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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2022
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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. |
format | Online Article Text |
id | pubmed-9156542 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
record_format | MEDLINE/PubMed |
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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