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Transforming growth factor beta and soluble endoglin in the healthy senior and in Alzheimer’s disease patients
Objectives Senescence of the immune system and of endothelial cells can contribute to age-dependent vascular and neurodegenerative disorders including Alzheimer’s disease. The aim of this study is an assessment of putative relationships of serum levels of transforming growth factor beta (TGFβ) and s...
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Published in: | The Journal of nutrition, health & aging health & aging, 2010-11, Vol.14 (9), p.758-761 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Objectives
Senescence of the immune system and of endothelial cells can contribute to age-dependent vascular and neurodegenerative disorders including Alzheimer’s disease. The aim of this study is an assessment of putative relationships of serum levels of transforming growth factor beta (TGFβ) and soluble endoglin (sCD105) and neurodegeneration, and of changes of these molecules in the course of ageing.
Design
The subjects of the study consisted of three groups, the first one was 63 otherwise healthy middle-aged participants, 31 females, 32 males, of average age 35 years. The second group was formed by 58 healthy, self-dependent inhabitants of nursing homes, 44 females and 14 males, average age 83.5 years. The third group comprised of 129 Alzheimer’s disease patients, 86 females, 43 males, of average age 80 years, with MMSE score that ranged from 16 to 20.
Measurement
Serum levels of TGF beta and soluble endoglin were measured by the ELISA method in samples of peripheral blood using commercial kits.
Results
The serum level of TGFβ was 34,339 ± 6,420 pg/ml in the healthy younger group, 37,555 ± 11,944 pg/ml in the healthy seniors, and 29,057 ± 11,455 pg/ml in Alzheimer’s disease patients. Compared to healthy seniors, the serum level of TGFβ was significantly decreased in Alzheimer’s disease patients (p |
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ISSN: | 1279-7707 1760-4788 |
DOI: | 10.1007/s12603-010-0325-1 |