Tarabeih Nader, Kalinkovich Alexander, Shalata Adel, Cherny Stacey S, Livshits Gregory
Department of Anatomy and Anthropology, Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel.
Maale HaCarmel Mental Health Center, Affiliated to Rappaport Faculty of Medicine Technion, Israel Institute of Technology, Haifa, Israel.
J Pain Res. 2022 Jan 29;15:215-227. doi: 10.2147/JPR.S349251. eCollection 2022.
Low back pain (LBP) is one of the major disabling health conditions in aging societies presenting significant cost burdens to health and social care systems. Its complications and associated disability are often accompanied by mental disorders, metabolic comorbidities, changed body composition, and inflammation. However, their mutual relationships in LBP-associated disability remain unclear.
In the present case-control study, a self-report validated questionnaire was used to collect LBP disability data in an ethnically homogeneous Israeli Arab sample (489 males and 589 females). Body composition parameters were assessed through bioelectrical impedance analysis and plasma levels of soluble markers by EISA. Comorbidity status was assessed in personal interview and from the individual medical files.
Our mixed multiple regression analysis identified that GDF-15 (β = 0.160, p = 2.95×10-8), vaspin (β = 0.085, p = 0.003), follistatin (β = 0.076, p = 0.001), extracellular water (β = 0.096, p = 0.001), waist hip ratio (β = 0.072, p = 0.009), mental disorders (β = 0.077, p = 0.001), and metabolic comorbidities (β = 0.059, p = 0.02) were significantly associated with LBP disability scores, when controlling for age and sex effects. Additive Bayesian network modelling further suggests that LBP disability appears to be directly influenced by age, sex, GDF-15, and extracellular water, and indirectly by mental and metabolic disorders, waist-hip ratio, and follistatin. LBP, in turn, seems to affect the vaspin levels directly.
Our data suggest the existence of a complex, age-associated, and probably hierarchical, relationship between LBP disability and mental and metabolic disorders, inflammation-related soluble markers, and body composition parameters.
腰痛(LBP)是老龄化社会中导致残疾的主要健康问题之一,给卫生和社会护理系统带来了巨大的成本负担。其并发症和相关残疾常伴有精神障碍、代谢合并症、身体成分改变和炎症。然而,它们在LBP相关残疾中的相互关系仍不清楚。
在本病例对照研究中,使用一份经过验证的自我报告问卷,在种族同质的以色列阿拉伯样本(489名男性和589名女性)中收集LBP残疾数据。通过生物电阻抗分析评估身体成分参数,并通过酶联免疫吸附测定法(EISA)测定可溶性标志物的血浆水平。在个人访谈和个人医疗档案中评估合并症状况。
我们的混合多元回归分析确定,在控制年龄和性别影响后,生长分化因子15(GDF-15)(β = 0.160,p = 2.95×10-8)、内脏脂肪素(vaspin)(β = 0.085,p = 0.003)、卵泡抑素(follistatin)(β = 0.076,p = 0.001)、细胞外液(β = 0.096,p = 0.001)、腰臀比(β = 0.072,p = 0.009)、精神障碍(β = 0.077,p = 0.001)和代谢合并症(β = 0.059,p = 0.02)与LBP残疾评分显著相关。加性贝叶斯网络建模进一步表明,LBP残疾似乎直接受年龄、性别、GDF-15和细胞外液的影响,间接受精神和代谢障碍、腰臀比和卵泡抑素的影响。反过来,LBP似乎直接影响内脏脂肪素水平。
我们的数据表明,LBP残疾与精神和代谢障碍、炎症相关可溶性标志物以及身体成分参数之间存在复杂的、与年龄相关的、可能是分层的关系。