Literature DB >> 16164199

Abnormal sympathetic innervation of the heart in a patient with Emery-Dreifuss muscular dystrophy.

Takashi Fujiita1, Masami Shimizu, Bunji Kaku, Hounin Kanaya, Yuki Horita, Yoshihide Uno, Tsukasa Yamazaki, Takio Ohka, Kenji Sakata, Hiroshi Mabuchi.   

Abstract

A 33-year-old man was admitted for general malaise and vomiting. An electrocardiogram showed a complete atrioventricular block and an echocardiogram showed right atrial dilatation and normal wall motion of left ventricle (LV). Gene analysis showed nonsense mutation in the STA gene, which codes for emerin, and Emery-Dreifuss muscular dystrophy was diagnosed. An endomyocardial biopsy of right ventricle showed mild hypertrophy of myocytes. Myocardial scintigraphic studies with Tc-99m methoxyisobutylisonitrile (MIBI) and I-123-betamethyl-p-iodophenylpentadecanoic acid (BMIPP) scintigrams showed no abnormalities. In contrast, I-123 metaiodobenzylguanidine (MIBG) scintigrams showed a diffuse and severe decrease in accumulation of MIBG in the heart. Six months later, his LV wall motion on echocardiograms developed diffuse hypokinesis. These results suggest that the abnormality on I-123 MIBG myocardial scintigrams may predict LV dysfunction in Emery-Dreifuss muscular dystrophy.

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Year:  2005        PMID: 16164199     DOI: 10.1007/bf03027407

Source DB:  PubMed          Journal:  Ann Nucl Med        ISSN: 0914-7187            Impact factor:   2.668


  2 in total

Review 1.  Autonomic dysfunction in muscular dystrophy: a theoretical framework for muscle reflex involvement.

Authors:  Scott A Smith; Ryan M Downey; Jon W Williamson; Masaki Mizuno
Journal:  Front Physiol       Date:  2014-02-18       Impact factor: 4.566

2.  Autonomic regulation in muscular dystrophy.

Authors:  Corrado Angelini; Rita Di Leo; Paola Cudia
Journal:  Front Physiol       Date:  2013-09-20       Impact factor: 4.566

  2 in total

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