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1.
Can J Psychiatry ; 64(5): 356-374, 2019 05.
Article in English | MEDLINE | ID: mdl-31095435

ABSTRACT

This position paper has been substantially revised by the Canadian Psychiatric Association's Professional Standards and Practice Committee and approved for republication by the CPA's Board of Directors on July 26, 2018. The original position paper1 was first approved by the Board of Directors on January 25, 2003. It was subsequently reviewed and approved for republication with minor revisions on June 2, 2009.


Subject(s)
Ambulatory Care/standards , Mandatory Programs/standards , Mental Disorders/therapy , Mental Health Services/standards , Psychiatry/standards , Societies, Medical/standards , Canada , Humans
2.
Psychiatr Serv ; 69(7): 791-796, 2018 07 01.
Article in English | MEDLINE | ID: mdl-29695223

ABSTRACT

OBJECTIVE: Community treatment orders (CTOs) refer to a variety of legal schemes that require a person with a serious mental illness to follow a plan of treatment and supervision while living in the community. Use of CTOs has been controversial, and they have been the subject of a considerable amount of quantitative and qualitative research. This article reports the results of a systematic review of qualitative studies focused on understanding the views and experiences of clinicians who work with individuals on CTOs. METHODS: Relevant databases and gray literature were searched for articles that used a qualitative methodology for data collection and analysis to examine clinicians' perspectives. CTOs were defined as various legal schemes, including court-ordered outpatient commitment and renewable conditional-leave provisions initiated while a person is an inpatient in a psychiatric unit. Mandatory treatment and supervision required after a person has been charged with or convicted of committing a criminal offense was not considered. RESULTS: Fourteen articles met inclusion criteria. They represented the views of more than 700 clinicians from six international jurisdictions. Three themes were identified: endorsement of the benefits of CTOs despite tensions both within and between clinicians concerning several aspects of CTOs; belief that medication compliance is a central aspect of CTOs; and acknowledgment that there is room for improvement in CTO implementation, monitoring, and administration. Strategies for reducing tensions and improving administration of CTOs are discussed. CONCLUSIONS: Clinicians view CTOs as providing benefits to their clients but struggle with the coercive nature of these tools.


Subject(s)
Commitment of Mentally Ill/legislation & jurisprudence , Community Mental Health Services , Health Personnel/psychology , Involuntary Treatment , Coercion , Health Knowledge, Attitudes, Practice , Humans , Mental Disorders/therapy , Qualitative Research
4.
BMC Med Genomics ; 8: 17, 2015 May 06.
Article in English | MEDLINE | ID: mdl-25943100

ABSTRACT

BACKGROUND: Despite their singular origin, monozygotic twin pairs often display discordance for complex disorders including schizophrenia. It is a common (1%) and often familial disease with a discordance rate of ~50% in monozygotic twins. This high discordance is often explained by the role of yet unknown environmental, random, and epigenetic factors. The involvement of DNA methylation in this disease appears logical, but remains to be established. METHODS: We have used blood DNA from two pairs of monozygotic twins discordant for schizophrenia and their parents in order to assess genome-wide methylation using a NimbleGen Methylation Promoter Microarray. RESULTS: The genome-wide results show that differentially methylated regions (DMRs) exist between members representing discordant monozygotic twins. Some DMRs are shared with parent(s) and others appear to be de novo. We found twenty-seven genes affected by DMR changes that were shared in the affected member of two discordant monozygotic pairs from unrelated families. Interestingly, the genes affected by pair specific DMRs share specific networks. Specifically, this study has identified two networks; "cell death and survival" and a "cellular movement and immune cell trafficking". These two networks and the genes affected have been previously implicated in the aetiology of schizophrenia. CONCLUSIONS: The results are compatible with the suggestion that DNA methylation may contribute to the discordance of monozygotic twins for schizophrenia. Also, this may be accomplished by the direct effect of gene specific methylation changes on specific biological networks rather than individual genes. It supports the extensive genetic, epigenetic and phenotypic heterogeneity implicated in schizophrenia.


