Diabetes Metab J.  2024 Mar;48(2):170-183. 10.4093/dmj.2023.0272.

One-Carbon Metabolism Nutrients, Genetic Variation, and Diabetes Mellitus

Affiliations
  • 1Nutrition and Foods Program, School of Family and Consumer Sciences, Texas State University, San Marcos, TX, USA
  • 2Institute for Translational Epidemiology & Division of Liver Diseases, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, USA
  • 3Department of Mathematics, Texas State University, San Marcos, TX, USA
  • 4Department of Obstetrics and Gynecology, Vagelos College of Physician and Surgeons, Columbia University, New York, NY, USA
  • 5Department of Epidemiology, Mailman School of Public Health, Columbia University, New York, NY, USA

Abstract

Diabetes mellitus (DM) affects about 9.3% of the population globally. Hyperhomocysteinemia (HHcy) has been implicated in the pathogenesis of DM, owing to its promotion of oxidative stress, β-cell dysfunction, and insulin resistance. HHcy can result from low status of one-carbon metabolism (OCM) nutrients (e.g., folate, choline, betaine, vitamin B6, B12), which work together to degrade homocysteine by methylation. The etiology of HHcy may also involve genetic variation encoding key enzymes in OCM. This review aimed to provide an overview of the existing literature assessing the link between OCM nutrients status, related genetic factors, and incident DM. We also discussed possible mechanisms underlying the role of OCM in DM development and provided recommendations for future research and practice. Even though the available evidence remains inconsistent, some studies support the potential beneficial effects of intakes or blood levels of OCM nutrients on DM development. Moreover, certain variants in OCM-related genes may influence metabolic handling of methyl-donors and presumably incidental DM. Future studies are warranted to establish the causal inference between OCM and DM and examine the interaction of OCM nutrients and genetic factors with DM development, which will inform the personalized recommendations for OCM nutrients intakes on DM prevention.

Keyword

Betaine; Choline; Diabetes mellitus; Folic acid; Genes; Homocysteine; Riboflavin; Vitamin B 6; Vitamin B 12; Zinc

Figure

  • Fig. 1. One-carbon metabolism. SAM, S-adenosylmethionine; PE, phosphatidylethanolamine; ChAT, choline acetyltransferase; DMG, dimethylglycine; MT, methyltransferase; PEMT, phosphatidylethanolamine N-methyltransferase; CK, choline kinase; CHDH, choline dehydrogenase; BHMT, betaine-homocysteine S-methyltransferase; Zn, zinc; SAH, S-adenosylhomocysteine; PC, phosphatidylcholine; CPT, cholinephosphotransferase; CDP, cytidine diphosphate; Choline-P, phosphocholine; CT, cytidylyltransferase; BADH, betaine aldehyde dehydrogenase; CBS, cystathionine β-synthase; CTH, cystathionine γ-lyase; THF, tetrahydrofolate; DHFR, dihydrofolate reductase; DHF, dihydrofolate; MS, methionine synthase; 10-formyl THF, 10-formyl-tetrahydrofolate; SHMT, serine hydroxymethyltransferase; dTMP, thymidine monophosphate; TS, thymidylate synthase; 5-MTHF, 5-methyl- tetrahydrofolate; MTHFR, methylenetetrahydrofolate reductase; dUMP, deoxyuridine monophosphate; 5,10-MTHF, 5,10-methylenetetrahydrofolate.


