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Parent-of-origin Effect in Schizophrenia and Non-affective Psychoses: Evidence from Dermatoglyphics

OBJECTIVE: This study aims at examining “parent-of-origin effect” (POE) in dermatoglyphic patterns among patients with schizophrenia and non-affective psychoses. MATERIALS AND METHODS: Dermatoglyphic comparison was carried out for schizophrenia patients (n=200) and healthy controls (HC) (n=100). In...

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Autores principales: Divakaran, Anjith, Narayanaswamy, Janardhanan C., Kalmadi, Sunil V., Narayan, Vidya, Rao, Naren P., Venkatasubramanian, Ganesan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3821203/
https://www.ncbi.nlm.nih.gov/pubmed/24249928
http://dx.doi.org/10.4103/0253-7176.119481
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author Divakaran, Anjith
Narayanaswamy, Janardhanan C.
Kalmadi, Sunil V.
Narayan, Vidya
Rao, Naren P.
Venkatasubramanian, Ganesan
author_facet Divakaran, Anjith
Narayanaswamy, Janardhanan C.
Kalmadi, Sunil V.
Narayan, Vidya
Rao, Naren P.
Venkatasubramanian, Ganesan
author_sort Divakaran, Anjith
collection PubMed
description OBJECTIVE: This study aims at examining “parent-of-origin effect” (POE) in dermatoglyphic patterns among patients with schizophrenia and non-affective psychoses. MATERIALS AND METHODS: Dermatoglyphic comparison was carried out for schizophrenia patients (n=200) and healthy controls (HC) (n=100). In addition, the effect of family history and POE was examined in the dermatoglyphic pattern. RESULTS: Schizophrenia patients compared to HC had significantly lower left total finger ridge count (LTFRC) (t=3.63, P<0.001), right total finger ridge count (RTFRC) (t=4.86, P<0.001), and absolute finger ridge count (ATFRC) (t=4.80, P<0.001) compared to HC. It was also noted that patient group had significantly higher average number of arches (t=2.20, P=0.03). The comparison between the same sex POE group and the opposite sex POE group revealed that significant differences exist in LTFRC (t=2.91, P<0.01) and ATFRC (t=2.30, P=0.02). The same sex group also had lesser number of whorls compared to opposite sex group (t=2.04, P=0.04). CONCLUSIONS: The same sex parental inheritance group seem to be more developmentally compromised than the opposite sex parental inheritance group indicating a significant POE. Complex epigenetic mechanisms along with hormonal modulation could explain the sex specific disease phenotype expression, which is a plausible explanation as in the present study.
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spelling pubmed-38212032013-11-18 Parent-of-origin Effect in Schizophrenia and Non-affective Psychoses: Evidence from Dermatoglyphics Divakaran, Anjith Narayanaswamy, Janardhanan C. Kalmadi, Sunil V. Narayan, Vidya Rao, Naren P. Venkatasubramanian, Ganesan Indian J Psychol Med Original Article OBJECTIVE: This study aims at examining “parent-of-origin effect” (POE) in dermatoglyphic patterns among patients with schizophrenia and non-affective psychoses. MATERIALS AND METHODS: Dermatoglyphic comparison was carried out for schizophrenia patients (n=200) and healthy controls (HC) (n=100). In addition, the effect of family history and POE was examined in the dermatoglyphic pattern. RESULTS: Schizophrenia patients compared to HC had significantly lower left total finger ridge count (LTFRC) (t=3.63, P<0.001), right total finger ridge count (RTFRC) (t=4.86, P<0.001), and absolute finger ridge count (ATFRC) (t=4.80, P<0.001) compared to HC. It was also noted that patient group had significantly higher average number of arches (t=2.20, P=0.03). The comparison between the same sex POE group and the opposite sex POE group revealed that significant differences exist in LTFRC (t=2.91, P<0.01) and ATFRC (t=2.30, P=0.02). The same sex group also had lesser number of whorls compared to opposite sex group (t=2.04, P=0.04). CONCLUSIONS: The same sex parental inheritance group seem to be more developmentally compromised than the opposite sex parental inheritance group indicating a significant POE. Complex epigenetic mechanisms along with hormonal modulation could explain the sex specific disease phenotype expression, which is a plausible explanation as in the present study. Medknow Publications & Media Pvt Ltd 2013 /pmc/articles/PMC3821203/ /pubmed/24249928 http://dx.doi.org/10.4103/0253-7176.119481 Text en Copyright: © Indian Journal of Psychological Medicine http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Divakaran, Anjith
Narayanaswamy, Janardhanan C.
Kalmadi, Sunil V.
Narayan, Vidya
Rao, Naren P.
Venkatasubramanian, Ganesan
Parent-of-origin Effect in Schizophrenia and Non-affective Psychoses: Evidence from Dermatoglyphics
title Parent-of-origin Effect in Schizophrenia and Non-affective Psychoses: Evidence from Dermatoglyphics
title_full Parent-of-origin Effect in Schizophrenia and Non-affective Psychoses: Evidence from Dermatoglyphics
title_fullStr Parent-of-origin Effect in Schizophrenia and Non-affective Psychoses: Evidence from Dermatoglyphics
title_full_unstemmed Parent-of-origin Effect in Schizophrenia and Non-affective Psychoses: Evidence from Dermatoglyphics
title_short Parent-of-origin Effect in Schizophrenia and Non-affective Psychoses: Evidence from Dermatoglyphics
title_sort parent-of-origin effect in schizophrenia and non-affective psychoses: evidence from dermatoglyphics
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3821203/
https://www.ncbi.nlm.nih.gov/pubmed/24249928
http://dx.doi.org/10.4103/0253-7176.119481
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