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Water Supplementation Reduces Copeptin and Plasma Glucose in Adults With High Copeptin: The H2O Metabolism Pilot Study

Abstract

Objective: Because elevated copeptin, a marker of vasopressin, is linked to low water intake and high diabetes risk, we tested the effect of water supplementation on copeptin and fasting glucose.

Design, Setting, And Participants: Thirty-one healthy adults with high copeptin (>10.7 pmol · L-1 in men and >6.1 pmol·L-1 in women) identified in a population-based survey from 2013 to 2015 and with a current 24-hour urine osmolality of >600 mOsm · kg-1 were included.

Intervention: Addition of 1.5 L water daily on top of habitual fluid intake for 6 weeks.

Main Outcome Measure: Pre- and postintervention fasting plasma copeptin concentrations.

Results: Reported mean water intake increased from 0.43 to 1.35 L · d-1 (P < 0.001), with no other observed changes in diet. Median (interquartile range) urine osmolality was reduced from 879 (705, 996) to 384 (319, 502) mOsm · kg-1 (P < 0.001); urine volume increased from 1.06 (0.90, 1.20) to 2.27 (1.52, 2.67) L · d-1 (P < 0.001); and baseline copeptin decreased from 12.9 (7.4, 21.9) pmol · L-1 to 7.8 (4.6;11.3) pmol · L-1 (P < 0.001). Water supplementation reduced fasting plasma glucose from a mean (SD) of 5.94 (0.44) to 5.74 (0.51) (P = 0.04). The water-associated reduction of both fasting copeptin and glucose concentration in plasma was most pronounced in participants in the top tertile of baseline copeptin.

Conclusions: Water supplementation in persons with habitually low water consumption and high copeptin levels is effective in lowering copeptin. It appears a safe and promising intervention with the potential of lowering fasting plasma glucose and thus reducing diabetes risk. Further investigations are warranted to support these findings.

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References
1.
Laakso M . Hyperglycemia and cardiovascular disease in type 2 diabetes. Diabetes. 1999; 48(5):937-42. DOI: 10.2337/diabetes.48.5.937. View

2.
Coutinho M, Gerstein H, Wang Y, Yusuf S . The relationship between glucose and incident cardiovascular events. A metaregression analysis of published data from 20 studies of 95,783 individuals followed for 12.4 years. Diabetes Care. 1999; 22(2):233-40. DOI: 10.2337/diacare.22.2.233. View

3.
Bankir L . Antidiuretic action of vasopressin: quantitative aspects and interaction between V1a and V2 receptor-mediated effects. Cardiovasc Res. 2001; 51(3):372-90. DOI: 10.1016/s0008-6363(01)00328-5. View

4.
Abu-Basha E, Yibchok-anun S, Hsu W . Glucose dependency of arginine vasopressin-induced insulin and glucagon release from the perfused rat pancreas. Metabolism. 2002; 51(9):1184-90. DOI: 10.1053/meta.2002.34052. View

5.
Tanoue A, Ito S, Honda K, Oshikawa S, Kitagawa Y, Koshimizu T . The vasopressin V1b receptor critically regulates hypothalamic-pituitary-adrenal axis activity under both stress and resting conditions. J Clin Invest. 2004; 113(2):302-9. PMC: 311433. DOI: 10.1172/JCI19656. View