TY - JOUR
T1 - Effect of Progressive Weight Loss on Lactate Metabolism
T2 - A Randomized Controlled Trial
AU - Chondronikola, Maria
AU - Magkos, Faidon
AU - Yoshino, Jun
AU - Okunade, Adewole L.
AU - Patterson, Bruce W.
AU - Muehlbauer, Michael J.
AU - Newgard, Christopher B.
AU - Klein, Samuel
N1 - Publisher Copyright:
© 2018 The Obesity Society
PY - 2018/4
Y1 - 2018/4
N2 - Objective: Lactate is an intermediate of glucose metabolism that has been implicated in the pathogenesis of insulin resistance. This study evaluated the relationship between glucose kinetics and plasma lactate concentration ([LAC]) before and after manipulating insulin sensitivity by progressive weight loss. Methods: Forty people with obesity (BMI = 37.9 ± 4.3 kg/m2) were randomized to weight maintenance (n = 14) or weight loss (n = 19). Subjects were studied before and after 6 months of weight maintenance and before and after 5%, 11%, and 16% weight loss. A hyperinsulinemic-euglycemic clamp procedure in conjunction with [6,6-2H2]glucose tracer infusion was used to assess glucose kinetics. Results: At baseline, fasting [LAC] correlated positively with endogenous glucose production rate (r = 0.532; P = 0.001) and negatively with insulin sensitivity, assessed as the insulin-stimulated glucose disposal (r = −0.361; P = 0.04). Progressive (5% through 16%) weight loss caused a progressive decrease in fasting [LAC], and the decrease in fasting [LAC] after 5% weight loss was correlated with the decrease in endogenous glucose production (r = 0.654; P = 0.002) and the increase in insulin sensitivity (r = −0.595; P = 0.007). Conclusions: This study demonstrates the interrelationships among weight loss, hepatic and muscle glucose kinetics, insulin sensitivity, and [LAC], and it suggests that [LAC] can serve as an additional biomarker of glucose-related insulin resistance.
AB - Objective: Lactate is an intermediate of glucose metabolism that has been implicated in the pathogenesis of insulin resistance. This study evaluated the relationship between glucose kinetics and plasma lactate concentration ([LAC]) before and after manipulating insulin sensitivity by progressive weight loss. Methods: Forty people with obesity (BMI = 37.9 ± 4.3 kg/m2) were randomized to weight maintenance (n = 14) or weight loss (n = 19). Subjects were studied before and after 6 months of weight maintenance and before and after 5%, 11%, and 16% weight loss. A hyperinsulinemic-euglycemic clamp procedure in conjunction with [6,6-2H2]glucose tracer infusion was used to assess glucose kinetics. Results: At baseline, fasting [LAC] correlated positively with endogenous glucose production rate (r = 0.532; P = 0.001) and negatively with insulin sensitivity, assessed as the insulin-stimulated glucose disposal (r = −0.361; P = 0.04). Progressive (5% through 16%) weight loss caused a progressive decrease in fasting [LAC], and the decrease in fasting [LAC] after 5% weight loss was correlated with the decrease in endogenous glucose production (r = 0.654; P = 0.002) and the increase in insulin sensitivity (r = −0.595; P = 0.007). Conclusions: This study demonstrates the interrelationships among weight loss, hepatic and muscle glucose kinetics, insulin sensitivity, and [LAC], and it suggests that [LAC] can serve as an additional biomarker of glucose-related insulin resistance.
UR - http://www.scopus.com/inward/record.url?scp=85042460211&partnerID=8YFLogxK
U2 - 10.1002/oby.22129
DO - 10.1002/oby.22129
M3 - Article
C2 - 29476613
AN - SCOPUS:85042460211
SN - 1930-7381
VL - 26
SP - 683
EP - 688
JO - Obesity
JF - Obesity
IS - 4
ER -