Trastorno esquizoafectivo: ¿Cuánto de esquizofrenia? ¿Cuánto de bipolar? / Schizoaffective disorder: How much belongs to schizophrenia? How much belongs to bipolar disorder?

Introduction: Schizoaffective Disorder represents a controversial clinical entity, in regard to nosology and classification criteria. It has been considered as a variant of Schizophrenia, as a mixed entity between Schizophrenia and Bipolar Disorder and as a Bipolar Disorder subtype Method: Classificatory, clinical issues, neuropsychology and genetics research contributions are reviewed. Discussion and Conclusion: Schizoaffective Disorder concept at present time, differs from its original description, maintaining lack of definitive clarity with respect to its nosology. Considering neurocognitive impairment within its course, Schizoaffective Disorder looks much closer to affective psychosis than to Schizophrenia. From genetic research field emerges data that challenge the classic dichotomist distinction between affective psychosis and Schizophrenia established by E. Kraepelin, raising again the question about thinking in psychosis as a continuum in which Schizoaffective Disorder could represent an intermediate state...

Introducción: El Trastorno Esquizoafectivo constituye un área de controversias respecto a su nosología y criterios para su clasificación. Ha sido considerado como una variante de la Esquizofrenia, un cuadro mixto en el cual coexisten la Esquizofrenia y el Trastorno Bipolar y como un subtipo del Trastorno Bipolar. Método: Se revisan aspectos diagnósticos, clasificatorios y características psicopatológicas del trastorno en su concepción actual y aportes desde la perspectiva de la investigación neuropsicológica y la genética. Discusión y Conclusiones: El concepto actual de Trastorno Esquizoafectivo, difiere de su descripción original manteniéndose la falta de claridad definitiva respecto a su nosología. Tomando en consideración las alteraciones neurocognitivas que acompañan su evolución, el Trastorno Esquizoafectivo guardaría una mayor afinidad con las psicosis afectivas que con la Esquizofrenia. Desde la investigación genética surgen datos que cuestionan la distinción dicotómica clásica entre las psicosis afectivas y la Esquizofrenia establecida por E. Kraepelin, replanteándose la formulación de la psicosis en un continuum del cual el Trastorno Esquizoafectivo podría representar un estadio intermedio...

Uso de clozapina en trastorno bipolar refractario / Clozapine in refractory bipolar disorder

Background: The combination of multiple agents including lithium, mood stabilizers and antipsychotics, represents the most commonly strategy in bipolar disorder treatment. Lack of response, breakthrough episodes during adequate maintenance treatment, functional impairment, including re-hospitalization, suicide attempts and intolerance of medication are considered clinical inclusion criteria for treatment resistance in bipolar disorder. In bipolar disorder, Clozapine as mono-therapy or in combination treatment, remains as a efficacious second line agent, with few clinical data available, mainly including short observational periods, small samples and uncontrolled trials. Methods: We analyze retrospectively clinical data about five female bipolar refractory patients who were under combined treatment including atypical antipsychotics. Due to this combined first line treatment resistance, Clozapine was indicated as an add-on agent. Equivalent analysis periods were established for each patient, previous and under Clozapine use. These periods extends from 8 months to 5 years and 2 months. Results: Clozapine average daily dose was 260 mgs. No adverse effects were noticed. Total hospitalization days decrease from 979 days to 118 days andsu icide attempts decrease from 14 ep isodes in pre Clozap ine period to 1 episode in the Clozapine treatment period. No re-hospitalization neither self harm attempts with Clozapine add on treatment were reported in 3 patients. Conclusion: Clozapine efficacy, in treatment resistance bipolar patients, should be considered as a second line option in combination therapy with insufficient response. Therapeutic benefits of Clozapine may include potential decrease of self harm conduct in bipolar patients as in schizophrenia and schizoaffective disorder.

