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Post-challenge hyperglycemia in older adults is associated with increased cardiovascular risk profile
Jill P Crandall1, Harry Shamoon, Hillel W Cohen
1The Institute of Aging Research, Albert Einstein College of Medicine, Bronx, New York 10461, USA. crandall@aecom.yu.edu
Insights
Post-challenge hyperglycemia (PCH) in older adults is linked to metabolic issues and increased cardiovascular disease risk. This study reveals PCH is associated with significant metabolic dysregulation and a proatherosclerotic vascular profile.
Area of Science:
- Gerontology
- Endocrinology
- Cardiovascular Medicine
Background:
- Post-challenge hyperglycemia (PCH) is prevalent in older adults, yet often unrecognized clinically.
- PCH is associated with elevated cardiovascular disease (CVD) risk and mortality.
- The specific glycemic exposure and CVD risk profile in elderly individuals with PCH remain underexplored.
Purpose of the Study:
- To characterize the metabolic and CVD risk profile of elderly individuals with PCH.
- To determine the impact of acute postprandial metabolic changes on vascular biomarkers in this population.
Main Methods:
- A cross-sectional study design was employed.
- Participants included older adults with normal glucose tolerance (n=30) and PCH (n=28).
- Fasting and postprandial levels of glucose, insulin, lipids, inflammatory markers (hs-CRP, PAI-1, adiponectin), and endothelial function (EndoPat) were assessed after a standard meal challenge.
Main Results:
- Subjects with PCH exhibited higher fasting glucose, glycosylated hemoglobin, and insulin resistance compared to controls.
- PCH was associated with elevated fasting high-sensitivity C-reactive protein (hs-CRP) and lower adiponectin levels.
- Postprandial glucose, insulin, and lipid responses were amplified in the PCH group, alongside increased plasminogen activator inhibitor-1 (PAI-1).
- Endothelial function, measured by reactive hyperemia peripheral arterial tonometry (RHPAT), declined postprandially exclusively in the PCH group.
Conclusions:
- Older adults with PCH demonstrate substantial fasting and postprandial metabolic dysregulation.
- This metabolic derangement is accompanied by a vascular profile that is both proatherosclerotic and prothrombotic.
- These findings highlight the clinical significance of identifying and managing PCH in the elderly to mitigate cardiovascular risk.
Context:
Post-challenge hyperglycemia (PCH) is common in older adults and is associated with increased cardiovascular disease (CVD) risk and total mortality. However, PCH is rarely recognized in clinical settings, and the glycemic exposure and CVD risk profile of elderly individuals with PCH has not been defined.
Objective:
The aim of the study was to characterize metabolic and CVD risk profile of elderly subjects with PCH and to determine the effect of acute postprandial metabolic changes on vascular biomarkers.
Design:
We conducted a cross-sectional study with a standard meal challenge protocol.
Participants:
Older adults with normal glucose tolerance (n = 30) or PCH (fasting glucose <126 mg/dl and 2-h glucose >or=170 mg/dl; n = 28) participated in the study.
Main Outcome Measures:
We assessed fasting and postprandial levels of glucose, insulin, lipids, high sensitivity C-reactive protein, plasminogen activator inhibitor-1, and adiponectin and endothelial function using reactive hyperemia peripheral arterial tonometry.
Results:
Normal glucose tolerance and PCH subjects were matched for age, sex, body mass index, and ethnicity. Fasting glucose (102 +/- 3 vs. 93 +/- 2 mg/dl; P < 0.001) and glycosylated hemoglobin (5.7 vs. 5.4%; P = 0.01) were modestly higher in the PCH group, which was also more insulin resistant (homeostasis model assessment for insulin resistance, 7.0 +/- 1.3 vs. 4.1 +/- 0.6; P = 0.03). Fasting high sensitivity C-reactive protein was higher (2.6 +/- 0.5 vs. 1.3 +/- 0.2 mg/dl; P = 0.05), and adiponectin was lower (11.6 +/- 1.6 vs. 14.0 +/- 1.3 microg/ml; P = 0.03) in subjects with PCH. Peak and 6-h postprandial area under the curve glucose, insulin, and lipids were higher in PCH subjects, who also had higher fasting and postprandial levels of plasminogen activator inhibitor-1. Reactive hyperemia peripheral arterial tonometry declined postprandially only in PCH.
Conclusions:
Older adults with PCH experience significant fasting and postprandial metabolic dysregulation, which is accompanied by a proatherosclerotic and prothrombotic vascular profile.
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