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大学・研究所にある論文を検索できる 「Clinical and genetic determinants of urinary glucose excretion in patients with diabetes mellitus」の論文概要。リケラボ論文検索は、全国の大学リポジトリにある学位論文・教授論文を一括検索できる論文検索サービスです。

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Clinical and genetic determinants of urinary glucose excretion in patients with diabetes mellitus

物部 圭介 近畿大学

2022.02.28

概要

Aims/Introduction:
Glucosuria is a representative symptom in diabetes patients with poor glycemic control and in those treated with sodium–glucose cotransporter 2 inhibitors. Renal threshold levels of glucose excretion are known to vary among individuals, but factors contributing to glucosuria are not well characterized. The present study aimed to clarify clinical and genetic determinants of glucosuria in individuals with diabetes mellitus.

Materials and Methods:
The 24-h urinary glucose excretion was measured in 135 hospitalized patients on admission, with continuous measurement for five consecutive days in 75 patients. Genetic and clinical factors contributing to glucosuria were studied. As a genetic factor, SLC5A2 polymorphism was genotyped. A total of 476 participants (266 participants with type 2 diabetes and 210 healthy controls) were additionally genotyped for the association study of SLC5A2 with type 2 diabetes. A meta-analysis was carried out with the present study and previous association studies.

Results:
Multiple regression analysis showed that the independent variables of average blood glucose (b = 0.41, P = 1.4 9 10-7 ), estimated glomerular filtration rate (b = 0.28, P = 6.0 9 10-5 ), sex (b = 0.28, P = 5.7 9 10-5 ) and SLC5A2 rs9934336 polymorphism (b = 0.17, P = 0.02) were significantly correlated with urinary glucose excretion. The frequency of the A allele of rs9934336 tended to be lower in participants with type 2 diabetes than in controls (odds ratio 0.78, 95% confidence interval 0.53–1.13, not significant), and meta-analysis showed a significant association between the A allele and type 2 diabetes (summary odds ratio for minor allele [A] 0.86, 95% confidence interval 0.78–0.94, P < 0.002).

Conclusions:
Blood glucose, estimated glomerular filtration rate, sex and SLC5A2 polymorphism were independent determinants of glucosuria in diabetes mellitus.

参考文献

1. Stumvoll M, Chintalapudi U, Perriello G, et al. Uptake and release of glucose by the human kidney. Postabsorptive rates and responses to epinephrine. J Clin Invest 1995; 96: 2528–2533.

2. Gerich JE, Meyer C, Woerle HJ, et al. Renal gluconeogenesis: Its importance in human glucose homeostasis. Diabetes Care 2001; 24: 382–391.

3. Gamba G, Miyanoshita A, Lombardi M, et al. Molecular cloning, primary structure, and characterization of two members of the mammalian electroneutral sodium- (potassium)-chloride cotransporter family expressed in kidney. J Biol Chem 1994; 269: 17713–17722.

4. Butterfield WJ, Keen H, Whichelow MJ. Renal glucose threshold variations with age. Br Med J 1967; 4: 505–507.

5. Kanai Y, Lee WS, You G, et al. The human kidney low affinity na+/glucose cotransporter sglt2. Delineation of the major renal reabsorptive mechanism for d-glucose. J Clin Invest 1994; 93: 397–404.

6. Wright EM. Renal na(+)-glucose cotransporters. Am J Physiol Renal Physiol 2001; 280: F10–F18.

7. Mogensen CE. Maximum tubular reabsorption capacity for glucose and renal hemodynamcis during rapid hypertonic glucose infusion in normal and diabetic subjects. Scand J Clin Lab Invest 1971; 28: 101–109.

8. Rahmoune H, Thompson PW, Ward JM, et al. Glucose transporters in human renal proximal tubular cells isolated from the urine of patients with non-insulin-dependent diabetes. Diabetes 2005; 54: 3427–3434.

