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Outcome predictability of biomarkers of protein-energy wasting and inflammation in moderate and advanced chronic kidney disease.中晚期慢性肾脏病患者蛋白质能量消耗和炎症生物标志物的预后可预测性
Am J Clin Nutr. 2009 Aug;90(2):407-14. doi: 10.3945/ajcn.2008.27390. Epub 2009 Jun 17.
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Rosuvastatin and cardiovascular events in patients undergoing hemodialysis.瑞舒伐他汀与血液透析患者的心血管事件
N Engl J Med. 2009 Apr 2;360(14):1395-407. doi: 10.1056/NEJMoa0810177. Epub 2009 Mar 30.
3
Effect of atorvastatin on inflammation and outcome in patients with type 2 diabetes mellitus on hemodialysis.阿托伐他汀对2型糖尿病血液透析患者炎症及预后的影响
Kidney Int. 2008 Dec;74(11):1461-7. doi: 10.1038/ki.2008.484. Epub 2008 Sep 24.
4
Long-term effects of renin-angiotensin system-blocking therapy and a low blood pressure goal on progression of hypertensive chronic kidney disease in African Americans.肾素-血管紧张素系统阻断疗法及低血压目标对非裔美国人高血压慢性肾病进展的长期影响。
Arch Intern Med. 2008 Apr 28;168(8):832-9. doi: 10.1001/archinte.168.8.832.
5
N-terminal prohormone brain natriuretic peptide as a predictor of cardiovascular disease and mortality in blacks with hypertensive kidney disease: the African American Study of Kidney Disease and Hypertension (AASK).N末端前体脑钠肽作为高血压肾病黑人心血管疾病和死亡率的预测指标:非裔美国人肾脏疾病与高血压研究(AASK)
Circulation. 2008 Apr 1;117(13):1685-92. doi: 10.1161/CIRCULATIONAHA.107.724187. Epub 2008 Mar 24.
6
Factor analysis of risk variables associated with low-grade inflammation.与低度炎症相关的风险变量的因子分析
Atherosclerosis. 2008 Sep;200(1):206-12. doi: 10.1016/j.atherosclerosis.2007.12.008. Epub 2008 Feb 20.
7
A proposed nomenclature and diagnostic criteria for protein-energy wasting in acute and chronic kidney disease.急性和慢性肾脏病中蛋白质能量消耗的拟议命名法和诊断标准
Kidney Int. 2008 Feb;73(4):391-8. doi: 10.1038/sj.ki.5002585. Epub 2007 Dec 19.
8
The Framingham predictive instrument in chronic kidney disease.慢性肾脏病中的弗雷明汉预测工具。
J Am Coll Cardiol. 2007 Jul 17;50(3):217-24. doi: 10.1016/j.jacc.2007.03.037. Epub 2007 Jul 2.
9
The inflammation hypothesis and its potential relevance to statin therapy.炎症假说及其与他汀类药物治疗的潜在相关性。
Am J Cardiol. 2007 Mar 1;99(5):732-8. doi: 10.1016/j.amjcard.2006.09.125. Epub 2007 Jan 10.
10
Inverse association between lipid levels and mortality in men with chronic kidney disease who are not yet on dialysis: effects of case mix and the malnutrition-inflammation-cachexia syndrome.尚未接受透析的慢性肾脏病男性患者血脂水平与死亡率之间的负相关:病例组合及营养不良-炎症-恶病质综合征的影响
J Am Soc Nephrol. 2007 Jan;18(1):304-11. doi: 10.1681/ASN.2006060674. Epub 2006 Dec 13.

营养不良-炎症改变了胆固醇与心血管疾病的关系。

Malnutrition-inflammation modifies the relationship of cholesterol with cardiovascular disease.

机构信息

Department of Medicine, Division of Nephrology and Hypertension, University of Miami Miller School of Medicine, 1120 NW 14th Street, Suite 360E, Miami, FL 33136, USA.

出版信息

J Am Soc Nephrol. 2010 Dec;21(12):2131-42. doi: 10.1681/ASN.2009121285. Epub 2010 Sep 23.

DOI:10.1681/ASN.2009121285
PMID:20864686
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3014026/
Abstract

In moderate and severe CKD, the association of cholesterol with subsequent cardiovascular disease (CVD) is weak. We examined whether malnutrition or inflammation (M-I) modifies the risk relationship between cholesterol levels and CVD events in African Americans with hypertensive CKD and a GFR between 20 and 65 ml/min per 1.73 m². We stratified 990 participants by the presence or absence of M-I, defined as body mass index <23 kg/m² or C-reactive protein >10 mg/L at baseline. The primary composite outcome included cardiovascular death or first hospitalization for coronary artery disease, stroke, or congestive heart failure occurring during a median follow-up of 77 months. Baseline total cholesterol (212 ± 48 versus 212 ± 44 mg/dl) and overall incidence of the primary CVD outcome (19 versus 21%) were similar in participants with (n = 304) and without (n = 686) M-I. In adjusted analyses, the CVD composite outcome exhibited a significantly stronger relationship with total cholesterol for participants without M-I than for participants with M-I at baseline (P < 0.02). In the non-M-I group, the cholesterol-adjusted hazard ratio (HR) for CVD increased progressively across cholesterol levels: HR = 1.19 [95% CI; 0.77, 1.84] and 2.18 [1.43, 3.33] in participants with cholesterol 200 to 239 and ≥240 mg/dl, respectively (reference: cholesterol <200). In the M-I group, the corresponding HRs did not vary significantly by cholesterol level. In conclusion, the presence of M-I modifies the risk relationship between cholesterol level and CVD in African Americans with hypertensive CKD.

摘要

在中重度 CKD 中,胆固醇与随后的心血管疾病(CVD)之间的关联较弱。我们研究了在肾小球滤过率(GFR)为 20 至 65 ml/min/1.73m²之间的患有高血压性 CKD 的非裔美国人中,营养不良或炎症(M-I)是否会改变胆固醇水平与 CVD 事件之间的风险关系。我们根据基线时是否存在 M-I 将 990 名参与者分层,M-I 定义为体质指数<23kg/m²或 C 反应蛋白>10mg/L。主要复合结局包括心血管死亡或因冠状动脉疾病、中风或充血性心力衰竭而首次住院,在中位随访 77 个月期间发生。基线总胆固醇(212±48 与 212±44mg/dl)和主要 CVD 结局的总体发生率(19%与 21%)在存在(n=304)和不存在(n=686)M-I 的参与者中相似。在调整后的分析中,与 M-I 无关的参与者的 CVD 复合结局与总胆固醇的关系明显强于存在 M-I 的参与者(P<0.02)。在非-M-I 组中,胆固醇调整后的 CVD 危险比(HR)随着胆固醇水平的升高呈逐渐增加趋势:HR=1.19[95%CI;0.77,1.84]和 2.18[1.43,3.33],胆固醇在 200 至 239mg/dl 和≥240mg/dl 的参与者中分别为(参考:胆固醇<200mg/dl)。在 M-I 组中,相应的 HR 随胆固醇水平变化不显著。结论,M-I 的存在改变了高血压性 CKD 的非裔美国人中胆固醇水平与 CVD 之间的风险关系。