Subject(s)
DNA Methylation , Genetic Predisposition to Disease , Psychotic Disorders/genetics , Schizophrenia/genetics , Twins, Monozygotic/genetics , Adult , CpG Islands , Diseases in Twins , Epigenesis, Genetic , Female , Gene Expression Profiling , Gene Expression Regulation , Genome, Human , Histones/chemistry , Humans , Middle Aged , Multigene Family , Pedigree , Phenotype , Promoter Regions, Genetic
5.
Epigenomics ; 7(1): 67-74, 2015.
Article in English | MEDLINE | ID: mdl-25687467

ABSTRACT

Evidence for involvement of DNA methylation in psychosis forms the focus of this perspective. Of interest are results from two independent sets of experiments including rats treated with antipsychotic drugs and monozygotic twins discordant for schizophrenia. The results show that DNA methylation is increased in rats treated with antipsychotic drugs, reflecting the global effect of the drugs. Some of these changes are also seen in affected schizophrenic twins that were treated with antipsychotics. The genes and pathways identified in the unrelated experiments are relevant to neurodevelopment and psychiatric disorders. The common cause is hypothesized to be aberrations resulting from medication use. However, this needs to be established by future studies that address the origin of methylation changes in psychosis.


Subject(s)
DNA Methylation , Psychotic Disorders/genetics , Animals , Antipsychotic Agents/therapeutic use , DNA Methylation/drug effects , Humans , Psychotic Disorders/drug therapy , Rats
6.
BMC Bioinformatics ; 15: 114, 2014 Apr 21.
Article in English | MEDLINE | ID: mdl-24750645

ABSTRACT

BACKGROUND: Studies involving the analysis of structural variation including Copy Number Variation (CNV) have recently exploded in the literature. Furthermore, CNVs have been associated with a number of complex diseases and neurodevelopmental disorders. Common methods for CNV detection use SNP, CNV, or CGH arrays, where the signal intensities of consecutive probes are used to define the number of copies associated with a given genomic region. These practices pose a number of challenges that interfere with the ability of available methods to accurately call CNVs. It has, therefore, become necessary to develop experimental protocols to test the reliability of CNV calling methods from microarray data so that researchers can properly discriminate biologically relevant data from noise. RESULTS: We have developed a workflow for the integration of data from multiple CNV calling algorithms using the same array results. It uses four CNV calling programs: PennCNV (PC), Affymetrix® Genotyping Console™ (AGC), Partek® Genomics Suite™ (PGS) and Golden Helix SVS™ (GH) to analyze CEL files from the Affymetrix® Human SNP 6.0 Array™. To assess the relative suitability of each program, we used individuals of known genetic relationships. We found significant differences in CNV calls obtained by different CNV calling programs. CONCLUSIONS: Although the programs showed variable patterns of CNVs in the same individuals, their distribution in individuals of different degrees of genetic relatedness has allowed us to offer two suggestions. The first involves the use of multiple algorithms for the detection of the largest possible number of CNVs, and the second suggests the use of PennCNV over all other methods when the use of only one software program is desirable.


Subject(s)
DNA Copy Number Variations , Twins, Monozygotic/genetics , Algorithms , Chromosomes, Human , Genome, Human , Genome-Wide Association Study , Genomics , Genotype , Humans , Polymorphism, Single Nucleotide , Reproducibility of Results , Software
7.
Twin Res Hum Genet ; 17(2): 108-20, 2014 Apr.
Article in English | MEDLINE | ID: mdl-24556202

