RESUMEN
AIMS: To evaluate safety, efficacy and glucose turnover during closed-loop with meal announcement using reduced prandial insulin boluses in adolescents with type 1 diabetes (T1D). METHODS: We conducted a randomized crossover study comparing closed-loop therapy with standard prandial insulin boluses versus closed-loop therapy with prandial boluses reduced by 25%. Eight adolescents with T1D [3 males; mean (standard deviation) age 15.9 (1.5) years, glycated haemoglobin 74 (17) mmol/mol; median (interquartile range) total daily dose 0.9 (0.7, 1.1) IU/kg/day] were studied on two 36-h-long visits. In random order, subjects received closed-loop therapy with either standard or reduced insulin boluses administered with main meals (50-80 g carbohydrates) but not with snacks (15-30 g carbohydrates). Stable-label tracer dilution methodology measured total glucose appearance (Ra_total) and glucose disposal (Rd). RESULTS: The median (interquartile range) time spent in target (3.9-10 mmol/l) was similar between the two interventions [74 (66, 84)% vs 80 (65, 96)%; p = 0.87] as was time spent above 10 mmol/l [21.8 (16.3, 33.5)% vs 18.0 (4.1, 34.2)%; p = 0.87] and below 3.9 mmol/l [0 (0, 1.5)% vs 0 (0, 1.8)%; p = 0.88]. Mean plasma glucose was identical during the two interventions [8.4 (0.9) mmol/l; p = 0.98]. Hypoglycaemia occurred once 1.5 h post-meal during closed-loop therapy with standard bolus. Overall insulin delivery was lower with reduced prandial boluses [61.9 (55.2, 75.0) vs 72.5 (63.6, 80.3) IU; p = 0.01] and resulted in lower mean plasma insulin concentration [186 (171, 260) vs 252 (198, 336) pmol/l; p = 0.002]. Lower plasma insulin was also documented overnight [160 (136, 192) vs 191 (133, 252) pmol/l; p = 0.01, pooled nights]. Ra_total was similar [26.3 (21.9, 28.0) vs 25.4 (21.0, 29.2) µmol/kg/min; p = 0.19] during the two interventions as was Rd [25.8 (21.0, 26.9) vs 25.2 (21.2, 28.8) µmol/kg/min; p = 0.46]. CONCLUSIONS: A 25% reduction in prandial boluses during closed-loop therapy maintains similar glucose control in adolescents with T1D whilst lowering overall plasma insulin levels. It remains unclear whether closed-loop therapy with a 25% reduction in prandial boluses would prevent postprandial hypoglycaemia.
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Glucemia/análisis , Diabetes Mellitus Tipo 1/tratamiento farmacológico , Hipoglucemia/prevención & control , Hipoglucemiantes/administración & dosificación , Sistemas de Infusión de Insulina , Insulina/administración & dosificación , Monitoreo Fisiológico , Adolescente , Algoritmos , Estudios Cruzados , Diabetes Mellitus Tipo 1/sangre , Diabetes Mellitus Tipo 1/metabolismo , Esquema de Medicación , Inglaterra/epidemiología , Femenino , Carga Glucémica , Humanos , Hiperinsulinismo/inducido químicamente , Hiperinsulinismo/epidemiología , Hiperinsulinismo/prevención & control , Hipoglucemia/inducido químicamente , Hipoglucemia/epidemiología , Hipoglucemiantes/efectos adversos , Hipoglucemiantes/sangre , Hipoglucemiantes/uso terapéutico , Inyecciones Subcutáneas , Insulina/efectos adversos , Insulina/sangre , Insulina/uso terapéutico , Resistencia a la Insulina , Masculino , Comidas , RiesgoRESUMEN
Idiopathic normal pressure hydrocephalus (iNPH) is the most common cause of hydrocephalus in adults. The diagnosis may be challenging, requiring collaborative efforts between different specialists. According to the International Society for Hydrocephalus and Cerebrospinal Fluid Disorders, iNPH should be considered in the differential of any unexplained gait failure with insidious onset. Recognizing iNPH can be even more difficult in the presence of comorbid neurologic disorders. Among these, idiopathic Parkinson's disease (PD) is one of the major neurologic causes of gait dysfunction in the elderly. Both conditions have their peak prevalence between the 6th and the 7th decade. Importantly, postural instability and gait dysfunction are core clinical features in both iNPH and PD. Therefore, diagnosing iNPH where diagnostic criteria of PD have been met represents an additional clinical challenge. Here, we report a patient with parkinsonism initially consistent with PD who subsequently displayed rapidly progressive postural instability and gait dysfunction leading to the diagnosis of concomitant iNPH. In the following sections, we will review the clinical features of iNPH, as well as the overlapping and discriminating features when degenerative parkinsonism is in the differential diagnosis. Understanding and recognizing the potential for concomitant disease are critical when treating both conditions.
