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1.
J Endocrinol Invest ; 46(8): 1673-1684, 2023 Aug.
Article in English | MEDLINE | ID: mdl-36749450

ABSTRACT

INTRODUCTION: Severe short stature is a feature of acrodysostosis, but data on growth are sparse. Treatment with recombinant human growth hormone (rhGH) is used in some centers to increase final height, but no studies have been published so far. Our objective was to conduct a multicenter, retrospective, cohort study to investigate growth in individuals with both types of acrodysostosis, treated with rhGH or not; we used the new nomenclature to describe acrodysostosis, as this disease belongs to the large group of inactivating PTH/PTHrP signaling disorders (iPPSD); acrodysostosis refers to iPPSD4 (acrodysostosis type 1 due to PRKAR1A mutations) and iPPSD5 (acrodysostosis type 2, due to PDE4D mutations). METHODS: We present auxological data from individuals with genetically characterized iPPSD4, and participants with clinical features of iPPSD5. RESULTS: We included 20 and 17 individuals with iPPSD4 and iPPSD5, respectively. The rhGH-treated iPPSD4 patients (n = 9) were smaller at birth than those who did not receive rhGH (median - 2.2 SDS vs. - 1.7 SDS); they showed a trend to catch-up growth during rhGH therapy (median 0.5 SDS in the first year). The rhGH-treated patients (n = 5) reached a better final height compared to those who did not receive rhGH (n = 4) (median - 2.8 SDS vs. - 3.9 SDS), suggesting that rhGH is efficient to increase height in those patients. The difference in target height to final height ranged between 1.6 and 3.0 SDS for iPPSD4 not treated with rhGH (n = 4), 2.1-2.8 SDS for rhGH-treated iPPSD4 (n = 5), 0.6-5.5 SDS for iPPSD5 not treated with rhGH (n = 5) and 2.5-3.1 for rhGH-treated iPPSD5 (n = 2). CONCLUSION: Final height may be positively influenced by rhGH in patients with acrodysostosis/iPPSD. Our rhGH-treated cohort started therapy relatively late, which might explain, at least in part, the limited effect of rhGH on height.


Subject(s)
Human Growth Hormone , Infant, Newborn , Humans , Human Growth Hormone/therapeutic use , Human Growth Hormone/pharmacology , Growth Hormone/therapeutic use , Retrospective Studies , Cohort Studies , Growth Disorders/drug therapy , Growth Disorders/etiology , Body Height , Recombinant Proteins/therapeutic use
2.
J Maxillofac Oral Surg ; 14(3): 653-8, 2015 Sep.
Article in English | MEDLINE | ID: mdl-26225058

ABSTRACT

OBJECTIVE: The objective of this study was to evaluate the difference between the combination agent of xylitol, beatine and olive oil in a chewable capsule versus the control agent of a sorbitol tablet in subjects with hyposalivation and xerostomia. MATERIALS AND METHODS: The subjects had xerostomia over 3 months and a measured hyposalivation. The study was 3 weeks in duration, with 2 treatment phases of 1 week and a 7 day wash out period in between. At the end of each treatment phase, subjects returned for a follow up evaluation. At this visit they were given the subjective sensation questionnaire, as well as their unstimulated whole salivary flow and stimulated whole salivary flow were measured. RESULTS: There was a greater increase in the unstimulated and stimulated whole salivary flow rate, although the results were not statistically significant. The subjective evaluation as measured by the questionnaire showed that both agents reduced the mean score as compared to the baseline, although only the findings in the active agent was statistically significant (p = 0.0015). CONCLUSION: The significant conclusions found in this study were that the active agent provided a significant subjective improvement in speech, swallowing, and decreased subjective xerostomia as compared to the control tablet. CLINICAL RELEVANCE: This combination agent has a significant effect on patients with subjective xerostomia but does not have a significant effect on objective hyposalivation.