ABSTRACT

We have evaluated copy number variants (CNVs) in six monozygotic twin pairs discordant for schizophrenia. The data from Affymetrix® Human SNP 6.0 arrays™ were analyzed using Affymetrix® Genotyping Console™, Partek® Genomics Suite™, PennCNV, and Golden Helix SVS™. This yielded both program-specific and overlapping results. Only CNVs called by Affymetrix Genotyping Console, Partek Genomics Suite, and PennCNV were used in further analysis. This analysis included an assessment of calls in each of the six twin pairs towards identification of unique CNVs in affected and unaffected co-twins. Real time polymerase chain reaction (PCR) experiments confirmed one CNV loss at 7q11.21 that was found in the affected patient but not in the unaffected twin. The results identified CNVs and genes that were previously implicated in mental abnormalities in four of the six twin pairs. It included PYY (twin pairs 1 and 5), EPHA3 (twin pair 3), KIAA1211L (twin pair 4), and GPR139 (twin pair 5). They represent likely candidate genes and CNVs for the discordance of four of the six monozygotic twin pairs for this heterogeneous neurodevelopmental disorder. An explanation for these differences is ontogenetic de novo events that differentiate in the monozygotic twins during development.


Subject(s)
DNA Copy Number Variations , Schizophrenia/genetics , Twins, Monozygotic/genetics , Adolescent , Adult , Female , Humans , Male , Young Adult
8.
Int Psychiatry ; 11(3): 65-67, 2014 Aug.
Article in English | MEDLINE | ID: mdl-31507766

ABSTRACT

In Canada the ten provinces and three territories are responsible for their own health laws and services. The 13 mental health acts have core similarities, but there are clinically significant differences. In most Canadian jurisdictions legislation is based on common law; in Quebec, it is based on a civil code. Canadian jurisdictions favour voluntary admission and sometimes make this explicit in their mental health acts. For involuntary admission or compulsory in-patient or community treatment to be valid, three elements must be applied correctly: the process, the criteria and the rights procedures. These are reviewed in this paper.

10.
Aust N Z J Psychiatry ; 44(12): 1126-31, 2010 Dec.
Article in English | MEDLINE | ID: mdl-21070108

ABSTRACT

OBJECTIVE: The main objective of this paper is to compare the mental health Acts of the eight Australian jurisdictions and the 13 Canadian jurisdictions on three major issues: involuntary admission criteria, treatment authorization/consent and compulsory treatment in the community, in the light of international trends towards patients' rights. METHOD: The legislation was examined against the background of rights instruments such as the Canadian Charter of Rights and Freedoms and the United Nations Convention on the Rights of Persons with Disabilities. RESULTS: It was found that some Canadian involuntary admission criteria require the likelihood of bodily harm whereas all Australian Acts have broad harm and deterioration criteria. Unlike all Australian jurisdictions, some Canadian jurisdictions allow for the refusal of treatment that may be required for discharge. In addition, Canadian community treatment orders are much more restrictive than in Australia because they require a person to have considerable previous hospitalization despite meeting the committal criteria. Australian jurisdictions can use community treatment orders as a least restrictive alternative to inpatient status without prior hospitalization. CONCLUSIONS: The paper concludes that there are significant philosophical differences regarding the purpose of involuntary admission between Australian and some Canadian jurisdictions where treatment refusal is possible. Australian mental health Acts have a relatively stronger 'treatment' focus than some Canadian Acts. The apparently stronger 'rights' focus of some Canadian laws (such as the permission of treatment refusal) can paradoxically result in a denial of liberty rights. The way in which the relevant legislation is shaped in both countries will increasingly be affected by international trends towards the rights of individuals with disabilities.


Subject(s)
Commitment of Mentally Ill/legislation & jurisprudence , Informed Consent/legislation & jurisprudence , Mental Health Services/legislation & jurisprudence , Treatment Refusal/legislation & jurisprudence , Australia , Canada , Humans , Patient Rights/legislation & jurisprudence , United Nations
11.
Int J Law Psychiatry ; 32(5): 315-22, 2009.
Article in English | MEDLINE | ID: mdl-19643478

