Jacob E Aronoff, Carrie L Jenkins, Angela R Garcia, Stephanie V Koebele, Suhail Ghafoor, Kate L Woolard, Mia Charifson, Ivan M Suarez, Daniel Eid Rodriguez, Bret Beheim, Daniel K Cummings, Paul L Hooper, Thomas K Kraft, Kenneth Buetow, Caleb E Finch, Maximilien Franck, Alan A Cohen, Jonathan Stieglitz, Michael Gurven, Hillard Kaplan, Benjamin C Trumble
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IL-6 was positively associated with age (<i>β</i> = 0.013, <i>p</i> < 0.01). However, other pro-inflammatory markers, including IL-1β and TNF-α, did not increase with age (<i>β</i> = -0.005 and <i>β</i> = -0.001, respectively). We then compared the Moseten, a neighbouring population that has experienced greater market integration (423 samples from <i>n</i> = 380 individuals, age 39-85, 48.2% female). The Moseten also showed a positive age association for IL-6 that attenuated at later ages (age <i>β</i> = 0.025, <i>p</i> < 0.01; age<sup>2</sup> <i>β</i> = -0.001, <i>p</i> < 0.05). Further, IL-1β and TNF-α were both positively associated with age (<i>β</i> = 0.021, <i>p</i> < 0.05 and <i>β</i> = 0.011, <i>p</i> < 0.01, respectively). Our results demonstrate minimal inflammaging in the Tsimane, highlighting variation across populations in this age-related process. They also suggest that inflammaging is exacerbated by lifestyle shifts.</p>","PeriodicalId":520757,"journal":{"name":"Proceedings. 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引用次数: 0
摘要
晚年慢性全身性炎症(称为炎症)的增加与健康风险有关。然而,目前尚不清楚炎症是否会在所有人群中发展,或者是否是环境不匹配的产物。我们评估了玻利维亚亚马逊地区Tsimane采集园艺者的炎症,主要采用横断面样本(来自n = 714个个体的1134个样本,年龄39-94岁,51.3%为女性)的血清细胞因子。IL-6与年龄呈正相关(β = 0.013, p < 0.01)。然而,其他促炎标志物,包括IL-1β和TNF-α,并没有随着年龄的增长而增加(β = -0.005和β = -0.001)。然后,我们比较了Moseten,一个经历了更大市场一体化的邻近人口(423个样本,来自n = 380个人,年龄39-85岁,48.2%为女性)。Moseten与IL-6呈年龄正相关,随着年龄的增长逐渐减弱(age β = 0.025, p < 0.01; age2 β = -0.001, p < 0.05)。IL-1β和TNF-α均与年龄呈正相关(β = 0.021, p < 0.05)。我们的研究结果表明,Tsimane的炎症最小,突出了在这个与年龄相关的过程中不同人群的差异。他们还指出,生活方式的改变会加剧炎症。
Inflammaging is minimal among forager-horticulturalists in the Bolivian Amazon.
An increase in chronic systemic inflammation in later life, termed inflammaging, is implicated in health risk. However, it is unclear whether inflammaging develops in all human populations, or if it is the product of environmental mismatch. We assessed inflammaging in Tsimane forager-horticulturalists of the Bolivian Amazon, using serum cytokines in a primarily cross-sectional sample (1134 samples from n = 714 individuals, age 39-94, 51.3% female). IL-6 was positively associated with age (β = 0.013, p < 0.01). However, other pro-inflammatory markers, including IL-1β and TNF-α, did not increase with age (β = -0.005 and β = -0.001, respectively). We then compared the Moseten, a neighbouring population that has experienced greater market integration (423 samples from n = 380 individuals, age 39-85, 48.2% female). The Moseten also showed a positive age association for IL-6 that attenuated at later ages (age β = 0.025, p < 0.01; age2β = -0.001, p < 0.05). Further, IL-1β and TNF-α were both positively associated with age (β = 0.021, p < 0.05 and β = 0.011, p < 0.01, respectively). Our results demonstrate minimal inflammaging in the Tsimane, highlighting variation across populations in this age-related process. They also suggest that inflammaging is exacerbated by lifestyle shifts.