3.
Arch Virol ; 160(8): 1909-21, 2015 Aug.
Article in English | MEDLINE | ID: mdl-26026955

ABSTRACT

In Argentina, classical vaccines are used to control infectious bursal disease virus (IBDV); however, outbreaks of IBDV are frequently observed. This could be due to failures in the vaccination programs or to the emergence of new strains, which would be able to break through the protection given by vaccines. Hence, genetic characterization of the viruses responsible for the outbreaks that occurred in recent years is crucial for the evaluation of the control programs and the understanding of the epidemiology and evolution of IBDV. In this study, we characterized 51 field samples collected in Argentina (previously identified as IBDV positive) through the analysis of previously identified apomorphic sequences. Phylogenetic analysis of regVP2 showed that 42 samples formed a unique cluster (Argentinean lineage), seven samples were typical classical strains (one of them was a vaccine strain), and two belonged to the very virulent lineage (vvIBDV). Interestingly, when the analysis was performed on the regVP1 sequences, the field samples segregated similarly to regVP2; thus, we observed no evidence of a reassortment event in the Argentinean samples. Amino acid sequence analysis of regVP2 showed a particular pattern of residues in the Argentinean lineage, particularly the presence of T272, P289 and F296, which had not been reported before as signature sequences for any IBDV phenotype. Notably, the residue S254, characteristic of the antigenic variant, was not present in any of the Argentinean samples.


Subject(s)
Birnaviridae Infections/veterinary , Infectious bursal disease virus/genetics , Infectious bursal disease virus/isolation & purification , Poultry Diseases/virology , Amino Acid Sequence , Animals , Argentina/epidemiology , Birnaviridae Infections/epidemiology , Birnaviridae Infections/virology , Chickens , Disease Outbreaks , Infectious bursal disease virus/chemistry , Infectious bursal disease virus/classification , Molecular Sequence Data , Phylogeny , Poultry Diseases/epidemiology , Sequence Alignment , Viral Structural Proteins/chemistry , Viral Structural Proteins/genetics , Virulence
4.
Neuroscience ; 285: 166-93, 2015 Jan 29.
Article in English | MEDLINE | ID: mdl-25451276

ABSTRACT

Gap junctions provide for direct intercellular electrical and metabolic coupling. The abundance of gap junctions at "large myelinated club ending (LMCE)" synapses on Mauthner cells (M-cells) of the teleost brain provided a convenient model to correlate anatomical and physiological properties of electrical synapses. There, presynaptic action potentials were found to evoke short-latency electrical "pre-potentials" immediately preceding their accompanying glutamate-induced depolarizations, making these the first unambiguously identified "mixed" (i.e., chemical plus electrical) synapses in the vertebrate CNS. We recently showed that gap junctions at these synapses exhibit asymmetric electrical resistance (i.e., electrical rectification), which we correlated with total molecular asymmetry of connexin composition in their apposing gap junction hemiplaques, with connexin35 (Cx35) restricted to axon terminal hemiplaques and connexin34.7 (Cx34.7) restricted to apposing M-cell plasma membranes. We now show that similarly heterotypic neuronal gap junctions are abundant throughout goldfish brain, with labeling exclusively for Cx35 in presynaptic hemiplaques and exclusively for Cx34.7 in postsynaptic hemiplaques. Moreover, the vast majority of these asymmetric gap junctions occur at glutamatergic axon terminals. The widespread distribution of heterotypic gap junctions at glutamatergic mixed synapses throughout goldfish brain and spinal cord implies that pre- vs. postsynaptic asymmetry at electrical synapses evolved early in the chordate lineage. We propose that the advantages of the molecular and functional asymmetry of connexins at electrical synapses that are so prominently expressed in the teleost CNS are unlikely to have been abandoned in higher vertebrates. However, to create asymmetric coupling in mammals, where most gap junctions are composed of connexin36 (Cx36) on both sides, would require some other mechanism, such as differential phosphorylation of connexins on opposite sides of the same gap junction or on asymmetric differences in the complement of their scaffolding and regulatory proteins.


Subject(s)
Brain/metabolism , Gap Junctions/metabolism , Glutamic Acid/metabolism , Goldfish/metabolism , Synapses/metabolism , Animals , Axons/metabolism , Dendrites/metabolism , Fish Proteins/metabolism , Immunohistochemistry , Microscopy, Confocal , Microscopy, Electron
5.
Zoonoses Public Health ; 61(1): 4-17, 2014 Feb.
Article in English | MEDLINE | ID: mdl-23556412

ABSTRACT

Pigs and humans have shared influenza A viruses (IAV) since at least 1918, and many interspecies transmission events have been documented since that time. However, despite this interplay, relatively little is known regarding IAV circulating in swine around the world compared with the avian and human knowledge base. This gap in knowledge impedes our understanding of how viruses adapted to swine or man impacts the ecology and evolution of IAV as a whole and the true impact of swine IAV on human health. The pandemic H1N1 that emerged in 2009 underscored the need for greater surveillance and sharing of data on IAV in swine. In this paper, we review the current state of IAV in swine around the world, highlight the collaboration between international organizations and a network of laboratories engaged in human and animal IAV surveillance and research, and emphasize the need to increase information in high-priority regions. The need for global integration and rapid sharing of data and resources to fight IAV in swine and other animal species is apparent, but this effort requires grassroots support from governments, practicing veterinarians and the swine industry and, ultimately, requires significant increases in funding and infrastructure.


