Olsalazine, consisting of two salicylate radicals linked by an azo-bond, is effective in the treatment of active ulcerative colitis. To test its effect in patients with mild to moderate attacks of Crohn's disease, the International Organization for the Study of Inflammatory Bowel Disease (IOIBD) des
Randomized, placebo-controlled, double-blind pilot trial of ramipril in McArdle's disease
✍ Scribed by Andrea Martinuzzi; Alexandra Liava; Enrico Trevisi; Mara Frare; Caterina Tonon; Emil Malucelli; David Manners; Graham J. Kemp; Claudia Testa; Bruno Barbiroli; Raffaele Lodi
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 182 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0148-639X
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✦ Synopsis
Abstract
McArdle's disease causes limitation in exercise capacity as well as disability, the severity of which has been associated with the angiotensin‐converting enzyme (ACE) insertion (I)/deletion (D) haplotype—patients with the genotype associated with higher ACE activity show the most severe phenotype. Modulation of ACE activity through the use of inhibitors may thus positively affect disease expression. In a double‐blind, randomized, placebo‐controlled trial, we assessed the efficacy of an ACE inhibitor (2.5 mg ramipril) in 8 patients with McArdle's disease. End‐points were changes in parameters of exercise physiology (cycloergometer and muscle ^31^P‐magnetic resonance spectroscopy), quality of life (QoL) according to the Short Form 36 (SF‐36), and disability according to the World Health Organization–Disability Assessment Scale II (WHO‐DAS II). Patients had lower QoL and higher disability than controls. Measures of exercise physiology were not changed by ramipril in the whole group, but treatment induced higher peak VO~2~ (P = 0.017) in ACE D/D patients, yet not in I/D patients. Treatment significantly improved disability (P < 0.05). McArdle's disease is a disabling condition affecting patients' QoL. Treatment with ramipril improves disability and modifies exercise physiology only in D/D patients, raising the possibility of a differential haplotype‐linked sensitivity to the treatment. Muscle Nerve, 2008
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