Clinical and familial correlates of tardive dyskinesia in India and Israel
Background: Antipsychotic drugs are widely used for the treatment of psychosis, especially schizophrenia. Their long-term use can result at times in serious side-effects such as Tardive Dyskinesia (TD). Since over 80% of schizophrenia sufferers (lifetime prevalence 1%) receive long-term antipsychoti...
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creator | Bhatia T, Sabeeha MR, Shriharsh V, Garg K, Segman RH, Uriel HL, Strous R, Nimgaonkar VL, Bernard L, Deshpande SmitaN |
description | Background: Antipsychotic drugs are widely used for the treatment of
psychosis, especially schizophrenia. Their long-term use can result at
times in serious side-effects such as Tardive Dyskinesia (TD). Since
over 80% of schizophrenia sufferers (lifetime prevalence 1%) receive
long-term antipsychotic drug treatment, the extent of the problem is
potentially large. Increasing age is the most consistently demonstrated
risk factor for TD. Aims: To assess effect of different clinical
factors and demographic variables in India and Israel and sib pair
concordance of Tardive Dyskinesia (TD) in India. Settings and Design:
The study was conducted simultaneously among Indian and Israeli
subjects: ascertainment was family-based in India and hospital-based in
Israel. Methods and Material: In India the instruments used were:
Diagnostic Interview for Genetic Studies (DIGS), Positive and Negative
Syndrome Scale (PANSS), Abnormal Involuntary Movement Scale (AIMS), and
Simpson Angus Scale (SAS). The last three instruments were also used in
Israel. Statistical Analysis: Regression analysis and Pearson's
correlation. Results and Conclusions: TD symptoms were present in 40.4%
of 151 Israeli subjects and 28.7% of 334 Indian subjects. While age at
onset and total scores on PANSS were significant predictors of TD in
both the samples, lower scores on the Global Assessment of Functioning
Scale (GAF), diagnostic sub-group and male gender were significant
predictors among Indians. There was no concordance of TD symptoms among
33 affected sib-pairs from India. |
format | Article |
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psychosis, especially schizophrenia. Their long-term use can result at
times in serious side-effects such as Tardive Dyskinesia (TD). Since
over 80% of schizophrenia sufferers (lifetime prevalence 1%) receive
long-term antipsychotic drug treatment, the extent of the problem is
potentially large. Increasing age is the most consistently demonstrated
risk factor for TD. Aims: To assess effect of different clinical
factors and demographic variables in India and Israel and sib pair
concordance of Tardive Dyskinesia (TD) in India. Settings and Design:
The study was conducted simultaneously among Indian and Israeli
subjects: ascertainment was family-based in India and hospital-based in
Israel. Methods and Material: In India the instruments used were:
Diagnostic Interview for Genetic Studies (DIGS), Positive and Negative
Syndrome Scale (PANSS), Abnormal Involuntary Movement Scale (AIMS), and
Simpson Angus Scale (SAS). The last three instruments were also used in
Israel. Statistical Analysis: Regression analysis and Pearson's
correlation. Results and Conclusions: TD symptoms were present in 40.4%
of 151 Israeli subjects and 28.7% of 334 Indian subjects. While age at
onset and total scores on PANSS were significant predictors of TD in
both the samples, lower scores on the Global Assessment of Functioning
Scale (GAF), diagnostic sub-group and male gender were significant
predictors among Indians. There was no concordance of TD symptoms among
33 affected sib-pairs from India.</description><identifier>ISSN: 0022-3859</identifier><identifier>EISSN: 0972-2823</identifier><identifier>PMID: 15377799</identifier><language>eng</language><publisher>India: Medknow Publications and Staff Society of Seth GS Medical College and KEM Hospital, Mumbai, India</publisher><subject>Adult ; Antipsychotic Agents - adverse effects ; Antipsychotic drugs ; Dyskinesia, Drug-Induced - epidemiology ; Dyskinesia, Drug-Induced - etiology ; Female ; Genetic aspects ; Humans ; India - epidemiology ; Israel - epidemiology ; Male ; Neuropsychological Tests ; Psychiatric Status Rating Scales ; Risk factors ; Tardive dyskinesia ; Tardive dyskinesia, schizophrenia, genetic, familial</subject><ispartof>Journal of postgraduate medicine (Bombay), 2004-07, Vol.50 (3), p.167</ispartof><rights>Copyright 2004 Journal of Postgraduate Medicine.