Suppr超能文献

炎症标志物随年龄变化,但不会降至报告的正常范围以下。

Inflammatory Markers Change with Age, but do not Fall Beyond Reported Normal Ranges.

作者信息

Wyczalkowska-Tomasik Aleksandra, Czarkowska-Paczek Bozena, Zielenkiewicz Magdalena, Paczek Leszek

机构信息

Department of Immunology, Transplantology, and Internal Diseases, Medical University of Warsaw, Warsaw, Poland.

Department of Clinical Nursing, Medical University of Warsaw, E. Ciolka 27, 01-445, Warsaw, Poland.

出版信息

Arch Immunol Ther Exp (Warsz). 2016 Jun;64(3):249-54. doi: 10.1007/s00005-015-0357-7. Epub 2015 Aug 18.

Abstract

We examined the serum levels of IL-6, IL-8, TNF, IL-6R, TNF-R1, and CRP and the dynamics of changes in these levels according to age. The study included healthy individuals of 20-90 years of age. Participants were divided into subgroups based on their decade of life, and into subgroups of ≥65 or <65 years. Serum cytokine levels were assayed by ELISA, and CRP using an immunoturbidimetric method. Serum CRP levels were within the normal range for all subgroups. The 60- to 70-year age group showed higher CRP than the 20- to 30- (p = 0.003), 30- to 40- (p = 0.009), and 40- to 50- (p = 0.030) year age groups. Serum cytokine levels were low. It was greater in the 60- to 70-year age group than in the 20- to 30- (p = 0.008) and 30- to 40- (p = 0.040) year groups, and was greater in the 70- to 90-year group than the 20- to 30-year group (p = 0.043). Serum TNF-R1 level in the 70- to 90-year group was greater than in all other age groups (p = 0.000 for all comparisons). Other measured parameters did not differ between groups. Serum levels of IL-6, CRP, and TNF-R1 were greater in participants ≥65 than <65 years of age. Healthy older people showed low serum levels of CRP and pro-inflammatory cytokines, but higher than in younger population. Therefore, the adjustment of normal ranges in the elderly should be considered. Serum levels of pro-inflammatory cytokines elevated beyond normal ranges indicate particular diseases.

摘要

我们检测了白细胞介素-6(IL-6)、白细胞介素-8(IL-8)、肿瘤坏死因子(TNF)、IL-6受体(IL-6R)、TNF受体1(TNF-R1)和C反应蛋白(CRP)的血清水平,以及这些水平随年龄变化的动态情况。该研究纳入了年龄在20至90岁的健康个体。参与者根据其生活年代分为亚组,并分为年龄≥65岁或<65岁的亚组。采用酶联免疫吸附测定法(ELISA)检测血清细胞因子水平,采用免疫比浊法检测CRP。所有亚组的血清CRP水平均在正常范围内。60至70岁年龄组的CRP水平高于20至30岁(p = 0.003)、30至40岁(p = 0.009)和40至50岁(p = 0.030)年龄组。血清细胞因子水平较低。60至70岁年龄组的水平高于20至30岁(p = 0.008)和30至40岁(p = 0.040)年龄组,70至90岁年龄组的水平高于20至30岁年龄组(p = 0.043)。70至90岁年龄组的血清TNF-R1水平高于所有其他年龄组(所有比较的p = 0.000)。其他测量参数在各年龄组之间无差异。年龄≥65岁参与者的血清IL-6、CRP和TNF-R1水平高于<65岁者。健康老年人的血清CRP和促炎细胞因子水平较低,但高于年轻人群。因此,应考虑调整老年人的正常范围。促炎细胞因子血清水平超过正常范围表明患有特定疾病。