9. Freitas HS, Anhe GF, Melo KF, et al. Na(+) -glucose transporter-2 messenger ribonucleic acid expression in kidney of diabetic rats correlates with glycemic levels: Involvement of hepatocyte nuclear factor-1alpha expression and activity. Endocrinology 2008; 149: 717–724.

10. Santer R, Kinner M, Lassen CL, et al. Molecular analysis of the sglt2 gene in patients with renal glucosuria. J Am Soc Nephrol 2003; 14: 2873–2882.

11. Gong S, Guo J, Han X, et al. Clinical and genetic features of patients with type 2 diabetes and renal glycosuria. J Clin Endocrinol Metab 2017; 102: 1548–1556.

12. Yu L, Wu M, Hou P, et al. Slc5a2 mutations, including two novel mutations, responsible for renal glucosuria in chinese families. BMC Nephrol 2020; 21: 69.

13. Haneda M, Noda M, Origasa H, et al. Japanese clinical practice guideline for diabetes 2016. J Diabetes Investig 2018; 9: 657–697.

14. Ordelheide AM, Bohm A, Kempe-Teufel D, et al. Common variation in the sodium/glucose cotransporter 2 gene slc5a2 does neither affect fasting nor glucose-suppressed plasma glucagon concentrations. PLoS One 2017; 12: e0177148.

15. Mantel N, Haenszel W. Statistical aspects of the analysis of data from retrospective studies of disease. J Natl Cancer Inst 1959; 22: 719–748.

16. Enigk U, Breitfeld J, Schleinitz D, et al. Role of genetic variation in the human sodium-glucose cotransporter 2 gene (sglt2) in glucose homeostasis. Pharmacogenomics 2011; 12: 1119–1126.

17. Drexel H, Leiherer A, Saely CH, et al. Are sglt2 polymorphisms linked to diabetes mellitus and cardiovascular disease? Prospective study and meta-analysis. Biosci Rep 2019; 39: BSR20190299.

18. Zimdahl H, Haupt A, Brendel M, et al. Influence of common polymorphisms in the slc5a2 gene on metabolic traits in subjects at increased risk of diabetes and on response to empagliflozin treatment in patients with diabetes. Pharmacogenet Genomics 2017; 27: 135–142.

19. Ogna VF, Ogna A, Vuistiner P, et al. New anthropometrybased age- and sex-specific reference values for urinary 24- hour creatinine excretion based on the adult Swiss population. Bmc Med 2015; 13: 40.

20. Hosoya T, Toshima R, Icida K, et al. Changes in renal function with aging among Japanese. Intern Med 1995; 34: 520–527.

21. Sabolic I, Vrhovac I, Eror DB, et al. Expression of na+-dglucose cotransporter sglt2 in rodents is kidney-specific and exhibits sex and species differences. Am J Physiol Cell Physiol 2012; 302: C1174–C1188.

22. Magen D, Sprecher E, Zelikovic I, et al. A novel missense mutation in slc5a2 encoding sglt2 underlies autosomalrecessive renal glucosuria and aminoaciduria. Kidney Int 2005; 67: 34–41.

23. Yu L, Xu Q, Hou P, et al. Decreased expression and function of sodium-glucose co-transporter 2 from a novel c-terminal mutation: A case report. BMC Nephrol 2016; 17: 31.

24. Hwang YC, Kim JH, Lee BW, et al. A lower baseline urinary glucose excretion predicts a better response to the sodium glucose cotransporter 2 inhibitor. Diabetes Metab J 2019; 43: 898–905.

25. The GTEx Consortium. The Genotype-Tissue Expression (GTEx) pilot analysis: Multitissue gene regulation in humans. Science 2015; 348: 648–660.

26. Yakovleva T, Sokolov V, Chu L, et al. Comparison of the urinary glucose excretion contributions of SGLT2 and SGLT1: A quantitative systems pharmacology analysis in healthy individuals and patients with type 2 diabetes treated with SGLT2 inhibitors. Diabetes Obes Metab 2019; 21: 2684–2693.

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