Do Psychosocial Interventions Improve Quality of Life and Wellbeing in Adults with Neuromuscular Disorders? A Systematic Review and Narrative Synthesis

Background: Quality of life and well-being are frequently restricted in adults with neuromuscular disorders. As such, identification of appropriate interventions is imperative. Objective: The objective of this paper was to systematically review and critically appraise quantitative studies (RCTs, controlled trials and cohort studies) of psychosocial interventions designed to improve quality of life and well-being in adults with neuromuscular disorders. Method: A systematic review of the published and unpublished literature was conducted. Studies meeting inclusion criteria were appraised using a validated quality assessment tool and results presented in a narrative synthesis. Results: Out of 3,136 studies identified, ten studies met criteria for inclusion within the review. Included studies comprised a range of interventions including: cognitive behavioural therapy, dignity therapy, hypnosis, expressive disclosure, gratitude lists, group psychoeducation and psychologically informed rehabilitation. Five of the interventions were for patients with Amyotrophic Lateral Sclerosis (ALS). The remainder were for patients with post-polio syndrome, muscular dystrophies and mixed disorders, such as Charcot-Marie-Tooth disease, myasthenia gravis and myotonic dystrophy. Across varied interventions and neuromuscular disorders, seven studies reported a short-term beneficial effect of intervention on quality of life and well-being. Whilst such findings are encouraging, widespread issues with the methodological quality of these studies significantly compromised the results. Conclusion: There is no strong evidence that psychosocial interventions improve quality of life and well-being in adults with neuromuscular disorders, due to a paucity of high quality research in this field. Multi-site, randomised controlled trials with active controls, standardised outcome measurement and longer term follow-ups are urgently required.

Ocular manifestations of microcephaly with or without chorioretinopathy, lymphedema or intellectual disability (MCLID) syndrome associated with mutations in KIF11

Purpose Microcephaly with or without chorioretinopathy, lymphedema or intellectual disability (MCLID) is an autosomal dominant condition. Mutations in KIF11 have been found to be causative in approximately 75% of cases. This study describes the ocular phenotype in patients with confirmed KIF11 mutations. Methods Standard ophthalmic examination and investigation including visual acuity, refraction and fundus examination was carried out in all patients. Fundus autofluorescence imaging (FAF) was performed in three patients, and four patients underwent spectral domain optical coherence tomography (OCT). Flash electroretinography (ERG) was performed in seven patients, and five underwent additional pattern electroretinography (PERG). Results The patients ranged in age from 2 to 10 years. Most presented with visual acuity loss. Fundus examination revealed lacunae of chorioretinal atrophy. Pigmentary macular changes and optic disc pallor were present in three of seven patients. Fundus autofluorescence demonstrated hypoautofluorescence at the macula in two of three patients. The lacunae of chorioretinal atrophy were hypoautofluorescent. The OCT showed atrophic maculae in three of four patients. Follow-up in one patient showed no deterioration of the vision over a 9-year period. The lesions appear not to be progressive on the follow-up imaging. Electrophysiology showed generalized rod and cone dysfunction and severe macular dysfunction. Inner retinal dysfunction was evident in three of seven patients. Conclusions Patients with KIF11 mutations show a specific ocular phenotype with variable expressivity and intrafamilial variability. Macular atrophy and dysfunction have not been consistently documented before. The fundus lesions appear non-progressive. The findings assist in providing an accurate diagnosis and thus improving the management and follow-up of patients with this syndrome.

Lipofilling in skin affected by radiodermatitis: clinical and ultrasound aspects. Case report

In recent years, lipofilling has established itself as one of the most effective and least invasive techniques to treat connective dystrophy subsequent to radiotherapy. We report the case of a patient diagnosed with intraductal carcinoma of the right breast in 1996, at the age of 41. The patient underwent quadrantectomy with ipsilateral axillary lymph node dissection and adjuvant chemotherapy and radiotherapy. Four years later, a recurrence led the patient to undergo a subcutaneous mastectomy and immediate reconstruction, involving the submuscular insertion of a permanent implant. In 2007 the patient suffered both radiodermatitis and capsular contracture around the implant, causing constant pain and significant functional limitation. She first took a leukotriene inhibitor (Zafirlukast, 20 mg daily for 8 months) to reduce the capsular contracture. She then underwent lipofilling (Coleman’s technique) of the area affected by radiodermatitis, in which the skin was considerably thinned and visibly ischemic. A second session followed four months later. Clinical, photographic and ultrasound examination revealed clear and lasting thickening of the superficial tissues, increased coverage of the implant, and reduced skin discoloration and tension.