Subject(s)
Endemic Diseases , Influenza A Virus, H1N1 Subtype/isolation & purification , Influenza A virus/isolation & purification , Influenza, Human/epidemiology , Orthomyxoviridae Infections/veterinary , Swine Diseases/epidemiology , Animals , Biomedical Research , Humans , Influenza A Virus, H1N1 Subtype/physiology , Influenza A virus/physiology , Influenza, Human/transmission , International Cooperation , Orthomyxoviridae Infections/epidemiology , Orthomyxoviridae Infections/transmission , Public Health , Public Health Surveillance , Swine , Swine Diseases/transmission , Swine Diseases/virology , Zoonoses
6.
J Gen Virol ; 94(Pt 3): 652-662, 2013 Mar.
Article in English | MEDLINE | ID: mdl-23152367

ABSTRACT

Bluetongue is an insect-transmitted viral disease of ruminant species, which represents a major barrier to the international trade of animals and their products. Bluetongue virus (BTV) has a genome composed of ten linear segments of dsRNA, which code for at least ten different viral proteins. In South America, serological evidence for the presence of BTV has been found in Peru, Argentina, Brazil, Ecuador and Chile. Brazil and Argentina are the only South American countries where BTV has been isolated. In Brazil, only one BTV isolate, serotype 12, has been reported, whereas in Argentina five BTV serotype 4 isolates have been obtained from cattle without clinical signs. Three of these five isolates were isolated during 1999-2001, whereas two of them were obtained as part of the present work. This study describes sequence comparisons and phylogenetic analyses of segment (Seg)-2, Seg-3, Seg-6, Seg-7 and Seg-10 of the first Argentinian field isolates of BTV. The analysis of Seg-2 and Seg-6 resulted in a single cluster of Argentinian sequences into the serotype 4 clade. In addition, the Argentinian sequences grouped within the nucleotype A clade, along with reference strains. The analysis of Seg-3, Seg-7 and Seg-10 showed that the Argentinian isolates grouped into the western topotype, indicating that the circulating virus had an African/European origin. Phylogenetic analysis revealed that the Argentinian sequences present a South American genetic identity, suggesting an independent lineage evolution.


Subject(s)
Bluetongue virus/classification , Bluetongue virus/genetics , Bluetongue/virology , Cattle Diseases/virology , Phylogeny , Animals , Argentina/epidemiology , Biological Evolution , Bluetongue/epidemiology , Cattle , Cattle Diseases/epidemiology , Cell Line , Cricetinae , Gene Expression Regulation, Viral , Molecular Epidemiology , Molecular Sequence Data
7.
Avian Dis ; 53(3): 331-5, 2009 Sep.
Article in English | MEDLINE | ID: mdl-19848068

ABSTRACT

Chicken infectious anemia virus (CAV) is a worldwide-distributed infectious agent that affects commercial poultry. Although this agent was first detected in Argentina in 1994, no further studies on CAV in this country were reported after that. The recent increased occurrence of clinical cases of immunosuppression that could be caused by CAV has prompted this study. Our results confirmed that CAV is still circulating in commercial flocks in Argentina. Phylogenetic analysis focusing on the VP1 nucleotide sequence showed that all Argentinean isolates grouped together in a cluster, sharing a high similarity (> 97%) with genotype B reference strains. However, Argentinean isolates were distantly related to other strains commonly used for vaccination in this country, such as Del-Ros and Cux-1. Sequence analysis of predicted VP1 peptides showed that most of the Argentinean isolates have a glutamine residue at positions 139 and 144, suggesting that these isolates might have a reduced spread in cell culture compared with Cux-1. In addition, a particular amino acid substitution at position 290 is present in all studied Argentinean isolates, as well as in several VP1 sequences from Malaysia, Australia, and Japan isolates. Our results indicate that it is possible to typify CAV strains by comparison of VPI nucleotide sequences alone because the same tree topology was obtained when using the whole genome sequence. The molecular analysis of native strains sheds light into the epidemiology of CAV in Argentinean flocks. In addition, this analysis could be considered in future control strategies focused not only on breeders but on broilers and layer flocks.