Reference

1. Saeedi P, Petersohn I, Salpea P, Malanda B, Karuranga S, Unwin N, et al. Global and regional diabetes prevalence estimates for 2019 and projections for 2030 and 2045: results from the International Diabetes Federation Diabetes Atlas, 9th edition. Diabetes Res Clin Pract. 2019; 157:107843.
Article
2. Glier MB, Green TJ, Devlin AM. Methyl nutrients, DNA methylation, and cardiovascular disease. Mol Nutr Food Res. 2014; 58:172–82.
3. Finer S, Saravanan P, Hitman G, Yajnik C. The role of the onecarbon cycle in the developmental origins of type 2 diabetes and obesity. Diabet Med. 2014; 31:263–72.
4. Zhu J, Wu Y, Tang Q, Leng Y, Cai W. The effects of choline on hepatic lipid metabolism, mitochondrial function and antioxidative status in human hepatic C3A cells exposed to excessive energy substrates. Nutrients. 2014; 6:2552–71.
Article
5. Huang T, Ren J, Huang J, Li D. Association of homocysteine with type 2 diabetes: a meta-analysis implementing Mendelian randomization approach. BMC Genomics. 2013; 14:867.
Article
6. Zhu J, Chen C, Lu L, Shikany JM, D’Alton ME, Kahe K. Folate, vitamin B6, and vitamin B12 status in association with metabolic syndrome incidence. JAMA Netw Open. 2023; 6:e2250621.
7. Song Y, Cook NR, Albert CM, Van Denburgh M, Manson JE. Effect of homocysteine-lowering treatment with folic acid and B vitamins on risk of type 2 diabetes in women: a randomized, controlled trial. Diabetes. 2009; 58:1921–8.
8. Qin X, Li J, Zhang Y, Chen D, Wang B, He M, et al. Effect of folic acid supplementation on risk of new-onset diabetes in adults with hypertension in China: findings from the China Stroke Primary Prevention Trial (CSPPT). J Diabetes. 2016; 8:286–94.
Article
9. Ranasinghe P, Wathurapatha WS, Galappatthy P, Katulanda P, Jayawardena R, Constantine GR. Zinc supplementation in prediabetes: a randomized double-blind placebo-controlled clinical trial. J Diabetes. 2018; 10:386–97.
10. Al-Maskari MY, Waly MI, Ali A, Al-Shuaibi YS, Ouhtit A. Folate and vitamin B12 deficiency and hyperhomocysteinemia promote oxidative stress in adult type 2 diabetes. Nutrition. 2012; 28:e23–6.
Article
11. Hong SM, Woo HW, Kim MK, Kim SY, Lee YH, Shin DH, et al. A prospective association between dietary folate intake and type 2 diabetes risk among Korean adults aged 40 years or older: the Korean Multi-Rural Communities Cohort (MRCohort) Study. Br J Nutr. 2017; 118:1078–88.
Article
12. Eshak ES, Iso H, Muraki I, Tamakoshi A. Among the water-soluble vitamins, dietary intakes of vitamins C, B2 and folate are associated with the reduced risk of diabetes in Japanese women but not men. Br J Nutr. 2019; 121:1357–64.
Article
13. Zhu J, Chen C, Lu L, Yang K, Reis J, He K. Intakes of folate, vitamin B6, and vitamin B12 in relation to diabetes incidence among American young adults: a 30-year follow-up study. Diabetes Care. 2020; 43:2426–34.
Article
14. Virtanen JK, Tuomainen TP, Voutilainen S. Dietary intake of choline and phosphatidylcholine and risk of type 2 diabetes in men: the Kuopio Ischaemic Heart Disease Risk Factor Study. Eur J Nutr. 2020; 59:3857–61.
Article
15. Dibaba DT, Johnson KC, Kucharska-Newton AM, Meyer K, Zeisel SH, Bidulescu A. The association of dietary choline and betaine with the risk of type 2 diabetes: the Atherosclerosis Risk in Communities (ARIC) Study. Diabetes Care. 2020; 43:2840–6.
Article
16. Greenberg JA, Jiang X, Tinker LF, Snetselaar LG, Saquib N, Shadyab AH. Eggs, dietary cholesterol, choline, betaine, and diabetes risk in the Women’s Health Initiative: a prospective analysis. Am J Clin Nutr. 2021; 114:368–77.
Article
17. Lu X, Huang R, Li S, Fang A, Chen Y, Chen S, et al. Associations between serum betaine, methyl-metabolizing genetic polymorphisms and risk of incident type 2 diabetes: a prospective cohort study in community-dwelling Chinese adults. Nutrients. 2022; 14:362.
Article
