AI Article Synopsis

  • Patients with type 2 diabetes (T2D) have a high prevalence of non-alcoholic fatty liver disease (NAFLD), with 184 out of 204 screened patients showing risk.
  • The study compared existing international and national guidelines for diagnosing and referring patients for NAFLD, finding high referral rates (60-77%) based on fibrosis scores using the EASL-EASD-EASO and DGVS guidelines.
  • Simpler referral strategies, like the FAST score, showed comparable sensitivity and reduced the need for specialist referrals to 35%, suggesting more efficient screening methods can be effective.

Article Abstract

Patients with type 2 diabetes (T2D) are at risk for non-alcoholic fatty liver disease (NAFLD) and associated complications. This study evaluated the performance of international (EASL-EASD-EASO) and national (DGVS) guidelines for NAFLD risk stratification. Patients with T2D prospectively underwent ultrasound, liver stiffness measurement (LSM) and serum-based fibrosis markers. Guideline-based risk classification and referral rates for different screening approaches were compared and the diagnostic properties of simplified algorithms, genetic markers and a new NASH surrogate (FAST score) were evaluated. NAFLD risk was present in 184 of 204 screened patients (age 64.2 ± 10.7 years; BMI 32.6 ± 7.6 kg/m). EASL-EASD-EASO recommended specialist referral for 60-77% depending on the fibrosis score used, only 6% were classified as low risk. The DGVS algorithm required LSM for 76%; 25% were referred for specialised care. The sensitivities of the diagnostic pathways were 47-96%. A simplified referral strategy revealed a sensitivity/specificity of 46/88% for fibrosis risk. Application of the FAST score reduced the referral rate to 35%. This study (a) underlines the high prevalence of fibrosis risk in T2D, (b) demonstrates very high referral rates for in-depth hepatological work-up, and (c) indicates that simpler referral algorithms may produce comparably good results and could facilitate NAFLD screening.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7591877PMC
http://dx.doi.org/10.1038/s41598-020-75227-xDOI Listing

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