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Blood DNA methylation at TXNIP and glycemic changes in response to weight-loss diet interventions: the POUNDS Lost Trial

BACKGROUND: Thioredoxin Interacting Protein (TXNIP) functions as a master regulator for glucose homeostasis. Hypomethylation at the 5’-cytosine-phosphate-guanine-3’ (CpG) site cg19693031 of TXNIP has been consistently related to islet dysfunction, hyperglycemia, and type 2 diabetes. DNA methylation...

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Autores principales: Li, Xiang, Shao, Xiaojian, Bazzano, Lydia A., Xue, Qiaochu, Kosewa, Boryana S., Grundberg, Elin, Shai, Iris, Bray, George A., Sacks, Frank M., Qi, Lu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9156542/
https://www.ncbi.nlm.nih.gov/pubmed/35165382
http://dx.doi.org/10.1038/s41366-022-01084-5
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author Li, Xiang
Shao, Xiaojian
Bazzano, Lydia A.
Xue, Qiaochu
Kosewa, Boryana S.
Grundberg, Elin
Shai, Iris
Bray, George A.
Sacks, Frank M.
Qi, Lu
author_facet Li, Xiang
Shao, Xiaojian
Bazzano, Lydia A.
Xue, Qiaochu
Kosewa, Boryana S.
Grundberg, Elin
Shai, Iris
Bray, George A.
Sacks, Frank M.
Qi, Lu
author_sort Li, Xiang
collection PubMed
description BACKGROUND: Thioredoxin Interacting Protein (TXNIP) functions as a master regulator for glucose homeostasis. Hypomethylation at the 5’-cytosine-phosphate-guanine-3’ (CpG) site cg19693031 of TXNIP has been consistently related to islet dysfunction, hyperglycemia, and type 2 diabetes. DNA methylation (DNAm) may reveal the missing mechanistic link between obesity and type 2 diabetes. We hypothesize that baseline DNAm level at TXNIP in blood may be associated with glycemic traits and their changes in response to weight-loss diet interventions. METHODS: We included 639 adult participants with overweight or obesity, who participated in a 2-year randomized weight-loss diet intervention. Baseline blood DNAm levels were profiled by high-resolution methylC-capture sequencing. We defined the regional DNAm level of TXNIP as the average methylation level over CpGs within 500 bp of cg19693031. Generalized linear regression models were used for main analyses. RESULTS: We found that higher regional DNAm at TXNIP was significantly correlated with lower fasting glucose, HbA1c, and Homeostatic Model Assessment of Insulin Resistance (HOMA-IR) at baseline (P<0.05 for all). Significant interactions were observed between dietary protein intake and DNAm on changes in insulin (P-interaction=0.007) and HOMA-IR (P-interaction=0.009) at 6 months. In participants with the highest tertile of regional DNAm at TXNIP, average protein (15%) intake was associated with a greater reduction in insulin (β: −0.14; 95% CI: −0.24, −0.03; P=0.011) and HOMA-IR (β: −0.15; 95% CI: −0.26, −0.03; P=0.014) than high protein (25%) intake, whereas no significant associations were found in those with the lower tertiles (P>0.05). The interaction was attenuated to be non-significant at 2 years, presumably related to decreasing adherence to the diet intervention. CONCLUSIONS: Our data indicate that higher regional DNAm level at TXNIP was significantly associated with better fasting glucose, HbA1c, and HOMA-IR; and people with higher regional DNAm levels benefited more in insulin and HOMA-IR improvement by taking the average-protein weight-loss diet.
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spelling pubmed-91565422022-08-14 Blood DNA methylation at TXNIP and glycemic changes in response to weight-loss diet interventions: the POUNDS Lost Trial Li, Xiang Shao, Xiaojian Bazzano, Lydia A. Xue, Qiaochu Kosewa, Boryana S. Grundberg, Elin Shai, Iris Bray, George A. Sacks, Frank M. Qi, Lu Int J Obes (Lond) Article BACKGROUND: Thioredoxin Interacting Protein (TXNIP) functions as a master regulator for glucose homeostasis. Hypomethylation at the 5’-cytosine-phosphate-guanine-3’ (CpG) site cg19693031 of TXNIP has been consistently related to islet dysfunction, hyperglycemia, and type 2 diabetes. DNA methylation (DNAm) may reveal the missing mechanistic link between obesity and type 2 diabetes. We hypothesize that baseline DNAm level at TXNIP in blood may be associated with glycemic traits and their changes in response to weight-loss diet interventions. METHODS: We included 639 adult participants with overweight or obesity, who participated in a 2-year randomized weight-loss diet intervention. Baseline blood DNAm levels were profiled by high-resolution methylC-capture sequencing. We defined the regional DNAm level of TXNIP as the average methylation level over CpGs within 500 bp of cg19693031. Generalized linear regression models were used for main analyses. RESULTS: We found that higher regional DNAm at TXNIP was significantly correlated with lower fasting glucose, HbA1c, and Homeostatic Model Assessment of Insulin Resistance (HOMA-IR) at baseline (P<0.05 for all). Significant interactions were observed between dietary protein intake and DNAm on changes in insulin (P-interaction=0.007) and HOMA-IR (P-interaction=0.009) at 6 months. In participants with the highest tertile of regional DNAm at TXNIP, average protein (15%) intake was associated with a greater reduction in insulin (β: −0.14; 95% CI: −0.24, −0.03; P=0.011) and HOMA-IR (β: −0.15; 95% CI: −0.26, −0.03; P=0.014) than high protein (25%) intake, whereas no significant associations were found in those with the lower tertiles (P>0.05). The interaction was attenuated to be non-significant at 2 years, presumably related to decreasing adherence to the diet intervention. CONCLUSIONS: Our data indicate that higher regional DNAm level at TXNIP was significantly associated with better fasting glucose, HbA1c, and HOMA-IR; and people with higher regional DNAm levels benefited more in insulin and HOMA-IR improvement by taking the average-protein weight-loss diet. 2022-06 2022-02-14 /pmc/articles/PMC9156542/ /pubmed/35165382 http://dx.doi.org/10.1038/s41366-022-01084-5 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: https://www.springernature.com/gp/open-research/policies/accepted-manuscript-terms
spellingShingle Article
Li, Xiang
Shao, Xiaojian
Bazzano, Lydia A.
Xue, Qiaochu
Kosewa, Boryana S.
Grundberg, Elin
Shai, Iris
Bray, George A.
Sacks, Frank M.
Qi, Lu
Blood DNA methylation at TXNIP and glycemic changes in response to weight-loss diet interventions: the POUNDS Lost Trial
title Blood DNA methylation at TXNIP and glycemic changes in response to weight-loss diet interventions: the POUNDS Lost Trial
title_full Blood DNA methylation at TXNIP and glycemic changes in response to weight-loss diet interventions: the POUNDS Lost Trial
title_fullStr Blood DNA methylation at TXNIP and glycemic changes in response to weight-loss diet interventions: the POUNDS Lost Trial
title_full_unstemmed Blood DNA methylation at TXNIP and glycemic changes in response to weight-loss diet interventions: the POUNDS Lost Trial
title_short Blood DNA methylation at TXNIP and glycemic changes in response to weight-loss diet interventions: the POUNDS Lost Trial
title_sort blood dna methylation at txnip and glycemic changes in response to weight-loss diet interventions: the pounds lost trial
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9156542/
https://www.ncbi.nlm.nih.gov/pubmed/35165382
http://dx.doi.org/10.1038/s41366-022-01084-5
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