18. Gao X, Randell E, Tian Y, Zhou H, Sun G. Low serum choline and high serum betaine levels are associated with favorable components of metabolic syndrome in Newfoundland population. J Diabetes Complications. 2019; 33:107398.
Article
19. Nie H, Hu H, Li Z, Wang R, He J, Li P, et al. Associations of plasma metal levels with type 2 diabetes and the mediating effects of microRNAs. Environ Pollut. 2022; 292(Pt B):118452.
Article
20. Cheng Y, Wang C, Zhang X, Zhao Y, Jin B, Wang C, et al. Circulating homocysteine and folate concentrations and risk of type 2 diabetes: a retrospective observational study in Chinese adults and a Mendelian randomization analysis. Front Cardiovasc Med. 2022; 9:978998.
Article
21. Ding L, Yang Q, Sun Z, Liu L, Meng Z, Zhao X, et al. Association between dietary intake of one-carbon metabolism nutrients and hyperglycemia in coal-burning fluorosis areas of Guizhou, China. Front Nutr. 2022; 9:1002044.
Article
22. Sun X, Chen Y, Shu J, Li Z, Yu D, Peng W, et al. The association between methionine intake and diabetes in Chinese Adults: results from the China Health and Nutrition Survey. Nutrients. 2022; 15:116.
Article
23. Doshi SN, McDowell IF, Moat SJ, Lang D, Newcombe RG, Kredan MB, et al. Folate improves endothelial function in coronary artery disease: an effect mediated by reduction of intracellular superoxide? Arterioscler Thromb Vasc Biol. 2001; 21:1196–202.
24. Doshi SN, McDowell IF, Moat SJ, Payne N, Durrant HJ, Lewis MJ, et al. Folic acid improves endothelial function in coronary artery disease via mechanisms largely independent of homocysteine lowering. Circulation. 2002; 105:22–6.
Article
25. Mangoni AA, Sherwood RA, Asonganyi B, Swift CG, Thomas S, Jackson SH. Short-term oral folic acid supplementation enhances endothelial function in patients with type 2 diabetes. Am J Hypertens. 2005; 18(2 Pt 1):220–6.
Article
26. Sheu WH, Chin HM, Lee WJ, Wan CJ, Su HY, Lang HF. Prospective evaluation of folic acid supplementation on plasma homocysteine concentrations during weight reduction: a randomized, double-blinded, placebo-controlled study in obese women. Life Sci. 2005; 76:2137–45.
Article
27. Villa P, Perri C, Suriano R, Cucinelli F, Panunzi S, Ranieri M, et al. L-folic acid supplementation in healthy postmenopausal women: effect on homocysteine and glycolipid metabolism. J Clin Endocrinol Metab. 2005; 90:4622–9.
Article
28. Moat SJ, Madhavan A, Taylor SY, Payne N, Allen RH, Stabler SP, et al. High- but not low-dose folic acid improves endothelial function in coronary artery disease. Eur J Clin Invest. 2006; 36:850–9.
Article
29. Solini A, Santini E, Ferrannini E. Effect of short-term folic acid supplementation on insulin sensitivity and inflammatory markers in overweight subjects. Int J Obes (Lond). 2006; 30:1197–202.
Article
30. Title LM, Ur E, Giddens K, McQueen MJ, Nassar BA. Folic acid improves endothelial dysfunction in type 2 diabetes: an effect independent of homocysteine-lowering. Vasc Med. 2006; 11:101–9.
Article
31. Moens AL, Claeys MJ, Wuyts FL, Goovaerts I, Van Hertbruggen E, Wendelen LC, et al. Effect of folic acid on endothelial function following acute myocardial infarction. Am J Cardiol. 2007; 99:476–81.
Article
32. Cagnacci A, Cannoletta M, Volpe A. High-dose short-term folate administration modifies ambulatory blood pressure in postmenopausal women: a placebo-controlled study. Eur J Clin Nutr. 2009; 63:1266–8.
Article
33. Gargari BP, Aghamohammadi V, Aliasgharzadeh A. Effect of folic acid supplementation on biochemical indices in overweight and obese men with type 2 diabetes. Diabetes Res Clin Pract. 2011; 94:33–8.
Article
34. Grigoletti SS, Guindani G, Moraes RS, Ribeiro JP, Sprinz E. Short-term folinic acid supplementation improves vascular reactivity in HIV-infected individuals: a randomized trial. Nutrition. 2013; 29:886–91.
Article
35. Asemi Z, Karamali M, Esmaillzadeh A. Metabolic response to folate supplementation in overweight women with polycystic ovary syndrome: a randomized double-blind placebo-controlled clinical trial. Mol Nutr Food Res. 2014; 58:1465–73.
