From the Lipoprotein and Atherosclerosis Laboratory, Baker IDI Heart & Diabetes Institute, Melbourne, Australia (P.J.N.); NHMRC Clinical Trials Centre, University of Sydney, Sydney, Australia (E.H.B., J.S., M.F.); Department of Epidemiology & Preventative Medicine, Monash University, Melbourne, Australia (A.M.T.); Green Lane Cardiovascular Research Unit, Auckland City Hospital, Auckland, New Zealand (H.D.W.); Department of Medicine, University of Queensland, Brisbane, Australia (D.M.C.); Department of General and Interventional Cardiology, University Heart Centre Hamburg, Hamburg, Germany (S.B.); and Royal Prince Alfred Hospital Department of Biochemistry, Sydney, Australia (D.R.S.).
Arterioscler Thromb Vasc Biol. 2013 Dec;33(12):2902-8. doi: 10.1161/ATVBAHA.113.302479. Epub 2013 Oct 3.
Association between lipoprotein(a) (Lp(a)) level and a first-ever coronary (CHD) event is recognized. Less is evident in patients with overt CHD and stable symptoms in whom we investigated associations between Lp(a) and future events.
Relationships between Lp(a) concentration and CHD and cardiovascular disease outcomes during 6 years' median follow-up were evaluated in the Long-Term Intervention with Pravastatin in Ischaemic Disease (LIPID) study. Lp(a) concentrations were measured in plasma from 7863 patients who had sustained a previous coronary event and been randomized to pravastatin or placebo. Lp(a) levels were categorized by lowest half, third quartile, 75th to 90th percentile, and highest decile. The prognostic value of Lp(a) on outcomes was assessed by fitting a Cox proportional-hazards model after adjustment for other risk factors and baseline cardiovascular disorders. The prognostic value of a change in Lp(a) at year 1 categorized by quartiles was assessed using Cox regression in a landmark model incorporating the above factors and baseline levels. Baseline Lp(a) concentration was associated with total CHD events (P<0.001), total cardiovascular disease events (P=0.002), and coronary events (P=0.03). Greatest risk occurred at >73 mg/dL, upper decile. For events after year 1, an increase in Lp(a) at 1 year was associated with adverse outcomes for total CHD events and total cardiovascular disease events (P=0.002 each).
In the LIPID study, baseline Lp(a) was associated with future cardiovascular disease and CHD events. Increased Lp(a) concentrations after 1 year were also associated with future events, supporting measurement of Lp(a) for risk assessment of patients with known CHD.
脂蛋白 (a)(Lp(a))水平与首次发生的冠心病 (CHD) 事件之间存在关联。在有明显 CHD 和稳定症状的患者中,这种关联不太明显,我们在这些患者中研究了 Lp(a) 与未来事件之间的关系。
在长期依泽替米贝治疗缺血性疾病 (LIPID) 研究中,评估了 Lp(a) 浓度与 6 年中位随访期间 CHD 和心血管疾病结局之间的关系。该研究纳入了 7863 例先前发生过冠状动脉事件并随机接受普伐他汀或安慰剂治疗的患者,从他们的血浆中测量了 Lp(a) 浓度。根据最低半分位数、第三四分位数、第 75 至 90 百分位数和最高十分位数对 Lp(a) 水平进行分类。通过拟合 Cox 比例风险模型,在调整其他危险因素和基线心血管疾病后,评估 Lp(a) 对结局的预测价值。使用 Cox 回归在包含上述因素和基线水平的 landmark 模型中对第 1 年按四分位数分类的 Lp(a) 变化的预后价值进行评估。基线 Lp(a) 浓度与总 CHD 事件(P<0.001)、总心血管疾病事件(P=0.002)和冠状动脉事件(P=0.03)相关。最大风险发生在 >73mg/dL,最高十分位数。对于第 1 年后的事件,第 1 年 Lp(a) 的增加与总 CHD 事件和总心血管疾病事件的不良结局相关(P=0.002 各)。
在 LIPID 研究中,基线 Lp(a) 与未来的心血管疾病和 CHD 事件相关。第 1 年后 Lp(a) 浓度的增加也与未来事件相关,支持对已知 CHD 患者进行 Lp(a) 测量以进行风险评估。