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      Cardiac involvement of the systemic disorder myotonic dystrophy type II - detection by CMR

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      1 , , 1 , 2 , 1 , 1 , 3 , 2 , 1
      Journal of Cardiovascular Magnetic Resonance
      BioMed Central
      17th Annual SCMR Scientific Sessions
      16-19 January 2014

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          Abstract

          Background Myotonic dystrophy type II (formerly denoted as proximal myotonic myopathy (PROMM)) is an autosomal dominantly inherited disease [1]. Sufferers are afflicted with skeletal muscle (SM) symptoms. Histopathologic changes of the SM include mild fibrosis and fatty degeneration[2]. The multisystemic disorder is also characterized by endocrine and metabolism disorder such as hypercholesterolemia and diabetes mellitus type II as well as cardiac arrhythmias [1]. The aim of this study is to evaluate myocardial structural abnormalities in preserved ejection fraction (EF). Methods We prospectively enrolled 28 subjects (age 53.1 ± 10.7 y, 20 women) with a genetically confirmed diagnosis of PROMM. The criteria for exclusion were known cardiac diseases and contraindication for CMR. We assessed biplanar left-ventricular (LV) volumes, mass and function applying cine imaging (TR 247.42 ms, TE 1.14 ms, FOV 340 ms, matrix 192×192, slice thickness 6 mm) using a 1.5 T Scanner (Avanto, Siemens Healthcare, Germany, 12 channel surface coil). Late enhancement imaging (LGE) (GRE, TR 800 ms, TE 5.02 ms, FOV 350 ms, matrix 256×256, slice thickness 7 mm) was performed to detect myocardial fibrosis about 10 minutes after injection of gadoteridol (0.2 mmol/kgbw). Furthermore, we used a previously described fat/water sequence[3] (multi-echo GRE, 4-echos, TE 1.53-8.42 ms, FOV 360 mm, matrix 256×256, slice thickness 6 mm) to identify myocardial fat deposits. Data were analyzed using cvi42 (circle cardiovascular imaging Inc., Canada). Results 24 data sets were completed (age 53.8 ± 10.9 y, EF 65.2 ± 5.8%, 17 women). All applied sequences were evaluable besides 3 fat/water images due to artifacts. None of the patients had wall motion abnormalities. Myocardial fibrosis were noticeable in 5 of the 24 subjects (2 women). No significant differences of age (p = 0.24) and LVEF (p = 0.09) were found between positive and negative LGE (Figure 1). These fibrous changes were mostly localized subepicardial inferolateral basal. No fat deposit was found in this region (Figure 1). Interestingly, small myocardial fat deposits were identified in the apical portion of the interventricular septum in 2 patients (Figure 2). Figure 1 (A) Detected subepicardial LGE (arrows) in a patient with PROMM. (B) Comparison of LGE positive to negative subjects. BMI: Body mass index, EF: ejection fraction, LV-EDV-Index: left-ventricular-enddiastolic volume-index. Figure 2 (A) Indicated fat deposit (arrows) in a patient with PROMM. The view shows both the water and the fat-seperated image. (B) Comparison of the subjects who have fat deposits with those who have no detected myocardial fat. BMI: Body mass index, EF: ejection fraction, LV-EDV-Index: left-ventricular-enddiastolic volume-index. Conclusions To the best of our knowledge this is the first systematic CMR study in patients with PROMM. Although all patients had preserved LVEF we could detect myocardial fibrosis in one fifth of all patients, suggesting CMR is feasible to detect such subclinical myocardial manifestations. Interestingly, we could also detect fat deposits. Further studies to look for diffuse alterations and correlations to clinical events should come next. Funding University funding hold by Schulz-Menger, J.

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          Myotonic dystrophy type 2: molecular, diagnostic and clinical spectrum.

          Myotonic dystrophy types 1 (DM1) and 2 (DM2/proximal myotonic myopathy PROMM) are dominantly inherited disorders with unusual multisystemic clinical features. The authors have characterized the clinical and molecular features of DM2/PROMM, which is caused by a CCTG repeat expansion in intron 1 of the zinc finger protein 9 (ZNF9) gene. Three-hundred and seventy-nine individuals from 133 DM2/PROMM families were evaluated genetically, and in 234 individuals clinical and molecular features were compared. Among affected individuals 90% had electrical myotonia, 82% weakness, 61% cataracts, 23% diabetes, and 19% cardiac involvement. Because of the repeat tract's unprecedented size (mean approximately 5,000 CCTGs) and somatic instability, expansions were detectable by Southern analysis in only 80% of known carriers. The authors developed a repeat assay that increased the molecular detection rate to 99%. Only 30% of the positive samples had single sizeable expansions by Southern analysis, and 70% showed multiple bands or smears. Among the 101 individuals with single expansions, repeat size did not correlate with age at disease onset. Affected offspring had markedly shorter expansions than their affected parents, with a mean size difference of -17 kb (-4,250 CCTGs). DM2 is present in a large number of families of northern European ancestry. Clinically, DM2 resembles adult-onset DM1, with myotonia, muscular dystrophy, cataracts, diabetes, testicular failure, hypogammaglobulinemia, and cardiac conduction defects. An important distinction is the lack of a congenital form of DM2. The clinical and molecular parallels between DM1 and DM2 indicate that the multisystemic features common to both diseases are caused by CUG or CCUG expansions expressed at the RNA level.
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            Myocardial Fat Imaging

            The presence of intramyocardial fat may form a substrate for arrhythmias, and fibrofatty infiltration of the myocardium has been shown to be associated with sudden death. Therefore, noninvasive detection could have high prognostic value. Fat-water–separated imaging in the heart by MRI is a sensitive means of detecting intramyocardial fat and characterizing fibrofatty infiltration. It is also useful in characterizing fatty tumors and delineating epicardial and/or pericardial fat. Multi-echo methods for fat and water separation provide a sensitive means of detecting small concentrations of fat with positive contrast and have a number of advantages over conventional chemical-shift fat suppression. Furthermore, fat and water–separated imaging is useful in resolving artifacts that may arise due to the presence of fat. Examples of fat-water–separated imaging of the heart are presented for patients with ischemic and nonischemic cardiomyopathies, as well as general tissue classification.
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              Muscle pathology in 57 patients with myotonic dystrophy type 2.

              We evaluated muscle biopsies from 57 patients with genetically confirmed myotonic dystrophy type 2/proximal myotonic myopathy (DM2/PROMM). Light microscopy showed myopathic together with "denervation-like" changes in almost all biopsies obtained from four different muscles: increased fiber size variation, internal nuclei, small angulated fibers, pyknotic nuclear clumps, and predominant type 2 fiber atrophy. Quantitative morphometry in 18 biopsies that were immunostained for myosin heavy chain confirmed a predominance of nonselective type 2 fiber atrophy. These histological changes were similar in all patients regardless of the site of biopsy, the predominant clinical symptoms and signs, and the clinical course. It is likely that, in a number of undiagnosed patients, DM2 is the underlying disorder. With a better understanding of the histopathological pattern in DM2, biopsies from patients with undiagnosed neuromuscular disorders can now be reevaluated.
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                Author and article information

                Conference
                J Cardiovasc Magn Reson
                J Cardiovasc Magn Reson
                Journal of Cardiovascular Magnetic Resonance
                BioMed Central
                1097-6647
                1532-429X
                2014
                16 January 2014
                : 16
                : Suppl 1
                : P390
                Affiliations
                [1 ]Working Group on Cardiovascular Magnetic Resonance, Experimental and Clinical Research Center a joint cooperation between the Charité Medical Faculty and the Max-Delbrueck Center for Molecular Medicine HELIOS Klinikum Berlin Buch, Department of Cardiology and Nephrology, Berlin, Germany
                [2 ]Muscle Research Unit, Experimental and Clinical Research Center a joint cooperation between the Charité Medical Faculty and the Max-Delbrueck Center for Molecular Medicine, Berlin, Germany
                [3 ]Laboratory of Cardiac Energetics, National Institutes of Health/NHLBI, Bethesda, Maryland, USA
                Article
                1532-429X-16-S1-P390
                10.1186/1532-429X-16-S1-P390
                4045020
                9c5cca52-88c7-4a54-a852-9f6e5e8325e4
                Copyright © 2014 Grosse et al.; licensee BioMed Central Ltd.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. 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 stated.

                17th Annual SCMR Scientific Sessions
                New Orleans, LA, USA
                16-19 January 2014
                History
                Categories
                Poster Presentation

                Cardiovascular Medicine
                Cardiovascular Medicine

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