CLC number: R684.3
On-line Access: 2024-08-27
Received: 2023-10-17
Revision Accepted: 2024-05-08
Crosschecked: 2019-11-05
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Dong Zhan, Aree Tanavalee, Saran Tantavisut, Srihatach Ngarmukos, Steven W. Edwards, Sittisak Honsawek. Relationships between blood leukocyte mitochondrial DNA copy number and inflammatory cytokines in knee osteoarthritis[J]. Journal of Zhejiang University Science B, 2020, 21(1): 42-52.
@article{title="Relationships between blood leukocyte mitochondrial DNA copy number and inflammatory cytokines in knee osteoarthritis",
author="Dong Zhan, Aree Tanavalee, Saran Tantavisut, Srihatach Ngarmukos, Steven W. Edwards, Sittisak Honsawek",
journal="Journal of Zhejiang University Science B",
volume="21",
number="1",
pages="42-52",
year="2020",
publisher="Zhejiang University Press & Springer",
doi="10.1631/jzus.B1900352"
}
%0 Journal Article
%T Relationships between blood leukocyte mitochondrial DNA copy number and inflammatory cytokines in knee osteoarthritis
%A Dong Zhan
%A Aree Tanavalee
%A Saran Tantavisut
%A Srihatach Ngarmukos
%A Steven W. Edwards
%A Sittisak Honsawek
%J Journal of Zhejiang University SCIENCE B
%V 21
%N 1
%P 42-52
%@ 1673-1581
%D 2020
%I Zhejiang University Press & Springer
%DOI 10.1631/jzus.B1900352
TY - JOUR
T1 - Relationships between blood leukocyte mitochondrial DNA copy number and inflammatory cytokines in knee osteoarthritis
A1 - Dong Zhan
A1 - Aree Tanavalee
A1 - Saran Tantavisut
A1 - Srihatach Ngarmukos
A1 - Steven W. Edwards
A1 - Sittisak Honsawek
J0 - Journal of Zhejiang University Science B
VL - 21
IS - 1
SP - 42
EP - 52
%@ 1673-1581
Y1 - 2020
PB - Zhejiang University Press & Springer
ER -
DOI - 10.1631/jzus.B1900352
Abstract: osteoarthritis (OA) is a degenerative articular disorder manifested by cartilage destruction, subchondral sclerosis, osteophytes, and synovitis, resulting in chronic joint pain and physical disability in the elderly. The purpose of this study was to investigate mitochondrial DNA copy number (mtDNACN) and inflammatory cytokines in primary knee OA patients and healthy volunteers. A total of 204 knee OA patients and 169 age-matched healthy volunteers were recruited. Their relative blood leukocyte mtDNACN was assessed by quantitative real-time polymerase chain reaction (qRT-PCR), and ten inflammatory cytokines in their plasma were detected by multiplex immunoassay. blood leukocyte mtDNACN in the OA group was significantly lower than that in the control group. Leukocyte mtDNACN in the control group was negatively correlated with their age (r=−0.380, P<0.0001), whereas mtDNACN in the OA group was positively correlated with their age (r=0.198, P<0.001). Plasma interleukin-4 (IL-4) and IL-6 were significantly higher in the knee OA group than in the control group. The plasma IL-6 level was positively correlated with blood leukocyte mtDNACN in the OA group (r=0.547, P=0.0014). IL-5 showed as a major factor (coefficient 0.69) in the second dimension of principle components analysis (PCA)-transformed data and was significantly higher in the OA group (P<0.001) as well as negatively correlated with mtDNACN (r=−0.577, P<0.001). These findings suggest that elevation of plasma IL-4 and IL-6 and a relative reduction in mtDNACN might be effective biomarkers for knee OA. IL-5 is a plausible factor responsible for decreasing blood leukocyte mtDNACN in knee OA patients.
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