Center for Research and Education in Special Environments, Department of Exercise and Nutrition Sciences, University at Buffalo, Buffalo, New York.
Department of Physiology and Biophysics, Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, Buffalo, New York.
J Appl Physiol (1985). 2020 Apr 1;128(4):715-728. doi: 10.1152/japplphysiol.00787.2019. Epub 2020 Feb 20.
Occupational heat stress increases the risk of acute kidney injury (AKI) and kidney disease. This study tested the hypothesis that attenuating the magnitude of hyperthermia (i.e., increase in core temperature) and/or dehydration during prolonged physical work in the heat attenuates increases in AKI biomarkers. Thirteen healthy adults (3 women, 23 ± 2 yr) exercised for 2 h in a 39.7 ± 0.6°C, 32 ± 3% relative-humidity environmental chamber. In four trials, subjects received water to remain euhydrated (), continuous upper-body cooling (), a combination of both (), or no intervention (). The magnitude of hyperthermia (increased core temperature of 1.9 ± 0.3°C; < 0.01) and dehydration (percent loss of body mass of -2.4 ± 0.5%; < 0.01) were greatest in the group. There were greater increases in the urinary biomarkers of AKI in the trial: albumin (increase of 13 ± 11 μg/mL; ≤ 0.05 compared with other trials), neutrophil gelatinase-associated lipocalin (NGAL) (increase of 16 ± 14 ng/dL, ≤ 0.05 compared with and groups), and insulin-like growth factor-binding protein 7 (IGFBP7) (increase of 227 ± 190 ng/mL; ≤ 0.05 compared with other trials). Increases in IGFBP7 in the trial persisted after correcting for urine production/concentration. There were no differences in the AKI biomarker tissue inhibitor of metalloproteinase 2 (TIMP-2) between trials ( ≥ 0.11). Our findings indicate that the risk of AKI is highest with greater magnitudes of hyperthermia and dehydration during physical work in the heat. Additionally, the differential findings between IGFBP7 (preferentially secreted in proximal tubules) and TIMP-2 (distal tubules) suggest the proximal tubules as the location of potential renal injury. We demonstrate that the risk for acute kidney injury (AKI) is higher in humans with greater magnitudes of hyperthermia and dehydration during physical work in the heat and that alleviating the hyperthermia and/or limiting dehydration equally reduce the risk of AKI. The biomarker panel employed in this study suggests the proximal tubules as the location of potential renal injury.
职业热应激会增加急性肾损伤 (AKI) 和肾脏疾病的风险。本研究旨在验证以下假设,即在长时间的热环境下体力劳动中,减轻体温升高(即核心温度升高)和/或脱水的幅度可降低 AKI 生物标志物的增加。13 名健康成年人(3 名女性,23±2 岁)在 39.7±0.6°C、32±3%相对湿度的环境室中运动 2 小时。在四项试验中,受试者接受水以保持水平衡()、连续上身冷却()、两者的组合()或不干预()。在 组中,体温升高(核心温度升高 1.9±0.3°C; < 0.01)和脱水(体重损失百分比为-2.4±0.5%; < 0.01)的幅度最大。在 试验中,AKI 的尿生物标志物增加幅度更大:白蛋白(增加 13±11μg/mL;与其他试验相比, ≤ 0.05)、中性粒细胞明胶酶相关脂质运载蛋白(NGAL)(增加 16±14ng/dL,与 和 组相比, ≤ 0.05)和胰岛素样生长因子结合蛋白 7(IGFBP7)(增加 227±190ng/mL;与其他试验相比, ≤ 0.05)。在 试验中,IGFBP7 的增加在校正尿液产生/浓度后仍然存在。在试验之间,AKI 生物标志物金属蛋白酶组织抑制剂 2(TIMP-2)没有差异( ≥ 0.11)。我们的研究结果表明,在热环境中进行体力劳动时,体温升高和脱水幅度越大,AKI 的风险越高。此外,IGFBP7(优先在近端肾小管中分泌)和 TIMP-2(在远端肾小管中分泌)之间的差异发现表明近端肾小管是潜在肾损伤的部位。我们证明,在热环境中进行体力劳动时,体温升高和脱水幅度较大的人发生急性肾损伤(AKI)的风险更高,而缓解体温升高和/或限制脱水同样可以降低 AKI 的风险。本研究中使用的生物标志物谱表明近端肾小管是潜在肾损伤的部位。