Cargando…

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

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 validate...

Descripción completa

Detalles Bibliográficos
Autores principales: Furthner, Dieter, Anderwald, Christian-Heinz, Bergsten, Peter, Forslund, Anders, Kullberg, Joel, Ahlström, Håkan, Manell, Hannes, Ciba, Iris, Mangge, Harald, Maruszczak, Katharina, Koren, Pia, Schütz, Sebastian, Brunner, Susanne Maria, Schneider, Anna Maria, Weghuber, Daniel, Mörwald, Katharina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8848352/
https://www.ncbi.nlm.nih.gov/pubmed/35185803
http://dx.doi.org/10.3389/fendo.2022.830012
_version_ 1784652230102614016
author Furthner, Dieter
Anderwald, Christian-Heinz
Bergsten, Peter
Forslund, Anders
Kullberg, Joel
Ahlström, Håkan
Manell, Hannes
Ciba, Iris
Mangge, Harald
Maruszczak, Katharina
Koren, Pia
Schütz, Sebastian
Brunner, Susanne Maria
Schneider, Anna Maria
Weghuber, Daniel
Mörwald, Katharina
author_facet Furthner, Dieter
Anderwald, Christian-Heinz
Bergsten, Peter
Forslund, Anders
Kullberg, Joel
Ahlström, Håkan
Manell, Hannes
Ciba, Iris
Mangge, Harald
Maruszczak, Katharina
Koren, Pia
Schütz, Sebastian
Brunner, Susanne Maria
Schneider, Anna Maria
Weghuber, Daniel
Mörwald, Katharina
author_sort Furthner, Dieter
collection PubMed
description 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.
format Online
Article
Text
id pubmed-8848352
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-88483522022-02-17 Single Point Insulin Sensitivity Estimator in Pediatric Non-Alcoholic Fatty Liver Disease Furthner, Dieter Anderwald, Christian-Heinz Bergsten, Peter Forslund, Anders Kullberg, Joel Ahlström, Håkan Manell, Hannes Ciba, Iris Mangge, Harald Maruszczak, Katharina Koren, Pia Schütz, Sebastian Brunner, Susanne Maria Schneider, Anna Maria Weghuber, Daniel Mörwald, Katharina Front Endocrinol (Lausanne) Endocrinology 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. Frontiers Media S.A. 2022-02-02 /pmc/articles/PMC8848352/ /pubmed/35185803 http://dx.doi.org/10.3389/fendo.2022.830012 Text en Copyright © 2022 Furthner, Anderwald, Bergsten, Forslund, Kullberg, Ahlström, Manell, Ciba, Mangge, Maruszczak, Koren, Schütz, Brunner, Schneider, Weghuber and Mörwald https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
Furthner, Dieter
Anderwald, Christian-Heinz
Bergsten, Peter
Forslund, Anders
Kullberg, Joel
Ahlström, Håkan
Manell, Hannes
Ciba, Iris
Mangge, Harald
Maruszczak, Katharina
Koren, Pia
Schütz, Sebastian
Brunner, Susanne Maria
Schneider, Anna Maria
Weghuber, Daniel
Mörwald, Katharina
Single Point Insulin Sensitivity Estimator in Pediatric Non-Alcoholic Fatty Liver Disease
title Single Point Insulin Sensitivity Estimator in Pediatric Non-Alcoholic Fatty Liver Disease
title_full Single Point Insulin Sensitivity Estimator in Pediatric Non-Alcoholic Fatty Liver Disease
title_fullStr Single Point Insulin Sensitivity Estimator in Pediatric Non-Alcoholic Fatty Liver Disease
title_full_unstemmed Single Point Insulin Sensitivity Estimator in Pediatric Non-Alcoholic Fatty Liver Disease
title_short Single Point Insulin Sensitivity Estimator in Pediatric Non-Alcoholic Fatty Liver Disease
title_sort single point insulin sensitivity estimator in pediatric non-alcoholic fatty liver disease
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8848352/
https://www.ncbi.nlm.nih.gov/pubmed/35185803
http://dx.doi.org/10.3389/fendo.2022.830012
work_keys_str_mv AT furthnerdieter singlepointinsulinsensitivityestimatorinpediatricnonalcoholicfattyliverdisease
AT anderwaldchristianheinz singlepointinsulinsensitivityestimatorinpediatricnonalcoholicfattyliverdisease
AT bergstenpeter singlepointinsulinsensitivityestimatorinpediatricnonalcoholicfattyliverdisease
AT forslundanders singlepointinsulinsensitivityestimatorinpediatricnonalcoholicfattyliverdisease
AT kullbergjoel singlepointinsulinsensitivityestimatorinpediatricnonalcoholicfattyliverdisease
AT ahlstromhakan singlepointinsulinsensitivityestimatorinpediatricnonalcoholicfattyliverdisease
AT manellhannes singlepointinsulinsensitivityestimatorinpediatricnonalcoholicfattyliverdisease
AT cibairis singlepointinsulinsensitivityestimatorinpediatricnonalcoholicfattyliverdisease
AT manggeharald singlepointinsulinsensitivityestimatorinpediatricnonalcoholicfattyliverdisease
AT maruszczakkatharina singlepointinsulinsensitivityestimatorinpediatricnonalcoholicfattyliverdisease
AT korenpia singlepointinsulinsensitivityestimatorinpediatricnonalcoholicfattyliverdisease
AT schutzsebastian singlepointinsulinsensitivityestimatorinpediatricnonalcoholicfattyliverdisease
AT brunnersusannemaria singlepointinsulinsensitivityestimatorinpediatricnonalcoholicfattyliverdisease
AT schneiderannamaria singlepointinsulinsensitivityestimatorinpediatricnonalcoholicfattyliverdisease
AT weghuberdaniel singlepointinsulinsensitivityestimatorinpediatricnonalcoholicfattyliverdisease
AT morwaldkatharina singlepointinsulinsensitivityestimatorinpediatricnonalcoholicfattyliverdisease