Caffeine intake enhances the benefits of sodium glucose transporter 2 inhibitor

被引:4
作者
Hashimoto, Yoshitaka [1 ]
Tanaka, Muhei [1 ]
Yamazaki, Masahiro [1 ]
Nakano, Koji [2 ]
Ushigome, Emi [1 ]
Okada, Hiroshi [3 ]
Oda, Yohei [1 ]
Nakamura, Naoto [1 ]
Fukui, Michiaki [1 ]
机构
[1] Kyoto Prefectural Univ Med, Grad Sch Med Sci, Dept Endocrinol & Metab, Kyoto, Japan
[2] Kyoto Yamashiro Gen Med Ctr, Dept Endocrinol & Metab, Kyoto, Japan
[3] Japanese Red Cross Kyoto Daini Hosp, Div Metab Nephrol & Rheumatol, Kyoto, Japan
关键词
caffeine; type; 2; diabetes; sodium glucose cotransporter; hydration; glomerular filtration rate; urinary glucose excretion; GLOMERULAR-FILTRATION-RATE; COFFEE CONSUMPTION; TYPE-2; ASSOCIATION; VASOPRESSIN; ADENOSINE; DISEASE; TRIAL;
D O I
10.1002/dmrr.2789
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BackgroundThe effect of sodium glucose transporter 2 (SGLT-2) inhibitors is dependent on the glomerular filtration rate. It has been reported that caffeine intake increases glomerular filtration rate. However, the effect of caffeine intake on urinary glucose excretion in patients who take SGLT-2 inhibitors is unclear. MethodsSix patients with type 2 diabetes took part in a randomized, open-label, crossover pilot study. The patients took SGLT-2 inhibitors (ipragliflozin) for 9days. On day 3, 6 and 9, the patients were assigned to one of three studies: Water 500, patients drank 500mL of water in 3h; Water 1500, patients drank 1500mL of water in 3h; and Caffeine 500, patients drank 500mL of water with 400mg of caffeine in 3h. In all of the studies, the patients' urine was collected over a 6-h period. In addition, we enrolled 60 patients with type 2 diabetes who newly took SGLT-2 inhibitors in a 3-month follow-up cohort study to investigate the effect of caffeine intake on glucose control. Caffeine intake was evaluated using questionnaires. ResultsThe 6-h median (interquartile range) urinary glucose excretion was 9.5 (8.5-9.7)g in Water 500, 12.2 (10.3-27.2)g in Water 1500 and 15.7 (11.4-21.4)g in Caffeine 500 (p=0.005 vs Water 500). In the cohort study, multiple regression analysis demonstrated that log (caffeine intake) was associated with a change in HbA(1c) (=-0.299, p=0.043) after adjusting for covariates. ConclusionsCaffeine intake enhanced the effect of SGLT-2 inhibitors. Copyright (c) 2016 John Wiley & Sons, Ltd.
引用
收藏
页码:694 / 699
页数:6
相关论文
共 23 条
  • [1] Aikawa T, 2007, YANYOUSYOUKENNKYU, V12, P45
  • [2] Effects of coffee on type 2 diabetes mellitus
    Akash, Muhammad Sajid Hamid
    Rehman, Kanwal
    Chen, Shuqing
    [J]. NUTRITION, 2014, 30 (7-8) : 755 - 763
  • [3] Bouby N, 1996, J AM SOC NEPHROL, V7, P842
  • [4] Caffeine IQ, 2014, HARV HLTH LETT, V39, P5
  • [5] Urine Volume and Change in Estimated GFR in a Community-Based Cohort Study
    Clark, William F.
    Sontrop, Jessica M.
    Macnab, Jennifer.
    Surf, Rita S.
    Moist, Louise
    Salvadori, Marina
    Garg, Amit X.
    [J]. CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2011, 6 (11): : 2634 - 2641
  • [6] Caffeinated and Decaffeinated Coffee Consumption and Risk of Type 2 Diabetes: A Systematic Review and a Dose-Response Meta-analysis
    Ding, Ming
    Bhupathiraju, Shilpa N.
    Chen, Mu
    van Dam, Rob M.
    Hu, Frank B.
    [J]. DIABETES CARE, 2014, 37 (02) : 569 - 586
  • [7] Renal Glucose Handling Impact of chronic kidney disease and sodium-glucose cotransporter 2 inhibition in patients with type 2 diabetes
    Ferrannini, Ele
    Veltkamp, Stephan A.
    Smulders, Ronald A.
    Kadokura, Takeshi
    [J]. DIABETES CARE, 2013, 36 (05) : 1260 - 1265
  • [8] RENAL EFFECTS OF THEOPHYLLINE AND CAFFEINE IN NEWBORN RABBITS
    GOUYON, JB
    GUIGNARD, JP
    [J]. PEDIATRIC RESEARCH, 1987, 21 (06) : 615 - 618
  • [9] Global estimates of diabetes prevalence for 2013 and projections for 2035
    Guariguata, L.
    Whiting, D. R.
    Hambleton, I.
    Beagley, J.
    Linnenkamp, U.
    Shaw, J. E.
    [J]. DIABETES RESEARCH AND CLINICAL PRACTICE, 2014, 103 (02) : 137 - 149
  • [10] Mortality from coronary heart disease in subjects with type 2 diabetes and in nondiabetic subjects with and without prior myocardial infarction
    Haffner, SM
    Lehto, S
    Rönnemaa, T
    Pyörälä, K
    Laakso, M
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1998, 339 (04) : 229 - 234