Subject(s)
Chicken anemia virus/genetics , Chickens , Circoviridae Infections/veterinary , Poultry Diseases/virology , Amino Acid Sequence , Animals , Argentina/epidemiology , Base Sequence , Capsid Proteins/genetics , Capsid Proteins/metabolism , Circoviridae Infections/epidemiology , Circoviridae Infections/virology , Gene Expression Regulation, Viral , Molecular Epidemiology , Phylogeny , Poultry Diseases/epidemiology
8.
Equine Vet J ; 40(6): 593-5, 2008 Sep.
Article in English | MEDLINE | ID: mdl-19031515

ABSTRACT

State of latency, well known for several herpesviruses, has been proposed for equine herpesvirus-3 (EHV-3) and supported by epidemiological observations. No detailed assessment about reactivation, patterns of excretion and reexcretion has been formally reported. An experimental reactivation study by corticosteroid treatment in previously naturally infected horses was therefore carried out. Two polo mares with clinical and virologically confirmed history of equine coital exanthema were injected with dexamethasone and prednisolone on 3 successive days. Clinical signs, body temperature and clinical samples for virological and serological studies were obtained daily. Mares did not show any systemic clinical signs or hyperthermia. EHV-3 shedding, seroconversion and the presence of a small lesion were observed in one of the mares under study 2 weeks after corticosteroid treatment. The results demonstrate that this virus exhibits a latency-reactivation behaviour similar to that of other alpha herpesviruses. Reactivation of latency may have an important bearing on the appearance of clinical signs in mares and/or stallions during the breeding season without the actual evidence of transfer from mare to stallion or vice versa.


Subject(s)
Adrenal Cortex Hormones/pharmacology , Herpesviridae Infections/veterinary , Herpesvirus 3, Equid/physiology , Horse Diseases/virology , Virus Latency , Animals , DNA, Viral/analysis , Dexamethasone/pharmacology , Female , Herpesviridae Infections/virology , Horses , Polymerase Chain Reaction/methods , Polymerase Chain Reaction/veterinary , Prednisolone/pharmacology , Virus Latency/drug effects
9.
J Intellect Disabil Res ; 52(12): 1091-101, 2008 Dec.
Article in English | MEDLINE | ID: mdl-18557967

ABSTRACT

BACKGROUND: Access to employment for people with intellectual disability (ID) has become a social priority. The aim of the present study is to try to determine which variables [sociodemographic variables, intelligence quotient (IQ), presence or absence of a psychiatric disorder, functioning, self-determination, and behavioural problems] could most reliably account for access to remunerated employment of people with ID. METHODS: Two groups of people with ID participated in this study: (1) 69 workers in a sheltered-employment programme; and (2) 110 clients of programmes in sheltered workshops. Both programmes were run by the Pardo-Valcarce Foundation in Madrid (Spain). The following variables were assessed for every participant: IQ, functioning, behavioural problems, self-determination and presence of psychiatric symptoms. A binary logistic regression analysis was carried out in order to identify the variables that best explained work outcome (sheltered workshop programme vs. sheltered employment programme). RESULTS: Although IQ showed no significant differences between the two groups of participants, the remaining variables did: behavioural problems, functioning, psychiatric symptoms and self-determination significantly explained work outcome. As for sociodemographic variables, whereas gender did not show any significant relationship with the labour status of the participants, significant differences were found when considering variables such as age and pension benefits. CONCLUSIONS: All the main variables considered, except IQ, turned out to be significant. Our findings should be considered encouraging, as they apparently show that both personal and social efforts can help individuals to overcome their low intellectual functioning in order to achieve access to employment. Such study highlights the importance of a prior psychopathological evaluation and efforts to enhance self-determination in order to improve work inclusion for people with ID.


