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. 1995 Oct 28;311(7013):1124–1127. doi: 10.1136/bmj.311.7013.1124

Increased risk of non-insulin dependent diabetes mellitus at low plasma vitamin E concentrations: a four year follow up study in men.

J T Salonen 1, K Nyyssönen 1, T P Tuomainen 1, P H Mäenpää 1, H Korpela 1, G A Kaplan 1, J Lynch 1, S P Helmrich 1, R Salonen 1
PMCID: PMC2551054  PMID: 7580706

Abstract

OBJECTIVE--To investigate whether low vitamin E status is a risk factor for incident non-insulin dependent diabetes mellitus. DESIGN--Population based follow up study with diabetes assessed at baseline and at four years. SETTING--Eastern Finland. SUBJECTS--Random sample of 944 men aged 42-60 who had no diabetes at the baseline examination. INTERVENTION--Oral glucose tolerance test at four year follow up. MAIN OUTCOME MEASURES--A man was defined diabetic if he had either (a) a fasting blood glucose concentration > or = 6.7 mmol/l, or (b) a blood glucose concentration > or = 10.0 mmol/l two hours after a glucose load, or (c) a clinical diagnosis of diabetes with either dietary, oral, or insulin treatment. RESULTS--45 men developed diabetes during the follow up period. In a multivariate logistic regression model including the strongest predictors of diabetes, a low lipid standardised plasma vitamin E (below median) concentration was associated with a 3.9-fold (95% confidence interval 1.8-fold to 8.6-fold) risk of incident diabetes. A decrement of 1 mumol/l of uncategorised unstandardised vitamin E concentration was associated with an increment of 22% in the risk of diabetes when allowing for the strongest other risk factors as well as serum low density lipoprotein cholesterol and triglyceride concentrations. CONCLUSIONS--There was a strong independent association between low vitamin E status before follow up and an excess risk of diabetes at four years. This supports the theory that free radical stress has a role in the causation of non-insulin dependent diabetes mellitus.

