Evidence map›Paper›PMID 35185803›Full record

ArticleFrontiers in endocrinology2022

Single Point Insulin Sensitivity Estimator in Pediatric Non-Alcoholic Fatty Liver Disease.

Dieter Furthner, Christian-Heinz Anderwald, Peter Bergsten, Anders Forslund, Joel Kullberg, Håkan Ahlström, Hannes Manell, Iris Ciba, Harald Mangge, Katharina Maruszczak and 6 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in endocrinology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

11 citing papers in PubMed, 10 citations in OpenAlex.

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  7. Identification of pediatric MASLD using insulin resistance indices.JHEP reports : innovation in hepatology · 2025
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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

16 authors at 4 institutions in 2 countries.

Dieter FurthnerDepartment of Pediatrics, Salzkammergutklinikum Voecklabruck, Voecklabruck, Austria.
Christian-Heinz AnderwaldObesity Research Unit, University Hospital Salzburg, Paracelsus Medical University, Salzburg, Austria.
Peter BergstenDepartment of Medical Cell Biology, Uppsala University, Uppsala, Sweden.
Anders ForslundDepartment of Women's and Children's Health, Uppsala University, Uppsala, Sweden.
Joel KullbergDepartment of Surgical Sciences, Radiology, Uppsala University, Uppsala, Sweden.
Håkan AhlströmDepartment of Surgical Sciences, Radiology, Uppsala University, Uppsala, Sweden.
Hannes ManellDepartment of Medical Cell Biology, Uppsala University, Uppsala, Sweden.
Iris CibaDepartment of Women's and Children's Health, Uppsala University, Uppsala, Sweden.
Harald ManggeClinical Institute of Medical and Chemical Laboratory Diagnosis, Medical University of Graz, Graz, Austria.
Katharina MaruszczakObesity Research Unit, University Hospital Salzburg, Paracelsus Medical University, Salzburg, Austria.
Pia KorenObesity Research Unit, University Hospital Salzburg, Paracelsus Medical University, Salzburg, Austria.
Sebastian SchützObesity Research Unit, University Hospital Salzburg, Paracelsus Medical University, Salzburg, Austria.
Susanne Maria BrunnerResearch Program for Receptor Biochemistry and Tumor Metabolism, Department of Pediatrics, University Hospital of the Paracelsus Medical University, Salzburg, Austria.
Anna Maria SchneiderObesity Research Unit, University Hospital Salzburg, Paracelsus Medical University, Salzburg, Austria.
Daniel WeghuberObesity Research Unit, University Hospital Salzburg, Paracelsus Medical University, Salzburg, Austria.
Katharina MörwaldObesity Research Unit, University Hospital Salzburg, Paracelsus Medical University, Salzburg, Austria.
Paracelsus Medical University · ATUppsala University · SEMedical University of Graz · ATMedical University of Vienna · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Attenuated insulin-sensitivity (IS) is a central feature of pediatric non-alcoholic fatty liver disease (NAFLD). We recently developed a new index, single point insulin sensitivity estimator (SPISE), based on triglycerides, high-density-lipoprotein and body-mass-index (BMI), and validated by euglycemic-hyperinsulinemic clamp-test (EHCT) in adolescents. This study aims to assess the performance of SPISE as an estimation of hepatic insulin (in-)sensitivity. Our results introduce SPISE as a novel and inexpensive index of hepatic insulin resistance, superior to established indices in children and adolescents with obesity. Materials and Methods: Ninety-nine pubertal subjects with obesity (13.5 ± 2.0 years, 59.6% males, overall mean BMI-SDS + 2.8 ± 0.6) were stratified by MRI (magnetic resonance imaging) into a NAFLD (>5% liver-fat-content; male n=41, female n=16) and non-NAFLD (≤5%; male n=18, female n=24) group. Obesity was defined according to WHO criteria (> 2 BMI-SDS). EHCT were used to determine IS in a subgroup (n=17). Receiver-operating-characteristic (ROC)-curve was performed for diagnostic ability of SPISE, HOMA-IR (homeostatic model assessment for insulin resistance), and HIRI (hepatic insulin resistance index), assuming null hypothesis of no difference in area-under-the-curve (AUC) at 0.5. Results: SPISE was lower in NAFLD (male: 4.8 ± 1.2, female: 4.5 ± 1.1) than in non-NAFLD group (male 6.0 ± 1.6, female 5.6 ± 1.5; P< 0.05 {95% confidence interval [CI]: male NAFLD 4.5, 5.2; male non-NAFLD 5.2, 6.8; female NAFLD 4.0, 5.1, female non-NAFLD 5.0, 6.2}). In males, ROC-AUC was 0.71 for SPISE (P=0.006, 95% CI: 0.54, 0.87), 0.68 for HOMA-IR (P=0.038, 95% CI: 0.48, 0.88), and 0.50 for HIRI (P=0.543, 95% CI: 0.27, 0.74). In females, ROC-AUC was 0.74 for SPISE (P=0.006), 0.59 for HOMA-IR (P=0.214), and 0.68 for HIRI (P=0.072). The optimal cutoff-level for SPISE between NAFLD and non-NAFLD patients was 5.18 overall (Youden-index: 0.35; sensitivity 0.68%, specificity 0.67%). Conclusion: SPISE is significantly lower in juvenile patients with obesity-associated NAFLD. Our results suggest that SPISE indicates hepatic IR in pediatric NAFLD patients with sensitivity and specificity superior to established indices of hepatic IR.

Indexed as

Insulin ResistanceNon-alcoholic Fatty Liver DiseaseAdolescentBody Mass IndexChildFemaleHumansInsulinMaleTriglyceridesInsulinTriglycerideshepatic insulin resistance indexHOMA-IRinsulin resistancepediatric obesityreceiver-operating-characteristic curve

Identifiers

PMID35185803
PMCPMC8848352
OpenAlexW4210415750

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.