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Changes in the lipidome in type 1 diabetes following low carbohydrate diet: Post‐hoc analysis of a randomized crossover trial

AIMS: Lipid metabolism might be compromised in type 1 diabetes, and the understanding of lipid physiology is critically important. This study aimed to compare the change in plasma lipid concentrations during carbohydrate dietary changes in individuals with type 1 diabetes and identify links to early...

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Autores principales: Al‐Sari, Naba, Schmidt, Signe, Suvitaival, Tommi, Kim, Min, Trošt, Kajetan, Ranjan, Ajenthen G., Christensen, Merete B., Overgaard, Anne J., Pociot, Flemming, Nørgaard, Kirsten, Legido‐Quigley, Cristina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8029500/
https://www.ncbi.nlm.nih.gov/pubmed/33855215
http://dx.doi.org/10.1002/edm2.213
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author Al‐Sari, Naba
Schmidt, Signe
Suvitaival, Tommi
Kim, Min
Trošt, Kajetan
Ranjan, Ajenthen G.
Christensen, Merete B.
Overgaard, Anne J.
Pociot, Flemming
Nørgaard, Kirsten
Legido‐Quigley, Cristina
author_facet Al‐Sari, Naba
Schmidt, Signe
Suvitaival, Tommi
Kim, Min
Trošt, Kajetan
Ranjan, Ajenthen G.
Christensen, Merete B.
Overgaard, Anne J.
Pociot, Flemming
Nørgaard, Kirsten
Legido‐Quigley, Cristina
author_sort Al‐Sari, Naba
collection PubMed
description AIMS: Lipid metabolism might be compromised in type 1 diabetes, and the understanding of lipid physiology is critically important. This study aimed to compare the change in plasma lipid concentrations during carbohydrate dietary changes in individuals with type 1 diabetes and identify links to early‐stage dyslipidaemia. We hypothesized that (1) the lipidomic profiles after ingesting low or high carbohydrate diet for 12 weeks would be different; and (2) specific annotated lipid species could have significant associations with metabolic outcomes. METHODS: Ten adults with type 1 diabetes (mean ± SD: age 43.6 ± 13.8 years, diabetes duration 24.5 ± 13.4 years, BMI 24.9 ± 2.1 kg/m(2), HbA(1c) 57.6 ± 2.6 mmol/mol) using insulin pumps participated in a randomized 2‐period crossover study with a 12‐week intervention period of low carbohydrate diet (< 100 g carbohydrates/day) or high carbohydrate diet (> 250 g carbohydrates/day), respectively, separated by a 12‐week washout period. A large‐scale non‐targeted lipidomics was performed with mass spectrometry in fasting plasma samples obtained before and after each diet intervention. Longitudinal lipid levels were analysed using linear mixed‐effects models. RESULTS: In total, 289 lipid species were identified from 14 major lipid classes. Comparing the two diets, 11 lipid species belonging to sphingomyelins, phosphatidylcholines and LPC(O‐16:0) were changed. All the 11 lipid species were significantly elevated during low carbohydrate diet. Two lipid species were most differentiated between diets, namely SM(d36:1) (β ± SE: 1.44 ± 0.28, FDR = 0.010) and PC(P‐36:4)/PC(O‐36:5) (β ± SE: 1.34 ± 0.25, FDR = 0.009) species. Polyunsaturated PC(35:4) was inversely associated with BMI and positively associated with HDL cholesterol (p < .001). CONCLUSION: Lipidome‐wide outcome analysis of a randomized crossover trial of individuals with type 1 diabetes following a low carbohydrate diet showed an increase in sphingomyelins and phosphatidylcholines which are thought to reduce dyslipidaemia. The polyunsaturated phosphatidylcholine 35:4 was inversely associated with BMI and positively associated with HDL cholesterol (p < .001). Results from this study warrant for more investigation on the long‐term effect of single lipid species in type 1 diabetes.
