Yavuz Bunyamin, Ertugrul Derun Taner, Cil Hicran, Ata Naim, Akin Kadir Okhan, Yalcin Ahmet Arif, Kucukazman Metin, Dal Kursad, Hokkaomeroglu Murat Sevket, Yavuz Burcu Balam, Tutal Emre
Kecioren Teaching and Research Hospital, Department of Cardiology, Ankara, Turkey.
Cardiovasc Drugs Ther. 2009 Aug;23(4):295-9. doi: 10.1007/s10557-009-6181-8.
Low levels of 25-hydroxyvitamin D are associated with higher risk of cardiovascular morbidity and mortality. Large trials demonstrated that statins significantly decrease cardiovascular morbidity and mortality. 7-dehydrocholesterol is the precursor of both cholesterol and vitamin D. The aim of this study was to investigate the possible effect of rosuvastatin on vitamin D metabolism.
The study was performed in a prospective cohort design. The study group consisted of 91 hyperlipidemic patients who had not been treated with lipid lowering medications. Lipid parameters, 25 hydroxyvitamin-D, 1,25-dihydroxyvitamin D, and bone alkaline phosphatase were obtained at baseline and after 8 weeks of rosuvastatin treatment.
None of the subjects withdrew from the study because of the adverse effects. The mean age was 59.9 +/- 12.5 years. The majority of the patients were male (55, 60%). Seventeen patients were diabetic, and 43 patients had systemic hypertension. There was a significant increase in 25-hydroxyvitamin D, from mean 14.0 (range 3.7- 67) to mean 36.3 (range 3.8 -117) ng/ml (p < 0.001), and also an increase of 1,25-dihydroxyvitamin D from mean 22.9 +/- 11.2 to 26.6 +/- 9.3 pg/dl (p = 0.023). Bone alkaline phosphatase decreased after 8 weeks of rosuvastatin treatment, mean 17.7 (range 2.6-214) to mean 9.5 (range 2.3-19.1) u/l (p < 0.001) rosuvastatin treatment.
This study has shown an effect of rosuvastatin on vitamin D metabolism, with an increase in both 25-hydroxyvitamin D and 1,25-dihydroxyvitamin D. This may be an important pleiotropic effect whereby rosuvastatin reduces mortality in patients with coronary artery disease. Further studies are needed to clarify the relationship between statins and vitamin D metabolism.
25-羟基维生素D水平较低与心血管疾病发病率和死亡率较高相关。大型试验表明,他汀类药物可显著降低心血管疾病发病率和死亡率。7-脱氢胆固醇是胆固醇和维生素D的前体。本研究的目的是探讨瑞舒伐他汀对维生素D代谢的可能影响。
本研究采用前瞻性队列设计。研究组由91例未接受过降脂药物治疗的高脂血症患者组成。在基线时以及瑞舒伐他汀治疗8周后,获取血脂参数、25-羟基维生素D、1,25-二羟基维生素D和骨碱性磷酸酶。
没有受试者因不良反应退出研究。平均年龄为59.9±12.5岁。大多数患者为男性(55例,60%)。17例患者患有糖尿病,43例患者患有系统性高血压。25-羟基维生素D显著升高,从平均14.0(范围3.7 - 67)ng/ml升至平均36.3(范围3.8 - 117)ng/ml(p < 0.001),1,25-二羟基维生素D也从平均22.9±11.2 pg/dl升至26.6±9.3 pg/dl(p = 0.023)。瑞舒伐他汀治疗8周后骨碱性磷酸酶降低,从平均17.7(范围2.6 - 214)u/l降至平均9.5(范围2.3 - 19.1)u/l(p < 0.001)。
本研究显示瑞舒伐他汀对维生素D代谢有影响,25-羟基维生素D和1,25-二羟基维生素D均升高。这可能是一种重要的多效性作用,通过该作用瑞舒伐他汀可降低冠心病患者的死亡率。需要进一步研究以阐明他汀类药物与维生素D代谢之间的关系。