Subject(s)
Intellectual Disability/rehabilitation , Rehabilitation, Vocational , Activities of Daily Living/psychology , Adult , Aged , Comorbidity , Disability Evaluation , Female , Humans , Intelligence , Male , Middle Aged , Personal Autonomy , Prognosis , Sheltered Workshops , Social Behavior , Spain
10.
J Intellect Disabil Res ; 51(Pt 11): 892-901, 2007 Nov.
Article in English | MEDLINE | ID: mdl-17910541

ABSTRACT

BACKGROUND: There is little information on the psychometric properties of instruments for assessing family care burden in adults with intellectual disabilities (ID). The aim of this study is therefore to analyse the usefulness of the 'Subjective and Objective Family Burden Interview' (SOFBI) in the assessment of principal caregivers in Spain. METHODS: The SOFBI was administered to 166 principal caregivers of adults with ID in a vocational centre. The psychometric analysis included: internal consistency, inter-rater and test-retest reliability, construct validity, convergent validity with the World Health Organization's Disability Assessment Schedule II, and feasibility. RESULTS: The Cronbach's alpha was 0.88 for the overall interview and always above 0.7 in the quantitative subdomains. The Kappa coefficients for test-retest were between 0.5 and 0.8, whereas inter-rater agreement was nearly perfect. Maximum-likelihood factor analysis showed four well-defined factors, which fitted the previously designed domains. Feasibility was also good. CONCLUSIONS: The SOFBI is a multi-domain, modular instrument which is feasible, reliable and valid for measuring the burden of family caregivers to adults with ID living in the community.


Subject(s)
Caregivers/psychology , Cost of Illness , Intellectual Disability/psychology , Interview, Psychological , Activities of Daily Living/psychology , Adolescent , Adult , Feasibility Studies , Female , Humans , Intellectual Disability/rehabilitation , Intelligence , Male , Psychometrics/statistics & numerical data , Rehabilitation, Vocational , Reproducibility of Results , Socioeconomic Factors , Spain , Surveys and Questionnaires
11.
Pediátrika (Madr.) ; 27(1): 5-8, ene. 2007. tab
Article in Es | IBECS | ID: ibc-64693

ABSTRACT

Una parte importante del dolor abdominal recurrentela constituyen los trastornos funcionales recogidosen los criterios de Roma. El objetivo de esteartículo es comentar las modificaciones más destacablesrealizadas en la última actualización, es decir,del Roma II de 1999 al Roma III del 2006. Sontres las modificaciones globales más destacables: a)se excluye a la aerofagia; b) se acorta el tiempo deduración de los síntomas necesario para el diagnóstico,pasando de tres a dos meses y c) exclusión delgrado de madurez en el desarrollo cognitivo del niñocomo criterio diagnóstico, incluyéndose niños a partirde los 4 años. Las modificaciones específicas paracada grupo más destacables son: a) dispepsiafuncional: se elimina la necesidad de realizar unaendoscopia digestiva alta para el diagnóstico; b) migrañaabdominal: se reduce la frecuencia y duraciónde los síntomas que deben afectar la actividad habitual.Los antecedentes familiares de migraña soncriterio de apoyo, no de diagnóstico; c) dolor abdominalfuncional: reducción de la frecuencia de la sintomatologíay la posibilidad de relacionarse coneventos psicosociales, pudiendo o no afectar a laactividad habitual del niño y c) no existen modificacionespara el síndrome de intestino irritable


Functional disorders, gathered in Rome criteria,constitute an important part of recurrent abdominalpain. The aim of this article is to comment the mostremarkable modifications made in the last update,that is, from the 1996 Rome II criteria to 2006 RomeIII criteria. Three are the most remarkable global modifications:a) aerophagia is excluded; b) durationterm of symptoms is reduced from three to twomonths and c) children cognitive mature degree isexcluded, including children older than 4 years. Themore remarkable modifications made in each specificgroup are: a) functional dyspepsia: the necessityof making an upper digestive endoscopy for thediagnosis is eliminated; b) abdominal migraine: frequencyand duration of symptoms that affect thenormal activity are reduced. Familiar antecedents ofmigraine are support criterion, they are not diagnosiscriterion; c) functional abdominal pain: reduction ofthe symptoms frequency, and the possibility to relatewith psycho – social events, that may affect the childrenhabitual activity, or may not; and d) there areno modifications about the irritable bowel syndrome


Subject(s)
Humans , Male , Female , Child , Abdominal Pain/etiology , Abdominal Pain/classification , Dyspepsia/diagnosis , Migraine Disorders/diagnosis , Irritable Bowel Syndrome/diagnosis , International Classification of Diseases/trends
12.
Pediátrika (Madr.) ; 27(1): 9-17, ene. 2007. ilus, tab
Article in Es | IBECS | ID: ibc-64694

