Literature DB >> 24618072

Gender difference in limb-girdle muscular dystrophy: a muscle fiber morphometric study in 101 patients.

Marina Fanin, Anna C Nascimbeni, Corrado Angelini.   

Abstract

AIMS: Limb girdle muscular dystrophies (LGMD), a genetically and clinically heterogeneous group of neuromuscular disorders, may show gender differences in the disease severity. We aimed to measure the extent of muscle fiber atrophy and evaluate possible gender differences at fiber level.
METHODS: We conducted a thorough morphometric analysis of muscle fiber size and fiber area in 101 muscles from patients with various forms of LGMD (43 LGMD2A, 30 LGMD2B, 21 LGMD2C-2D-2E, 7 LGMD1C) and 12 normal controls.
RESULTS: Reduced fiber size (atrophy) was pronounced in LGMD2A and LGMD2B, while LGMD1C showed a significant fiber hypertrophy. When we compared LGMD patients and controls of the same gender, males with LGMD2A and LGMD2B showed significantly higher fiber atrophy than control males, whereas female LGMD patients had similar values to female controls, suggesting a gender difference in muscle fiber atrophy. DISCUSSION: Less recovery to disuse atrophy in men than in women has been attributed to the possibility that in women a smaller initial muscle size associated to endocrine factors could attenuate gender-specific muscle loss. The possibility that males with LGMD may be clinically more severely affected than females has been explored, but the mechanism remains elusive.

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Mesh:

Year:  2014        PMID: 24618072     DOI: 10.5414/NP300728

Source DB:  PubMed          Journal:  Clin Neuropathol        ISSN: 0722-5091            Impact factor:   1.368


  11 in total

1.  European muscle MRI study in limb girdle muscular dystrophy type R1/2A (LGMDR1/LGMD2A).

Authors:  Andrea Barp; Pascal Laforet; Luca Bello; Giorgio Tasca; John Vissing; Mauro Monforte; Enzo Ricci; Ariane Choumert; Tanya Stojkovic; Edoardo Malfatti; Elena Pegoraro; Claudio Semplicini; Roberto Stramare; Olivier Scheidegger; Jana Haberlova; Volker Straub; Chiara Marini-Bettolo; Nicoline Løkken; Jordi Diaz-Manera; Jon A Urtizberea; Eugenio Mercuri; Martin Kynčl; Maggie C Walter; Robert Y Carlier
Journal:  J Neurol       Date:  2019-09-25       Impact factor: 4.849

2.  Neuromuscular disease. Diagnosis and discovery in limb-girdle muscular dystrophy.

Authors:  Corrado Angelini
Journal:  Nat Rev Neurol       Date:  2015-12-16       Impact factor: 42.937

Review 3.  Spinal muscular atrophy: Broad disease spectrum and sex-specific phenotypes.

Authors:  Natalia N Singh; Shaine Hoffman; Prabhakara P Reddi; Ravindra N Singh
Journal:  Biochim Biophys Acta Mol Basis Dis       Date:  2021-01-05       Impact factor: 5.187

Review 4.  Promising Perspective to Facioscapulohumeral Muscular Dystrophy Treatment: Nutraceuticals and Phytochemicals.

Authors:  Ceren Hangül; Sibel Berker Karaüzüm; Esra Küpeli Akkol; Devrim Demir-Dora; Zafer Çetin; Eyüp İlker Saygılı; Gökhan Evcili; Eduardo Sobarzo-Sánchez
Journal:  Curr Neuropharmacol       Date:  2021       Impact factor: 7.708

Review 5.  Muscle fatigue, nNOS and muscle fiber atrophy in limb girdle muscular dystrophy.

Authors:  Corrado Angelini; Elisabetta Tasca; Anna Chiara Nascimbeni; Marina Fanin
Journal:  Acta Myol       Date:  2014-12

6.  Natural history of LGMD2A for delineating outcome measures in clinical trials.

Authors:  Isabelle Richard; Jean-Yves Hogrel; Daniel Stockholm; Christine A M Payan; Françoise Fougerousse; Bruno Eymard; Claude Mignard; Adolfo Lopez de Munain; Michel Fardeau; Jon Andoni Urtizberea
Journal:  Ann Clin Transl Neurol       Date:  2016-03-04       Impact factor: 4.511

7.  Childhood Pompe disease: clinical spectrum and genotype in 31 patients.

Authors:  C I van Capelle; J C van der Meijden; J M P van den Hout; J Jaeken; M Baethmann; T Voit; M A Kroos; T G J Derks; M E Rubio-Gozalbo; M A Willemsen; R H Lachmann; E Mengel; H Michelakakis; J C de Jongste; A J J Reuser; A T van der Ploeg
Journal:  Orphanet J Rare Dis       Date:  2016-05-18       Impact factor: 4.123

8.  Effects of metformin on congenital muscular dystrophy type 1A disease progression in mice: a gender impact study.

Authors:  Cibely C Fontes-Oliveira; Bernardo M Soares Oliveira; Zandra Körner; Vahid M Harandi; Madeleine Durbeej
Journal:  Sci Rep       Date:  2018-11-02       Impact factor: 4.379

9.  Mitochondrial aberrations during the progression of disuse atrophy differentially affect male and female mice.

Authors:  Megan E Rosa-Caldwell; Seongkyun Lim; Wesley S Haynie; Jacob L Brown; David E Lee; Kirsten R Dunlap; Lisa T Jansen; Tyrone A Washington; Michael P Wiggs; Nicholas P Greene
Journal:  J Cachexia Sarcopenia Muscle       Date:  2021-09-29       Impact factor: 12.910

10.  Cross-Sectional Transcriptional Analysis of the Aging Murine Heart.

Authors:  Matthew Greenig; Andrew Melville; Derek Huntley; Mark Isalan; Michal Mielcarek
Journal:  Front Mol Biosci       Date:  2020-09-25
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