AI Article Synopsis

  • - The study aimed to assess how accurately diffusion tensor imaging (DTI) measures, specifically mean diffusivity (MD) and fractional anisotropy (FA), can distinguish between glioma recurrence and pseudoprogression.
  • - A systematic review of seven high-quality studies with 246 patients revealed that MD had a pooled sensitivity of 81% and specificity of 82%, while FA had a sensitivity of 74% and specificity of 79%.
  • - The results suggest that both MD and FA are effective markers for diagnosing glioma conditions, with MD showing slightly better diagnostic performance than FA.

Article Abstract

Purpose: To evaluate the diagnostic accuracy of diffusion tensor imaging (DTI)-derived metrics mean diffusivity (MD) and fractional anisotropy (FA) in differentiating glioma recurrence from pseudoprogression.

Methods: The Cochrane Library, Scopus, PubMed, and the Web of Science were systematically searched. Study selection and data extraction were done by two investigators independently. The quality assessment of diagnostic accuracy studies was applied to evaluate the quality of the included studies. Combined sensitivity (SEN) and specificity (SPE) and the area under the summary receiver operating characteristic curve (SROC) with the 95% confidence interval (CI) were calculated.

Results: Seven high-quality studies involving 246 patients were included. Quantitative synthesis of studies showed that the pooled SEN and SPE for MD were 0.81 (95% CI 0.70-0.88) and 0.82 (95% CI 0.70-0.90), respectively, and the value of the area under the SROC curve was 0.88 (95% CI 0.85-0.91). The pooled SEN and SPE for FA were 0.74 (95% CI 0.65-0.82) and 0.79 (95% CI 0.66-0.88), respectively, and the value of the area under the SROC curve was 0.84 (95% CI 0.80-0.87).

Conclusions: This meta-analysis showed that both MD and FA have a high diagnostic accuracy in differentiating glioma recurrence from pseudoprogression.

Registration: PROSPERO protocol: CRD42024501146.

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Source
http://dx.doi.org/10.1080/14737140.2024.2415404DOI Listing

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