Literature DB >> 16786213

Cardiac involvement in limb-girdle muscular dystrophy 2I : conventional cardiac diagnostic and cardiovascular magnetic resonance.

C Gaul1, M Deschauer, C Tempelmann, S Vielhaber, H U Klein, H J Heinze, S Zierz, F Grothues.   

Abstract

BACKGROUND: The C826A mutation in the fukutin-related protein (FKRP) gene is typically associated with autosomal recessive limb-girdle muscular dystrophy 2I (LGMD2I) but oligosymptomatic phenotypes and patients with predominant cardiac involvement are also described.
OBJECTIVE: To assess cardiac involvement in patients with LGMD2I. PATIENTS: Nine patients from 5 families (2 female, 7 male) homozygous for the 826C > A FKRP mutation were included.
METHODS: Additional to conventional cardiac investigations (electrocardiography and echocardiography) the patients underwent cardiovascular magnetic resonance imaging (CMR). RESULTS/
CONCLUSION: Cardiac involvement was detected by CMR in eight of nine patients (reduced left ventricular ejection fraction in 6, enlargement of left ventricular end-diastolic volume in 2 and left ventricular mass in 2) and in four patients by conventional cardiac diagnostic investigations. Two of the nine patients showed no muscle weakness or atrophy but suffered myalgias; both had cardiac manifestation of the disease. CMR is a sensitive method for detecting cardiac abnormalities in patients with LGMD2I and can be used for early detection of mild or subclinical cardiac involvement.

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Year:  2006        PMID: 16786213     DOI: 10.1007/s00415-006-0213-0

Source DB:  PubMed          Journal:  J Neurol        ISSN: 0340-5354            Impact factor:   4.849


  14 in total

1.  Quantification of right and left ventricular function by cardiovascular magnetic resonance.

Authors:  N G Bellenger; F Grothues; G C Smith; D J Pennell
Journal:  Herz       Date:  2000-06       Impact factor: 1.443

2.  FKRP (826C>A) frequently causes limb-girdle muscular dystrophy in German patients.

Authors:  M C Walter; J A Petersen; R Stucka; D Fischer; R Schröder; M Vorgerd; A Schroers; H Schreiber; C O Hanemann; U Knirsch; A Rosenbohm; A Huebner; N Barisic; R Horvath; S Komoly; P Reilich; W Müller-Felber; D Pongratz; J S Müller; E A Auerswald; H Lochmüller
Journal:  J Med Genet       Date:  2004-04       Impact factor: 6.318

3.  Dilated cardiomyopathy may be an early sign of the C826A Fukutin-related protein mutation.

Authors:  T Müller; M Krasnianski; R Witthaut; M Deschauer; S Zierz
Journal:  Neuromuscul Disord       Date:  2005-05       Impact factor: 4.296

4.  Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1C.

Authors:  M Brockington; Y Yuva; P Prandini; S C Brown; S Torelli; M A Benson; R Herrmann; L V Anderson; R Bashir; J M Burgunder; S Fallet; N Romero; M Fardeau; V Straub; G Storey; C Pollitt; I Richard; C A Sewry; K Bushby; T Voit; D J Blake; F Muntoni
Journal:  Hum Mol Genet       Date:  2001-12-01       Impact factor: 6.150

Review 5.  Defective glycosylation in muscular dystrophy.

Authors:  Francesco Muntoni; Martin Brockington; Derek J Blake; Silvia Torelli; Susan C Brown
Journal:  Lancet       Date:  2002-11-02       Impact factor: 79.321

6.  Cardiac and respiratory failure in limb-girdle muscular dystrophy 2I.

Authors:  Maja Poppe; John Bourke; Michelle Eagle; Patrick Frosk; Klaus Wrogemann; Cheryl Greenberg; Francesco Muntoni; Thomas Voit; Volker Straub; David Hilton-Jones; Cheerag Shirodaria; Kate Bushby
Journal:  Ann Neurol       Date:  2004-11       Impact factor: 10.422

Review 7.  Cardiac involvement in primary myopathies.

Authors:  J Finsterer; C Stöllberger
Journal:  Cardiology       Date:  2000       Impact factor: 1.869

8.  Assessment of mitral annulus velocity by Doppler tissue imaging in the evaluation of left ventricular diastolic function.

