49 research outputs found

    Content validity and clinical meaningfulness of the HFMSE in spinal muscular atrophy

    Get PDF
    © The Author(s). 2017 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise statedBACKGROUND: Reports on the clinical meaningfulness of outcome measures in spinal muscular atrophy (SMA) are rare. In this two-part study, our aim was to explore patients' and caregivers' views on the clinical relevance of the Hammersmith Functional Motor Scale Expanded- (HFMSE). METHODS: First, we used focus groups including SMA patients and caregivers to explore their views on the clinical relevance of the individual activities included in the HFMSE. Then we asked caregivers to comment on the clinical relevance of possible changes of HFMSE scores over time. As functional data of individual patients were available, some of the questions were tailored according to their functional level on the HFMSE. RESULTS: Part 1: Sixty-three individuals participated in the focus groups. This included 30 caregivers, 25 patients and 8 professionals who facilitated the discussion. The caregivers provided a comparison to activities of daily living for each of the HFMSE items. Part 2: One hundred and forty-nine caregivers agreed to complete the questionnaire: in response to a general question, 72% of the caregivers would consider taking part in a clinical trial if the treatment was expected to slow down deterioration, 88% if it would stop deterioration and 97% if the treatment was expected to produce an improvement. Caregivers were informed of the first three items that their child could not achieve on the HFMSE. In response 75% indicated a willingness to take part in a clinical trial if they could achieve at least one of these abilities, 89% if they could achieve two, and 100% if they could achieve more than 2. CONCLUSIONS: Our findings support the use of the HFMSE as a key outcome measure in SMA clinical trials because the individual items and the detected changes have clear content validity and clinical meaningfulness for patients and their caregivers.Peer reviewedFinal Published versio

    Developmental milestones in type I spinal muscular atrophy

    Get PDF
    The aim of this retrospective multicentric study was to assess developmental milestones longitudinally in type I SMA infants using the Hammersmith Infant Neurological Examination. Thirty-three type I SMA infants, who classically do not achieve the ability to sit unsupported, were included in the study. Our results confirmed that all patients had a score of 0 out of a scale of 4 on items assessing sitting, rolling, crawling, standing or walking. A score of more than 0 was only achieved in three items: head control (n = 13), kicking (n = 15) and hand grasp (n = 18). In these items, the maximal score achieved was 1 out of a scale of 4, indicating only partial achievement of the milestone. Infants with symptom onset after 6 months of age had longer preservation of a score of 1 when compared to those with onset before 6 months of age. Our results suggest that even when current standards of care are applied, developmental milestones are rarely even partially achieved as part of natural history in type I SMA infants. No infants in this study achieved a major milestone such as rolling over, or sitting independently, which would therefore represent robust outcomes in future interventional trials

    Mediterranean winter rainfall in phase with African monsoons during the past 1.36 million years

    Get PDF
    Mediterranean climates are characterized by strong seasonal contrasts between dry summers and wet winters. Changes in winter rainfall are critical for regional socioeconomic development, but are difficult to simulate accurately1 and reconstruct on Quaternary timescales. This is partly because regional hydroclimate records that cover multiple glacial–interglacial cycles2,3 with different orbital geometries, global ice volume and atmospheric greenhouse gas concentrations are scarce. Moreover, the underlying mechanisms of change and their persistence remain unexplored. Here we show that, over the past 1.36 million years, wet winters in the northcentral Mediterranean tend to occur with high contrasts in local, seasonal insolation and a vigorous African summer monsoon. Our proxy time series from Lake Ohrid on the Balkan Peninsula, together with a 784,000-year transient climate model hindcast, suggest that increased sea surface temperatures amplify local cyclone development and refuel North Atlantic low-pressure systems that enter the Mediterranean during phases of low continental ice volume and high concentrations of atmospheric greenhouse gases. A comparison with modern reanalysis data shows that current drivers of the amount of rainfall in the Mediterranean share some similarities to those that drive the reconstructed increases in precipitation. Our data cover multiple insolation maxima and are therefore an important benchmark for testing climate model performance

    Carriers of ADAMTS13 Rare Variants Are at High Risk of Life-Threatening COVID-19

    Get PDF
    Thrombosis of small and large vessels is reported as a key player in COVID-19 severity. However, host genetic determinants of this susceptibility are still unclear. Congenital Thrombotic Thrombocytopenic Purpura is a severe autosomal recessive disorder characterized by uncleaved ultra-large vWF and thrombotic microangiopathy, frequently triggered by infections. Carriers are reported to be asymptomatic. Exome analysis of about 3000 SARS-CoV-2 infected subjects of different severities, belonging to the GEN-COVID cohort, revealed the specific role of vWF cleaving enzyme ADAMTS13 (A disintegrin-like and metalloprotease with thrombospondin type 1 motif, 13). We report here that ultra-rare variants in a heterozygous state lead to a rare form of COVID-19 characterized by hyper-inflammation signs, which segregates in families as an autosomal dominant disorder conditioned by SARS-CoV-2 infection, sex, and age. This has clinical relevance due to the availability of drugs such as Caplacizumab, which inhibits vWF-platelet interaction, and Crizanlizumab, which, by inhibiting P-selectin binding to its ligands, prevents leukocyte recruitment and platelet aggregation at the site of vascular damage

    Properly discontinuous actions on Hilbert manifolds

    No full text
    In this article we study properly discontinuous actions on Hilbert manifolds giving new examples of complete Hilbert manifolds with nonnegative, respectively nonpositive, sectional curvature with infinite fundamental group. We also get examples of complete infinite dimensional Kähler manifolds with positive holomorphic sectional curvature and infinite fundamental group in contrastwith the finite dimensional case and we classify abelian groups acting linearly, isometrically and properly discontinuously on Stiefel manifolds. Finally, we classify homogeneous Hilbert manifolds with constant sectional curvature45433452CONSELHO NACIONAL DE DESENVOLVIMENTO CIENTÍFICO E TECNOLÓGICO - CNPQFUNDAÇÃO DE AMPARO À PESQUISA DO ESTADO DE SÃO PAULO - FAPESPsem informaçã

    Properly discontinuous actions on Hilbert manifolds

    No full text
    n this article we study properly discontinuous actions on Hilbert manifolds giving new examples of complete Hilbert manifolds with nonnegative, respectively nonpositive, sectional curvature with infinite fundamental group. We also get examples of complete infinite dimensional Kähler manifolds with positive holomorphic sectional curvature and infinite fundamental group in contrastwith the finite dimensional case and we classify abelian groups acting linearly, isometrically and properly discontinuously on Stiefel manifolds. Finally, we classify homogeneous Hilbert manifolds with constant sectional curvature

    Riemannian Hilbert manifolds

    No full text
    In this article we collect results obtained by the authors jointly with other authors and we discuss old and new ideas. In particular we discuss singularities of the exponential map, completeness and homogeneity for Riemannian Hilbert quotient manifolds. We also extend a Theorem due to Nomizu and Ozeki to infinite dimensional Riemannian Hilbert manifolds

    A note on tensor fields in Hilbert spaces

    No full text
    We discuss and extend to infinite dimensional Hilbert spaces a well-known tensoriality criterion for linear endomorphisms of the space of smooth vector fields in <IMG SRC="http:/img/fbpe/aabc/v74n2/m1img2.gif">n.<br>Discutimos e estendemos para espaços de Hilbert um critério de tensorialidade para endomorfismos do espaço dos campos vetoriais em Rpot(n)
    corecore