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  • 1
    Online-Ressource
    Online-Ressource
    Georg Thieme Verlag KG ; 2022
    In:  Journal of Pediatric Neurology Vol. 20, No. 04 ( 2022-08), p. 252-257
    In: Journal of Pediatric Neurology, Georg Thieme Verlag KG, Vol. 20, No. 04 ( 2022-08), p. 252-257
    Kurzfassung: Nusinersen is the first disease-modifying therapy for spinal muscular atrophy (SMA), but there are few data on potential long-term endocrinological and metabolic systemic effects of this novel treatment as well as metabolic alterations in SMA itself. In this retrospective and multicentric study, we analyzed anthropometric, endocrinological, and motor function data of 81 pediatric and adult patients with SMA1 to 3 undergoing treatment with nusinersen. In 39 patients (51%), we observed a slight increase in body mass index (BMI) centiles under treatment with nusinersen, especially in patients with SMA2 and in pediatric patients between 3.1 and 12 years. A correlation to the SMN2 copy number or motor function was not found. Additionally, length centiles decreased significantly under treatment. The results of longitudinal endocrinological assessments were interpreted as not clinically significant in most patients; in three patients, the signs of an altered glucose metabolism were present. Our study indicates a putative effect of treatment with nusinersen on BMI, which might be due to a conjoint effect of weight gain and reduction of height velocity, without evidence of correlation to increased muscle function. Further studies need to address specific effects of targeted therapies such as nusinersen or onasemnogene abeparvovec on body composition including fat and muscle mass.
    Materialart: Online-Ressource
    ISSN: 1304-2580 , 1875-9041
    Sprache: Englisch
    Verlag: Georg Thieme Verlag KG
    Publikationsdatum: 2022
    ZDB Id: 2130673-4
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 2
    Online-Ressource
    Online-Ressource
    Georg Thieme Verlag KG ; 1988
    In:  Thrombosis and Haemostasis Vol. 59, No. 01 ( 1988), p. 101-106
    In: Thrombosis and Haemostasis, Georg Thieme Verlag KG, Vol. 59, No. 01 ( 1988), p. 101-106
    Kurzfassung: An enzyme-linked immunosorbent assay (ELISA) was developed for the determination of thrombin-antithrombin III complex (TAT) in human plasma. The test system follows the sandwich principle and uses two different antibodies directed against human thrombin and human antithrombin III, respectively. The antibodies bind selectively to the corresponding antigen moieties of TAT. The assay was calibrated with definite concentrations of preformed purified TAT added to TAT-poor plasma. The lower limit of sensitivity of the assay was 0.5 μg/1. Mean coefficients of variation of 4.2% (intraassay) and 3.5% (interassay) were found for TAT concentrations between 2 and 60 μg/1. A reference range from 0.85 to 3.2 μg/1 was calculated from TAT concentration in plasma samples from 88 healthy donors (mean value ± SD: 1.45 ± 0.4 μg/I). In plasma samples from patients with pulmonary embolism (n = 17), TAT concentrations between 3 and 25 μg/1 were measured. In 15 patients with deep vein thrombosis, TAT was found up to 3 to 25 μg/1. From these data we conclude that measurement of TAT can be a sensitive parameter for specific detection of a latent activation of the clotting pathway.
    Materialart: Online-Ressource
    ISSN: 0340-6245 , 2567-689X
    Sprache: Englisch
    Verlag: Georg Thieme Verlag KG
    Publikationsdatum: 1988
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 3
    Online-Ressource
    Online-Ressource
    Georg Thieme Verlag KG ; 2014
    In:  Planta Medica Vol. 80, No. 18 ( 2014-11-5), p. 1739-1745
    In: Planta Medica, Georg Thieme Verlag KG, Vol. 80, No. 18 ( 2014-11-5), p. 1739-1745
    Materialart: Online-Ressource
    ISSN: 0032-0943 , 1439-0221
    URL: Issue
    Sprache: Englisch
    Verlag: Georg Thieme Verlag KG
    Publikationsdatum: 2014
    ZDB Id: 2037089-1
    SSG: 15,3
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 4
    Online-Ressource
    Online-Ressource
    Georg Thieme Verlag KG ; 1991
    In:  Thrombosis and Haemostasis Vol. 65, No. 02 ( 1991), p. 153-159
    In: Thrombosis and Haemostasis, Georg Thieme Verlag KG, Vol. 65, No. 02 ( 1991), p. 153-159
    Kurzfassung: The present investigation describes a novel approach to prepare a specific antibody against prothrombin activation fragment 1+2 (F 1+2). The antibody discriminates between native prothrombin and F 1+2 in plasma. A synthetic peptide from the negatively charged region of F 1+2, which becomes the carboxyterminal sequence after cleavage of prothrombin by factor Xa, was used for immunization of rabbits. Obtained antiserum was immunopurified and an enzyme-linked immunosorbent assay (ELISA) was constructed for determination of F 1+2. The test system follows the sandwich principle and uses two different antibodies directed against F 1+2 and prothrombin, respectively. The ELISA was calibrated with purified F 1+2 added to F 1+2-poor plasma. The lower limit of sensitivity of the assay was 0.02 nmol/1. Coefficients of variation of 6.9 to 10.4% (intraassay) and 6.7 to 11% (interassay) were found for F 1+2 concentrations between 0.08 and 4.9 nmol/1. A reference range from 0.32 to 1.2 nmol/l was calculated from 95 healthy donors (mean value ± SD: 0.67 ± 0.19 nmol/l). In patients with deep vein thrombosis (n = 7) confirmed by phlebography and in patients with pulmonary embolism (n = 8) confirmed by lung scan, F 1+2levels were found up to 1.5 to 9.5 nmol/l. In plasma samples of patients under oral anticoagulant therapy in the stable state F 1+2 concentrations were found to be in the range of 0.08 to 0.5 nmol/l. The results indicate that the antibody is specific and highly sensitive for quantification of F 1+2 in plasma. It can be supposed that the ELISA we have developed is a valuable tool for detection of both hypercoagulable as well as hypocoagulable states.
    Materialart: Online-Ressource
    ISSN: 0340-6245 , 2567-689X
    Sprache: Englisch
    Verlag: Georg Thieme Verlag KG
    Publikationsdatum: 1991
    Standort Signatur Einschränkungen Verfügbarkeit
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