Cross-sectional associations of pulmonary function with systemic inflammation and oxidative stress in individuals with chronic spinal cord injury

被引:18
|
作者
Hart, Jaime E. [1 ,2 ,3 ]
Morse, Leslie [4 ,5 ]
Tun, Carlos G. [6 ]
Brown, Robert [7 ,8 ]
Garshick, Eric [1 ,2 ,9 ]
机构
[1] Brigham & Womens Hosp, Dept Med, Channing Div Network Med, 75 Francis St, Boston, MA 02115 USA
[2] Harvard Med Sch, Boston, MA USA
[3] Harvard TH Chan Sch Publ Hlth, Dept Environm Hlth, Exposure Epidemiol & Risk Program, Boston, MA USA
[4] Harvard Med Sch, Spaulding Rehabil Hosp, Spaulding Harvard SCI Model Syst, Charlestown, MA USA
[5] Harvard Med Sch, Dept Phys Med & Rehabil, Charlestown, MA USA
[6] VA Boston Healthcare Syst, Rehabil Med Serv, West Roxbury, MA USA
[7] Massachusetts Gen Hosp, Pulm & Crit Care Med Unit, Boston, MA 02114 USA
[8] Massachusetts Gen Hosp, Dept Med, Boston, MA 02114 USA
[9] VA Boston Healthcare Syst, Med Serv, Pulm & Crit Care Med Sect, West Roxbury, MA USA
来源
JOURNAL OF SPINAL CORD MEDICINE | 2016年 / 39卷 / 03期
关键词
Pulmonary function; Inflammation; Oxidative stress; Spinal cord injury; C-REACTIVE PROTEIN; LUNG-FUNCTION DECLINE; SKELETAL-MUSCLE; LIPID-PEROXIDATION; BODY-COMPOSITION; VOLUMES; DISEASE; MARKERS; MEN; POPULATION;
D O I
10.1179/2045772315Y.0000000045
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Context/Objective: Systemic inflammation, and to a lesser extent oxidative stress, have been associated with reduced pulmonary function. Our objective was to evaluate the associations between biomarkers of inflammation (C-reactive protein (CRP), interleukin-6 (IL-6)) and novel makers of global oxidative stress (fluorescent oxidation products (FLOx)) with spirometric and lung volume measures in individuals with chronic spinal cord injury (SCI). Design: Cross-sectional study. Setting: Veterans Affairs Medical Center. Participants: One-hundred thirty-seven men with chronic SCI participating in an epidemiologic study. Methods: Participants provided a blood sample, completed health questionnaires, and underwent pulmonary function testing, including helium dilution measurement of functional residual capacity (FRC). General linear models were used to model associations between increasing quartiles of inflammation or oxidative stress with each outcome measure, after adjustment for a number of potential confounders. Outcome Measures: Percent-predicted forced vital capacity in one second (FEV1), percent-predicted forced vital capacity (FVC), FEV1/FVC, percent-predicted residual volume (RV), percent-predicted FRC, and percent-predicted total lung capacity (TLC). Results: After adjustment for a number of confounders, participants with higher levels of CRP and IL-6 had lower percent-predicted FEV1 and FVC measurements. There were no clear patterns of association with any of the oxidative stress biomarkers or other outcome measures. Conclusion: Increased systemic inflammation was associated with reductions in FEV1 and FVC independent of a number of covariates. Although the mechanism is uncertain, these results suggest that reductions in pulmonary function in SCI are associated with systemic inflammation.
引用
收藏
页码:344 / 352
页数:9
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