4.7 Article

Telomere Shortening and Increased Oxidative Stress in Lumbar Disc Degeneration

期刊

出版社

MDPI
DOI: 10.3390/ijms231710125

关键词

antioxidant; lumbar disc degeneration; oxidative stress; relative telomere length; severity

资金

  1. 90th Anniversary of Chulalongkorn University Scholarship [CUFRB65_hea(18)_025_30_06]
  2. Ratchadapiseksompotch Fund [CUGR 63953002]
  3. Center of Excellence in Osteoarthritis [GCE 6507230031-1]
  4. Musculoskeleton
  5. Graduate School, Chulalongkorn University

向作者/读者索取更多资源

This study found that patients with lumbar disc degeneration (LDD) had shorter telomeres, increased oxidative stress, and decreased antioxidant levels. The telomere length was negatively correlated with the severity of LDD, while oxidative stress markers (MDA and 8-OHdG) showed positive correlations with severity. These findings suggest that telomere length, as well as MDA and 8-OHdG levels, may be potential non-invasive biomarkers for assessing the severity of LDD.
Lumbar disc degeneration (LDD) contributes to low back pain. This study aimed to determine relative telomere length (RTL), oxidative stress status, and antioxidant levels and examine the relationships between RTL, oxidative stress, and the severity in LDD patients. A total of 100 subjects, 50 LDD patients and 50 healthy controls, were enrolled in the case-control study. Blood leukocyte RTL was analyzed using quantitative real-time polymerase chain reaction. Lipid peroxidation was determined by malondialdehyde (MDA) assay. Plasma 8-hydroxy 2 '-deoxyguanosine (8-OHdG) values were determined using enzyme-linked immunosorbent assay. Total antioxidant capacity (TAC) and ferric reducing antioxidant power (FRAP) in plasma were also measured. The LDD patients had significantly shorter telomeres than the healthy controls (p = 0.04). Blood leukocyte RTL was inversely correlated with the LDD severity (r = -0.41, p = 0.005). Additionally, plasma MDA and 8-OHdG levels were markedly greater in LDD patients than in the controls (p = 0.01 and p = 0.002, respectively). Furthermore, the plasma MDA level showed a positive correlation with the radiographic severity (r = 0.49, p = 0.001). There was a positive correlation between plasma 8-OHdG and the severity (r = 0.60, p < 0.001). Moreover, plasma TAC and FRAP levels were significantly lower in LDD patients than in the controls (p = 0.04). No significant differences in plasma TAC and FRAP were observed among the three groups of LDD severity. We found that RTL was negatively correlated with the severity while plasma MDA and 8-OHdG levels were positively correlated with the severity. These findings suggest that blood leukocyte RTL, plasma MDA, and 8-OHdG may have potential as noninvasive biomarkers for the assessment of severity in LDD.

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