Title |
Genetic determinants of statin intolerance
|
---|---|
Published in |
Lipids in Health and Disease, March 2007
|
DOI | 10.1186/1476-511x-6-7 |
Pubmed ID | |
Authors |
Jisun Oh, Matthew R Ban, Brooke A Miskie, Rebecca L Pollex, Robert A Hegele |
Abstract |
Statin-related skeletal muscle disorders range from benign myalgias--such as non-specific muscle aches or joint pains without elevated serum creatinine kinase (CK) concentration--to true myositis with >10-fold elevation of serum CK, to rhabdomyolysis and myoglobinuria. The genetic basis of statin-related muscle disorders is largely unknown. Because mutations in the COQ2 gene are associated with severe inherited myopathy, we hypothesized that common, mild genetic variation in COQ2 would be associated with inter-individual variation in statin intolerance. We studied 133 subjects who developed myopathy on statin monotherapy and 158 matched controls who tolerated statins without incident or complaint. |
X Demographics
Geographical breakdown
Country | Count | As % |
---|---|---|
United Kingdom | 2 | 100% |
Demographic breakdown
Type | Count | As % |
---|---|---|
Members of the public | 1 | 50% |
Practitioners (doctors, other healthcare professionals) | 1 | 50% |
Mendeley readers
Geographical breakdown
Country | Count | As % |
---|---|---|
Germany | 2 | 2% |
United States | 1 | 1% |
Australia | 1 | 1% |
Canada | 1 | 1% |
Unknown | 90 | 95% |
Demographic breakdown
Readers by professional status | Count | As % |
---|---|---|
Student > Bachelor | 18 | 19% |
Student > Ph. D. Student | 16 | 17% |
Researcher | 13 | 14% |
Other | 10 | 11% |
Student > Master | 8 | 8% |
Other | 24 | 25% |
Unknown | 6 | 6% |
Readers by discipline | Count | As % |
---|---|---|
Medicine and Dentistry | 41 | 43% |
Agricultural and Biological Sciences | 17 | 18% |
Biochemistry, Genetics and Molecular Biology | 10 | 11% |
Pharmacology, Toxicology and Pharmaceutical Science | 7 | 7% |
Nursing and Health Professions | 3 | 3% |
Other | 8 | 8% |
Unknown | 9 | 9% |