ABSTRACT

The Supreme Court of Canada's (SCC) first case involving capacity and the refusal of involuntary psychiatric treatment involved a self described "professor" who had been referred to as "Canada's Beautiful Mind". He had been found not criminally responsible on account of mental disorder for uttering death threats. While considered incapable of making a treatment decision by psychiatrists and a review board, three levels of court, including the SCC, found him to be capable. "Professor" Starson therefore continued to refuse treatment for his psychosis and spent over seven years detained because he refused the treatment required to become well enough to be released. This refusal of treatment is permitted under Ontario law, although it is not permitted in some other Canadian provinces, and in many other countries. This article describes Starson's situation, Ontario's law with respect to consent to treatment and relevant Canadian constitutional and criminal law. It provides an analysis of the Consent and Capacity Board decision and the court appeals. Implications from Starson's case are analyzed in relation to what happened to Starson, human rights and comparative law pertaining to involuntary patients' refusal of treatment, especially their relevance to the Canadian Charter of Rights and Freedoms, and laws in some other countries. Many Canadian and foreign jurisdictions where laws apparently accord with human rights codes do not allow a person to refuse the treatment required to restore their liberty. We conclude that a law that allows a person with a mental illness to be incarcerated indefinitely in a "hospital" because needed psychiatric treatment cannot, by law, be provided is not justifiable in a caring democratic jurisdiction.


Subject(s)
Commitment of Mentally Ill/legislation & jurisprudence , Insanity Defense , Jurisprudence , Mental Competency/legislation & jurisprudence , Psychotic Disorders/rehabilitation , Treatment Refusal/legislation & jurisprudence , Antipsychotic Agents/administration & dosage , Antipsychotic Agents/adverse effects , Human Rights/legislation & jurisprudence , Humans , Informed Consent/legislation & jurisprudence , Male , Middle Aged , Ontario , Patient Discharge/legislation & jurisprudence , Psychotic Disorders/diagnosis , Psychotic Disorders/psychology , Retreatment
12.
BMC Med Genet ; 9: 115, 2008 Dec 22.
Article in English | MEDLINE | ID: mdl-19102774

ABSTRACT

BACKGROUND: The synapsin III (SYN III) gene on chromosome 22q is a candidate gene for schizophrenia susceptibility due to its chromosome location, neurological function, expression patterns and functional polymorphisms. METHODS: This research has established the mRNA expression of SYN III in 22 adult human brain regions as well as the methylation specificity in the closest CpG island of this gene. The methylation specificity studied in 31 brain regions (from a single individual) was also assessed in 51 human blood samples (representing 20 people affected with schizophrenia and 31 normal controls) including a pair of monozygotic twin discordant for schizophrenia and 2 non-human primates. RESULTS: The results show that the cytosine methylation in this genomic region is 1) restricted to cytosines in CpG dinucleotides 2) similar in brain regions and blood and 3) appears conserved in primate evolution. Two cytosines (cytosine 8 and 20) localized as the CpG dinucleotide are partially methylated in all brain regions studied. The methylation of these sites in schizophrenia and control blood samples was variable. While cytosine 8 was partially methylated in all samples, the distribution of partial to complete methylation at the cytosine 20 was 22:9 in controls as compared to 18:2 in schizophrenia (p = 0.82). Also, there is no difference in methylation between the affected and unaffected member of a monozygotic twin pair. CONCLUSION: The variation in SYN III methylation studied is 1) not related to schizophrenia in the population sample or a monozygotic twin pair discordant for schizophrenia and 2) not related to the mRNA level of SYN IIIa in different human brain regions.


Subject(s)
DNA Methylation , Schizophrenia/genetics , Synapsins/genetics , Animals , Brain/metabolism , CpG Islands , Cytosine/metabolism , DNA/genetics , Gene Expression , Genetic Predisposition to Disease , Humans , Organ Specificity , RNA, Messenger/genetics , Reverse Transcriptase Polymerase Chain Reaction , Schizophrenia/metabolism , Sequence Analysis, DNA , Species Specificity , Sulfites , Synapsins/metabolism , Tissue Distribution
13.
Int J Law Psychiatry ; 31(1): 66-71, 2008.
Article in English | MEDLINE | ID: mdl-18191452

ABSTRACT

When advance directives are used to reject standard psychiatric treatment they have the potential to place civilly committed patients in a catch-22 where they need psychotropic medication to ameliorate their symptoms in order to regain liberty but are bound by their previously expressed wish that medication be withheld. The capacity to make an advance directive is higher than that required to make a contemporaneous treatment decision. Furthermore, unlike the assessment of contemporaneous capacity, it is very difficult to determine a person's capacity retrospectively or to determine if an advance directive was meant to apply in changed circumstances. The author argues that when an advance directive demands a course of action that is contrary to a person's best interests the onus should fall on the person rejecting the care to demonstrate that he or she was capable when executing the directive and that the directive is meant to apply in the current circumstances.


