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

被引:16
|
作者
Li, Xiang [1 ]
Shao, Xiaojian [2 ]
Bazzano, Lydia A. [1 ]
Xue, Qiaochu [1 ]
Koseva, Boryana S. [3 ]
Grundberg, Elin [3 ]
Shai, Iris [4 ]
Bray, George A. [5 ]
Sacks, Frank M. [6 ]
Qi, Lu [1 ,6 ]
机构
[1] Tulane Univ, Sch Publ Hlth & Trop Med, Dept Epidemiol, New Orleans, LA 70118 USA
[2] Natl Res Council Canada, Digital Technol Res Ctr, Ottawa, ON, Canada
[3] Childrens Mercy Kansas City, Dept Pediat, Genom Med Ctr, Kansas City, MO USA
[4] Ben Gurion Univ Negev, Fac Hlth Sci, Beer Sheva, Israel
[5] Louisiana State Univ, Pennington Biomed Res Ctr, Baton Rouge, LA 70808 USA
[6] Harvard TH Chan Sch Publ Hlth, Dept Nutr, Boston, MA 02115 USA
关键词
EPIGENOME-WIDE ASSOCIATION; DIABETES-MELLITUS; GLUCOSE; PROTEIN; OVERWEIGHT; EXPOSURE; INSULIN; ELEMENT; FAMINE; MODEL;
D O I
10.1038/s41366-022-01084-5
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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 methyiC-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 (beta: -0.14; 95% CI: -0.24, -0.03; P = 0.011) and HOMA-IR 0(beta: -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.
引用
收藏
页码:1122 / 1127
页数:6
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