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Though abnormalities of visuospatial function occur in Parkinson's disease, the impact of such deficits on functional independence and psychological wellbeing has been historically under- recognized, and effective treatments for this impairment are unknown. These symptoms can be encountered at any stage of the disease, affecting many activities of daily living, and negatively influencing mood, self-efficacy, independence, and overall quality of life. Furthermore, visuospatial dysfunction has been recently linked to gait impairment and falls, symptoms that are known to be poor prognostic factors. Here, we aim to present an original modality of neurorehabilitation designed to address visuospatial dysfunction and related symptoms in Parkinson's disease, known as "Art Therapy". Art creation relies on sophisticated neurologic mechanisms including shape recognition, motion perception, sensory-motor integration, abstraction, and eye-hand coordination. Furthermore, art therapy may enable subjects with disability to understand their emotions and express them through artistic creation and creative thinking, thus promoting self-awareness, relaxation, confidence and self-efficacy. The potential impact of this intervention on visuospatial dysfunction will be assessed by means of combined clinical, behavioral, gait kinematic, neuroimaging and eye tracking analyses. Potential favorable outcomes may drive further trials validating this novel paradigm of neurorehabilitation.
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Arteterapia , Rehabilitación Neurológica/métodos , Enfermedad de Parkinson/rehabilitación , Anciano , Anciano de 80 o más Años , Encéfalo/diagnóstico por imagen , Femenino , Fijación Ocular/fisiología , Humanos , Imagen por Resonancia Magnética , Masculino , Persona de Mediana Edad , Estudios Prospectivos , Navegación Espacial/fisiologíaRESUMEN
The Forkead Box G1 (FOXG1 in humans, Foxg1 in mice) gene encodes for a DNA-binding transcription factor, essential for the development of the telencephalon in mammalian forebrain. Mutations in FOXG1 have been reported to be involved in the onset of Rett Syndrome, for which sequence alterations of MECP2 and CDKL5 are known. While visual alterations are not classical hallmarks of Rett syndrome, an increasing body of evidence shows visual impairment in patients and in MeCP2 and CDKL5 animal models. Herein we focused on the functional role of FOXG1 in the visual system of animal models (Foxg1(+/Cre) mice) and of a cohort of subjects carrying FOXG1 mutations or deletions. Visual physiology of Foxg1(+/Cre) mice was assessed by visually evoked potentials, which revealed a significant reduction in response amplitude and visual acuity with respect to wild-type littermates. Morphological investigation showed abnormalities in the organization of excitatory/inhibitory circuits in the visual cortex. No alterations were observed in retinal structure. By examining a cohort of FOXG1-mutated individuals with a panel of neuro-ophthalmological assessments, we found that all of them exhibited visual alterations compatible with high-level visual dysfunctions. In conclusion our data show that Foxg1 haploinsufficiency results in an impairment of mouse and human visual cortical function.
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Factores de Transcripción Forkhead/genética , Factores de Transcripción Forkhead/metabolismo , Proteínas del Tejido Nervioso/genética , Proteínas del Tejido Nervioso/metabolismo , Trastornos de la Visión/genética , Trastornos de la Visión/fisiopatología , Animales , Preescolar , Estudios de Cohortes , Modelos Animales de Enfermedad , Potenciales Evocados Visuales/fisiología , Femenino , Haploinsuficiencia , Humanos , Lactante , Masculino , Ratones Endogámicos C57BL , Ratones Transgénicos , Mutación , Neuronas/patología , Neuronas/fisiología , Retina/patología , Retina/fisiopatología , Síndrome de Rett/patología , Síndrome de Rett/fisiopatología , Agudeza Visual/fisiología , Corteza Visual/patología , Corteza Visual/fisiopatología , Vías Visuales/patología , Vías Visuales/fisiopatología , Adulto JovenRESUMEN
True hermaphroditism is a very rare disorder of human sexual differentiation. In the medical literature, more than 450 cases are described, and about 250 true hermaphrodites have been subjected to chromosome studies. A 21-year-old "man" was examined because of genital and phenotypic abnormalities: clinical, surgical and laboratory investigations showed a true hermaphroditism, with a quadruple mosaicism 45,X/46,XX/46,XY/47,XXY. We believe that this is the first case in which this peculiar type of multiple mosaicism has been documented.