Antecedentes: La combinación de múltiples agentes incluyendo el litio, los estabilizadores del ánimo y los antipsicóticos, representa la estrategia más común en el tratamiento del trastorno bipolar. La falta de respuesta, la irrupción de nuevos episodios durante un adecuado tratamiento de mantención, el deterioro funcional incluyendo la re-hospitalización, los intentos de suicido y la intolerancia a la medicación se consideran criterios clínicos de inclusión para establecer la resistencia al tratamiento en el trastorno bipolar. En el trastorno bipolar, la Clozapina como terapia única o en tratamiento combinado, se mantiene como un agente de segunda línea eficaz, con pocos datos clínicos disponibles, incluyendo principalmente períodos cortos de observación, muestras pequeñas y ensayos no controlados. Métodos: Analizamos datos clínicos en forma retrospectiva de cinco pacientes mujeres bipolares refractarias que se sometieron a tratamiento combinado que incluyó antipsicóticos atípicos. Debido a resistencia a este tratamiento de primera línea, se indicó Clozapina como antipsicótico asociado al tratamiento. Se establecieron períodos de análisis equivalentes para cada paciente, previo y durante el uso de Clozapina. Estos períodos se extendieron de 8 meses a 5 años y 2 meses. Resultados: La dosis diaria promedio de Clozapina fue de 260 mg. No se observaron efectos adversos. Los días de hospitalización totales disminuyeron de 979 días a 118 días y los intentos de suicidio disminuyeron de 14 episodios en el período previo a Clozapina a 1 episodio durante el período de tratamiento con Clozapina. En tres pacientes no se informó de re-hospitalizaciones ni de intentos de auto agresiones con el tratamiento agregado de Clozapina. Conclusión: La eficacia de Clozapina en pacientes bipolares con resistencia al tratamiento debiera considerarse como una opción de segunda línea en terapia combinada con respuesta insuficiente. Los beneficios terapéuticos de Clozapina pueden inclui...

Solar disinfection of water for diarrhoeal prevention in southern India.

AIMS: To evaluate the efficacy and acceptability of solar irradiation in the prevention of diarrhoeal morbidity in children under 5 years of age, in an urban slum in Vellore, Tamil Nadu. METHODS: A total of 100 children were assigned to receive drinking water that had been subjected to solar disinfection in polyethylene terephthalate bottles. One hundred age and sex matched controls were also selected. Both groups were followed by weekly home visits for a period of six months for any diarrhoeal morbidity. At the end of the follow up period, the acceptability of the intervention was assessed by interviews, questionnaires, and focus group discussions. RESULTS: There was significant reduction in the incidence, duration, and severity of diarrhoea in children receiving solar disinfected water, despite 86% of the children drinking water other than that treated by the intervention. The incidence of diarrhoea in the intervention group was 1.7 per child-year, and among controls 2.7 per child-year, with an incidence rate ratio of 0.64 (95% CI -0.48 to 0.86). The risk of diarrhoea was reduced by 40% by using solar disinfection. In qualitative evaluation of acceptability, most women felt that solar disinfection was a feasible and sustainable method of disinfecting water. CONCLUSIONS: Solar disinfection of water is an inexpensive, effective, and acceptable method of increasing water safety in a resource limited environment, and can significantly decrease diarrhoeal morbidity in children.

Alteración del funcionamiento familiar en el trastorno bipolar / Family disruption in bipolar disorder

