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Joint effect of visit-to-visit variability in LDL-cholesterol, HDL-cholesterol and HbA1c on cardiovascular and total mortality in patients with diabetes.

基本信息

DOI:
10.1186/s13098-022-00905-x
发表时间:
2022-09-19
影响因子:
4.8
通讯作者:
Qin, Xianhui
中科院分区:
医学2区
文献类型:
Journal Article
作者: He, Panpan;Gan, Xiaoqin;Wu, Qimeng;Ye, Ziliang;Yang, Sisi;Zhang, Yanjun;Li, Huan;Zhou, Chun;Zhang, Yuanyuan;Liu, Mengyi;Qin, Xianhui研究方向: Endocrinology & MetabolismMeSH主题词: --
来源链接:pubmed详情页地址

文献摘要

We aimed to investigate the joint effect of visit-to-visit variability (VVV) in low-density lipoprotein cholesterol (LDL-C), high-density lipoprotein cholesterol (HDL-C), triglycerides and glycosylated hemoglobin (HbA1c) on cardiovascular mortality and total mortality in patients with diabetes. Among 5194 participants with type 2 diabetes enrolled in the ACCORD lipid trial, VVVs of LDL-C, triglycerides, HDL-C, and HbA1c were assessed from baseline to 2 years of follow-up and expressed as coefficient of variation (CV). The study outcomes included cardiovascular mortality and all-cause mortality. Over a median follow-up of 3.0 years from the end of variability measurements at years 2, there were 305 (5.9%) cases of all-cause mortality, of which, 144 were cardiovascular causes. The positive relations between LDL-C CV and cardiovascular mortality were significantly stronger among participants with higher HDL-C CV (P for interaction = 0.023), and higher HbA1c CV (P for interaction = 0.015). However, there were no significant interactions between LDL-C CV and triglycerides CV (P for interaction = 0.591). Similar trends were found for all-cause mortality. Consistently, there were graded trends in the risk of mortality with the increasing numbers of higher CV of the three variables: LDL-C, HbA1c, and HDL-C (P for trend = 0.008 for cardiovascular mortality, and P for trend < 0.001 for all-cause mortality). VVVs in LDL-C, HDL-C, and HbA1c may jointly affect the risks of cardiovascular and all-cause mortality in diabetes patients. Those with higher CVs of all three variables had the highest risks of cardiovascular and all-cause mortality. The online version contains supplementary material available at 10.1186/s13098-022-00905-x.
我们旨在研究低密度脂蛋白胆固醇(LDL - C)、高密度脂蛋白胆固醇(HDL - C)、甘油三酯和糖化血红蛋白(HbA1c)的随访间变异性(VVV)对糖尿病患者心血管死亡率和全因死亡率的联合影响。 在参与ACCORD脂质试验的5194名2型糖尿病参与者中,从基线到2年随访期间对LDL - C、甘油三酯、HDL - C和HbA1c的随访间变异性进行了评估,并以变异系数(CV)表示。研究结果包括心血管死亡率和全因死亡率。 从第2年变异性测量结束后的中位随访3.0年期间,共有305例(5.9%)全因死亡病例,其中144例是心血管原因导致的。在HDL - C变异系数较高(交互作用P = 0.023)和HbA1c变异系数较高(交互作用P = 0.015)的参与者中,LDL - C变异系数与心血管死亡率之间的正相关关系明显更强。然而,LDL - C变异系数和甘油三酯变异系数之间没有显著的交互作用(交互作用P = 0.591)。在全因死亡率方面也发现了类似的趋势。一致地,随着LDL - C、HbA1c和HDL - C这三个变量中较高变异系数的数量增加,死亡风险呈现分级趋势(心血管死亡率趋势P = 0.008,全因死亡率趋势P < 0.001)。 LDL - C、HDL - C和HbA1c的随访间变异性可能共同影响糖尿病患者心血管和全因死亡的风险。这三个变量变异系数都较高的患者心血管和全因死亡的风险最高。 在线版本包含补充材料,可在10.1186/s13098 - 022 - 00905 - x获取。
参考文献(25)
被引文献(0)
Effects of combination lipid therapy in type 2 diabetes mellitus.
DOI:
10.1056/nejmoa1001282
发表时间:
2010-04-29
期刊:
The New England journal of medicine
影响因子:
0
作者:
ACCORD Study Group;Ginsberg HN;Elam MB;Lovato LC;Crouse JR 3rd;Leiter LA;Linz P;Friedewald WT;Buse JB;Gerstein HC;Probstfield J;Grimm RH;Ismail-Beigi F;Bigger JT;Goff DC Jr;Cushman WC;Simons-Morton DG;Byington RP
通讯作者:
Byington RP
Blood pressure variability and cardiovascular disease: systematic review and meta-analysis.
DOI:
10.1136/bmj.i4098
发表时间:
2016-08-09
期刊:
BMJ (Clinical research ed.)
影响因子:
0
作者:
Stevens SL;Wood S;Koshiaris C;Law K;Glasziou P;Stevens RJ;McManus RJ
通讯作者:
McManus RJ
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DOI:
10.1056/nejmoa1012848
发表时间:
2012-01-26
期刊:
The New England journal of medicine
影响因子:
0
作者:
Berry JD;Dyer A;Cai X;Garside DB;Ning H;Thomas A;Greenland P;Van Horn L;Tracy RP;Lloyd-Jones DM
通讯作者:
Lloyd-Jones DM
Prognostic significance of visit-to-visit variability, and maximum and minimum LDL cholesterol in diabetes mellitus.
DOI:
10.1186/s12944-022-01628-8
发表时间:
2022-02-10
期刊:
Lipids in health and disease
影响因子:
4.5
作者:
Sheng CS;Miao Y;Ding L;Cheng Y;Wang D;Yang Y;Tian J
通讯作者:
Tian J
Effects of intensive glucose lowering in type 2 diabetes
DOI:
10.1056/nejmoa0802743
发表时间:
2008-06-12
期刊:
NEW ENGLAND JOURNAL OF MEDICINE
影响因子:
158.5
作者:
Gerstein, Hertzel C.;Miller, Michael E.;Friedewald, William T.
通讯作者:
Friedewald, William T.

数据更新时间:{{ references.updateTime }}

关联基金

同型半胱氨酸血症促进CKD心血管并发症的作用和机制研究
批准号:
81730019
批准年份:
2017
资助金额:
300.0
项目类别:
重点项目
维生素A、B(叶酸、B6和B12)、D、E水平及其关键遗传因素预测新发糖尿病肾病风险
批准号:
81973133
批准年份:
2019
资助金额:
55
项目类别:
面上项目
Qin, Xianhui
通讯地址:
Southern Med Univ, Guangdong Prov Key Lab Renal Failure Res,Guangdon, Guangdong Prov Clin Res Ctr Kidney Dis,State Key, Div Nephrol,Nanfang Hosp,Natl Clin Res Ctr Kidney, Guangzhou 510515, Peoples R China
所属机构:
Southern Med UnivnSouthern Medical University - ChinanSouthern Medical University Nanfang HospitalnNational Clinical Research Center of Kidney DiseasesnSouthern Medical University Nanfang Hospital
电子邮件地址:
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