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Trastornos del Desarrollo Sexual/genética , Mosaicismo , Femenino , Genitales/anomalías , Humanos , Cariotipificación , Masculino , Ovario/patología , Testículo/patologíaRESUMEN
Descreveu-se a morfologia do útero de cutias nulíparas e não nulíparas por meio de ovariossalpingoisterectomia. A análise macroscópica do útero foi realizada in loco e na peça retirada. Segmentos das porções proximal, média e distal do órgão foram colhidas, fixadas e preparadas histologicamente, sendo as amostras analisadas à microscopia de luz, e realizada a histomorfometria das camadas uterinas. Topograficamente, o útero localiza-se na região sublombar, caudalmente aos rins, em continuação aos ovários e às tubas uterinas, estendendo-se até à entrada da pelve, onde se posiciona dorsalmente à bexiga. Caracteriza-se como do tipo duplo, embora culmine em apenas um óstio cervical externo. Microscopicamente, a mucosa uterina é formada por variações do epitélio, de cilíndrico a pseudoestratificado, que se apoia em tecido conjuntivo frouxo, onde se observam glândulas endometriais revestidas por epitélio cilíndrico, além da presença de vasos sanguíneos. A camada muscular subdivide-se em interna ou submucosa, média ou vascular e externa ou subserosa. A camada serosa é composta por tecido conjuntivo e mesotélio. Na histomorfometria, verificou-se que a espessura uterina total e a espessura da camada mucosa, em média, foram maiores nas fêmeas não nulíparas.
The uterine morphology was studied through ovarysalpingohysterectomy in nulliparous and non nulliparous agoutis (Dasyprocta azare). The uterus macroscopic analysis was done "in loco" and in the removed specimens. Fragments of the proximal, media and distal portions of this viscerae were collected, fixed and histologically prepared, and the samples analyzed through light microscopy and through the histomorphometry of the uterine layers. Topographycally, the uterus of this rodent is located on the sub lumbar area, caudally to the kidneys, and following the ovaries and uterine horns, getting through the pelvic entrance, where it is located dorsally to the bladder. It is characterized as a double uterus, although there is only an external cervical os. Microscopically, the uterine mucous is formed by epithelial elevations, from cylindrical to pseudostratified epithelium, which is supported by a loose connective tissue where endometrial glands covered by cylindrical epithelium can be observed, besides blood vessels. The muscle layer is subdivided in inner or submuscous, median or vascular and outer or subserous. The serous layer is composed of a connective tissue and mesothelium. In the histomorphometry analysis, the total uterine thickness and the mucous layer thickness, in average, were bigger on non nulliparous females.
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Animales , Femenino , Útero/anatomía & histología , Procedimientos Quirúrgicos Ginecológicos/métodos , Roedores/clasificaciónRESUMEN
An innovative miniaturized kit based on the use of 2-week-old ozone-supersensitive tobacco germlings (Nicotiana tabacum L. cv. Bel-W3) raised in tissue culture plates was utilized, in conjunction with four calibrated automatic analyzers, to monitor the distribution of phytotoxic ground level ozone in Tuscany during the summer of 1993 at 27 sites differing in nature. Germlings of ozone-resistant Bel-B tobacco were also included in the protocol. The intensity of visible injury on the cotyledons of Bel-W3 was linearly correlated with several ozone statistical descriptors. The occurrence of phytotoxic levels of photochemical ozone was detected in all the monitoring sites, which included rural and remote areas, whose local sources of pollution were negligible. The suitability of the new methodology for low-cost, space-saving, user-friendly monitoring of ozone on a large geographical scale is discussed.
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The authors describe a case of true hermaphroditism of mainly female phenotype, ambiguous genitalia, and ovotestis. The cytogenetic revealed 45X/46XY mosaicism and an absence of Barr bodies.
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Trastornos del Desarrollo Sexual/genética , Mosaicismo , Aberraciones Cromosómicas Sexuales , Adolescente , Trastornos del Desarrollo Sexual/patología , Femenino , Humanos , Cariotipificación , Masculino , Ovario/patología , Fenotipo , Testículo/patologíaRESUMEN
A mentally retarded child with an extra small bisatellited acrocentric chromosome is described. The patient exhibited rather unspecific clinical signs such as strabismus, marked facial asymmetry, broad and prominent nasal bridge, hypertelorism, Brushfield's spots, malformed ears with atresia of the external auditory canal on the right side. Giemsa banding (R and G methods) did not allow a clear cytogenetic identification of the extra-chromosome. A tentative interpretation of the cytogenetic aberration as a trisomy of the proximal part of the long arm of chromosome 13 is discussed.
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Aberraciones Cromosómicas/genética , Cromosomas Humanos 13-15 , Trisomía , Anomalías Múltiples/genética , Aberraciones Cromosómicas/diagnóstico , Trastornos de los Cromosomas , Cromosomas Humanos 21-22 e Y , Oído Externo/anomalías , Femenino , Humanos , Lactante , Discapacidad Intelectual/genética , FenotipoRESUMEN
1. Alkaline phosphatase (AP) present in the liver of Helix nemoralis and of Octopus vulgaris; enzyme was purified by homogenization, ultracentrifugation, n-butanol treatment, acetone fractionation and Sephadex G-200 chromatography. 2. The two enzymes show a similar enzyme-substrate affinity, but differ in several properties (molecular weight, electrophoretic mobility, optimum pH, substrate inhibition); a possible correlation of them with different evolutionary adaptations is suggested. 3. Possible roles of AP in Mollusca are discussed.