Evidence map›Paper›PMID 42666198›Full record

ArticleFrontiers in endocrinology2026

Association of one-hour postload plasma glucose combined with metabolic dysfunction-associated steatotic liver disease and FIB-4 screening positivity with elevated LDL cholesterol and cerebrovascular stenosis.

Fengtong Zuo, XiaoYan Wang, Changan Xu

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Article in Frontiers in endocrinology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Fengtong ZuoDepartment of Cerebrovascular Diseases (Third Division), Cangzhou Central Hospital, Cangzhou, Hebei, China.
XiaoYan WangDepartment 2 of Neuroimmunology and Central Nervous System Infection, Cangzhou Central Hospital, Cangzhou, Hebei, China.
Changan XuDepartment of Endocrinology, Tianjin People's Hospital, Tianjin, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Metabolic dysfunction-associated steatotic liver disease (MASLD) is highly prevalent in type 2 diabetes mellitus (T2DM) and amplifies cardiovascular and metabolic burden. Elevated low-density lipoprotein cholesterol (LDL-C) is a key driver of atherosclerotic cerebrovascular stenosis, and MASLD-mediated hepatic lipid dysregulation is closely linked to LDL-C metabolism. One-hour postload plasma glucose (1h-PG) reflects early beta-cell dysfunction and may synergistically contribute to cerebrovascular injury alongside the MASLD/FIB-4 phenotype. Methods: This single-center retrospective cross-sectional study enrolled 312 treatment-naïve adults with newly diagnosed T2DM, of whom 278 completed a standardized 75-g oral glucose tolerance test (OGTT; age 24-78 years). The primary outcome was ultrasound-confirmed MASLD combined with age-specific FIB-4 screening positivity (age <65 years: FIB-4 ≥1.30; age ≥65 years: FIB-4 ≥2.00). Secondary outcomes included elevated LDL-C (≥3.4 mmol/L) and cerebrovascular stenosis (≥50% luminal narrowing in major intracranial or extracranial arteries). Results: Overall, 199 participants (71.6%) had MASLD and 64 (23.0%) met the primary outcome. Those meeting the primary outcome had significantly higher 1h-PG (17.7 ± 3.7 vs. 14.9 ± 3.8 mmol/L; P<0.001), with an adjusted OR of 1.15 per 1-mmol/L increment (95% CI 1.05-1.26; P = 0.003). Elevated LDL-C was present in 73 participants (26.3%) and cerebrovascular stenosis in 49 (17.6%). The composite group of high 1h-PG (≥Q3) plus MASLD/FIB-4 positivity had the highest stenosis rate (34.8% vs. 6.0%), with an adjusted OR of 2.61 (95% CI 1.23-5.55; P = 0.012). Adding LDL-C attenuated the OR from 3.42 to 2.61 (~24%), indicating partial mediation. The AUC improved from 0.661 (1h-PG alone) to 0.726 (combined model). Conclusions: In newly diagnosed T2DM, elevated 1h-PG was associated with MASLD/FIB-4 positivity; their combination was further linked to higher LDL-C and increased cerebrovascular stenosis risk, with LDL-C potentially acting as a partial mediator. The combined model showed improved discriminative ability, though validation in larger multicenter cohorts remains warranted.

Indexed as

Blood GlucoseCerebrovascular DisordersCholesterol, LDLDiabetes Mellitus, Type 2Fatty LiverAdultAgedConstriction, PathologicCross-Sectional StudiesFemaleGlucose Tolerance TestHumansMaleMiddle AgedRetrospective StudiesYoung AdultBlood GlucoseCholesterol, LDL1-hour postload plasma glucosecross-sectional analysisfibrosis-4 indexmetabolic dysfunction-associated steatotic liver diseasetype 2 diabetes mellitus

Identifiers

PMID42666198
PMCPMC13521856

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.