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spelling pubmed-80295002021-04-13 Changes in the lipidome in type 1 diabetes following low carbohydrate diet: Post‐hoc analysis of a randomized crossover trial Al‐Sari, Naba Schmidt, Signe Suvitaival, Tommi Kim, Min Trošt, Kajetan Ranjan, Ajenthen G. Christensen, Merete B. Overgaard, Anne J. Pociot, Flemming Nørgaard, Kirsten Legido‐Quigley, Cristina Endocrinol Diabetes Metab Original Research Articles AIMS: Lipid metabolism might be compromised in type 1 diabetes, and the understanding of lipid physiology is critically important. This study aimed to compare the change in plasma lipid concentrations during carbohydrate dietary changes in individuals with type 1 diabetes and identify links to early‐stage dyslipidaemia. We hypothesized that (1) the lipidomic profiles after ingesting low or high carbohydrate diet for 12 weeks would be different; and (2) specific annotated lipid species could have significant associations with metabolic outcomes. METHODS: Ten adults with type 1 diabetes (mean ± SD: age 43.6 ± 13.8 years, diabetes duration 24.5 ± 13.4 years, BMI 24.9 ± 2.1 kg/m(2), HbA(1c) 57.6 ± 2.6 mmol/mol) using insulin pumps participated in a randomized 2‐period crossover study with a 12‐week intervention period of low carbohydrate diet (< 100 g carbohydrates/day) or high carbohydrate diet (> 250 g carbohydrates/day), respectively, separated by a 12‐week washout period. A large‐scale non‐targeted lipidomics was performed with mass spectrometry in fasting plasma samples obtained before and after each diet intervention. Longitudinal lipid levels were analysed using linear mixed‐effects models. RESULTS: In total, 289 lipid species were identified from 14 major lipid classes. Comparing the two diets, 11 lipid species belonging to sphingomyelins, phosphatidylcholines and LPC(O‐16:0) were changed. All the 11 lipid species were significantly elevated during low carbohydrate diet. Two lipid species were most differentiated between diets, namely SM(d36:1) (β ± SE: 1.44 ± 0.28, FDR = 0.010) and PC(P‐36:4)/PC(O‐36:5) (β ± SE: 1.34 ± 0.25, FDR = 0.009) species. Polyunsaturated PC(35:4) was inversely associated with BMI and positively associated with HDL cholesterol (p < .001). CONCLUSION: Lipidome‐wide outcome analysis of a randomized crossover trial of individuals with type 1 diabetes following a low carbohydrate diet showed an increase in sphingomyelins and phosphatidylcholines which are thought to reduce dyslipidaemia. The polyunsaturated phosphatidylcholine 35:4 was inversely associated with BMI and positively associated with HDL cholesterol (p < .001). Results from this study warrant for more investigation on the long‐term effect of single lipid species in type 1 diabetes. John Wiley and Sons Inc. 2021-01-04 /pmc/articles/PMC8029500/ /pubmed/33855215 http://dx.doi.org/10.1002/edm2.213 Text en © 2021 The Authors. Endocrinology, Diabetes & Metabolism published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research Articles
Al‐Sari, Naba
Schmidt, Signe
Suvitaival, Tommi
Kim, Min
Trošt, Kajetan
Ranjan, Ajenthen G.
Christensen, Merete B.
Overgaard, Anne J.
Pociot, Flemming
Nørgaard, Kirsten
Legido‐Quigley, Cristina
Changes in the lipidome in type 1 diabetes following low carbohydrate diet: Post‐hoc analysis of a randomized crossover trial
title Changes in the lipidome in type 1 diabetes following low carbohydrate diet: Post‐hoc analysis of a randomized crossover trial
title_full Changes in the lipidome in type 1 diabetes following low carbohydrate diet: Post‐hoc analysis of a randomized crossover trial
title_fullStr Changes in the lipidome in type 1 diabetes following low carbohydrate diet: Post‐hoc analysis of a randomized crossover trial
title_full_unstemmed Changes in the lipidome in type 1 diabetes following low carbohydrate diet: Post‐hoc analysis of a randomized crossover trial
title_short Changes in the lipidome in type 1 diabetes following low carbohydrate diet: Post‐hoc analysis of a randomized crossover trial
title_sort changes in the lipidome in type 1 diabetes following low carbohydrate diet: post‐hoc analysis of a randomized crossover trial
topic Original Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8029500/
https://www.ncbi.nlm.nih.gov/pubmed/33855215
http://dx.doi.org/10.1002/edm2.213
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