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Vertebral endplate defect as initiating factor for Modic change in the general population (CROSBI ID 290842)

Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija

Määttä J.H. ; Rade M. ; Freidin M.B. ; Airaksinen O. ; Karppinen J. ; Williams F.M.K. Vertebral endplate defect as initiating factor for Modic change in the general population // Scientific reports, 8 (2018), 1; 16630, 8

Podaci o odgovornosti

Määttä J.H. ; Rade M. ; Freidin M.B. ; Airaksinen O. ; Karppinen J. ; Williams F.M.K.

engleski

Vertebral endplate defect as initiating factor for Modic change in the general population

Modic change (MC) is considered an independent risk factor for low back pain (LBP) but its aetiology remains unclear. In this cross- sectional, large-scale population-based study we sought to characterise associations between endplate defect (ED) and MC in a population sample of broad age range. The study population consisted of 831 twin volunteers (including 4155 discs and 8310 endplates) from TwinsUK. Lumbar T2-weighted MR images were coded for ED and MC. Total endplate (TEP) score was calculated at each intervertebral disc while receiver operating curves (ROC) were calculated to define critical endplate values predictive of MC. MC was detected in 32.1% of the subjects, with a significantly higher prevalence at lower lumbar levels (3.5% at L1/2-L3/4 vs. 15.9% at L4/5-L5/S1, p < 0.001). TEP score was strongly and independently associated with MC at each lumbar level (risk estimates from 1.49 to 2.44 ; all p ≤ 0.001) after adjustment for age, sex, BMI and twin pairing. ROC analysis showed a TEP score cut-off of 6 above which there was a significantly higher prevalence of MC. In conclusion, ED were strongly associated with MC at every lumbar level. These findings support the hypothesis that endplate defect is a major initiating factor for the cascade of events that may include disc degeneration (DD) and MC.

endplate, disc degeneration, modic changes, DD, low back pain

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Podaci o izdanju

8 (1)

2018.

16630

8

objavljeno

2045-2322

Povezanost rada

Kliničke medicinske znanosti, Temeljne medicinske znanosti

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