Article
36. Hashemi M, Heshmat-Ghahdarijani K, Zarean E, Baktash F, Mortazavi ZS. Evaluation of the effect of high-dose folic acid on endothelial dysfunction in pre-eclamptic patients: a randomized clinical trial. J Res Med Sci. 2016; 21:114.
Article
37. Aarsand AK, Carlsen SM. Folate administration reduces circulating homocysteine levels in NIDDM patients on long-term metformin treatment. J Intern Med. 1998; 244:169–74.
Article
38. Setola E, Monti LD, Galluccio E, Palloshi A, Fragasso G, Paroni R, et al. Insulin resistance and endothelial function are improved after folate and vitamin B12 therapy in patients with metabolic syndrome: relationship between homocysteine levels and hyperinsulinemia. Eur J Endocrinol. 2004; 151:483–9.
Article
39. Potter K, Hankey GJ, Green DJ, Eikelboom J, Jamrozik K, Arnolda LF. The effect of long-term homocysteine-lowering on carotid intima-media thickness and flow-mediated vasodilation in stroke patients: a randomized controlled trial and metaanalysis. BMC Cardiovasc Disord. 2008; 8:24.
Article
40. Kurt R, Yilmaz Y, Ermis F, Kalayoglu Besisik S, Polat N, Elitok A, et al. Folic acid and vitamin B12 supplementation improves coronary flow reserve in elderly subjects with vitamin B12 deficiency. Arch Med Res. 2010; 41:369–72.
Article
41. Palomba S, Falbo A, Giallauria F, Russo T, Tolino A, Zullo F, et al. Effects of metformin with or without supplementation with folate on homocysteine levels and vascular endothelium of women with polycystic ovary syndrome. Diabetes Care. 2010; 33:246–51.
Article
42. Mashavi M, Hanah R, Boaz M, Gavish D, Matas Z, Fux A, et al. Effect of homocysteine-lowering therapy on arterial elasticity and metabolic parameters in metformin-treated diabetic patients. Atherosclerosis. 2008; 199:362–7.
Article
43. Talari HR, Rafiee M, Farrokhian A, Raygan F, Bahmani F, Darooghegi Mofrad M, et al. The effects of folate supplementation on carotid intima-media thickness and metabolic status in patients with metabolic syndrome. Ann Nutr Metab. 2016; 69:41–50.
Article
44. Bahmani F, Rahimi Galougahi F, Vahedpoor Z, Jamilian M, Mahmoodi S, Baghban R, et al. The effects of folic acid supplementation on recurrence and metabolic status in endometrial hyperplasia: a randomized, double-blind, placebo-controlled trial. Arch Iran Med. 2018; 21:452–9.
45. Karamali M, Heidarzadeh Z, Seifati SM, Samimi M, Tabassi Z, Hajijafari M, et al. Zinc supplementation and the effects on metabolic status in gestational diabetes: a randomized, doubleblind, placebo-controlled trial. J Diabetes Complications. 2015; 29:1314–9.
Article
46. Attia JR, Holliday E, Weaver N, Peel R, Fleming KC, Hure A, et al. The effect of zinc supplementation on glucose homeostasis: a randomised double-blind placebo-controlled trial. Acta Diabetol. 2022; 59:965–75.
Article
47. Song Y, Manson JE, Tinker L, Howard BV, Kuller LH, Nathan L, et al. Insulin sensitivity and insulin secretion determined by homeostasis model assessment and risk of diabetes in a multiethnic cohort of women: the Women’s Health Initiative Observational Study. Diabetes Care. 2007; 30:1747–52.
Article
48. Kilicdag EB, Bagis T, Tarim E, Aslan E, Erkanli S, Simsek E, et al. Administration of B-group vitamins reduces circulating homocysteine in polycystic ovarian syndrome patients treated with metformin: a randomized trial. Hum Reprod. 2005; 20:1521–8.
Article
49. Asemi Z, Vahedpoor Z, Jamilian M, Bahmani F, Esmaillzadeh A. Effects of long-term folate supplementation on metabolic status and regression of cervical intraepithelial neoplasia: a randomized, double-blind, placebo-controlled trial. Nutrition. 2016; 32:681–6.
Article
50. Mao G, Hong X, Xing H, Liu P, Liu H, Yu Y, et al. Efficacy of folic acid and enalapril combined therapy on reduction of blood pressure and plasma glucose: a multicenter, randomized, double-blind, parallel-controlled, clinical trial. Nutrition. 2008; 24:1088–96.
Article
