Effects of insomnia disorder and knee osteoarthritis on resting and pain-evoked inflammatory markers.
Effects of insomnia disorder and knee osteoarthritis on resting and pain-evoked inflammatory markers.
复制标题
DOI:
10.1016/j.bbi.2014.12.010
复制
发表时间:
2015-07
影响因子:
15.1
通讯作者:
Smith, Michael T.
中科院分区:
文献类型:
--
作者:
Quartana, Phillip J.;Finan, Patrick H.;Page, Gayle G.;Smith, Michael T.
Osteoarthritis is the most prevalent arthritic condition. Systemic inflammatory cytokines appear to have an important role in the onset and maintenance of the disease. Sleep disturbances are prevalent in osteoarthritis and associated with alterations in systemic inflammatory cytokines, suggesting a common pathophysiology across these conditions. A comparative investigation of the effects of insomnia disorder and osteoarthritis on pain-evoked cytokine responses has yet to be undertaken. We examined the influence of symptomatic knee osteoarthritis and insomnia disorder on resting C-reactive protein (CRP), interleukin (IL)-6, and IL-10 levels, and pain-evoked IL-6 and IL-10 responses. Participants were N = 117 older adults (mean age = 59.7 years; 61.8% women) rigorously evaluated for knee osteoarthritis and insomnia disorder using established diagnostic guidelines. Results revealed no association of osteoarthritis or insomnia disorder with CRP. Resting IL-6 was greater in osteoarthritis participants versus those without osteoarthritis, although this association was largely attributable to BMI. IL-10 was highest among participants with osteoarthritis or insomnia disorder. Growth curve modeling revealed that participants with insomnia disorder had greater pain-evoked IL-6 responses than participants without insomnia disorder or osteoarthritis. These findings highlight the utility of laboratory pain testing methods for understanding individual differences in inflammatory cytokines. Moreover, our findings provide evidence for amplified pain-evoked pro-inflammatory cytokine reactivity among older adults with clinically diagnosed insomnia disorder, even after controlling for individual differences in BMI and age. Additional research will be required determine whether an amplified pain-related cytokine response contributes to OA, and possibly other age-related disease, associated with insomnia disorder.
登录
查看更多内容
影响因子:
2.6
作者:
Brydon, Lena
通讯作者:
Brydon, Lena
影响因子:
8.2
作者:
Dickerson SS;Gable SL;Irwin MR;Aziz N;Kemeny ME
通讯作者:
Kemeny ME
DOI:
10.1093/gerona/gln038
发表时间:
2009-04-01
影响因子:
5.1
作者:
Brinkley, Tina E.;Leng, Xiaoyan;Nicklas, Barbara J.
通讯作者:
Nicklas, Barbara J.
影响因子:
15.1
作者:
Burgos, I;Richter, L;Riemann, D
通讯作者:
Riemann, D
影响因子:
4.8
作者:
Bastien, Celyne H.;Vallieres, Annie;Morin, Charles M.
通讯作者:
Morin, Charles M.