BMC Psychiatry Research BACKGROUND: Psychiatric disorders are characterized by alteration in emotions, mood and behavior. Genetics is known to play a significant role in the development of psychiatric disorders. Genome-wide association studies have identified several loci associated with psychiatric illnesses. We hypothesize the existence of rare variants following Mendelian recessive mode of inheritance. These variants can be identified in families with multiple affected individuals born to unaffected consanguineous parents. METHODS: We visited psychiatric outpatient departments of multiple hospitals in Lahore, Pakistan. We focused on psychosis, as it can occur in several DSM disorders such as schizophrenia, dementia and bipolar disorder. After clinical diagnosis by an American trained psychiatrist, detailed clinical assessments using Diagnostic Interview for Genetic Studies (DIGS), Diagnostic Interview for Psychosis and Affective Disorders (DI-PAD), Positive and Negative Syndrome Scale (PANSS), Hamilton Depression and Anxiety Rating Scale (HAM-D; HAM-A) were administered to all willing affected and unaffected participants. RESULTS: We identified eight pedigrees with two or more psychotic individuals in each family. Clinical diagnoses determined by their psychiatrists included ten individuals with schizophrenia; four individuals with psychosis and bipolar disorder; and two patients with “unspecified psychosis.” The rating instruments rigorously confirmed the diagnosis of psychosis in the affected patients from the six families as well as the absence of psychotic disorders in unaffected individuals from the six families. We obtained DNA samples from willing members of all eight families for future genetic analyses. CONCLUSION: Our research highlights an alternative approach to discovery of rare recessively inherited genetic variants causing psychiatric disorders that have remained unidentified to date. These findings could illuminate underlying biological mechanisms leading toward development of targeted therapies in future. BioMed Central 2022-11-16 /pmc/articles/PMC9667425/ /pubmed/36384485 http://dx.doi.org/10.1186/s12888-022-04304-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Kanwal, Ambreen
Sheikh, Sohail A.
Iftikhar, Amina
Naz, Sadaf
Pardo, José V.
Preliminary studies on apparent mendelian psychotic disorders in consanguineous families
title Preliminary studies on apparent mendelian psychotic disorders in consanguineous families
title_full Preliminary studies on apparent mendelian psychotic disorders in consanguineous families
title_fullStr Preliminary studies on apparent mendelian psychotic disorders in consanguineous families
title_full_unstemmed Preliminary studies on apparent mendelian psychotic disorders in consanguineous families
title_short Preliminary studies on apparent mendelian psychotic disorders in consanguineous families
title_sort preliminary studies on apparent mendelian psychotic disorders in consanguineous families
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9667425/
https://www.ncbi.nlm.nih.gov/pubmed/36384485
http://dx.doi.org/10.1186/s12888-022-04304-4
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