# Adoption and validation of the European Association for the Study of the Liver algorithm for the noninvasive diagnosis of advanced fibrosis in metabolic dysfunction-associated steatotic liver disease in low-resource South Asian settings

**Authors:** Chamila Mettananda, Chamila Ranawaka, Thimira Egodage, Channaka Dantanarayana, Rumal Fernando, Lakmali Ranaweera, Dulani Kottahachchi, Shirom Siriwardhana, Arunasalam Pathmeswaran, Anuradha Dassanayake, Janaka de Silva, Sophia Martínez-Vázquez, Sophia Martínez-Vázquez, Sophia Martínez-Vázquez

PMC · DOI: 10.1371/journal.pone.0341364 · PLOS One · 2026-02-06

## TL;DR

The study adapts a liver fibrosis diagnostic algorithm for low-resource South Asian settings, reducing the need for specialized tests while maintaining diagnostic accuracy.

## Contribution

A revised cost-effective algorithm for diagnosing advanced liver fibrosis in low-resource settings, validated in South Asia.

## Key findings

- The revised algorithm reduced VCTE referrals by 13.5% in the study cohort and 15.5% in an external validation cohort.
- Key predictors of advanced fibrosis included diabetes duration ≥5 years, vascular complications, and BMI ≥25 kg/m².
- The new algorithm maintains diagnostic accuracy while being more cost-effective in resource-limited settings.

## Abstract

Patients with significant liver fibrosis (SF) are likely to progress to advanced chronic liver disease (ACLD). Therefore, liver-directed therapy is indicated. The European Association for the Study of the Liver-2024 (EASL) recommends annual screening of patients with diabetes for SF/ACLD using the FIB-4 score, followed by vibration-controlled transient elastography (VCTE) in patients with FIB-4 ≥ 1.3 in ≤65-year-olds and ≥2.0 in > 65-year-olds. Because VCTE is not freely available in resource-limited settings, we revised the EASL algorithm to prioritise referrals for VCTE in such settings and validated it in an external cohort.

We conducted a cross-sectional study of adults with type 2 diabetes (T2DM) and ultrasonographic evidence of steatotic liver disease (SDL) attending three outpatient medical clinics in the Gampaha District, Sri Lanka. FIB-4 scores were calculated, and those with scores ≥1.3 underwent VCTE. SF was defined as liver stiffness measure (LSM) ≥ 8.0 kPa. Factors significantly associated with SF/ACLD were identified using multiple logistic regression (LR). We then developed a new criterion for VCTE referral and compared the number of referrals for VCTE when using the new criterion-based algorithm with the EASL algorithm. We validated the new criterion-based algorithm in an external cohort of 372 patients with MASLD.

We studied 363 patients, and 128 had an FIB-4 score of≥1.3. Of them,121 underwent VCTE, and 76 had an LSM ≥ 8.0 kPa. On multivariable LR, VCTE-diagnosed SF/ACLD was independently associated with diabetes of ≥ 5 years duration (OR 3.8, p = 0.035), micro/macrovascular complications (OR 19.4, p = 0.016), and BMI of ≥ 25 kg/m2(OR 6.2, p = 0.003). We revised the VCTE referral criterion as “patients having EASL FIB-4 criterion plus one or more of the three other factors: diabetes of ≥ 5 years duration, presence of micro/macrovascular complications or BMI≥25 kg/m2,”. The number of VCTE referrals indicated using the EASL algorithm was 96, compared to 83 with the new criterion, resulting in a 13.5% reduction. In the external validation cohort, the new algorithm reduced the number requiring VCTE referral by 15.5%.

Adopting the new criterion for VCTE referral in patients with MASLD appears more cost-effective for detecting SF/ACLD in low-resource settings in South Asia.

## Linked entities

- **Diseases:** type 2 diabetes (MONDO:0005148), metabolic dysfunction-associated steatotic liver disease (MONDO:0013209)

## Full-text entities

- **Genes:** GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}
- **Diseases:** hemochromatosis (MESH:D006432), Type-2 Diabetes Mellitus (MESH:D003924), end-stage liver disease (MESH:D058625), neuropathy (MESH:D009422), -4 fibrosis (MESH:D005355), hepatocellular carcinoma (MESH:D006528), SF (MESH:D008103), obesity (MESH:D009765), stroke (MESH:D020521), LSM (MESH:D017093), Wilson disease (MESH:D006527), retinopathy (MESH:D058437), abdominal obesity (MESH:D056128), autoimmune hepatitis (MESH:D019693), hypertriglyceridemia (MESH:D015228), liver steatosis (MESH:D005234), nephropathy (MESH:D007674), peripheral vascular disease (MESH:D016491), ischaemic heart disease (MESH:D006331), Metabolic Dysfunction (MESH:D008659), Diabetes (MESH:D003920), CLCD (MESH:D002973), viral hepatitis (MESH:D014777), insulin resistance (MESH:D007333), CAP (MESH:C538265), vascular complications (MESH:D003925), VCTE (MESH:D053421), overweight (MESH:D050177), diabetic micro/macrovascular complications (MESH:D048909), ACLD (MESH:D008107)
- **Chemicals:** PONE-D-25-61395R1 (-), methotrexate (MESH:D008727), alcohol (MESH:D000438), tamoxifen (MESH:D013629)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

39 references — full list in the complete paper: https://tomesphere.com/paper/PMC12880717/full.md

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Source: https://tomesphere.com/paper/PMC12880717