Aging-associated inflammation in healthy Japanese individuals and patients with Werner syndrome

被引:25
作者
Goto, Makoto [1 ,2 ]
Sugimoto, Kazunori [3 ]
Hayashi, Seigaku [3 ]
Ogino, Tetsuhito [4 ]
Sugimoto, Masanobu
Furuichi, Yasuhiro
Matsuura, Masaaki [5 ]
Ishikawa, Yuichi [6 ]
Iwaki-Egawa, Sachiko [7 ]
Watanabe, Yasuhiro [7 ]
机构
[1] Toin Univ Yokohama, Fac Med Engn, Dept Med Technol, Div Antiageing & Longev Sci,Aoba Ku, Yokohama, Kanagawa 2258502, Japan
[2] Tokyo Womens Med Univ, E Clin Ctr, Dept Orthoped Surg & Rheumatol, Tokyo, Japan
[3] Fukui Gen Hosp, Dept Rheumatol, Fukui, Japan
[4] Kyoritsu Ogino Hosp, Tokyo, Japan
[5] Japanese Fdn Canc Res, Inst Canc, Div Canc Genom, Tokyo, Japan
[6] Japanese Fdn Canc Res, Inst Canc, Dept Pathol, Tokyo, Japan
[7] Hokkaido Pharmaceut Univ, Sch Pharm, Dept Life Sci, Sapporo, Hokkaido, Japan
基金
日本学术振兴会;
关键词
Aging; Werner syndrome; Inflammaging; Inflammation; hsCRP; C-REACTIVE PROTEIN; HUMAN MONOCYTES; DNA-DAMAGE; POPULATION;
D O I
10.1016/j.exger.2012.08.010
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Minor inflammation-driven aging (inflammaging) has been proposed to explain human aging mechanism. To study the inflammatory condition associated with normal human aging, highly sensitive CRP (hsCRP) was examined in the sera collected from 217 healthy Japanese individuals aged between 1 and 100 years and 41 mutation-proven Japanese Werner syndrome (WS) patients. The serum hsCRP was assayed by ELISA. The serum hsCRP level increased significantly (p<0.001) with normal aging from both sexes. The serum hsCRP was significantly elevated in WS (mean +/- SE: 11.0 +/- 1.6 mu g/ml) compared with age-matched normal population (1.3 +/- 0.3 mu g/ml, p<0.001) and normal elderly population ages between 71 and 100 years (4.2 +/- 0.7 mu g/ml, p<0.001). Both normal aging and WS were associated with minor inflammation that can be evaluated by serum hsCRP. WS may be a good candidate to study inflammaging. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:936 / 939
页数:4
相关论文
共 25 条
  • [1] [Anonymous], 1973, 2 INT S INF THEOR
  • [2] High-sensitivity C-reactive protein and coronary heart disease in a general population of Japanese - The Hisayama study
    Arima, Hisatomi
    Kubo, Michiaki
    Yonemoto, Koji
    Doi, Yasufumi
    Ninomiya, Toshiharu
    Tanizaki, Yumihiro
    Hata, Jun
    Matsumura, Kiyoshi
    Iida, Mitsuo
    Kiyohara, Yutaka
    [J]. ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2008, 28 (07) : 1385 - 1391
  • [3] Cancer - An inflammatory link
    Balkwill, F
    Coussens, LM
    [J]. NATURE, 2004, 431 (7007) : 405 - 406
  • [4] INDUCTION OF INFLAMMATORY CYTOKINE RELEASE FROM CULTURED HUMAN MONOCYTES BY C-REACTIVE PROTEIN
    BALLOU, SP
    LOZANSKI, G
    [J]. CYTOKINE, 1992, 4 (05) : 361 - 368
  • [5] The major receptor for C-reactive protein on leukocytes is Fcγ receptor II
    Bharadwaj, D
    Stein, MP
    Volzer, M
    Mold, C
    Du Clos, TW
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1999, 190 (04) : 585 - 590
  • [6] Comfort A., 1964, AGEING BIOL SENESCEN
  • [7] Werner syndrome as an example of inflamm-aging: Possible therapeutic opportunities for a progeroid syndrome?
    Davis, Terence
    Kipling, David
    [J]. REJUVENATION RESEARCH, 2006, 9 (03) : 402 - 407
  • [8] C-reactive protein as a regulator of autoimmunity and inflammation
    Du Clos, TW
    [J]. ARTHRITIS AND RHEUMATISM, 2003, 48 (06): : 1475 - 1477
  • [9] Franceschi C, 2000, ANN NY ACAD SCI, V908, P244
  • [10] C-reactive protein binds to apoptotic cells, protects the cells from assembly of the terminal complement components, and sustains an antiinflammatory innate immune response: Implications for systemic autoimmunity
    Gershov, D
    Kim, S
    Brot, N
    Elkon, KB
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 192 (09) : 1353 - 1363