Cited by 490Diabetes Management and ResearchDiabetes Treatment and ManagementDiabetes, Cardiovascular Risks, and Lipoproteins

The loss of postprandial glycemic control precedes stepwise deterioration of fasting with worsening diabetes

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Monnier, Louis, Colette, Claude, Dunseath, Gareth J., Owens, David R.·2007·Diabetes Care

Abstract

OBJECTIVE— The aim of the study was to determine whether the loss of fasting and postprandial glycemic control occurs in parallel or sequentially in the evolution of type 2 diabetes. RESEARCH DESIGN AND METHODS— In 130 type 2 diabetic patients, 24-h glucose profiles were obtained using a continuous glucose monitoring system. The individuals with type 2 diabetes were divided into five groups according to A1C levels: 1 (<6.5%, n = 30), 2 (6.5–6.9%, n = 17), 3 (7–7.9%, n = 32), 4 (8–8.9%, n = 25), and 5 (≥9%, n = 26). The glucose profiles between the groups were compared. The overall glucose concentrations for the diurnal, nocturnal, and morning periods, which represent the postprandial, fasting, and the dawn phenomenon states, respectively, were also compared. RESULTS— Glucose concentrations increased steadily from group 1 to 5 in a stepwise manner. The initial differences in mean glucose concentrations reaching statistical significance occurred 1) between groups 1 and 2 (6.4 vs. 7.7 mmol/l, P = 0.0004) for daytime postprandial periods, followed by differences; 2) between groups 2 and 3 (7.5 vs. 9.3 mmol/l, P = 0.0003) for the morning periods (dawn phenomenon); and finally 3) between groups 3 and 4 (6.3 vs. 8.4 mmol/l, P < 0.0001) for nocturnal fasting periods. CONCLUSIONS— The deterioration of glucose homeostasis in individuals with type 2 diabetes progressed from postprandial to fasting hyperglycemia following a three-step process. The first step related to the three diurnal postmeal periods considered as a whole, the second step occurred during the morning period, and the third and final step corresponded to sustained hyperglycemia over the nocturnal fasting periods. Such a description of the key stages in the evolution of type 2 diabetes may be of interest for implementing antidiabetes treatment.

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  • A 2-hour PPG <8.0 mmol/L correlates best with an A1C <7.0%.

    “Another study using continuous glucose monitoring (CGM) demonstrated that a 2-hour PPG <8.0 mmol/L correlates best with an A1C <7.0% (40).”

    From Targets for Glycemic Control (2018) · cites this paper as [40]

    The Comparison of daytime postprandial periods section reports CGM-derived mean postprandial glucose of 7.7 mmol/L in the group with A1C of 6.5–6.9%, supporting a relationship between postprandial glucose and A1C. It does not establish that a glucose value measured two hours after a meal below 8.0 mmol/L correlates best with A1C below 7.0%. Page numbers are unavailable in our copy. (LLM, conf=0.85)

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  • If an A1C target ≤7.0% cannot be achieved with a FPG target of 4.0-7.0 mmol/L and PPG target of 5.0-10.0 mmol/L, further FPG lowering to 4.0 to 5.5 mmol/L and/or PPG lowering to 5.0-8.0 mmol/L may be considered, but must be balanced against the risk of hypoglycemia.

    “If an A1C target ≤7.0%cannot be achieved with a FPG target of 4.0-7.0mmol/L and PPG target of 5.0-10.0mmol/L, further FPG lowering to 4.0 to 5.5 mmol/L and/or PPG lowering to 5.0-8.0 mmol/L may be considered, but must be balanced against the risk of hypoglycemia [Grade D, Level 4 (38) for FPG target for type 2 diabetes; Grade D, Consensus for FPG target for type 1 diabetes; Grade D, Level 4 (38,40”

    From Targets for Glycemic Control (2018) · cites this paper as [40]

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  • Postprandial hyperglycemia begins prior to type 2 diabetes occurring.

    “Firstly, postprandial hyperglycemia has been shown to begin prior to type 2 diabetes occurring [3–5]”

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Research works printed but not linked: 1

  1. [18]18. Zar JH: Testing for goodness of fit. In Bio- statistical Analysis. 4th ed. Upper Saddle River, NJ, Prentice Hall, 1999, p. 461- 485

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Authors
Monnier, L., Colette, C., Dunseath, G. J., & Owens, D. R.
Affiliations
  • Hôpital Lapeyronie (FR)
  • Laboratory of Human Nutrition and Atherogenesis, University Institute of Clinical Research, Montpellier, France
  • University Hospital Llandough (GB)
Venue
Diabetes Care
Published
2007-02-01
Volume
30
Issue
2
Pages
263-269
ISSN
  • 0149-5992 (ISSN-L)
  • 1935-5548
OpenAlex
W2127454519
Cited by
490
References
31
Citations by year
2026: 7 · 2025: 12 · 2024: 17 · 2023: 16 · 2022: 17 · 2021: 20 · 2020: 14 · 2019: 22 · 2018: 27 · 2017: 33 · 2016: 31 · 2015: 24 · 2014: 40 · 2013: 35 · 2012: 27
FWCI
28.26
Type
journal article
Language
en
Open access
Locations
  • Diabetes Care (publishedVersion)
  • PubMed (publishedVersion)
  • ORCA Online Research @Cardiff (Cardiff University) (submittedVersion)
Topics
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Management and Research
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Treatment and Management
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes, Cardiovascular Risks, and Lipoproteins
Keywords
type 2 diabetes, glycemic control, postprandial hyperglycemia, fasting hyperglycemia, dawn phenomenon, HbA1c, disease progression, glucose homeostasis, continuous glucose monitoring
MeSH terms
Blood Glucose, Blood Pressure, Energy Intake, Diabetes Mellitus, Type 2, Eating, Fasting, Female, Glycated Hemoglobin, Humans, Male, Middle Aged, Disease Progression, Monitoring, Ambulatory, Postprandial Period, Glycemic Index

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