Processos degenerativos do tecido cutâneo

Os processos degenerativos do tecido cutâneo estão amplamente associados ao seu envelhecimento natural, onde se verifica perda de tecido fibroso, renovação celular mais lenta e redução da rede vascular e glandular da pele. Alguns fatores externos ao organismo podem contudo acelerar estes processos, como por exemplo a exposição solar, consumo excessivo de álcool e tabaco, poluição ambiental e aumento de peso. De entre estes processos destacam-se o processo descamativo, um fenómeno natural do mecanismo de diferenciação dos queratinócitos. É um processo complexo que envolve essencialmente a degradação da coesão entre células da pele. A lipodistrofia ginóide é outro destes processos, comummente denominado de celulite, e que se caracteriza como uma distrofia celular complexa, com alterações do metabolismo hídrico que conferem uma aparência de "casca de laranja" à pele. A flacidez é um processo resultante da atrofia tecidular, onde se verifica a perda progressiva de massa muscular que é substituída por tecido adiposo. Está diretamente relacionada com a redução da produção de fibras de colagénio e fibras elásticas no tecido subcutâneo. Por fim, insuficiência venosa é um termo utilizado para caracterizar um processo que afeta o sistema venoso dos membros inferiores, que se desenvolve por aumento da pressão venosa em combinação com um retorno venoso ineficiente. Embora ainda não exista compreensão total destes mecanismos, já é possível encontrar uma série de tratamentos que visam minimizar ou mesmo tratá-los, de modo a que não se agravem e representem um risco sério para a saúde.

Effets du stress oxydatif induit par les rayons UVA et endogène sur la cornée humaine : étude des délétions de l’ADN mitochondrial, des modifications dans la matrice extracellulaire cornéenne et de la dystrophie cornéenne endothéliale de Fuchs

Le stress oxydatif peut provenir de sources exogènes comme les UVA ou de sources endogènes comme la chaîne respiratoire (OXPHOS). L’oxydation des composants cellulaires a été associée avec la dégénération, des phénotypes de vieillissement et des pertes de fonctionnalités des tissus. Les UVA sont les plus efficaces des rayons UV à induire de l’oxydation, tel que démontré par la formation de dommages oxydatifs à l’ADN et par l’apparition de délétions mitochondriales qui en résultent. La délétion mitochondriale de 4977 pb (ADNmtCD4977), la plus commune, et celle de 3895 pb (ADNmt3895) sont deux délétions reliées au photovieillissement cutané et à l’exposition au stress oxydant. Le phénomène de vieillissement dans la peau est bien documenté et se traduit par une dégradation de la matrice extracellulaire, une perte d’élasticité et la formation de rides. Toutefois, peu d’études portent sur la cornée humaine alors qu’elle est un tissu exposé directement aux rayonnements UV au même titre que la peau. Nous avons donc tenté mieux comprendre l’effet de l’oxydation exogène et endogène sur cette structure. L’analyse de la localisation des délétions ADNmtCD4977 et ADNmtCD4977 dans l’oeil humain a permis de révéler qu’elles se concentrent principalement dans le stroma cornéen et s’accumule avec l’âge. Le stroma cornéen est la couche cellulaire qui confère la transparence et la rigidité à la cornée humaine. Ces résultats nous ont suggéré une implication des UVA dans le photovieillissement de la cornée. Nous avons donc entrepris de vérifier les changements liés à l’exposition aux UVA dans le stroma cornéen puisque les UVA sont connus pour causer des altérations à la matrice extracellulaire (ECM) au niveau cutané. Nous avons donc créé un modèle de photovieillisement par une exposition chronique aux UVA sur des kératocytes avec lesquels nous avons fait sécréter une ECM. Nos résultats nous ont démontré qu’une exposition chronique aux UVA cause des altérations à l’ECM cornéen semblable à des phénotypes de photvieillissement. En effet, nous avons dénoté des changements transcriptomiques et protéomiques pour certains collagènes et protéoglycans. Une atteinte aux collagènes par le vieillissement cornéen se traduit entre autres par une rigidification, une opacification et un changement dans son pouvoir réfractif qui mène à une perte de la vision. Par ailleurs, notre avons également investigué l’implication du stress oxydatif dans la dystrophie cornéenne endothéliale de Fuchs (FECD), une maladie dégénérative de l’endothélium cornéen, qui mène à une perte de vision et est une cause principale de greffe cornéenne. L’étiologie de la maladie est encore inconnue, mais le stress oxydatif est soupçonné de jouer un rôle important dans la pathogenèse. Nos résultats ont amené de nouvelles évidences de l’implication de l’oxydation dans la maladie par l’augmentation de la quantité d’ADN mitochondrial et un raccourcissement des télomères dans des explants de cornées pathologiques. Nos résultats nous ont également démontré que la mise en culture de cellules FECD permettait la sélection de cellules fonctionnelles et comparables à des cellules saines en termes de quantité d’ADN mitochondrial et de son intégrité, de sensibilité à l’oxydation et de longueur télomérique. Les résultats obtenus soutiennent ainsi la possibilité d’employer les cellules FECD fonctionnelles sélectionnées pour utilisation en génie tissulaire afin de créer des cornées autologues pour pallier aux manques de greffes cornéennes. Enfin, nos résultats apportent de nouvelles évidences quant à l’implication du stress oxydatif dans le photovieillissement cornéen et dans l’étiologie de la FECD.

