Inflammation in Older Poles with Localized and Widespread Chronic Pain-Results from a Population-Based PolSenior Study.

老年波兰人局部和广泛性慢性疼痛的炎症——一项基于人群的波兰老年人研究的结果

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作者:Chudek Anna, Kotyla Przemysław, Kozak-Szkopek Elżbieta, Mossakowska Małgorzata, Wieczorowska-Tobis Katarzyna, Sulicka-Grodzicka Joanna, Olszanecka-Glinianowicz Magdalena, Chudek Jerzy, Owczarek Aleksander J
Background: Inflammation leads to a decrease in the excitation threshold and the sensitization of peripheral nociceptors. However, little is known about the effect of inflammation on the sensing of regional (CRegP) and widespread chronic pain (CWP) in older adults. This analysis aimed to characterize the prevalence and associates of both types of chronic pain in a population-based cohort. Methods: Our analysis was based on the Polish nationwide PolSenior study database. We excluded participants with moderate-to-severe dementia. Respondents answered questions concerning the occurrence of pain in 10 regions. CWP was defined as chronic pain present in the axial region (neck, upper back, lower back) and any part of both the lower (lower leg, hip, knee, foot) and upper (shoulder, hand) extremities. Inflammatory status was divided into three subgroups: no inflammation (CRP < 3 mg/dL), mild inflammation (CPR 3-10 mg/dL and IL-6 < 10 ng/mL), and significant inflammation (CRP ≥ 10 mg/dL or IL-6 ≥ 10 ng/mL). Results: CRegP was more frequent (33.9%) than CWP (8.8%). The occurrence of CWP was more frequent in subgroups with significant inflammation than in both subgroups with mild or no inflammation (11.4% vs. both 8.4%). Women (OR 3.67; 95% CI: 2.58-5.21) and subjects with major depression symptoms were more likely to experience CWP (OR 2.85; 95% CI: 1.68-4.82), while, malnourished participants were more likely to report CRegP (OR 2.00; 95% CI: 1.52-2.62). Conclusions: Significant inflammation is associated with increased occurrence of CWP in older adults. Female sex and major depression are the most significant associates of CWP, while malnutrition is the most significant associate of CRegP.

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