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Selected References

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  1. De Leenheer A. P., De Bevere V. O., De Ruyter M. G., Claeys A. E. Simultaneous determination of retinol and alpha-tocopherol in human serum by high-performance liquid chromatography. J Chromatogr. 1979 Mar 1;162(3):408–413. doi: 10.1016/s0378-4347(00)81528-5. [DOI] [PubMed] [Google Scholar]
  2. Flechner I., Maruta K., Burkart V., Kawai K., Kolb H., Kiesel U. Effects of radical scavengers on the development of experimental diabetes. Diabetes Res. 1990 Feb;13(2):67–73. [PubMed] [Google Scholar]
  3. Gallou G., Ruelland A., Legras B., Maugendre D., Allannic H., Cloarec L. Plasma malondialdehyde in type 1 and type 2 diabetic patients. Clin Chim Acta. 1993 Feb 28;214(2):227–234. doi: 10.1016/0009-8981(93)90114-j. [DOI] [PubMed] [Google Scholar]
  4. Gey K. F. Prospects for the prevention of free radical disease, regarding cancer and cardiovascular disease. Br Med Bull. 1993 Jul;49(3):679–699. doi: 10.1093/oxfordjournals.bmb.a072640. [DOI] [PubMed] [Google Scholar]
  5. Golay A., Felber J. P. Evolution from obesity to diabetes. Diabete Metab. 1994 Jan-Feb;20(1):3–14. [PubMed] [Google Scholar]
  6. Hayward A. R., Shriber M., Sokol R. Vitamin E supplementation reduces the incidence of diabetes but not insulitis in NOD mice. J Lab Clin Med. 1992 May;119(5):503–507. [PubMed] [Google Scholar]
  7. Kaplan G. A., Salonen J. T. Socioeconomic conditions in childhood and ischaemic heart disease during middle age. BMJ. 1990 Nov 17;301(6761):1121–1123. doi: 10.1136/bmj.301.6761.1121. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Kauhanen J., Julkunen J., Salonen J. T. Coping with inner feelings and stress: heavy alcohol use in the context of alexithymia. Behav Med. 1992 Fall;18(3):121–126. doi: 10.1080/08964289.1992.9936962. [DOI] [PubMed] [Google Scholar]
  9. Laakso M., Reunanen A., Klaukka T., Aromaa A., Maatela J., Pyörälä K. Changes in the prevalence and incidence of diabetes mellitus in Finnish adults, 1970-1987. Am J Epidemiol. 1991 May 1;133(9):850–857. doi: 10.1093/oxfordjournals.aje.a115965. [DOI] [PubMed] [Google Scholar]
  10. Lakka T. A., Salonen J. T. Intra-person variability of various physical activity assessments in the Kuopio Ischaemic Heart Disease Risk Factor Study. Int J Epidemiol. 1992 Jun;21(3):467–472. doi: 10.1093/ije/21.3.467. [DOI] [PubMed] [Google Scholar]
  11. Murthy V. K., Shipp J. C., Hanson C., Shipp D. M. Delayed onset and decreased incidence of diabetes in BB rats fed free radical scavengers. Diabetes Res Clin Pract. 1992 Oct;18(1):11–16. doi: 10.1016/0168-8227(92)90049-w. [DOI] [PubMed] [Google Scholar]
  12. Nishigaki I., Hagihara M., Tsunekawa H., Maseki M., Yagi K. Lipid peroxide levels of serum lipoprotein fractions of diabetic patients. Biochem Med. 1981 Jun;25(3):373–378. doi: 10.1016/0006-2944(81)90096-x. [DOI] [PubMed] [Google Scholar]
  13. Packer L. The role of anti-oxidative treatment in diabetes mellitus. This meeting was held in Frankfurt am Main, Germany. Diabetologia. 1993 Nov;36(11):1212–1213. doi: 10.1007/BF00401070. [DOI] [PubMed] [Google Scholar]
  14. Paolisso G., D'Amore A., Giugliano D., Ceriello A., Varricchio M., D'Onofrio F. Pharmacologic doses of vitamin E improve insulin action in healthy subjects and non-insulin-dependent diabetic patients. Am J Clin Nutr. 1993 May;57(5):650–656. doi: 10.1093/ajcn/57.5.650. [DOI] [PubMed] [Google Scholar]
  15. Salonen J. T. Is there a continuing need for longitudinal epidemiologic research? The Kuopio Ischaemic Heart Disease Risk Factor Study. Ann Clin Res. 1988;20(1-2):46–50. [PubMed] [Google Scholar]
  16. Salonen J. T., Salonen R., Seppänen K., Kantola M., Parviainen M., Alfthan G., Mäenpä P. H., Taskinen E., Rauramaa R. Relationship of serum selenium and antioxidants to plasma lipoproteins, platelet aggregability and prevalent ischaemic heart disease in Eastern Finnish men. Atherosclerosis. 1988 Mar;70(1-2):155–160. doi: 10.1016/0021-9150(88)90109-8. [DOI] [PubMed] [Google Scholar]
  17. Salonen J. T., Salonen R., Seppänen K., Rauramaa R., Tuomilehto J. HDL, HDL2, and HDL3 subfractions, and the risk of acute myocardial infarction. A prospective population study in eastern Finnish men. Circulation. 1991 Jul;84(1):129–139. doi: 10.1161/01.cir.84.1.129. [DOI] [PubMed] [Google Scholar]
  18. Sato Y., Hotta N., Sakamoto N., Matsuoka S., Ohishi N., Yagi K. Lipid peroxide level in plasma of diabetic patients. Biochem Med. 1979 Feb;21(1):104–107. doi: 10.1016/0006-2944(79)90061-9. [DOI] [PubMed] [Google Scholar]
  19. Sinclair A. J., Lunec J., Girling A. J., Barnett A. H. Modulators of free radical activity in diabetes mellitus: role of ascorbic acid. EXS. 1992;62:342–352. doi: 10.1007/978-3-0348-7460-1_34. [DOI] [PubMed] [Google Scholar]
  20. Tsai E. C., Hirsch I. B., Brunzell J. D., Chait A. Reduced plasma peroxyl radical trapping capacity and increased susceptibility of LDL to oxidation in poorly controlled IDDM. Diabetes. 1994 Aug;43(8):1010–1014. doi: 10.2337/diab.43.8.1010. [DOI] [PubMed] [Google Scholar]
  21. Tuomilehto J., Korhonen H. J., Kartovaara L., Salomaa V., Stengård J. H., Pitkänen M., Aro A., Javela K., Uusitupa M., Pitkäniemi J. Prevalence of diabetes mellitus and impaired glucose tolerance in the middle-aged population of three areas in Finland. Int J Epidemiol. 1991 Dec;20(4):1010–1017. doi: 10.1093/ije/20.4.1010. [DOI] [PubMed] [Google Scholar]
  22. Wolff S. P. Diabetes mellitus and free radicals. Free radicals, transition metals and oxidative stress in the aetiology of diabetes mellitus and complications. Br Med Bull. 1993 Jul;49(3):642–652. doi: 10.1093/oxfordjournals.bmb.a072637. [DOI] [PubMed] [Google Scholar]

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