Erosão dentária associada a distúrbios alimentares

Os distúrbios alimentares traduzem-se em comportamentos, quer pela falta, quer pelo excesso da ingestão de alimentos, sendo a anorexia nervosa e a bulimia as que mais frequentemente se verificam na população. O crescente aumento destes distúrbios, nomeadamente a obsessão pelos corpos magros, está relacionada com o impacto que os media têm na sociedade, uma vez que a magreza é vista como mecanismo de atracção sexual e de integração social. O diagnóstico das desordens alimentares não é fácil de ser efectuado, dado que os sinais são muitas vezes omitidos/ocultados pelos indivíduos. Os médicos dentistas podem ter um papel importante na sua detecção, dadas as manifestações precoces das alterações alimentares na cavidade oral. Há diversos sintomas comuns aos dois distúrbios alimentares como a erosão dentária, a hipersensibilidade dentinária, a hipertrofia das glândulas salivares e consequente hipossalivação, a cárie dentária, a doença periodontal, as mucosites, a candidíase oral e a queilite angular. Resultante do vómito induzido, há o aporte de ácido proveniente do conteúdo gástrico que induz alterações estruturais do esmalte e dentina, facilitando o processo de desgaste erosivo. Os fenómenos erosivos são uma das manifestações orais mais evidentes dos distúrbios alimentares. O conhecimento dos sinais, sintomas e da forma de evolução da erosão dentária, é imprescindível, e acaba por diferenciar a atuação profissional que possibilita um diagnóstico eficaz e o tratamento correto. A elaboração desta dissertação tem como objectivo reforçar a informação sobre estes fenómenos para que possam ser mais eficazmente prevenidos, diagnosticados e controlados/tratados. Para tal efectuou-se uma pesquisa na B-On, Medline/PubMed, sciELO, RCAAP e em livros, de informação válida sobre o tema. Interpôs-se limitação temporal e usaram-se as seguintes palavras-chave na seleção de artigos: “Dental erosion”, “Erosive wear”, “Anorexia”, “Bulimia”, “Eating disorders”.

