Evidence map›Paper›PMID 42116229›Full record

ArticleJournal of health, population, and nutrition2026

Effect of nutritional intervention on interleukin-18 and alpha-2-macroglobulin in women with obesity and metabolic dysfunction-associated fatty liver disease: a prospective cohort study.

Salwa M El Shebini, Eman R Youness, Nihad H Ahmed, Hisham A Orban, Rehab A Mohamed, Maha I A Moaty

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Article in Journal of health, population, and nutrition, 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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5 · Who and what money

Authors and funding

6 authors.

Salwa M El ShebiniDepartment of Nutrition and Food Sciences, National Research Centre, Dokki, Giza, Egypt.
Eman R YounessDepartment of Medical Biochemistry, National Research Centre, Dokki, 12622, Giza, Egypt.
Nihad H AhmedDepartment of Nutrition and Food Sciences, National Research Centre, Dokki, Giza, Egypt.
Hisham A OrbanDepartment of Medical Biochemistry, National Research Centre, Dokki, 12622, Giza, Egypt.
Rehab A MohamedDepartment of Medical Biochemistry, National Research Centre, Dokki, 12622, Giza, Egypt.
Maha I A MoatyDepartment of Nutrition and Food Sciences, National Research Centre, Dokki, Giza, Egypt. ibrahim.maha@yahoo.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMetabolic dysfunction-associated fatty liver disease (MAFLD) is closely linked to metabolic abnormalities, including central obesity, dyslipidaemia, hypertension, hyperglycaemia, and impaired liver function. Identifying effective lifestyle interventions and reliable noninvasive biomarkers remains a public health priority.

objectiveThis study aimed to evaluate the effect of dietary modification on metabolic and hepatic parameters in women with MAFLD and to assess the potential role of interleukin-18 (IL-18) and alpha-2-macroglobulin (A2M) as noninvasive biomarkers.

methodsA prospective interventional study was conducted on 54 women with obesity and at least one criterion of metabolic syndrome. Participants were categorized into mild MAFLD, moderate MAFLD, or healthy liver groups based on ultrasonographic findings. All participants followed a calorie-restricted, balanced diet (1000-1200 kcal/day) for eight weeks. Anthropometric measurements, 24-hour dietary recall, and biochemical parameters, including IL-18, A2M, and liver enzymes, were assessed at baseline and post-intervention.

resultsAt baseline, women with moderate MAFLD exhibited significantly higher body mass index (BMI), minimal waist circumference (MWC), low-density lipoprotein cholesterol (LDL-C), and LDL/HDL ratio, along with lower high-density lipoprotein cholesterol (HDL-C), reflecting an adverse metabolic profile. They also reported higher macronutrient intake and lower dietary fiber consumption. A strong positive correlation between IL-18 and A2M (p ≤ 0.01) was observed across all groups and was associated with an unfavorable metabolic status. Following the intervention, significant improvements (p ≤ 0.05) were observed in weight, BMI, MWC, LDL-C, and gamma-glutamyl transferase (GGT), along with increased HDL-C levels. A highly significant reduction (p ≤ 0.01) in IL-18 was observed only among participants with MAFLD, while A2M levels decreased significantly (p ≤ 0.05-0.01) across all groups. CONCLUIONS: A calorie-restricted, balanced diet significantly improves metabolic and hepatic parameters in women with MAFLD. These findings highlight the beneficial impact of dietary intervention on liver enzymes and inflammatory markers, particularly GGT, IL-18, and A2M, and support the potential utility of A2M as a noninvasive biomarker and therapeutic target.

Indexed as

alpha-MacroglobulinsDiet, ReducingFatty LiverInterleukin-18Metabolic SyndromeNon-alcoholic Fatty Liver DiseaseObesityAdultBiomarkersBody Mass IndexFemaleHumansMiddle AgedProspective Studiesalpha-MacroglobulinsBiomarkersInterleukin-18Alpha-2-macroglobulinDietary modificationInterleukin-18Metabolic dysfunction-associated fatty liver diseaseObesity

Identifiers

PMID42116229
PMCPMC13159282

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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.