En el curso de los últimos años se ha acumulado abundante evidencia sobre el beneficio de las intervenciones psicosociales en el tratamiento integral del trastorno bipolar. La psicoeducación a pacientes y familiares ha sido reportada por distintos grupos como un medio de reforzar la adherencia al tratamiento. En familias de pacientes bipolares se han descrito alteraciones en el funcionamiento psicosocial intrafamiliar. Nuestro servicio ha desarrollado un programa psicoeducativo aplicando el modelo de grupos multifamiliares con fines asistenciales tanto a familiares como pacientes. Se presentan los resultados de una exploración de variables del funcionamiento psicosocial que tuvieran relación con la presencia de trastorno bipolar en uno de los miembros del sistema familiar al interior de 40 familias de pacientes bipolares y se discutieron sus implicancias en el proceso psicoeducativo. Se exploró el funcionamiento social atendiendo a la estructura de relaciones en los subsistemas conyugales, procesos interaccionales entre los subsistemas familiares (comunicación, roles y reglas), impacto económico familiar y percepción del cuidador del paciente. En las familias del estudio, se encontró una alta frecuencia de ruptura en la relación conyugal siendo las separaciones comparativamente superiores en el caso de los matrimonios con hijos bipolares, a las observadas cuando era uno de los padres el enfermo y déficits en la calidad de la relación de los hermanos sanos con el paciente y de los hijos con el progenitor enfermo. El distanciamiento en la interacción intrafamiliar abarca tanto los periodos críticos como los intercríticos.

Impact of homozygosity for an amyloidogenic transthyretin mutation on phenotype and long term outcome.

Although amyloidogenic transthyretin (ATTR) mutations are common in several populations, such as black Americans, the small number of diagnosed patients homozygous for TTR amyloid and the short follow up in most studies has until now prevented an analysis of their phenotype. In Sweden, nine homozygous patients from eight families carrying the ATTR mutation Val30Met, which gives rise to fatal neuropathic amyloidosis (FAP), have been identified and have now been followed for up to 15 years. This has enabled an analysis of the phenotype of homozygous patients. Genetic testing and detection of amyloid deposits in the vitreous body or in intestinal or skin biopsies confirmed the diagnosis in all patients. The patients' symptoms were obtained from medical records. For comparison, we used a group of 35 heterozygous non-transplanted patients with FAP (18 men and 17 women), who had been evaluated at the Department of Medicine, Umeå University Hospital before their deaths. Vitreous amyloidosis was the most prevalent symptom in the homozygous group, and in two patients it was the only manifestation of the disease during their lifetime. The age at onset was not different from that of heterozygous patients, and their survival tended not to be shorter but actually longer than for heterozygotes. Homozygosity for the mutation associated with FAP, ATTR Val30Met, does not implicate a more severe phenotype for Swedish patients. The most common symptom was vitreous opacity, which may be the only manifestation of the disease. These findings point to the possibilities of different pathways for amyloid formation, or the presence of hitherto unknown genes operating in amyloid formation.

Discordant penetrance of the trait for familial amyloidotic polyneuropathy in two pairs of monozygotic twins.

BACKGROUND: Familial amyloidotic polyneuropathy (FAP) is caused by mutated transthyretin in which valine at position 30 is substituted by methionine (ATTR Val30Met). FAP is inherited as an autosomal dominant trait with variable penetrance. CASES: Two pairs of DNA confirmed monozygotic twin brothers, 63 and 37 years of age respectively, who are heterozygous for the ATTR Val30Met gene, have been identified in Sweden. In the first twin pair (A), the onset of typical FAP symptoms occurred at the age of 48 for twin A1, whilst his twin brother (A2) is still free from FAP symptoms 13 years later. In the second pair of twins (B), the onset of polyneuropathy occurred at the age of 34 for the proband (B1), whilst his brother (B2) is healthy 3 years after the onset of his brother's disease. DISCUSSION: In the following, a detailed description of the clinical presentation of the Swedish twin pairs is provided together with a discussion of possible environmental factors initiating the onset of the disease.

Hereditary transthyretin amyloidosis from a Scandinavian perspective.