Best Practice Guidelines on molecular diagnostics in Duchenne/Becker muscular dystrophies

Meeting participants: Rosário dos Santos, Porto, Portugal

Intellectual disability, coarse face, relative macrocephaly, and cerebellar hypotrophy in two sisters

We report on two Portuguese sisters with a very similar phenotype characterized by severe intellectual disability, absent speech, relative macrocephaly, coarse face, cerebellar hypotrophy, and severe ataxia. Additional common features include increased thickness of the cranial vault, delayed dental eruption, talipes equino-varus, clinodactyly, and camptodactyly of the fifth finger. The older sister has retinal dystrophy and the younger sister has short stature. Their parents are consanguineous. We suggest this condition constitutes a previously unreported autosomal recessive entity.

Frecuencia, manifestaciones clínicas y de laboratorio de infecciones respiratorias en pacientes con V.I.H./S.I.D.A. del Hospital Vicente Corral Moscoso de la ciudad de Cuenca período 2001-2007

Estudio descriptivo, se revisó y recolectó la información necesaria obtenidas de las historias clínicas de todos los pacientes diagnosticados de V.I.H.(+) en el departamento de clínica. Para el análisis estadístico: se utilizó los programas S.P.S.S. versión 10.0 para Windows y Microsoft Excel 2007, en la presentación de los datos se utilizó cuadros y gráficos en correspondencia con el tipo de variable y asociación que se deseó. Resultados: de un total de 7709 hospitalizados, 200 pacientes se encontraron infectados con V.I.H.(+), de los cuales 81 pacientes presentaron afección respiratoria, el 78de estos correspondió a los hombres, la mayoría se encontró entre los 26-35 años, la mortalidad se presentó en el 27,16; en los datos demográficos se encontró que los residentes de la sierra, católicos, solteros, un tipo de educación secundaria, la actividad manual sobresalían en los grupos de los pacientes; las principales patologías encontradas fueron Candidiasis Orofaríngea, Neumonía por P. Jirovecii, Tuberculosis Pulmonar y Neumonía Adquirida en la Comunidad. Se encontraron patrones en Radiología y Linfocitos CD4+ según principales patologías respiratorias. Conclusiones: el sexo masculino es el más frecuente dentro de los 81 pacientes V.I.H. que presentaron patologías respiratorias en el área de clínica, donde el sexo masculino fue el más frecuente, se presentó mortalidad alta en las primeras dos semanas de hospitalización, los datos demográficos son semejantes a nuestra región, la Candidiasis Oral y neumonía por P. Jirovecii fueron las principales afecciones en vías aéreas superior e inferior respectivamente, se encontró relación entre características radiológicas y linfocitos C.D.4+ asociadas con infecciones respiratorias en pacientes con VIH/SIDA

Aislamiento e identificación de Candida albicans de la cavidad oral, mediante el uso del Agar cromogénico en la población interna del Asilo San Antonio y Casa de la Misericordia de la ciudad de San Miguel