</rights><rights>COPYRIGHT 2004 Medknow Publications and Media Pvt. Ltd.</rights><rights>Copyright Medknow Publications Jul-Sep 2004</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,79173</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15377799$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bhatia T, Sabeeha MR, Shriharsh V, Garg K, Segman RH, Uriel HL, Strous R, Nimgaonkar VL, Bernard L, Deshpande SmitaN</creatorcontrib><title>Clinical and familial correlates of tardive dyskinesia in India and Israel</title><title>Journal of postgraduate medicine (Bombay)</title><addtitle>J Postgrad Med</addtitle><description>Background: Antipsychotic drugs are widely used for the treatment of
psychosis, especially schizophrenia. Their long-term use can result at
times in serious side-effects such as Tardive Dyskinesia (TD). Since
over 80% of schizophrenia sufferers (lifetime prevalence 1%) receive
long-term antipsychotic drug treatment, the extent of the problem is
potentially large. Increasing age is the most consistently demonstrated
risk factor for TD. Aims: To assess effect of different clinical
factors and demographic variables in India and Israel and sib pair
concordance of Tardive Dyskinesia (TD) in India. Settings and Design:
The study was conducted simultaneously among Indian and Israeli
subjects: ascertainment was family-based in India and hospital-based in
Israel. Methods and Material: In India the instruments used were:
Diagnostic Interview for Genetic Studies (DIGS), Positive and Negative
Syndrome Scale (PANSS), Abnormal Involuntary Movement Scale (AIMS), and
Simpson Angus Scale (SAS). The last three instruments were also used in
Israel. Statistical Analysis: Regression analysis and Pearson's
correlation. Results and Conclusions: TD symptoms were present in 40.4%
of 151 Israeli subjects and 28.7% of 334 Indian subjects. While age at
onset and total scores on PANSS were significant predictors of TD in
both the samples, lower scores on the Global Assessment of Functioning
Scale (GAF), diagnostic sub-group and male gender were significant
predictors among Indians. There was no concordance of TD symptoms among
33 affected sib-pairs from India.</description><subject>Adult</subject><subject>Antipsychotic Agents - adverse effects</subject><subject>Antipsychotic drugs</subject><subject>Dyskinesia, Drug-Induced - epidemiology</subject><subject>Dyskinesia, Drug-Induced - etiology</subject><subject>Female</subject><subject>Genetic aspects</subject><subject>Humans</subject><subject>India - epidemiology</subject><subject>Israel - epidemiology</subject><subject>Male</subject><subject>Neuropsychological Tests</subject><subject>Psychiatric Status Rating Scales</subject><subject>Risk factors</subject><subject>Tardive dyskinesia</subject><subject>Tardive dyskinesia, schizophrenia, genetic, familial</subject><issn>0022-3859</issn><issn>0972-2823</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>RBI</sourceid><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNptkE1LAzEQhoMoVqt_QRbvK9l8bo6l-FEpeNHzkk1mS2o2W5Ot0H9vpK1eygTmzeR5Z8KcoSusJClJTeh51piQktZcTdB1SmuMKyEYvUSTilMppVJX6HXuXXBG-0IHW3S6d97lixliBK9HSMXQFaOO1n1DYXfp0wVIThcuFItgs_i1LVLU4G_QRad9gttDnqKPp8f3-Uu5fHtezGfLsiWCj6UlCrLqWo5BMoIrKriUxuLaMGwUo7am1BhWqSo_W6Wp0hIkWN5WgnBOp-h-33cTh68tpLFZD9sY8siGUK4EFxhnqNxDK-2hcaEbxqjNCgJE7YcAncvlWUUY4TURKvMPJ_gcFnpnThruDr_Ytj3YZhNdr-OuOa72v2Prhrxj-CNMdLo5FtebfDDDnNEfdE6Ecg</recordid><startdate>200407</startdate><enddate>200407</enddate><creator>Bhatia T, Sabeeha MR, Shriharsh V, Garg K, Segman RH, Uriel HL, Strous R, Nimgaonkar VL, Bernard L, Deshpande SmitaN</creator><general>Medknow Publications and Staff Society of Seth GS Medical College and KEM Hospital, Mumbai, India</general><general>Medknow Publications and Media Pvt. Ltd</general><general>Medknow Publications & Media Pvt. Ltd</general><scope>RBI</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope></search><sort><creationdate>200407</creationdate><title>Clinical and familial correlates of tardive dyskinesia in India and Israel</title><author>Bhatia T, Sabeeha