The pace of biological aging helps explain the association between insomnia and chronic low back pain

被引:13
作者
Aroke, Edwin N. [1 ]
Wiggins, Asia M. [2 ]
Hobson, Joanna M. [2 ]
Srinivasasainagendra, Vinodh [3 ]
Quinn, Tammie L. [2 ]
Kottae, Pooja [3 ]
Tiwari, Hemant K. [3 ]
Sorge, Robert E. [2 ]
Goodin, Burel R. [4 ]
机构
[1] Univ Alabama Birmingham, Sch Nursing, 701 Univ Blvd, Birmingham, AL 35294 USA
[2] Univ Alabama Birmingham, Coll Arts & Sci, Dept Psychol, Birmingham, AL 35294 USA
[3] Univ Alabama Birmingham, Sch Publ Hlth, Dept Biostat, Birmingham, AL 35294 USA
[4] Washington Univ, Pain Ctr, Dept Anesthesiol, Sch Med, St Louis, MO USA
关键词
Biological clock; chronic low back pain; DunedinPACE; epigenetic aging; functional performance; insomnia; SLEEP; PREVALENCE; SEVERITY; SYMPTOMS;
D O I
10.1177/17448069231210648
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Chronic low back pain (cLBP) is associated with insomnia and advanced age. Emerging evidence suggests that the severity of both sleep disorders (like insomnia) and chronic pain are associated with a faster pace of biological aging. We aimed to determine whether the pace of biological age mediates the relationship between insomnia and the impact of cLBP in a sample of community-dwelling adults ages 19 to 85 years. Participants (49 with no pain, 32 with low-impact pain, and 37 with high-impact pain) completed sociodemographic, pain, insomnia, and short physical performance battery assessments. We calculated the pace of biological aging using DunedinPACE from blood leukocyte DNA. On average, individuals with high-impact cLBP had significantly faster biological aging than those with low-impact and no chronic pain (p < .001). Bivariate associations of DunedinPACE scores with insomnia severity and functional performance were significant at p < .01 (r(s) = 0.324 and -0.502, respectively). After adjusting for race and sex, the association of insomnia severity and the impact of cLBP was partially mediated by the pace of biological aging (beta = 0.070, p < .001). Also, the association of insomnia severity with functional performance was partially mediated by the pace of biological aging (beta = -0.105, p < .001). Thus, insomnia remains strongly predictive of cLBP outcomes, and the pace of biological aging helps explain this association. Future prospective studies with repeated assessments are needed to uncover the directionality of these complex relationships and ultimately develop interventions to manage cLBP.
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页数:9
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