51. Tsai MY, Loria CM, Cao J, Kim Y, Siscovick DS, Schreiner PJ, et al. Polygenic association with total homocysteine in the post-folic acid fortification era: the CARDIA study. Mol Genet Metab. 2009; 98:181–6.
Article
52. Huang T, Tucker KL, Lee YC, Crott JW, Parnell LD, Shen J, et al. Methylenetetrahydrofolate reductase variants associated with hypertension and cardiovascular disease interact with dietary polyunsaturated fatty acids to modulate plasma homocysteine in puerto rican adults. J Nutr. 2011; 141:654–9.
53. Huang T, Sun J, Chen Y, Xie H, Xu D, Li D. Associations of common variants in methionine metabolism pathway genes with plasma homocysteine and the risk of type 2 diabetes in Han Chinese. J Nutrigenet Nutrigenomics. 2014; 7:63–74.
Article
54. Meng Y, Liu X, Ma K, Zhang L, Lu M, Zhao M, et al. Association of MTHFR C677T polymorphism and type 2 diabetes mellitus (T2DM) susceptibility. Mol Genet Genomic Med. 2019; 7:e1020.
Article
55. Zhi X, Yang B, Fan S, Li Y, He M, Wang D, et al. Additive interaction of MTHFR C677T and MTRR A66G polymorphisms with being overweight/obesity on the risk of type 2 diabetes. Int J Environ Res Public Health. 2016; 13:1243.
Article
56. Wang H, Hu C, Xiao SH, Wan B. Association of tagging SNPs in the MTHFR gene with risk of type 2 diabetes mellitus and serum homocysteine levels in a Chinese population. Dis Markers. 2014; 2014:725731.
57. Savage DG, Lindenbaum J, Stabler SP, Allen RH. Sensitivity of serum methylmalonic acid and total homocysteine determinations for diagnosing cobalamin and folate deficiencies. Am J Med. 1994; 96:239–46.
Article
58. Cheng CK, Wang C, Shang W, Lau CW, Luo JY, Wang L, et al. A high methionine and low folate diet alters glucose homeostasis and gut microbiome. Biochem Biophys Rep. 2021; 25:100921.
Article
59. Pravenec M, Kozich V, Krijt J, Sokolova J, Zidek V, Landa V, et al. Folate deficiency is associated with oxidative stress, increased blood pressure, and insulin resistance in spontaneously hypertensive rats. Am J Hypertens. 2013; 26:135–40.
Article
60. Chong CR, Clarke K, Levelt E. Metabolic remodeling in diabetic cardiomyopathy. Cardiovasc Res. 2017; 113:422–30.
61. Assies J, Mocking RJ, Lok A, Ruhe HG, Pouwer F, Schene AH. Effects of oxidative stress on fatty acid- and one-carbon-metabolism in psychiatric and cardiovascular disease comorbidity. Acta Psychiatr Scand. 2014; 130:163–80.
Article
62. Esfahani PP, Mahdavinia M, Khorsandi L, Rezaei M, Nikravesh H, Khodayar MJ. Betaine protects against sodium arsenite-induced diabetes and hepatotoxicity in mice. Environ Sci Pollut Res Int. 2023; 30:10880–9.
Article
63. Li S, Wu D, Cao M, Yu Z, Wu M, Liu Y, et al. Effects of choline supplementation on liver biology, gut microbiota, and inflammation in Helicobacter pylori-infected mice. Life Sci. 2020; 259:118200.
Article
64. Mazaheri M, Aghdam AM, Heidari M, Zarrin R. Assessing the effect of zinc supplementation on the frequency of migraine attack, duration, severity, lipid profile and hs-CRP in adult women. Clin Nutr Res. 2021; 10:127–39.
Article
65. Anderson OS, Sant KE, Dolinoy DC. Nutrition and epigenetics: an interplay of dietary methyl donors, one-carbon metabolism and DNA methylation. J Nutr Biochem. 2012; 23:853–9.
Article
66. Jiang X, Greenwald E, Jack-Roberts C. Effects of choline on DNA methylation and macronutrient metabolic gene expression in in vitro models of hyperglycemia. Nutr Metab Insights. 2016; 9:11–7.
Article
67. National Institutes of Health Office of Dietary Supplements. Dietary supplement fact sheets. Available from: https://ods.od.nih.gov/factsheets/list-all/ (cited 2024 Feb 23).
68. U.S. Department of Agriculture, Agricultural Research Service. FoodData Central, 2019. Available from: https://fdc.nal.usda.gov/ (cited 2024 Feb 23).
69. Zeisel SH, Mar MH, Howe JC, Holden JM. Concentrations of choline-containing compounds and betaine in common foods. J Nutr. 2003; 133:1302–7.
Article
Full Text Links
  • DMJ
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr