Literature DB >> 3281058

Effect of chronic treatment with the calcium antagonist diltiazem in Duchenne muscular dystrophy.

T E Bertorini1, G M Palmieri, J W Griffin, M Igarashi, J McGee, R Brown, D F Nutting, A B Hinton, J G Karas.   

Abstract

We conducted a double-blind trial with the calcium antagonist, diltiazem (8 mg/kg/d), for 24 to 32 months in 22 boys with Duchenne muscular dystrophy, who were paired by functional activity and age. No adverse clinical or ECG effects of diltiazem were detected. In eight matched pairs, completing 28 months, manual muscle testing scores fell somewhat less in the diltiazem group (from 5.5 to 4.6) than in the placebo group (from 5.3 to 4.2), although the difference between groups was not significant (p = 0.06). The 95% confidence interval for the difference in slopes of regression lines obtained from trimonthly manual muscle tests on all subjects was markedly asymmetric in favor of the diltiazem group, but this difference was also not significant. There was less deterioration of functional activity of lower extremities in the diltiazem-treated group, when beginning and end values were analyzed (p = 0.03). However, the difference in slopes of regression lines obtained from trimonthly determinations was nonsignificant. Similarly, the beginning versus end comparisons of systolic and diastolic blood pressure showed a significantly (p less than 0.05) smaller elevation of blood pressure in the diltiazem-treated group, but no difference was observed when the slopes of all values were analyzed. All other clinical and laboratory variables were unaffected by diltiazem treatment. The findings in manual muscle tests and functional activity suggest a beneficial trend with chronic diltiazem treatment in DMD.

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Year:  1988        PMID: 3281058     DOI: 10.1212/wnl.38.4.609

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  7 in total

1.  Overexpression of SERCA1a in the mdx diaphragm reduces susceptibility to contraction-induced damage.

Authors:  Kevin J Morine; Meg M Sleeper; Elisabeth R Barton; H Lee Sweeney
Journal:  Hum Gene Ther       Date:  2010-12       Impact factor: 5.695

2.  The heart in muscular dystrophy: an electrocardiographic and ultrasound study of 20 patients.

Authors:  P Berlit; B Stegaru-Hellring
Journal:  Eur Arch Psychiatry Clin Neurosci       Date:  1991       Impact factor: 5.270

3.  Modulation by prednisolone of calcium handling in skeletal muscle cells.

Authors:  L Metzinger; A C Passaquin; W J Leijendekker; P Poindron; U T Rüegg
Journal:  Br J Pharmacol       Date:  1995-12       Impact factor: 8.739

4.  Dihydropyridine receptors in transverse tubules from normal and dystrophic chicken skeletal muscle.

Authors:  G Moro; A Saborido; J Delgado; F Molano; A Megias
Journal:  J Muscle Res Cell Motil       Date:  1995-10       Impact factor: 2.698

5.  Duchenne Muscular Dystrophy.

Authors:  Susan T. Iannaccone; Zohair Nanjiani
Journal:  Curr Treat Options Neurol       Date:  2001-03       Impact factor: 3.972

6.  Long-term blocking of calcium channels in mdx mice results in differential effects on heart and skeletal muscle.

Authors:  Louise H Jørgensen; Alison Blain; Elizabeth Greally; Steve H Laval; Andrew M Blamire; Benjamin J Davison; Heinrich Brinkmeier; Guy A MacGowan; Henrik D Schrøder; Kate Bushby; Volker Straub; Hanns Lochmüller
Journal:  Am J Pathol       Date:  2010-12-23       Impact factor: 4.307

Review 7.  Genetic evidence in the mouse solidifies the calcium hypothesis of myofiber death in muscular dystrophy.

Authors:  A R Burr; J D Molkentin
Journal:  Cell Death Differ       Date:  2015-06-19       Impact factor: 15.828

  7 in total

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