轴性腰痛的复合生物标志物、行为症状和合并症:系统综述。

Biological research for nursing Pub Date : 2023-10-01 Epub Date: 2023-05-04 DOI:10.1177/10998004231171146
Anitha Saravanan, Jinbing Bai, Prempreet Bajaj, Elizabeth Sterner, Mahalakshmi Rajagopal, Sameera Sanders, Anne Luckose, Michael Kushnick, Angela Starkweather
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引用次数: 0

摘要

目的:炎性细胞因子在慢性炎症和疼痛中起着关键作用,并导致行为症状(抑郁症状、焦虑、疲劳、睡眠障碍)和合并症(糖尿病、心脏病、癌症)。缺乏与这些行为症状/并发轴性腰痛(aLBP)的合并症相关的特异性促炎细胞因子的证据。这篇综述旨在系统地分析以下内容:(1)成人中与aLBP相关的特异性促炎细胞因子,为aLBP患者的未来诊断和干预目标开发一个新的临床框架。方法:检索2012年1月至2023年2月期间的电子数据库,包括PubMed/MEDLINE、ProQuest Nursing&Allied Health Source和CINAHL Complete(EBSCO)。符合条件的研究包括横断面、病例对照、纵向和队列研究,其中在18岁以上患有aLBP的成年人中报告了促炎细胞因子。干预研究和随机对照试验被排除在外。乔安娜·布里格斯研究所(JBI)标准用于质量评估。结果:11项研究显示,aLBP成年患者的3种促炎细胞因子与疼痛强度相关:C-反应蛋白(CRP)、肿瘤坏死因子(TNF-α)和白细胞介素(IL-6)。一些研究评估了促炎细胞因子与抑郁症状之间的关系;没有研究促炎细胞因子与aLBP中疲劳、焦虑、睡眠障碍或合并症(糖尿病、心脏病和癌症)的关系。需要进行精心设计的研究,评估慢性炎症、行为症状和合并症之间的关系。
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Composite Biomarkers, Behavioral Symptoms, and Comorbidities in Axial Low Back Pain: A Systematic Review.

Purpose: Proinflammatory cytokines play a critical role in chronic inflammation and pain and contribute to behavioral symptoms (depressive symptoms, anxiety, fatigue, sleep disturbance) and comorbidities (diabetes, cardiac diseases, cancer). Evidence is lacking on the specific proinflammatory cytokines associated with these behavioral symptoms/comorbidities co-occurring with axial low back pain (aLBP). This review aimed to systematically analyze the following: (1) specific proinflammatory cytokines associated with aLBP in adults, (2) associations among proinflammatory cytokines and behavioral symptoms in aLBP, and (3) relationships among proinflammatory cytokines and comorbidities in aLBP, to develop a new clinical framework for future diagnostic and intervention targets for patients with aLBP.

Methods: Electronic databases, including PubMed/MEDLINE, ProQuest Nursing & Allied Health Source, and CINAHL Complete (EBSCO) were searched for the period January 2012 to February 2023. Eligible studies included cross-sectional, case-control, longitudinal, and cohort studies in which proinflammatory cytokines were reported in adults above 18 years with aLBP. Intervention studies and randomized controlled trails were excluded. The Joanna Briggs Institute (JBI) criteria were used for quality evaluation.

Results: Findings from 11 studies showed 3 proinflammatory cytokines associated with pain intensity in adult patients with aLBP: C-Reactive Protein (CRP), Tumor Necrosis Factor (TNF-α), and Interleukin (IL-6). Some studies assessed associations between proinflammatory cytokines and depressive symptoms; none explored the association of proinflammatory cytokines with fatigue, anxiety, sleep disturbance, or comorbidities (diabetes, cardiac diseases, and cancer) in aLBP.

Conclusions: Proinflammatory cytokines in aLBP can serve as composite biomarkers for pain, associated symptoms, and comorbidities and may serve as a target for future interventions. There is need for well-designed studies assessing associations among chronic inflammation, behavioral symptoms, and comorbidities.

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