TY - JOUR
T1 - Impaired plasma glucose clearance is a key determinant of fasting hyperglycemia in people with obesity
AU - Mittendorfer, Bettina
AU - van Vliet, Stephan
AU - Smith, Gordon I.
AU - Petersen, Max C.
AU - Patterson, Bruce W.
AU - Klein, Samuel
N1 - Publisher Copyright:
© 2024 The Obesity Society.
PY - 2024/3
Y1 - 2024/3
N2 - Objective: The objective of this study was to evaluate the relative importance of the basal rate of glucose appearance (Ra) in the circulation and the basal rate of plasma glucose clearance in determining fasting plasma glucose concentration in people with obesity and different fasting glycemic statuses. Methods: The authors evaluated basal glucose kinetics in 33 lean people with normal fasting glucose (<100 mg/dL; Lean < 100 group) and 206 people with obesity and normal fasting glucose (Ob < 100 group, n = 118), impaired fasting glucose (100–125 mg/dL; Ob100–125 group, n = 66), or fasting glucose diagnostic of diabetes (≥126 mg/dL; Ob ≥ 126 group, n = 22). Results: Although there was a large (up to three-fold) range in glucose Ra within each group, the ranges in glucose concentration in the Lean < 100, Ob < 100, and Ob100–125 groups were small because of a close relationship between glucose Ra and clearance rate. However, the glucose clearance rate at any Ra value was lower in the hyperglycemic than the normoglycemic groups. In the Ob ≥ 126 group, plasma glucose concentration was primarily determined by glucose Ra, because glucose clearance was markedly attenuated. Conclusions: Fasting hyperglycemia in people with obesity represents a disruption of the precisely regulated integration of glucose production and clearance rates. (Figure presented.).
AB - Objective: The objective of this study was to evaluate the relative importance of the basal rate of glucose appearance (Ra) in the circulation and the basal rate of plasma glucose clearance in determining fasting plasma glucose concentration in people with obesity and different fasting glycemic statuses. Methods: The authors evaluated basal glucose kinetics in 33 lean people with normal fasting glucose (<100 mg/dL; Lean < 100 group) and 206 people with obesity and normal fasting glucose (Ob < 100 group, n = 118), impaired fasting glucose (100–125 mg/dL; Ob100–125 group, n = 66), or fasting glucose diagnostic of diabetes (≥126 mg/dL; Ob ≥ 126 group, n = 22). Results: Although there was a large (up to three-fold) range in glucose Ra within each group, the ranges in glucose concentration in the Lean < 100, Ob < 100, and Ob100–125 groups were small because of a close relationship between glucose Ra and clearance rate. However, the glucose clearance rate at any Ra value was lower in the hyperglycemic than the normoglycemic groups. In the Ob ≥ 126 group, plasma glucose concentration was primarily determined by glucose Ra, because glucose clearance was markedly attenuated. Conclusions: Fasting hyperglycemia in people with obesity represents a disruption of the precisely regulated integration of glucose production and clearance rates. (Figure presented.).
UR - http://www.scopus.com/inward/record.url?scp=85182483896&partnerID=8YFLogxK
U2 - 10.1002/oby.23963
DO - 10.1002/oby.23963
M3 - Article
C2 - 38228469
AN - SCOPUS:85182483896
SN - 1930-7381
VL - 32
SP - 540
EP - 546
JO - Obesity
JF - Obesity
IS - 3
ER -