相似文献

1
Inflammatory Markers Change with Age, but do not Fall Beyond Reported Normal Ranges.
Arch Immunol Ther Exp (Warsz). 2016 Jun;64(3):249-54. doi: 10.1007/s00005-015-0357-7. Epub 2015 Aug 18.
2
Evaluation of pro-inflammatory cytokines in frail Tunisian older adults.
PLoS One. 2020 Nov 9;15(11):e0242152. doi: 10.1371/journal.pone.0242152. eCollection 2020.
4
Inflammatory hypothesis as a link between Alzheimer's disease and diabetes mellitus.
Geriatr Gerontol Int. 2016 Oct;16(10):1161-1166. doi: 10.1111/ggi.12602. Epub 2015 Sep 3.
5
Inflammatory markers and cardiovascular disease (The Health, Aging and Body Composition [Health ABC] Study).
Am J Cardiol. 2003 Sep 1;92(5):522-8. doi: 10.1016/s0002-9149(03)00718-5.
6
Monocyte cytokine production in an elderly population: effect of age and inflammation.
J Gerontol A Biol Sci Med Sci. 1998 Jan;53(1):M20-6. doi: 10.1093/gerona/53a.1.m20.
7
Inflammatory markers in patients with rheumatoid arthritis.
Allergol Immunopathol (Madr). 2015 Jan-Feb;43(1):81-7. doi: 10.1016/j.aller.2013.11.003. Epub 2014 Mar 20.
8
[Effect of acupuncture on patients with cancer-related fatigue and serum levels of CRP, IL-6, TNF-α and sTNF-R1].
Zhongguo Zhen Jiu. 2020 May 12;40(5):505-9. doi: 10.13703/j.0255-2930.20190423-k0002.

引用本文的文献

2
Systemic C-reactive protein levels in patients with geographic atrophy stratified by sex.
Int J Ophthalmol. 2025 Aug 18;18(8):1498-1505. doi: 10.18240/ijo.2025.08.11. eCollection 2025.
4
Low-grade inflammation and serotonin 4 receptor binding in the healthy and the depressed brain.
Neurosci Appl. 2024 Jun 14;3:104078. doi: 10.1016/j.nsa.2024.104078. eCollection 2024.
6
Immunosenescence and Inflammaging in Dogs and Cats: A Narrative Review.
J Vet Intern Med. 2025 Jul-Aug;39(4):e70159. doi: 10.1111/jvim.70159.
8
Development and validation of an epigenetic signature of allostatic load.
Biosci Rep. 2025 Apr 9;45(4):247-62. doi: 10.1042/BSR20241663.
10

本文引用的文献

1
From inflammaging to healthy aging by dietary lifestyle choices: is epigenetics the key to personalized nutrition?
Clin Epigenetics. 2015 Mar 25;7(1):33. doi: 10.1186/s13148-015-0068-2. eCollection 2015.
2
Mechanisms of development of multimorbidity in the elderly.
Eur Respir J. 2015 Mar;45(3):790-806. doi: 10.1183/09031936.00229714. Epub 2015 Jan 22.
4
Ageing and myeloid-derived suppressor cells: possible involvement in immunosenescence and age-related disease.
Age (Dordr). 2014;36(6):9729. doi: 10.1007/s11357-014-9729-x. Epub 2014 Nov 16.
5
Low-grade systemic inflammation connects aging, metabolic syndrome and cardiovascular disease.
Interdiscip Top Gerontol. 2015;40:99-106. doi: 10.1159/000364934. Epub 2014 Oct 13.
7
The immune system and aging: a review.
Gynecol Endocrinol. 2014 Jan;30(1):16-22. doi: 10.3109/09513590.2013.852531. Epub 2013 Nov 12.
8
Toll-like receptors' pathway disturbances are associated with increased susceptibility to infections in humans.
Arch Immunol Ther Exp (Warsz). 2013 Dec;61(6):427-43. doi: 10.1007/s00005-013-0243-0. Epub 2013 Sep 22.
9
Chronic inflammation as a determinant of future aging phenotypes.
CMAJ. 2013 Nov 5;185(16):E763-70. doi: 10.1503/cmaj.122072. Epub 2013 Sep 16.
10
Proinflammatory cytokines, aging, and age-related diseases.
J Am Med Dir Assoc. 2013 Dec;14(12):877-82. doi: 10.1016/j.jamda.2013.05.009. Epub 2013 Jun 20.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验