Subject(s)
Advance Directives/psychology , Mental Competency , Mental Disorders/therapy , Antipsychotic Agents/therapeutic use , Humans , Ontario , Schizophrenia/drug therapy
15.
Int J Law Psychiatry ; 29(6): 516-24, 2006.
Article in English | MEDLINE | ID: mdl-17083974

ABSTRACT

This study examined the opinions of patients who have been placed on a community treatment order (CTO), their relatives, mental health clinicians and representatives of community agencies about the use of CTOs in Saskatchewan. Patients were assessed using indepth interviews, while their relatives, mental health professionals and representatives of community agencies took part in facilitated focus groups. Patients had contradictory feelings about CTOs. Most experienced some degree of coercion while on the orders but many believed that CTOs provided necessary structure in their lives. Clinicians were more consistently positive but recognized the difficult choices in balancing the subject's right to self-determination with the benefits of a treatment order. Family members viewed CTOs as necessary to control a chaotic situation caused by the subject's limited insight.


Subject(s)
Ambulatory Care/legislation & jurisprudence , Community Mental Health Services/statistics & numerical data , Mandatory Programs/legislation & jurisprudence , Mental Disorders/therapy , Case Management/legislation & jurisprudence , Coercion , Community Mental Health Services/legislation & jurisprudence , Community Mental Health Services/standards , Humans , Personal Autonomy , Saskatchewan , Social Support
16.
BMC Med Genet ; 7: 18, 2006 Mar 02.
Article in English | MEDLINE | ID: mdl-16512914

ABSTRACT

BACKGROUND: Chromosome 22q11.2 region is highly susceptible to rearrangement, specifically deletions that give rise to a variety of genomic disorders including velocardiofacial or DiGeorge syndrome. Individuals with this 22q11 microdeletion syndrome are at a greatly increased risk to develop schizophrenia. METHODS: Genotype analysis was carried out on the DNA from a patient with the 22q11 microdeletion using genetic markers and custom primer sets to define the deletion. Bioinformatic analysis was performed for molecular characterization of the deletion breakpoint sequences in this patient. RESULTS: This 22q11 deletion patient was established to have a novel 2.3 Mb deletion with a proximal breakpoint located between genetic markers RH48663 and RH48348 and a distal breakpoint between markers D22S1138 and SHGC-145314. Molecular characterization of the sequences at the breakpoints revealed a 270 bp shared sequence of the breakpoint regions (SSBR) common to both ends that share >90% sequence similarity to each other and also to short interspersed nuclear elements/Alu elements. CONCLUSION: This Alu sequence like SSBR is commonly in the proximity of all known deletion breakpoints of 22q11 region and also in the low copy repeat regions (LCRs). This sequence may represent a preferred sequence in the breakpoint regions or LCRs for intra-chromosomal homologous recombination mechanisms resulting in common 22q11 deletion.


Subject(s)
Alu Elements , Chromosome Breakage , Chromosome Deletion , Chromosomes, Human, Pair 22 , DiGeorge Syndrome/genetics , Adolescent , DiGeorge Syndrome/diagnosis , Humans , Male , Models, Genetic , Recombination, Genetic
17.
Psychiatr Serv ; 57(2): 179-81, 2006 Feb.
Article in English | MEDLINE | ID: mdl-16452694

ABSTRACT

Relationship management therapy allows patients to choose their own treatment. The model requires that patients who engage in or threaten self-harm or aggressive behavior are discharged from the inpatient part of the program for 24 hours. This study compared mean annual outcome rates for the 27 patients who were consecutively enrolled in the relationship management therapy program from 1998 to 2000. Significant reductions were found in restraint, constant nursing observation, self-harm incidents, and inpatient days. These results fill a gap in the literature about a treatment model that one day could be considered a best practice.