ABSTRACT

La prevalencia del dolor abdominal de larga duraciónen niños es desconocida. Supone el 2-4% delas consultas pediátricas. Un dolor cuya duraciónsupere las 2-6 semanas se denomina dolor abdominalcrónico y si persiste más de 3 meses se denominadolor abdominal recurrente. Puede ser orgánico,somatomorfo o funcional En los menores de 4 añosel dolor abdominal recurrente se establece como un“diagnóstico”, no pudiéndose establecer el diagnósticode funcional. En los mayores de 4 años el dolorabdominal recurrente es un “síntoma” y se estableceel diagnóstico de funcional según los criterios deRoma III, basados en un conjunto de síntomas.Un interrogatorio y un examen físico completosson los componentes de mayor importancia en lavaloración de cualquier enfermo con dolor abdominalcrónico o recurrente. La causa orgánica se debeconsiderar siempre en primer lugar, principalmenteen menores de 4 años. La presencia de síntomas osignos de alarma constituye una indicación parapracticar pruebas diagnósticas. Una vez descartadaenfermedad orgánica o trastorno por somatización,podemos establecer el diagnóstico de dolor abdominalfuncional, en base a los criterios de Roma III queestablece las siguientes categorías: dispepsia funcional,síndrome de intestino irritable, migraña abdominaly dolor abdominal funcional.El niño con dolor abdominal crónico o recurrentese debe tratar en el contexto de un modelo asistencialbiopsicosocial


Prevalence of long term abdominal pain is unknown.It supposes about 2-4% of the pediatric consultations.Pain that lasts more than 2-6 weeks is calledchronic abdominal pain, and if it lasts more than3 months, it is called recurrent abdominal pain. Itcan be an organic disorder, a somatization disorderor a functional disorder. In children younger than 4years recurrent abdominal pain sets up as a “diagnosis”,as it can’t be established as a functional disorder.In older children, recurrent abdominal pain isa “symptom”, and the diagnosis of functional disorderis established according to Rome III criteria, thatare based upon a set of symptoms.Complete examination and physical exploration arethe main components in the valuation of any patientwith chronic or recurrent abdominal pain. Organiccause should be always considered in first place, moreoverin children younger than 4 years. Presence ofalarm symptoms or signs constitutes and indication toperform diagnostic tests. Once discarded organic diseaseor somatization disorder, we can establish thefunctional abdominal pain diagnosis, based upon theRome III criteria, that sets up the following categories:functional dyspepsia, irritable bowel syndrome, abdominalmigraine and abdominal functional pain.Children with chronic or recurrent abdominal painshould be treated in the context of a biopsicosocial assistant model (AU)


Subject(s)
Humans , Male , Female , Child , Adolescent , Abdominal Pain/diagnosis , Abdominal Pain/therapy , Recurrence , Chronic Disease , International Classification of Diseases , Somatoform Disorders/diagnosis
13.
Psychol Med ; 37(5): 717-25, 2007 May.
Article in English | MEDLINE | ID: mdl-17094818

ABSTRACT

BACKGROUND: This study sought to evaluate the acceptance of two brief psychological interventions for depressed individuals, contacted through a community survey, and to look for predictors of adherence at the patient level. METHOD: The authors used data from the Outcomes of Depression International Network (ODIN) study, which included a randomized controlled trial in which depressed individuals from five European countries, and nine geographical areas were assigned to one of three groups: individual problem-solving treatment, group psychoeducation, or control group. In this analysis, we included all of the individuals who had been assigned to one of the psychological interventions. Compliance with intervention was defined in two different ways. Multiple logistic regression was used to see which variables might predict an individual's compliance with psychological treatment. RESULTS: Psychological intervention was offered to 236 subjects. Treatment was completed by 128 subjects and not by 108 (compliance definition A). Three variables were found to have an effect on compliance A: the presence of a confidant, the use of antidepressant medication during the previous 6 months, and the previous use of any social or health services. On the other hand, 164 subjects had agreed to at least start the treatment, and 72 had not (compliance definition B). The three factors associated with compliance B were presence of a confidant, previous use of services, and the 'desire for change' score. CONCLUSIONS: Social support and previous use of services are the main predictors of compliance with a psychological treatment in depressed individuals from the community. Implications for clinical practice and community programs are discussed.


