Biomarkers of antioxidant status and lipid peroxidation in elderly patients with hypertension
Open accessAbstract
OBJECTIVE: The objective of the present study was to examine selected parameters of the blood redox system in elderly patients with hypertension.examine selected parameters of the blood redox system in elderly patients with hypertension. METHODS: We analyzed differences in redox-associated molecules and enzymes among elderly hypertensive subjects (age above 65 years, n = 49) and two groups of normotensive subjects (<65 years old - Control group I; n = 27, and >65 - Control group II; n = 30). RESULTS: Decreased activity of antioxidant enzymes, increased lipid peroxidation and reduced production of nitric oxide were observed in hypertensive subjects, compared to healthy younger controls, or those of the same age. In healthy controls, an age-related decrease in the production of nitric oxide and the activities of SOD-1 and GPx-1 was also evident. The pathology of hypertension was characterised by further, significant decreases in the values of these parameters. When the subgroups of females and males were compared to their respective controls, a compromised redox balance was observed that was more evident in female hypertensives. DISCUSSION: Hypertension in elderly patients is accompanied by changes in biomarkers of antioxidant status and lipid peroxidation status, which significantly differ from those observed in healthy ageing subjects. Our study also suggests that the relationship of gender and changes in redox balance with regard to hypertension should be further explored.
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Erythrocyte MDA levels do not differ between healthy subjects aged ≤65 years (n = 27) and those aged ≥65 years (n = 30), as measured by TBARS assay.
“| Aging | Erythrocytes | Healthy subjects aged ≤65 years (n = 27) and ≥65 years (n = 30) | TBARS assay | No differences between the groups | [243] |”
From Protein oxidation - Formation mechanisms, detection and relevance as biomarkers in human diseases (2021) · cites this paper as [243]
The Results report similar erythrocyte TBARS concentrations in the two normotensive control groups (0.230 versus 0.238 μmol/gHb), and Laboratory methods describe a thiobarbituric-acid assay. The paper reports TBARS, not MDA specifically; it also defines the younger group as <65, rather than ≤65. No page numbers are available in our copy. (LLM, conf=0.84)
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- Authors
- Pawluk, H., Pawluk, R., Robaczewska, J., Kędziora-Kornatowska, K., & Kędziora, J.
- Affiliations
- Nicolaus Copernicus University (PL)
- Provincial Polyclinical Hospital in Toruń (PL)
- Department of Public Health, Nicolaus Copernicus University in Torun, Bydgoszcz, Poland
- Corresponding author
- Robaczewska, Joanna
- ORCID
- Pawluk, Hanna
- Venue
- Redox Report
- Publisher
- Informa UK Limited
- Published
- 2017-09-05
- Volume
- 22
- Issue
- 6
- Pages
- 542-546
- ISSN
- 1351-0002 (ISSN-L)
- 1743-2928
- PMC
- PMC8900620
- OpenAlex
- W2751538039
- Cited by
- 32
- References
- 29
- Citations by year
- 2026: 1 · 2025: 3 · 2024: 2 · 2023: 1 · 2022: 3 · 2021: 10 · 2020: 5 · 2019: 4 · 2018: 3
- FWCI
- 2.22
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- other-oa
- Locations
- Redox Report (publishedVersion, other-oa)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Biochemistry › Antioxidant Activity and Oxidative Stress
- Health Sciences › Medicine › Physiology › Nitric Oxide and Endothelin Effects
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
- Keywords
- hypertension, older adults, antioxidant status, lipid peroxidation, redox homeostasis, nitric oxide, superoxide dismutase, glutathione peroxidase, age-related decline, sex differences, oxidative stress biomarkers
- MeSH terms
- Superoxide Dismutase-1, Glutathione Peroxidase GPX1, Adult, Aged, Aged, 80 and over, Antioxidants, Catalase, Female, Glutathione, Glutathione Peroxidase, Humans, Hypertension, Male, Malondialdehyde, Middle Aged, Superoxide Dismutase, Lipid Peroxidation, Biomarkers
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