Subject(s)
Interpersonal Relations , Psychotherapy , Borderline Personality Disorder/diagnosis , Borderline Personality Disorder/therapy , Diagnostic and Statistical Manual of Mental Disorders , Humans
19.
Int J Law Psychiatry ; 28(1): 13-22, 2005.
Article in English | MEDLINE | ID: mdl-15710446

ABSTRACT

This paper addresses the principles underlying compulsory community treatment (CCT) and discusses the different provisions in Canada's twelve jurisdictions. Comparisons with different models of CCT in other countries are also drawn. CCT is not only intended to reduce relapses it is also a "least restrictive" alternative to in-patient detention. Seven of the twelve Canadian mental health acts allow conditional leave from hospital. Two jurisdictions provide community treatment orders, but require two or three previous in-patient admissions. Criteria for CCT, in most jurisdictions, includes that there is a "likelihood of significant mental or physical deterioration". The requirement for previous hospitalization for CCT in Canada, unlike other countries, precludes CCT for use with first episode patients. Some jurisdictions require consent for CCT. Most jurisdictions explicitly state that the services necessary for the CCT conditions must be available.


Subject(s)
Commitment of Mentally Ill/legislation & jurisprudence , Community Mental Health Services/legislation & jurisprudence , Community Mental Health Services/organization & administration , Health Care Reform/legislation & jurisprudence , Mental Disorders/therapy , Canada , Hospitalization/legislation & jurisprudence , Humans , Informed Consent , Patient Rights/legislation & jurisprudence , Secondary Prevention
20.
Am J Med Genet B Neuropsychiatr Genet ; 133B(1): 37-42, 2005 Feb 05.
Article in English | MEDLINE | ID: mdl-15635661

ABSTRACT

The catechol-o-methyltransferase (COMT) gene on chromosome 22q11 has been considered a strong candidate gene for schizophrenia (SZ) susceptibility. A functional Val/Met polymorphism in exon 4, with potential to affect COMT activity has been implicated in SZ, but the results remain inconclusive. We hypothesized that the association of COMT gene with SZ is not strictly a genetic alteration but could involve DNA methylation, as an epigenetic alteration. Thus, we chose to examine the cytosine DNA methylation profile of the human COMT promoter regions, which partially overlaps with the MB-COMT coding region and covers a total of 56 cytosines. Our analysis of 31 brain regions and 51 individual blood samples suggests that the cytosine methylation in his region is restricted to the CpG dinucleotides only. Also, the methylation pattern is nearly identical in the brain and blood with few exceptions. One cytosine (#27) is partially methylated in 5 brain regions and another cytosine (#23) is partially methylated in 81 of 82 samples studied. The exception being the blood DNA from a single SZ patient with prominent extreme negative symptoms, which was completely methylated. Interestingly, there was no difference in methylation at these sites in the blood DNA from three pairs of monozygotic twins discordant for SZ. The results support the use of blood DNA in methylation studies and rule out S-COMT promoter methylation as a common cause of SZ. The unique observation of a completely methylated cytosine 23 in one patient with SZ may have the potential to affect COMT mRNA transcription and gene activity, but remains to be evaluated.


Subject(s)
Brain/metabolism , Catechol O-Methyltransferase/genetics , DNA Methylation , Promoter Regions, Genetic/genetics , Schizophrenia/genetics , Adult , Base Sequence , CpG Islands/genetics , Cytosine/blood , Cytosine/metabolism , DNA/chemistry , DNA/genetics , DNA/metabolism , DNA Mutational Analysis , Humans , Molecular Sequence Data , Ontario , Polymorphism, Single Nucleotide , Schizophrenia/enzymology , Schizophrenia/pathology , Twins, Monozygotic/genetics
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