Relationship Between Fasting Plasma Insulin Level and Resistance to Insulin-Mediated Glucose Uptake in Normal and Diabetic Subjects
Abstract
We have previously shown that a significant inverse correlation exists between the height of the plasma insulin concentration and the efficiency of glucose uptake in the fasting state. Subsequently, we devised an infusion technic that provides a more specific measure of cellular resistance to insulin mediated glucose uptake. We have used this technic to study the relationship between fasting plasma insulin level and resistance to insulin mediated glucose uptake in twenty-two patients with normal oral glucose tolerance, fourteen patients with impaired glucose tolerance, and fourteen patients classified as having chemical diabetes mellitus. The results indicate a highly significant positive correlation between the degree of insulin resistance and fasting plasma insulin concentration (r = .69, p < .0001). A positive correlation (r = .43, p < .005) was also found between the degree of insulin resistance and the two hour plasma glucose level during an oral glucose tolerance test. However, no significant correlation was found between per cent adiposity and fasting insulin level, and the relationship between insulin resistance and fasting insulin level appeared to be independent of obesity or any other known cause of decreased insulin responsiveness. These studies indicate that: (1) increases in fasting insulin levels and increase in resistance to insulin mediated glucose uptake are closely related, and that these changes can occur in the absence of any of the “known” causes of decreased insulin responsiveness; (2) in the types of subjects we have studied, deterioration of glucose tolerance is closely related to increases in insulin resistance; and (3) the increases in fasting insulin levels which we have observed appear to be compensatory attempts to overcome the resistance to glucose uptake.
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Olefsky et al. showed that glucose utilization at basal glucose levels was diminished in obese, diabetic individuals.
“This result is consistent with the finding of Olefsky et al. (28) who showed that glucose utilization at basal glucose levels was diminished in obese, diabetic, individuals.”
Several studies, especially in normoglycaemic populations, have shown that HOMA-IR may be a better estimate of insulin sensitivity than fasting insulin.
“Although FI correlates with IR, several studies, especially in normoglycaemic populations [133, 134], have shown that HOMA-IR (calculated based on FI and FBG values) may be a better estimate of insulin sensitivity [135].”
From Exercise, or exercise and diet for the management of polycystic ovary syndrome: a systematic review and meta-analysis (2019) · cites this paper as [133]
Obesity is an important determinant of insulin sensitivity.
“It is well recognised that obesity is an important determinant of insulin sensitivity [9, 10, 29, 30, 31, 32].”
From The relative contributions of insulin resistance and beta-cell dysfunction to the pathophysiology of type 2 diabetes (2003) · cites this paper as [9]
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Identification of a Minimal Model of Glucose Disappearance for Estimating Insulin Sensitivity
Bergman, R. N., Bortolan, G., Cobelli, C., & TOFFOLO, G. M. (1979) · IFAC Proceedings Volumes · doi:10.1016/s1474-6670(17)65505-8 · Cited by 24 · see citing works
Does C‐reactive protein identify a subclinical metabolic disease in healthy subjects?
Bo, S., Gambino, R., Uberti, B., Mangiameli, M. P., Colosso, G., Repetti, E., Gentile, L., Cassader, M., & Pagano, G. F. (2005) · European Journal of Clinical Investigation · doi:10.1111/j.1365-2362.2005.01490.x · Cited by 24 · see citing works
- Authors
- Olefsky, J., Farquhar, J. W., & Reaven, G.
- Affiliations
- Stanford University (US)
- ORCID
- Olefsky, Jerrold
- Venue
- Diabetes
- Publisher
- American Diabetes Association
- Published
- 1973-07-01
- Volume
- 22
- Issue
- 7
- Pages
- 507-513
- ISSN
- 0012-1797 (ISSN-L)
- 1939-327X
- OpenAlex
- W2004880720
- Cited by
- 179
- References
- 0
- Citations by year
- 2026: 1 · 2025: 2 · 2024: 1 · 2023: 4 · 2022: 2 · 2021: 7 · 2020: 5 · 2019: 3 · 2018: 5 · 2017: 6 · 2016: 6 · 2015: 2 · 2014: 6 · 2013: 6 · 2012: 3
- FWCI
- 4.27
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Diabetes (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health
- School of Medicine, Stanford University
- NIH Clinical Center
- Topics
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes, Cardiovascular Risks, and Lipoproteins
- Health Sciences › Medicine › Surgery › Pancreatic function and diabetes
- Health Sciences › Medicine › Epidemiology › Adipokines, Inflammation, and Metabolic Diseases
- Keywords
- fasting insulin, insulin resistance, insulin-stimulated glucose uptake, impaired glucose tolerance, type 2 diabetes, oral glucose tolerance, adiposity, compensatory insulin secretion, hyperinsulinemia
- MeSH terms
- Adult, Blood Glucose, Diabetes Mellitus, Epinephrine, Female, Glucose, Glucose Tolerance Test, Humans, Hyperglycemia, Insulin, Insulin Resistance, Male, Middle Aged, Obesity, Propranolol
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