van Halm V P, Nielen M M J, Nurmohamed M T, van Schaardenburg D, Reesink H W, Voskuyl A E, Twisk J W R, van de Stadt R J, de Koning M H M T, Habibuw M R, van der Horst-Bruinsma I E, Dijkmans B A C
Departments of Internal Medicine and Rheumatology, VU University Medical Centre, PO Box 7057, 1007 MB Amsterdam, The Netherlands.
Ann Rheum Dis. 2007 Feb;66(2):184-8. doi: 10.1136/ard.2006.051672. Epub 2006 Jun 7.
Rheumatoid arthritis is characterised by inflammation and an increased cardiovascular risk. It was recently shown that active early rheumatoid arthritis is associated with dyslipidaemia, which may partially explain the enhanced cardiovascular risk. However, it is unknown when this dyslipidaemia starts.
To investigate the progression of the lipid profile over time and the influence of inflammatory parameters on this lipid profile, in people who later developed rheumatoid arthritis.
Levels of total cholesterol, high-density lipoprotein cholesterol (HDLc), triglycerides, apolipoprotein AI (apo AI), apolipoprotein B (apo B) and lipoprotein(a) (Lp(a)) were determined in 1078 stored, deep-frozen, serial blood bank samples, collected between 1984 and 1999, of 79 blood donors who later developed rheumatoid arthritis. These samples were compared with 1071 control samples of unselected blood donors, matched for age, sex and storage time.
Samples of patients who later developed rheumatoid arthritis showed, on average, 4% higher total cholesterol, 9% lower HDLc, 17% higher triglyceride and 6% higher apo B levels than matched controls (p< or =0.05). The magnitude of the differences in lipid levels between groups, explained by C reactive protein (CRP), was limited. For example, only 3.6% of the difference in HDLc levels between the groups was explained by the CRP concentrations.
Patients who later develop rheumatoid arthritis have a considerably more atherogenic lipid profile than matched blood donors at least 10 years before onset of symptoms. As inflammation only marginally explains the differences between the two groups, a modulating effect of lipids on inflammatory processes is hypothesised.
类风湿性关节炎的特征是炎症反应以及心血管疾病风险增加。最近研究表明,早期活动性类风湿性关节炎与血脂异常有关,这可能部分解释了心血管疾病风险增加的原因。然而,这种血脂异常何时开始尚不清楚。
研究日后发展为类风湿性关节炎的人群血脂水平随时间的变化以及炎症参数对血脂水平的影响。
对79名日后发展为类风湿性关节炎的献血者在1984年至1999年期间储存的1078份深度冷冻的系列血库样本进行检测,测定总胆固醇、高密度脂蛋白胆固醇(HDLc)、甘油三酯、载脂蛋白AI(apo AI)、载脂蛋白B(apo B)和脂蛋白(a)(Lp(a))的水平。将这些样本与1071份未选定的献血者对照样本进行比较,这些对照样本在年龄、性别和储存时间上相匹配。
日后发展为类风湿性关节炎的患者样本与匹配的对照组相比,总胆固醇平均高4%,HDLc低9%,甘油三酯高17%,apo B水平高6%(p≤0.05)。由C反应蛋白(CRP)解释的两组血脂水平差异幅度有限。例如,两组间HDLc水平差异中只有3.6%可由CRP浓度解释。
日后发展为类风湿性关节炎的患者在症状出现前至少10年,其血脂谱比匹配的献血者更具致动脉粥样硬化性。由于炎症只能勉强解释两组之间的差异,因此推测血脂对炎症过程有调节作用。