Evidence map›Paper›PMID 36941617›Full record

ArticleDiabetology & metabolic syndrome2023

Clinical and diagnostic characteristics of non-alcoholic fatty liver disease among Egyptian children and adolescents with type1 diabetes.

Hanaa Reyad Abdallah, Eman Refaat Youness, Manar Maher Bedeir, Marwa W Abouelnaga, Wafaa M Ezzat, Yasser Elhosary, Hazem Mohamed El-Hariri, Mona Abd Elmotaleb A Hussein, Heba R Ahmed, Rasha Eladawy

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Article in Diabetology & metabolic syndrome, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.7field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 8 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

Hanaa Reyad AbdallahBiological Anthropology Department, Medical Research and Clinical Studies Institute, National Research Centre, Cairo, Egypt. hanaareyad@yahoo.com.
Eman Refaat YounessMedical Biochemistry Department, Medical Research and Clinical Studies Institute, National Research Centre, Cairo, Egypt.
Manar Maher BedeirChild Health Department, Medical Research and Clinical Studies Institute, National Research Centre, Cairo, Egypt.
Marwa W AbouelnagaChild Health Department, Medical Research and Clinical Studies Institute, National Research Centre, Cairo, Egypt.
Wafaa M EzzatInternal Medicine Department, Medical Research and Clinical Studies Institute, National Research Centre, Cairo, Egypt.
Yasser ElhosaryInternal Medicine Department, Medical Research and Clinical Studies Institute, National Research Centre, Cairo, Egypt.
Hazem Mohamed El-HaririCommunity Medicine Department, Medical Research and Clinical Studies Institute, National Research Centre, Cairo, Egypt.
Mona Abd Elmotaleb A HusseinNational Institute of Diabetes and Endocrinology, Cairo, Egypt.
Heba R AhmedNational Institute of Diabetes and Endocrinology, Cairo, Egypt.
Rasha EladawyFaculty of Medicine, Ain Shams University, Cairo, Egypt.
National Research Centre · EGAin Shams University · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundType 1 diabetes mellitus (T1DM) patients are at an increased risk for non-alcoholic fatty liver disease (NAFLD). This study aimed to evaluate the clinical criteria associated with the diagnosis of Non-Alcoholic Fatty Liver Disease (NAFLD) among T1DM Egyptian children and adolescents.

methods74 T1DM patients aged 8-18 year were enrolled in this cross sectional study. Assessments of Clinical status, anthropometric measures, lipid profile, glycated haemoglobin (HbA1c) and liver enzymes were done. Abdominal Ultrasound evaluation of hepatic steatosis was done. Accordingly, patients were divided into two groups (NAFLD and normal liver group) and compared together. Assessment of liver fibrosis using acoustic radiation force impulse elastography (ARFI) was done. Statistical analysis included; independent t-test, Chi square and Fisher's Exact, Pearson and Spearman tests and Logistic regression models for factors associated with fatty liver were used when appropriate.

resultsIn this study; 74 patients were enrolled; 37 males (50%) and 37 females with mean age 14.3 ± 3.0 year. The mean insulin dose was 1.1 ± 0.4 U/kg and mean disease duration was 6.3 ± 3.0 year. NAFLD was detected in 46 cases while 28 cases had normal liver as diagnosed by abdominal ultrasound. Cases with NAFLD had statistically significant higher BMI-Z scores, waist/hip, waist/height and sum of skin fold thicknesses compared to those with normal liver (P < 0.05). The mean value of HbA1c % was significantly higher in NAFLD group (P = 0.003). Total cholesterol, triglycerides and LDL serum levels were significantly elevated (p < 0.05), while the HDL level was significantly lower in NAFLD cases (p = 0.001). Although, serum levels of liver enzymes; ALT and AST were significantly higher among cases with NAFLD than in normal liver group (p < 0.05), their means were within normal. Using the ARFI elastography; NAFLD cases exhibited significant fibrosis (F2, 3 and 4). BMI, patient age and female gender were among risk factors for NAFLD.

conclusionsNAFLD represents a serious consequence in type 1 diabetic children and adolescents that deserves attention especially with poor glycemic control. NAFLD has the potential to evolve to fibrosis. This study demonstrated a very high prevalence of NAFLD in T1D children and adolescents using US which was (62.2%) with the percent of liver fibrosis among the NAFLD cases (F2-F4) using ARFI elastography was 26%. BMI, age of patients and female gender were detected as risk factors for NAFLD.

Indexed as

Acoustic radiation force impulse elastography (ARFI)Anthropometric measuresHepatopathyNon-alcoholic fatty liver disease (NAFLD)Type1 diabetes

Identifiers

PMID36941617
PMCPMC10029237
OpenAlexW4328049352

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.