Subject(s)
Antidepressive Agents/therapeutic use , Community Mental Health Services/statistics & numerical data , Depressive Disorder, Major/epidemiology , Depressive Disorder, Major/therapy , Patient Compliance/statistics & numerical data , Psychotherapy/statistics & numerical data , Quality of Life/psychology , Social Support , Adult , Canada/epidemiology , Depressive Disorder, Major/drug therapy , Double-Blind Method , Female , Humans , Male , Middle Aged , Patient Education as Topic/statistics & numerical data , Prevalence , Problem Solving , Program Evaluation , Prospective Studies , Psychotherapy/methods , Time Factors , Treatment Outcome
15.
Acta pediatr. esp ; 64(1): 2-6, ene. 2006. tab
Article in Es | IBECS | ID: ibc-043523

ABSTRACT

El reflujo gastroesofágico(RGE) es un proceso fisiológico que se manifiesta clínicamente en mayor o menor grado. La enfermedad por reflujo gastroesofágico(ERGE), entendido como el conjunto de signos y síntomas derivados del RGE, es poco frecuente. Se revisan los mecanismos fisiopatológicos implicados en estos procesos, los procedimientos diagnósticos y el tratamiento


Gastroesophageal reflux (GER)is a physiologic process that has a variable expression. We understand gastroesophageal reflux disease(GERD), as the clinical picture that appears secondary to GER. We have reviewed physiopathologic mechanisms involved, as well as the diagnosis procedures and treatment


Subject(s)
Male , Female , Infant , Infant, Newborn , Humans , Gastroesophageal Reflux/diagnosis , Gastroesophageal Reflux/physiopathology , Antacids/therapeutic use , Hydrogen-Ion Concentration , Ranitidine/therapeutic use , Cisapride/therapeutic use , Metoclopramide/therapeutic use , Vomiting/complications , Vomiting/diagnosis , Pepsin A/physiology , Antacids/toxicity , Duodenogastric Reflux/complications , Duodenogastric Reflux/epidemiology , Gastroesophageal Reflux/epidemiology
17.
Virus Res ; 110(1-2): 111-8, 2005 Jun.
Article in English | MEDLINE | ID: mdl-15845261

ABSTRACT

To date, there is little information concerning the epidemiological situation of classical swine fever (CSF) in the Americas. Besides summarizing the available data, genotyping of isolates from outbreaks in domestic pigs in several countries of South and Central America was performed. For this, a 190 base fragment of the E2 envelope glycoprotein gene was used. European strains and isolates, and historical isolates from the United States (US) were included for comparison. In contrast to the situation in most parts of Europe, where group 2 isolates predominate, it was found that all the isolates from the American continent analyzed belonged to group 1 and were further resolved into three subgroups. The Cuban isolates clustered in subgroup 1.2, whereas the isolates from Honduras and Guatemala clustered in subgroup 1.3. The remaining isolates from Argentina, Brazil, Colombia and Mexico generated four poorly resolved clusters in subgroup 1.1, together with the vaccine strains, with historical European and US isolates, and with a recent Russian isolate. While the vaccine strains and the historical European isolates formed a relatively distinct cluster, one of the US isolates clustered together with the Mexican, and another one with Colombian isolates. Historically, CSF (hog cholera) was observed almost simultaneously in the US and in Europe in the first half of the 19th century, and its origin remains a matter of discussion. Our results showed that the US isolates are closely related to isolates from South America, while appearance of isolates in Cuba on one hand and in Honduras and Guatemala on the other hand, seems to have been due to unrelated events. This allows to speculate that at least in the American continent, CSF virus may have appeared independently in several regions, and spreading may have been a secondary effect.


Subject(s)
Classical Swine Fever Virus/genetics , Classical Swine Fever Virus/isolation & purification , Classical Swine Fever/epidemiology , Classical Swine Fever/virology , Disease Outbreaks/veterinary , Animals , Central America/epidemiology , Classical Swine Fever Virus/classification , DNA, Viral/chemistry , Genotype , Molecular Epidemiology , Molecular Sequence Data , Phylogeny , Sequence Analysis, DNA , South America/epidemiology , Sus scrofa/virology , Viral Envelope Proteins/genetics
18.
J Neurocytol ; 33(1): 131-51, 2004 Jan.
Article in English | MEDLINE | ID: mdl-15173637