Hereditary transthyretin (TTR) amyloidosis is a rare often fatal form of systemic amyloidosis, that until recently was considered intractable, with the patients dying from the disease 5-15 years after onset. The phenotype of the disease varies according to the type of mutation, but generally the heart and/or the nervous system is affected. Liver and in some cases heart transplantation has now been shown to stop the progress of the disease, but the outcome depends on the patients' status at the time of operation, as no substantial improvement of the patients' symptoms has been noted after the procedure. Thus an early diagnosis is of importance for the outcome. In the following, we summarize our knowledge of the amyloidogenic TTR mutations found in the Scandinavian countries, their symptoms, how to settle the diagnosis and the outcome of transplantation. Besides, the problems arising from our capability to genetically test asymptomatic members of affected families for the trait will be discussed.

Identification of a susceptibility locus for migraine with and without aura on 6p12.2-p21.1.

Migraine is the most common type of chronic episodic headache. To find novel susceptibility genes for familial migraine with and without aura, a genomewide screen was performed in a large family from northern Sweden. Evidence of linkage was obtained on chromosome 6p12.2-p21.1, with a maximum two-point lod score of 5.41 for marker D6S452. The patients with migraine shared a common haplotype of 10 Mb between markers D6S1650 and D6S1960.

Identification of numerical and structural chromosome aberrations in 15 high hyperdiploid childhood acute lymphoblastic leukemias using spectral karyotyping.

Spectral karyotyping (SKY) on metaphase spreads from 15 high hyperdiploid (>51 chromosomes) childhood acute lymphoblastic leukemias (ALL), which typically display a poor chromosome morphology, was performed in order to investigate the pattern of numerical abnormalities, reveal the chromosomal origin of marker chromosomes, and identify translocations and other interchromosomal rearrangements not detected by G-banding analysis. In all cases the numerical changes could be fully characterized, and a non-random pattern of chromosomal gain was identified, with chromosomes X, 21, 14, 17, 6, 18, 4, and 10 being most frequently gained. The numerical changes had been partly misinterpreted in 12 of the 15 ALL patients using G-banding, and the present study hence emphasizes the importance of SKY in identifying such anomalies, some of which, i.e. +4 and +10, have been suggested to be prognostically important. The chromosomal origin of all marker chromosomes and of seven structural rearrangements, one of which was the prognostically important Philadelphia chromosome, could be identified. Five rearrangements [der(1)t(1;14)(q32;q21), der(2)t(2;8)(q36;?), der(3)t(2;3)(q21;?), der(8)t(8;14)(?;?), and t(9;21)(q12;q22)] have previously not been reported in ALL, emphasizing the value of SKY in identifying novel chromosomal rearrangements.

Human ameloblastin gene: genomic organization and mutation analysis in amelogenesis imperfecta patients.

A gene encoding the enamel protein ameloblastin (AMBN) was recently localized to a region on chromosome 4q21 containing a gene for the inherited enamel defect local hypoplastic amelogenesis imperfecta (AIH2). Ameloblastin protein is located at the Tomes processes of secretory ameloblasts and in the sheath space between rod-interrod enamel, and the AMBN gene therefore represents a viable candidate gene for local hypoplastic amelogenesis imperfecta (AI). In this study, the genomic organization of human AMBN was characterized. The gene was shown to consist of 13 exons and 12 introns. An alternatively spliced 45 bp sequence was shown not to represent a separate exon and is most likely spliced by the use of a cryptic splice site. The finding that there were no recombinations between an intragenic microsatellite and AIH2 encouraged us to evaluate this gene's potential role as a candidate gene for local hypoplastic AI. Mutation screening was performed on all 13 exons in 20 families and 8 sporadic cases with 6 different forms of AI. DNA variants were found but none that was associated exclusively with local hypoplastic AI or any of the other variants of AI in the identified Swedish families. This study excludes the coding regions and the splice sites of AMBN from a causative role in the pathogenesis of AIH2.

Scavenger treatment of free radical injury in familial amyloidotic polyneuropathy: a study on Swedish transplanted and non-transplanted patients.