MR, Shriharsh V, Garg K, Segman RH, Uriel HL, Strous R, Nimgaonkar VL, Bernard L, Deshpande SmitaN</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b265t-d29eb26fb50e7420136577cd08c40c943d833cc4191742d9a39a7e7ed5b162553</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Adult</topic><topic>Antipsychotic Agents - adverse effects</topic><topic>Antipsychotic drugs</topic><topic>Dyskinesia, Drug-Induced - epidemiology</topic><topic>Dyskinesia, Drug-Induced - etiology</topic><topic>Female</topic><topic>Genetic aspects</topic><topic>Humans</topic><topic>India - epidemiology</topic><topic>Israel - epidemiology</topic><topic>Male</topic><topic>Neuropsychological Tests</topic><topic>Psychiatric Status Rating Scales</topic><topic>Risk factors</topic><topic>Tardive dyskinesia</topic><topic>Tardive dyskinesia, schizophrenia, genetic, familial</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bhatia T, Sabeeha MR, Shriharsh V, Garg K, Segman RH, Uriel HL, Strous R, Nimgaonkar VL, Bernard L, Deshpande SmitaN</creatorcontrib><collection>Bioline International</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Psychology</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><jtitle>Journal of postgraduate medicine (Bombay)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bhatia T, Sabeeha MR, Shriharsh V, Garg K, Segman RH, Uriel HL, Strous R, Nimgaonkar VL, Bernard L, Deshpande SmitaN</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Clinical and familial correlates of tardive dyskinesia in India and Israel</atitle><jtitle>Journal of postgraduate medicine (Bombay)</jtitle><addtitle>J Postgrad Med</addtitle><date>2004-07</date><risdate>2004</risdate><volume>50</volume><issue>3</issue><spage>167</spage><pages>167-</pages><issn>0022-3859</issn><eissn>0972-2823</eissn><abstract>Background: Antipsychotic drugs are widely used for the treatment of
psychosis, especially schizophrenia. Their long-term use can result at
times in serious side-effects such as Tardive Dyskinesia (TD). Since
over 80% of schizophrenia sufferers (lifetime prevalence 1%) receive
long-term antipsychotic drug treatment, the extent of the problem is
potentially large. Increasing age is the most consistently demonstrated
risk factor for TD. Aims: To assess effect of different clinical
factors and demographic variables in India and Israel and sib pair
concordance of Tardive Dyskinesia (TD) in India. Settings and Design:
The study was conducted simultaneously among Indian and Israeli
subjects: ascertainment was family-based in India and hospital-based in
Israel. Methods and Material: In India the instruments used were:
Diagnostic Interview for Genetic Studies (DIGS), Positive and Negative
Syndrome Scale (PANSS), Abnormal Involuntary Movement Scale (AIMS), and
Simpson Angus Scale (SAS). The last three instruments were also used in
Israel. Statistical Analysis: Regression analysis and Pearson's
correlation. Results and Conclusions: TD symptoms were present in 40.4%
of 151 Israeli subjects and 28.7% of 334 Indian subjects. While age at
onset and total scores on PANSS were significant predictors of TD in
both the samples, lower scores on the Global Assessment of Functioning
Scale (GAF), diagnostic sub-group and male gender were significant
predictors among Indians. There was no concordance of TD symptoms among
33 affected sib-pairs from India.</abstract><cop>India</cop><pub>Medknow Publications and Staff Society of Seth GS Medical College and KEM Hospital, Mumbai, India</pub><pmid>15377799</pmid><oa>free_for_read</oa></addata></record> |
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issn | 0022-3859 0972-2823 |
language | eng |
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source | MEDLINE; Bioline International; EZB-FREE-00999 freely available EZB journals |
subjects | Adult Antipsychotic Agents - adverse effects Antipsychotic drugs Dyskinesia, Drug-Induced - epidemiology Dyskinesia, Drug-Induced - etiology Female Genetic aspects Humans India - epidemiology Israel - epidemiology Male Neuropsychological Tests Psychiatric Status Rating Scales Risk factors Tardive dyskinesia Tardive dyskinesia, schizophrenia, genetic, familial |
title | Clinical and familial correlates of tardive dyskinesia in India and Israel |
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