# Prevalence of high-risk for advanced liver fibrosis using non-invasive scores among type 2 diabetes mellitus patients in the United Arab Emirates: a retrospective cross-sectional study

**Authors:** Najma Yaqoob, Shaikha Salah Alhaj, Ayah Maher Al Obid, Amna Alketbi, Meera Alsuwaidi, Alia Ali Galadari, Amna Ahmad, Heitham Ajlouni, Dima Kamal Abdelmannan

PMC · DOI: 10.3389/fendo.2026.1719626 · Frontiers in Endocrinology · 2026-02-17

## TL;DR

This study finds that a small but significant portion of type 2 diabetes patients in the UAE are at high risk for advanced liver fibrosis, highlighting the need for non-invasive screening.

## Contribution

The study provides new data on liver fibrosis risk in T2DM patients in the UAE using non-invasive scores.

## Key findings

- 2.7% of T2DM patients in the UAE were at high risk for advanced liver fibrosis.
- Higher BMI was significantly associated with increased liver fibrosis risk (p=.002).

## Abstract

Advanced liver fibrosis is a major determinant of liver-related morbidity and mortality and occurs more frequently in individuals with type 2 diabetes mellitus (T2DM). While metabolic dysfunction–associated steatotic liver disease (MASLD) is highly prevalent among patients with T2DM, data on the risk of advanced liver fibrosis in this population in the United Arab Emirates (UAE) remain limited. Non-invasive fibrosis scores offer a pragmatic approach for risk stratification in routine clinical practice.

To determine the prevalence of high risk for advanced liver fibrosis and its clinical associations among patients with T2DM in the UAE using validated non-invasive fibrosis scores.

A retrospective cross-sectional study was conducted between October to December 2023, enrolling T2DM patients who attended at the Diabetic Care Centre in Dubai, UAE. Data was extracted from the Dubai Health electronic medical records, Epic (Salama). Liver fibrosis risk was assessed using the fibrosis-4 (FIB-4) score and Nonalcoholic Fatty Liver Disease (NAFLD) fibrosis score, with chi-square tests determining the statistical difference across liver fibrosis risk groups. Analyses were performed at a 5% significance level.

Among 373 patients, there was a slight female predominance (53%). Overall, 2.7% were at high risk of advanced liver fibrosis, while 56% had suspected hepatitis steatosis (MASLD), which aligns with global MASLD estimates in T2DM. Higher BMI was significantly associated with greater liver fibrosis risk (p=.002).

A small but clinically relevant proportion of patients with T2DM in the UAE are at high risk for advanced liver fibrosis. Incorporating non-invasive fibrosis risk assessment into routine diabetes care may facilitate early detection and specialist referral.

## Linked entities

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

## Full-text entities

- **Genes:** IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, TM6SF2 (transmembrane 6 superfamily member 2) [NCBI Gene 53345], GGT1 (gamma-glutamyltransferase 1) [NCBI Gene 2678] {aka CD224, D22S672, D22S732, GGT, GGT 1, GGTD}, PNPLA3 (patatin like domain 3, 1-acylglycerol-3-phosphate O-acyltransferase) [NCBI Gene 80339] {aka ADPN, C22orf20, iPLA(2)epsilon}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}
- **Diseases:** hypertension (MESH:D006973), COVID-19 infection (MESH:D000086382), Insulin resistance (MESH:D007333), T2DM (MESH:D003924), organ damage (MESH:D000092124), hepatic fibrogenesis (MESH:D056486), liver injury (MESH:D017093), chronic inflammation (MESH:D007249), Lean MASLD (MESH:D008107), Fibrosis (MESH:D005355), hyperglycemia (MESH:D006943), dyslipidemia (MESH:D050171), mitochondrial dysfunction (MESH:D028361), NAFLD (MESH:D065626), Gut dysbiosis (MESH:D064806), Diabetes (MESH:D003920), Liver fibrosis (MESH:D008103), prediabetes (MESH:D011236), Fatty liver (MESH:D005234), Obesity (MESH:D009765), vitamin D deficiency (MESH:D014808), fat (MESH:D004620), metabolic dysfunction (MESH:D008659), visceral adiposity (MESH:D007418)
- **Chemicals:** HDL (-), alcohol (MESH:D000438), glucose (MESH:D005947), Triglycerides (MESH:D014280), alanine (MESH:D000409), free fatty acid (MESH:D005230), cholesterol (MESH:D002784)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** C>G, rs738409

## Full text

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## References

58 references — full list in the complete paper: https://tomesphere.com/paper/PMC12953101/full.md

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Source: https://tomesphere.com/paper/PMC12953101