ABSTRACT

Combined confocal microscopy and freeze-fracture replica immunogold labeling (FRIL) were used to examine the connexin identity at electrical synapses in goldfish brain and rat retina, and to test for "co-localization" vs. "close proximity" of connexins to other functionally interacting proteins in synapses of goldfish and mouse brain and rat retina. In goldfish brain, confocal microscopy revealed immunofluorescence for connexin35 (Cx35) and NMDA-R1 (NR1) glutamate receptor protein in Mauthner Cell/Club Ending synapses. By FRIL double labeling, NR1 glutamate receptors were found in clusters of intramembrane particles in the postsynaptic membrane extraplasmic leaflets, and these distinctive postsynaptic densities were in close proximity (0.1-0.3 microm) to neuronal gap junctions labeled for Cx35, which is the fish ortholog of connexin36 (Cx36) found at neuronal gap junctions in mammals. Immunogold labeling for Cx36 in adult rat retina revealed abundant gap junctions, including several previously unrecognized morphological types. As in goldfish hindbrain, immunogold double labeling revealed NR1-containing postsynaptic densities localized near Cx36-labeled gap junction in rat inferior olive. Confocal immunofluorescence microscopy revealed widespread co-localization of Cx36 and ZO-1, particularly in the reticular thalamic nucleus and amygdala of mouse brain. By FRIL, ZO-1 immunoreactivity was co-localized with Cx36 at individual gap junction plaques in rat retinal neurons. As cytoplasmic accessory proteins, ZO-1 and possibly related members of the membrane-associated guanylate kinase (MAGUK) family represent scaffolding proteins that may bind to and regulate the activity of many neuronal gap junctions. These data document the power of combining immunofluorescence confocal microscopy with FRIL ultrastructural imaging and immunogold labeling to determine the relative proximities of proteins that are involved in short- vs. intermediate-range molecular interactions in the complex membrane appositions at synapses between neurons.


Subject(s)
Brain Mapping/methods , Connexins/analysis , Eye Proteins/analysis , Membrane Proteins/analysis , Phosphoproteins/analysis , Proteomics/methods , Receptors, N-Methyl-D-Aspartate/analysis , Animals , Connexins/biosynthesis , Eye Proteins/biosynthesis , Goldfish , Immunohistochemistry , Membrane Proteins/biosynthesis , Mice , Mice, Knockout , Phosphoproteins/biosynthesis , Rats , Rats, Sprague-Dawley , Receptors, N-Methyl-D-Aspartate/biosynthesis , Zonula Occludens-1 Protein , Gap Junction delta-2 Protein
20.
Cell Commun Adhes ; 10(4-6): 419-23, 2003.
Article in English | MEDLINE | ID: mdl-14681051

ABSTRACT

Auditory afferents terminating as mixed, electrical, and chemical, synapses on the goldfish Mauthner cells constitute an ideal experimental model to study the properties of gap junctions in the nervous system as well as to explore possible functional interactions with the other major form of interneuronal communication--chemically mediated synapses. By combining confocal microscopy and freeze-fracture replica immunogold labeling (FRIL), we found that gap junctions at these synapses contain connexin35 (Cx35), the fish ortholog of the neuron-specific human and mouse connexin36 (Cx36). Conductance of gap junction channels at these endings is known to be dynamically modulated by the activity of their co-localized chemically mediated glutamatergic synapses. By using simultaneous pre- and postsynaptic recordings at these single terminals, we demonstrate that such functional interaction takes place in the same ending, within a few micrometers. Accordingly, we also found evidence by confocal and FRIL double-immunogold labeling that the NR1 subunit of the NMDA glutamate receptor, proposed to be a key regulatory element, is present at postsynaptic densities closely associated with gap junction plaques containing Cx35. Given the widespread distribution of Cx35- and Cx36-mediated electrical synapses and glutamatergic synapses, our data suggest that the local functional interactions observed at these identifiable junctions may also apply to other electrical synapses, including those in mammalian brain.


Subject(s)
Connexins/physiology , Eye Proteins/physiology , Gap Junctions/physiology , Goldfish/physiology , Receptors, N-Methyl-D-Aspartate/metabolism , Synaptic Transmission/physiology , Animals , Connexins/genetics , Electric Conductivity , Excitatory Postsynaptic Potentials/physiology , Eye Proteins/genetics , Freeze Fracturing , Presynaptic Terminals/physiology , Gap Junction delta-2 Protein
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