Authors:  D W Sohn; I H Chai; D J Lee; H C Kim; H S Kim; B H Oh; M M Lee; Y B Park; Y S Choi; J D Seo; Y W Lee
Journal:  J Am Coll Cardiol       Date:  1997-08       Impact factor: 24.094

9.  Estimation of human myocardial mass with MR imaging.

Authors:  J Katz; M C Milliken; J Stray-Gundersen; L M Buja; R W Parkey; J H Mitchell; R M Peshock
Journal:  Radiology       Date:  1988-11       Impact factor: 11.105

10.  Asymptomatic carriers for homozygous novel mutations in the FKRP gene: the other end of the spectrum.

Authors:  Flavia de Paula; Natássia Vieira; Alessandra Starling; Lydia Uraco Yamamoto; Bruno Lima; Rita de Cássia Pavanello; Mariz Vainzof; Vincenzo Nigro; Mayana Zatz
Journal:  Eur J Hum Genet       Date:  2003-12       Impact factor: 4.246

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  14 in total

1.  AAV-mediated transfer of FKRP shows therapeutic efficacy in a murine model but requires control of gene expression.

Authors:  Evelyne Gicquel; Natacha Maizonnier; Steven J Foltz; William J Martin; Nathalie Bourg; Fedor Svinartchouk; Karine Charton; Aaron M Beedle; Isabelle Richard
Journal:  Hum Mol Genet       Date:  2017-05-15       Impact factor: 6.150

2.  Post-Natal knockdown of fukutin-related protein expression in muscle by long-termRNA interference induces dystrophic pathology [corrected].

Authors:  Chi-Hsien Wang; Yiumo Michael Chan; Ru-Hang Tang; Bin Xiao; Peijuan Lu; Elizabeth Keramaris-Vrantsis; Hui Zheng; Chunping Qiao; Jiangang Jiang; Juan Li; Hsin-I Ma; Qilong Lu; Xiao Xiao
Journal:  Am J Pathol       Date:  2010-12-23       Impact factor: 4.307

Review 3.  Cardiac involvement in patients with muscular dystrophies: magnetic resonance imaging phenotype and genotypic considerations.

Authors:  David Verhaert; Kathryn Richards; Jill A Rafael-Fortney; Subha V Raman
Journal:  Circ Cardiovasc Imaging       Date:  2011-01       Impact factor: 7.792

Review 4.  Neuromuscular diseases and their cardiac manifestations under the spectrum of cardiovascular imaging.

Authors:  Georgios M Alexandridis; Efstathios D Pagourelias; Nikolaos Fragakis; Maria Kyriazi; Efthymia Vargiami; Dimitrios Zafeiriou; Vassilios P Vassilikos
Journal:  Heart Fail Rev       Date:  2022-07-20       Impact factor: 4.654

5.  Cardiac pathology exceeds skeletal muscle pathology in two cases of limb-girdle muscular dystrophy type 2I.

Authors:  Marta Margeta; Anne M Connolly; Thomas L Winder; Alan Pestronk; Steven A Moore
Journal:  Muscle Nerve       Date:  2009-11       Impact factor: 3.217

6.  Further evidence of Fukutin mutations as a cause of childhood onset limb-girdle muscular dystrophy without mental retardation.

Authors:  Rebecca L Puckett; Steven A Moore; Thomas L Winder; Tobias Willer; Stephen G Romansky; Kelly King Covault; Kevin P Campbell; Jose E Abdenur
Journal:  Neuromuscul Disord       Date:  2009-04-01       Impact factor: 4.296

Review 7.  Therapeutic possibilities in the autosomal recessive limb-girdle muscular dystrophies.

Authors:  Volker Straub; Kate Bushby
Journal:  Neurotherapeutics       Date:  2008-10       Impact factor: 7.620

8.  Respiratory and cardiac function in congenital muscular dystrophies with alpha dystroglycan deficiency.

Authors:  M Pane; S Messina; G Vasco; A R Foley; L Morandi; E Pegoraro; T Mongini; A D'Amico; F Bianco; M E Lombardo; R Scalise; C Bruno; A Berardinelli; A Pini; I Moroni; M Mora; A Toscano; M Moggio; G Comi; F M Santorelli; E Bertini; F Muntoni; E Mercuri
Journal:  Neuromuscul Disord       Date:  2012-06-22       Impact factor: 4.296

9.  Cardiovascular magnetic resonance of cardiomyopathy in limb girdle muscular dystrophy 2B and 2I.

Authors:  Xiomara Q Rosales; Sean J Moser; Tam Tran; Beth McCarthy; Nicholas Dunn; Philip Habib; Orlando P Simonetti; Jerry R Mendell; Subha V Raman
Journal:  J Cardiovasc Magn Reson       Date:  2011-08-04       Impact factor: 5.364

10.  Zebrafish models for human FKRP muscular dystrophies.

Authors:  Genri Kawahara; Jeffrey R Guyon; Yukio Nakamura; Louis M Kunkel
Journal:  Hum Mol Genet       Date:  2009-12-01       Impact factor: 6.150

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