La investigación se realizó en la población con los adultos mayores del Asilo San Antonio y Casa de la Misericordia de la Ciudad de San Miguel, en el período de Junio a Julio de 2015. El Objetivo de la investigación fue aislar e identificar Candida albicans en muestras de la cavidad oral, mediante el uso del agar cromogénico de la población interna del Asilo San Antonio y Casa de la Misericordia de la Ciudad de San Miguel. El diseño metodológico es de tipo descriptivo, prospectivo, transversal, y de laboratorio, para el cual se tomaron 61 muestras de la cavidad oral de los internos en el Asilo San Antonio y Casa de la Misericordia de la Ciudad de San Miguel a través de un hisopado bucal con el que se realizó un examen directo al fresco con Solución Salina estéril al 0.85% en la búsqueda de levaduras; posteriormente se procedió a sembrar en el agar cromogénico Brilliance Candida, para observar el crecimiento de colonias verdes, las cuales indican la presencia de Candida albicans, como agente causal de Candidiasis oral. Resultados: De las 61 muestras procesadas a 26 se les aisló e identificó Candida albicas con un porcentaje de 42.7%. De los 22 adultos mayores que presentaban lesiones sugestivas a candidiasis oral a 20 se les aisló e identificó Candida albicans de los cuales 15 (88.2%) pertenecen al Asilo San Antonio y 5 (100%) pertenecen a la Casa de la Misericordia. De los 10 adultos mayores que reportaron que no practican el aseo bucal se les aisló e identificó Candida albicans a 3 (33.3%) de ellos que se encuentran en el Asilo San Antonio. A 5 internos que reportaron practicar algunas veces el aseo bucal también se les aisló e identificó Candida albicans, 4 (44.4%) pertenecen al Asilo San Antonio y 1 (50%) a la Casa de la Misericordia. De los 18 adultos mayores que usan prótesis dentales a 7 (53.8%) se les aisló e identificó Candida albicans en el Asilo San Antonio y en la Casa de la Misericordia a 5 (100%) internos se les aisló e identificó Candida albicans. De 35 adultos mayores que reportaron que usan antibiótico a 14 (46.7%) que se encuentran en el Asilo San Antonio se les aisló e identificó Candida albicans. Con respecto Casa de la Misericordia de los 5 (100%) que reportaron que usan antibiótico no se les aisló Candida albicans. En 16 (26.2%) muestras no se observó crecimiento de ninguna especie de Candida. Conclusiones: Se estudió a la población interna del Asilo San Antonio y Casa de La Misericordia debido a que los adultos mayores son vulnerables a las infecciones por hongos oportunistas ya que su sistema inmunológico se encuentra disminuido unido a una serie de factores predisponentes, como el uso de prótesis dentales, antibióticos, mal higiene bucal y diabetes. Mediante el uso del agar Brilliance Candida se logró diferenciar otras especies del género Candida como Candida tropicalis 26.2%, Candida krusei 3.3% y Candida glabrata 1.6%. De acuerdo a estos resultados y las conclusiones de la investigación se plantean algunas recomendaciones orientadas principalmente al personal de salud para brindar apoyo a este tipo de estudios.

Candidaemia or Candidasis: Controversy of Staphylococcus Sexually Transmitted Infection?

Herbal medications are becoming increasingly popular but a most-extraordinary claim by traditional/herbal medical practitioners relates to a Gram-positive bacterium, Staphylococcus , which has been depicted as a deadly sexually transmitted disease that manifest in the form of worms and other symptoms; with contributory roles including infertility, sexual dysfunction and impotency. They further boasted that they are the only ones that possessed the remedy (herbal) for the Staphylococcus sexually transmitted scourge. In the absence of distinguishing phenotypic taxonomic tools, Staphylococcus and Candida spp. may be confused for each other. However, Staphylococcus is a bacterium and not an infection; therefore, there must be more to the traditional medical practitioners’ boasts in ability to cure an infection that was not an infection in the first place. In conclusion, the common sense is that candiaemia or candidiasis is most likely the misdiagnosed sexually transmitted Staphylococcus disease, which is of significant human clinical health issue.

Estudio de la patogenicidad de Candida y de la actividad de los fármacos antifúngicos en un modelo animal en Caenorhabditis elegans

171 p.

First description of Candida nivariensis in Brazil: antifungal susceptibility profile and potential virulence attributes

This study evaluated the antifungal susceptibility profile and the production of potential virulence attributes in a clinical strain of Candida nivariensis for the first time in Brazil, as identified by sequencing the internal transcribed spacer (ITS)1-5.8S-ITS2 region and D1/D2 domains of the 28S of the rDNA. For comparative purposes, tests were also performed with reference strains. All strains presented low planktonic minimal inhibitory concentrations (PMICs) to amphotericin B (AMB), caspofungin (CAS), and voriconazole. However, our strain showed elevated planktonic MICs to posaconazole (POS) and itraconazole, in addition to fluconazole resistance. Adherence to inert surfaces was conducted onto glass and polystyrene. The biofilm formation and antifungal susceptibility on biofilmgrowing cells were evaluated by crystal violet staining and a XTT reduction assay. All fungal strains were able to bind both tested surfaces and form biofilm, with a binding preference to polystyrene (p < 0.001). AMB promoted significant reductions (≈50%) in biofilm production by our C. nivariensis strain using both methodologies. This reduction was also observed for CAS and POS, but only in the XTT assay. All strains were excellent protease producers and moderate phytase producers, but lipases were not detected. This study reinforces the pathogenic potential of C. nivariensis and its possible resistance profile to the azolic drugs generally used for candidiasis management.

