Insulin resistance and systemic inflammation, but not metabolic syndrome phenotype, predict 9 years mortality in older adults

被引:29
作者
Zuliani, Giovanni [1 ]
Morieri, Mario Luca [1 ]
Volpato, Stefano [1 ]
Maggio, Marcello [2 ]
Cherubini, Antonio [3 ]
Francesconi, Daniela [1 ]
Bandinelli, Stefania [4 ,5 ]
Paolisso, Giuseppe [6 ]
Guralnik, Jack M. [7 ]
Ferrucci, Luigi [8 ]
机构
[1] Univ Ferrara, Dept Med Sci, Sect Internal & CardioResp Med, I-44100 Ferrara, Italy
[2] Univ Parma, Dept Internal Med & Biomed Sci, Sect Geriatr, I-43100 Parma, Italy
[3] INNRCA, Inst Gerontol & Geriatr, Ancona, Italy
[4] ASF Geriatr Rehabil, Florence, Italy
[5] IOT, Tuscany Reg Hlth Agcy, Florence, Italy
[6] Univ Naples 2, Dept Gerontol Geriatr & Metab Dis, Naples, Italy
[7] Univ Maryland, Sch Med, Dept Epidemiol & Publ Hlth, Baltimore, MD 21201 USA
[8] NIA, Longitudinal Studies Sect, Clin Res Branch, NIH, Baltimore, MD 21224 USA
基金
美国国家卫生研究院;
关键词
Insulin resistance; C reactive protein; Mortality; Metabolic syndrome; Elderly; C-REACTIVE PROTEIN; CORONARY-HEART-DISEASE; CARDIOVASCULAR-DISEASE; RISK; POPULATION; HEALTH; MEN; INTERLEUKIN-6; INDIVIDUALS; SENSITIVITY;
D O I
10.1016/j.atherosclerosis.2014.05.959
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Although metabolic syndrome (MS) is a typical condition of middle-aged/older person, the association between MS and mortality risk has not been confirmed in people over 65 years. We hypothesized that while in the elderly MS phenotype might lose its value in predicting mortality risk, the two core factors of MS, i.e. insulin resistance (IR) and low grade systemic inflammation (LGSI) would not. Methods: 1011 community-dwelling older individuals (InCHIANTI study) were included. MS phenotype was defined by NCEP-ATP-III criteria. IR was calculated by HOMA; high-sensitivity C reactive protein was measured by ELISA. Subjects were divided into four groups based on presence/absence of IR (HOMA >= 2.27) and LGSI (hs-CRP >= 3 g/L): Group 1: no IR/LGSI (reference); Group 2: LGSI only; Group 3: IR only; Group 4: IR + LGSI. Hazard Ratios (HR) for 9-years cardiovascular (CVD) and total mortality, according to IR/LGSI groups, were estimated in subjects with (n. 311) and without MS by Cox model. Results: 31.8% of subjects with MS phenotype had no IR, 45.3% had no LGSI; moreover, 51% of subjects with both IR and LGSI didn't display the MS phenotype. MS phenotype was not associated with CVD (HR: 1.29; 95% C. I.: 0.92-1.81) or total (HR: 1.07; 95% C. I.: 0.86-1.34) mortality risk, whereas the presence of IR plus LGSI was associated with increased CVD (no MS: HR 2.07, 95% CI: 1.12-3.72; MS: HR 9.88, 95% CI: 2.18 -4), and overall (no MS: HR 1.72, 95% CI: 1.001-3.17; MS: HR 1.51, 95% CI: 1.02-2.28) mortality risk. The presence of IR (HR: 6.90, 95% CI: 1.45-32) or LGSI (HR 7.56, 95% CI: 1.63-35) was associated with CVD mortality, only among individuals with MS phenotype. Conclusions: Among community-dwelling older individuals, IR and LGSI, but not MS phenotype, was associated with 9-years overall and CVD mortality risk. Since a reduced "overlap" between MS phenotype and its physiopathological core (IR and LGSI) might be present with aging, we suggest that the definition of MS might be more holistic in advanced age, and probably comprise the measurement of IR and LGSI. (C) 2014 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:538 / 545
页数:8
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