The association between fatigue and inflammatory marker levels in cancer patients: A quantitative review

被引:263
作者
Schubert, Christian [1 ]
Hong, Suzi
Natarajan, Loki
Mills, Paul J.
Dimsdale, Joel E.
机构
[1] Univ Innsbruck, Clin Dept Med Psychol & Psychotherapy, A-6020 Innsbruck, Austria
[2] Univ Calif San Diego, Dept Psychiat, La Jolla, CA 92093 USA
[3] Univ Calif San Diego, Moores Canc Ctr, La Jolla, CA 92093 USA
基金
美国国家卫生研究院;
关键词
cancer; cytokines; fatigue; interleukin; quantitative review; quality of life; tumor necrosis factor;
D O I
10.1016/j.bbi.2006.11.004
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
increased cytokine and neopterin levels may be responsible for cancer-related fatigue, the most common complaint among cancer patients. We quantitatively reviewed empirical findings on this topic, focusing on studies not using immunotherapy. PubMed, PsychINFO and BIOSIS were searched for articles published until July 2006. Studies remained unweighted or were weighted according to study quality and sample size. The correlation coefficient r was used for statistical analyses. Heterogeneity among the studies was examined using the I-2 index. Eighteen studies (1037 participants) of moderately high methodological quality were located and statistically analyzed. Most studies measured more than one inflammatory marker, resulting in a total of 58 correlation estimates. In 31 of these, we had to impute a null correlation because results had been simply reported as nonsignificant and no further statistical information was available. General analyses based on weighting according to sample size showed a significantly positive correlation between fatigue and circulating levels of inflammatory markers (r = 0.11, p < 0.0001). Analyses of individual inflammatory markers revealed significantly positive correlations between fatigue and IL-6 (r= 0.12, p =0.004), fatigue and IL-1ra (r=0.24, p=0.0005), and fatigue and neopterin (r=0.22, p= 0.0001). Fatigue did not correlate significantly with IL-l beta (r=0.05,p= 0.42) or TNF-alpha (r=0.04,p= 0.34). Given its preliminary nature due to the limited available data, this quantitative review showed a positive association between cancer-related fatigue and circulating levels of IL-6, IL-1ra and neopterin. Future studies examining the relationship between cancer related fatigue and inflammation would benefit from multiple rather than single blood sampling and from repeated daily ratings of the multidimensional nature of fatigue. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:413 / 427
页数:15
相关论文
共 74 条
  • [1] Ahlberg Karin, 2004, Biol Res Nurs, V5, P203, DOI 10.1177/1099800403259500
  • [2] [Anonymous], COCHRANE REV HDB 4 2
  • [3] CYTOKINES AND CYTOKINE INHIBITORS OR ANTAGONISTS IN RHEUMATOID-ARTHRITIS
    AREND, WP
    DAYER, JM
    [J]. ARTHRITIS AND RHEUMATISM, 1990, 33 (03): : 305 - 315
  • [4] AUZEBY A, 1988, CLIN CHEM, V34, P1866
  • [5] Cancer-related anemia: Biological findings, clinical implications and impact on quality of life
    Blohmer, JU
    Dunst, J
    Harrison, L
    Johnston, P
    Khayat, D
    Ludwig, H
    O'Brien, M
    Van Belle, S
    Vaupel, P
    [J]. ONCOLOGY, 2005, 68 : 12 - 21
  • [6] TAXOL, A MICROTUBULE-STABILIZING ANTINEOPLASTIC AGENT, INDUCES EXPRESSION OF TUMOR-NECROSIS-FACTOR-ALPHA AND INTERLEUKIN-1 IN MACROPHAGES
    BOGDAN, C
    DING, A
    [J]. JOURNAL OF LEUKOCYTE BIOLOGY, 1992, 52 (01) : 119 - 121
  • [7] Fatigue and proinflammatory cytokine activity in breast cancer survivors
    Bower, JE
    Ganz, PA
    Aziz, N
    Fahey, JL
    [J]. PSYCHOSOMATIC MEDICINE, 2002, 64 (04): : 604 - 611
  • [8] Bruera E, 1989, J Pain Symptom Manage, V4, P59, DOI 10.1016/0885-3924(89)90023-7
  • [9] Acute phase responses and cytokine secretion in chronic fatigue syndrome
    Cannon, JG
    Angel, JB
    Ball, RW
    Abad, LW
    Fagioli, L
    Komaroff, AL
    [J]. JOURNAL OF CLINICAL IMMUNOLOGY, 1999, 19 (06) : 414 - 421
  • [10] Inflammatory biomarkers for persistent fatigue in breast cancer survivors
    Collado-Hidalgo, A
    Bower, JE
    Ganz, PA
    Cole, SW
    Irwin, MR
    [J]. CLINICAL CANCER RESEARCH, 2006, 12 (09) : 2759 - 2766