The DOI matches its Crossref record; 37 of the 37 references it cites were found in a registry or an index.
Insulin Resistance in Essential Hypertension
Abstract
High blood pressure is prevalent in obesity and in diabetes, both conditions with insulin resistance. To test whether hypertension is associated with insulin resistance independently of obesity and glucose intolerance, we measured insulin sensitivity (using the euglycemic insulin-clamp technique), glucose turnover (using [3H]glucose isotope dilution), and whole-body glucose oxidation (using indirect calorimetry) in 13 young subjects (38 +/- 2 years [+/- SEM]) with untreated essential hypertension (165 +/- 6/112 +/- 3 mm Hg), normal body weight, and normal glucose tolerance. In the postabsorptive state, all measures of glucose metabolism were normal. During steady-state euglycemic hyperinsulinemia (about 60 microU per milliliter), hepatic glucose production and lipolysis were effectively suppressed, and glucose oxidation and potassium disposal were normally stimulated. However, total insulin-induced glucose uptake was markedly impaired (3.80 +/- 0.32 vs. 6.31 +/- 0.42 mg per minute per kilogram of body weight in 11 age- and weight-matched controls, P less than 0.001). Thus, reduced nonoxidative glucose disposal (glycogen synthesis and glycolysis) accounted for virtually all the defect in overall glucose uptake (1.19 +/- 0.24 vs. 3.34 +/- 0.44 mg per minute per kilogram, P less than 0.001). Total glucose uptake was inversely related to systolic or mean blood pressure (r = 0.76 for both, P less than 0.001). These results provide preliminary evidence that essential hypertension is an insulin-resistant state. We conclude that this insulin resistance involves glucose but not lipid or potassium metabolism, is located in peripheral tissues but not the liver, is limited to nonoxidative pathways of intracellular glucose disposal, and is directly correlated with the severity of hypertension.
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“Insulin resistance in skeletal muscle also can develop independent of family history of T2DM.”
From Pathogenesis of insulin resistance in skeletal muscle (2010) · cites this paper as [35]
In the citing paper
“Thus, obese NGT subjects without a family history for T2DM [33, 34] and individuals with essential hypertension [35] and ischemic heart disease [36] also have a 35–50% decrease in whole body insulin-mediated glucose disposal (Figure 3).”
From Pathogenesis of insulin resistance in skeletal muscle (2010) · cites this paper as [35]
In the citing paper
“Insulin resistance and compensatory hyperinsulinaemia are frequently found with essential hypertension [1,2].”
From The sympathetic response to euglycaemic hyperinsulinaemia: Evidence from microelectrode nerve recordings in healthy subjects (1992) · cites this paper as [1]
In the citing paper
“many subsequent clinical and population-based studies showed an association of insulin levels and ⁄ or insulin resistance with hypertension in both obese and nonobese people.12,13”
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Cited by
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Role of Insulin Resistance in Human Disease
Reaven, G. M. (1988) · Diabetes · doi:10.2337/diab.37.12.1595 · Cited by 12,154
Eckel, R. H., Alberti, K., Grundy, S. M., & Zimmet, P. (2010) · The Lancet · doi:10.1016/s0140-6736(09)61794-3 · Cited by 6,317
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Metadata
- Authors
- Ferrannini, E., Buzzigoli, G., Bonadonna, R., Giorico, M. A., Oleggini, M., Graziadei, L., Pedrinelli, R., Brandi, L., & Bevilacqua, S.
- Venue
- New England Journal of Medicine
- Publisher
- Massachusetts Medical Society
- Published
- 1987-08-06
- Volume
- 317
- Issue
- 6
- Pages
- 350-357
- ISSN
- 0028-4793 (ISSN-L)
- 1533-4406
- OpenAlex
- W2319850088
- Semantic Scholar
- 8f94bc06901b356e0488337d786981d8352e8bf1
- Cited by
- 2,344
- References
- 37
- Citations by year
- 2026: 7 · 2025: 16 · 2024: 17 · 2023: 22 · 2022: 21 · 2021: 25 · 2020: 12 · 2019: 23 · 2018: 21 · 2017: 40 · 2016: 28 · 2015: 31 · 2014: 39 · 2013: 47 · 2012: 45
- FWCI
- 45.05
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- New England Journal of Medicine (publishedVersion)
- PubMed (publishedVersion)
- CINECA IRIS Institutial research information system (University of Pisa) (submittedVersion)
- Topics
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes, Cardiovascular Risks, and Lipoproteins
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Blood Pressure and Hypertension Studies
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiovascular Function and Risk Factors
- Keywords
- insulin resistance, essential hypertension, insulin sensitivity, glucose uptake, nonoxidative glucose disposal, hepatic glucose production, lipolysis, glucose turnover, glucose oxidation, blood pressure, obesity, impaired glucose tolerance
- MeSH terms
- Adult, Blood Glucose, Female, Humans, Hypertension, Insulin, Insulin Resistance, Male
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