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...
Autores principales: | , , , , , , , , , , , , , , , |
---|---|
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 |