Since oxidative stress has been implicated in amyloid diseases, a study of scavenger treatment of hereditary transthyretin amyloidosis was undertaken on 23 familial amyloidotic polyneuropathy (FAP) patients. Nine patients had undergone a liver transplantation for the disease. Twenty patients completed the 6-month study period of scavenger treatment (vitamin C, 1 g, three times daily, vitamin E, 0.1 g, three times daily and acetylcysteine, 0.2 g three times daily). They were evaluated clinically and by immunohistochemical measurement of hydroxynonenal (HNE), a product of lipid peroxidation, in biopsy specimens. For non-transplanted patients, no improvement was found for HNE in relation to the amyloid content in biopsy specimens, whereas a tendency to a decreased amount was noted for transplanted patients. Clinically, no differences were found for non-transplanted patients, but an increased nutritional status, measured by a modified body mass index (mBMI) was noted for transplanted patients. In summary, scavenger treatment with the drugs and doses used in the present study appears to be unable to decrease lipid peroxidation in amyloid-rich tissue in non-transplanted FAP patients. For transplanted patients, lipid peroxidation tended to decrease, and the nutritional status measured by mBMI improved, even though the findings may be explained by liver transplantation alone, scavenger treatment may facilitate recovery after transplantation.

Spectrum of CLCN1 mutations in patients with myotonia congenita in Northern Scandinavia.

Myotonia congenita is a non-dystrophic muscle disorder affecting the excitability of the skeletal muscle membrane. It can be inherited either as an autosomal dominant (Thomsen's myotonia) or an autosomal recessive (Becker's myotonia) trait. Both types are characterised by myotonia (muscle stiffness) and muscular hypertrophy, and are caused by mutations in the muscle chloride channel gene, CLCN1. At least 50 different CLCN1 mutations have been described worldwide, but in many studies only about half of the patients showed mutations in CLCN1. Limitations in the mutation detection methods and genetic heterogeneity might be explanations. In the current study, we sequenced the entire CLCN1 gene in 15 Northern Norwegian and three Northern Swedish MC families. Our data show a high prevalence of myotonia congenita in Northern Norway similar to Northern Finland, but with a much higher degree of mutation heterogeneity. In total, eight different mutations and three polymorphisms (T87T, D718D, and P727L) were detected. Three mutations (F287S, A331T, and 2284+5C>T) were novel while the others (IVS1+3A>T, 979G>A, F413C, A531V, and R894X) have been reported previously. The mutations F413C, A531V, and R894X predominated in our patient material. Compound heterozygosity for A531V/R894X was the predominant genotype. In two probands, three mutations cosegregated with myotonia. No CLCN1 mutations were identified in two families. Our data support the presence of genetic heterogeneity and additional modifying factors in myotonia congenita.

A major locus for myoclonus-dystonia maps to chromosome 7q in eight families.

Myoclonus-dystonia (M-D) is an autosomal dominant disorder characterized by myoclonic and dystonic muscle contractions that are often responsive to alcohol. The dopamine D2 receptor gene (DRD2) on chromosome 11q has been implicated in one family with this syndrome, and linkage to a 28-cM region on 7q has been reported in another. We performed genetic studies, using eight additional families with M-D, to assess these two loci. No evidence for linkage was found for 11q markers. However, all eight of these families showed linkage to chromosome 7 markers, with a combined multipoint LOD score of 11.71. Recombination events in the families define the disease gene within a 14-cM interval flanked by D7S2212 and D7S821. These data provide evidence for a major locus for M-D on chromosome 7q21.

Knowing when but not how!--mothers' perceptions and use of antibiotics in a rural area of Viet Nam.