Evolution of developmental gene regulatory networks in echinoids

Developmental gene regulatory networks (dGRNs) are assemblages of regulatory genes that direct embryonic development of animal body plans and their morpho-logical structures. dGRNs exhibit recursively-wired circuitry that is encoded in the genome and executed during development. Alteration to the regulatory architecture of dGRNs causes variation in developmental programs both during the development of an individual organism and during the evolution of an individual lineage. The ex-planatory power of these networks is best exemplified by the global dGRN directing early development of the euechinoid sea urchin Strongylocentrotus purpuratus. This network consists of numerous regulatory genes engaging in hundreds of genomic regulatory transactions that collectively direct the delineation of early embryonic domains and the specification of cell lineages. Research on closely-related euechi-noid sea urchins, e.g. Lytechinus variegatus and Paracentrotus lividus, has revealed marked conservation of dGRN architecture in echinoid development, suggesting little appreciable alteration has occurred since their divergence in evolution at least 90 million years ago (mya).

We sought to test whether this observation extends to all sea urchins (echinoids) and undertook a systematic analysis of over 50 regulatory genes in the cidaroid sea urchin Eucidaris tribuloides, surveing their regulatory activity and function in a sea urchin that diverged from euechinoid sea urchins at least 268 mya. Our results revealed extensive alterations have occurred to all levels of echinoid dGRN archi-tecture since the cidaroid-euechinoid divergence. Alterations to mesodermal sub-circuits were particularly striking, including functional di˙erences in specification of non-skeletogenic mesenchyme (NSM), skeletogenic mesenchyme (SM), and en-domesodermal segregation. Specification of endomesodermal embryonic domains revealed that, while their underlying network circuitry had clearly diverged, regu-latory states established in pregastrular embryos of these two groups are strikingly similar. Analyses of E. tribuloides specification leading to the estab-lishment of dorsal-ventral (aboral-oral) larval polarity indicated that regulation of regulatory genes expressed in mesodermal embryonic domains had incurred significantly more alterations than those expressed in endodermal and ectodermal domains. Taken together, this study highlights the ability of dGRN architecture to buffer extensive alterations in the evolution and early development of echinoids and adds further support to the notion that alterations can occur at all levels of dGRN architecture and all stages of embryonic development.

Epothilone-d rescues cognition and attenuates alzheimer’s disease-like pathology in APP/PS1 mice

AIMS: Cognitive decline in Alzheimer's disease (AD) patients has been linked to synaptic damage and neuronal loss. Hyperphosphorylation of tau protein destabilizes microtubules leading to the accumulation of autophagy/vesicular material and the generation of dystrophic neurites, thus contributing to axonal/synaptic dysfunction. In this study, we analyzed the effect of a microtubule-stabilizing compound in the progression of the disease in the hippocampus of APP751SL/PS1M146L transgenic model. METHODS: APP/PS1 mice (3 month-old) were treated with a weekly intraperitoneal injection of 2 mg/kg epothilone-D (Epo-D) for 3 months. Vehicle-injected animals were used as controls. Mice were tested on the Morris water maze, Y-maze and object-recognition tasks for memory performance. Abeta, AT8, ubiquitin and synaptic markers levels were analyzed by Western-blots. Hippocampal plaque, synaptic and dystrophic loadings were quantified by image analysis after immunohistochemical stainings. RESULTS: Epo-D treated mice exhibited a significant improvement in the memory tests compared to controls. The rescue of cognitive deficits was associated to a significant reduction in the AD-like hippocampal pathology. Levels of Abeta, APP and ubiquitin were significantly reduced in treated animals. This was paralleled by a decrease in the amyloid burden, and more importantly, in the plaque-associated axonal dystrophy pathology. Finally, synaptic levels were significantly restored in treated animals compared to controls. CONCLUSION: Epo-D treatment promotes synaptic and spatial memory recovery, reduces the accumulation of extracellular Abeta and the associated neuritic pathology in the hippocampus of APP/PS1 model. Therefore, microtubule stabilizing drugs could be considered therapeutical candidates to slow down AD progression. Supported by FIS-PI12/01431 and PI15/00796 (AG),FIS-PI12/01439 and PI15/00957(JV)