Given the world-wide focus on how to rationally use antibiotics, national drug policy programmes have been developed in many countries in order to minimize the environmental antibiotic pressure and thereby hopefully limit increasing bacterial resistance. This study investigated perceptions of antibiotics in a health system with weak drug regulation. The study was conducted in two rural communes in Viet Nam, with a drug market characterized by the increased accessibility and consumption of pharmaceuticals. The study focused on rural mothers' perceptions and use of antibiotics in the treatment of acute respiratory infections (ARI) in children 5 years and under. A combination of qualitative and quantitative methods were used including key informant interviews, focus group discussions, and interviews with mothers and drug vendors. The study demonstrated that using a combination of qualitative and quantitative methods gives a better understanding of the prevailing perceptions and use of antibiotics in communities. The results showed that the mothers recognized well the signs of severe ARI and that antibiotics were reserved for more severe illness episodes, where penicillin V and ampicillin were first drugs of choice. However, the mothers' perceptions and use of antibiotics reflects indigenization of antibiotics into traditional Vietnamese thinking and medical practice. This resulted in self-medication and a respect for antibiotics from the mothers' point of view. A first step towards the rational use of antibiotics is already taken where mothers, as the health decision-maker, know when to initiate antibiotic treatment and try to limit unnecessary use of antibiotics. The next step is to develop a well-functioning health education programme in order to promote the correct use of antibiotics for a successful clinical outcome. This requires acknowledgement of the mothers' culture based behaviour.

Heart failure caused by a novel amyloidogenic mutation of the transthyretin gene: ATTR Ala45Ser.

Cardiac failure in transthyretin (TTR) amyloidosis patients has been shown to be caused by different mutations in the TTR gene. In the present case, a 73-year-old man from Northern Sweden was evaluated for heart failure. Amyloid deposits were found in subcutaneous fat and in intestinal biopsies. The presence of a variant form of TTR was detected in the plasma by electrospray ionisation mass spectrometry (ESI-MS). The mutation was located by single-strand conformation polymorphism (SSCP) analysis of the TTR gene where a band shift was seen in exon 2. Direct sequencing of exon 2 revealed a single base-pair substitution (G1724T). This transversion results in an amino acid substitution at codon 45, alanine to serine (ATTR Ala45Ser). Mass spectrometry analysis excluded that the variant is a polymorphism, since no similar shift in molecular weight has been present in more than 200 control samples. Congo red and immunostaining of duodenum biopsy specimens confirmed the presence of systemic ATTR amyloidosis, and clinical examination, including echocardiography, found evidence of a restrictive cardiomyopathy. He had 10 years previously been operated for a bilateral carpal tunnel syndrome, but otherwise no symptoms were present that could be attributed to his systemic amyloidosis. No axonal polyneuropathy was noted at nerve conduction studies. This novel mutation is the second amyloidogenic TTR mutation found in the Swedish population.

Enhancement of AA-amyloid formation in mice by transthyretin amyloid fragments and polyethylene glycol.

The mechanism behind amyloid formation is unknown in all types of amyloidosis. Several substances can enhance amyloid formation in animal experiments. To induce secondary systemic amyloid (AA-type amyloid) formation, we injected silver nitrate into mice together with either amyloid fibrils obtained from patients with familial polyneuropathy (FAP) type I or polyethylene glycol (PEG). Mice injected with silver nitrate only served as controls. Amyloid deposits were detectable at day 3 in animals injected with amyloid fibrils and in those injected with PEG, whereas in control mice, deposits were not noted before day 12. Our results indicate that amyloid fibrils from FAP patients and even a non-sulfate containing polysaccharide (PEG) have the potential to act as amyloid-enhancing factors.

Evaluation of the role of the D2 dopamine receptor in myoclonus dystonia.

A novel Val154-->Ile mutation in the D2 dopamine receptor (DRD2) on chromosome 11q23 has recently been shown to be associated with myoclonus dystonia (M-D) in one large family. Sequence analysis of the DRD2 gene in 5 M-D patients from different families did not reveal any mutations, nor was there evidence of linkage to the 11q23 region in the DRD2 gene in four other families. Receptor binding and signal transduction assays of the DRD2 mutant and wild-type receptors revealed identical agonist and antagonist affinities and functional responses. These studies suggest that M-D is genetically heterogeneous. The molecular mechanisms through which the Val-->Ile mutation may contribute to M-D remain to be determined.