Exploring the Interplay between Carotenoids, Lipid Oxidation, and Cognitive Impairment in Aging

Abstract Background Alzheimer's disease (AD) is a progressive neurodegenerative disorder characterised by cognitive decline, memory loss, and impaired daily functioning. As the global population ages, the prevalence of AD continues to rise, emphasising the urgent need for effective preventive and therapeutic strategies. Carotenoids, a group of naturally occurring pigments with antioxidant properties, have gained attention for their potential neuroprotective effects. Carotenoids interrupt the oxidative process by scavenging free radicals and quenching singlet oxygen, ultimately reducing lipid oxidation and preserving the integrity of lipids in biological systems. This project investigated the relationship between blood carotenoid levels, lipid oxidation and their impact on cognitive impairment. Method Serum samples were collected from 49 healthy individuals (17 male, 32 female) who are 65 years or older. Serum carotenoids (Retinol, Lutein, Zeaxanthin, Lycopene, Alpha‐Tocopherol, β‐Carotene) were analysed by reversed phase HPLC method using methanol/acetonitrile/water gradient. Method validation was performed to establish linearity, sensitivity, recovery, and accuracy. Lipid oxidation products (oxysterols and oxidised phospholipids) were analysed using targeted mass spectrometry methods developed in our laboratory. Cognitive functions were measured using Montreal Cognitive Assessment, Trail Making Tests, letter fluency, category fluency and CogState. Result HPLC assay for carotenoids assay showed a linear dynamic range (R2 > 0.94) of 0.01 µM‐20 µM for the six carotenoids that were tested. High intra‐ and inter‐day precision (CV < 9%) and high concentration accuracy (< 15% absolute error) were observed for the QC plasma samples. Correlation analyses did not show any relationship between cognitive status with serum carotenoids or oxysterols; 7‐ketocholesterol, 7β hydroxycholesterol and 25‐hydroxycholesterol and 27‐hydroxycholesterol). 27‐hydroxycholesterol was increased in individuals >80 years old. Conclusion Our data suggests some lipid oxidation products such as 27‐ hydroxycholesterol may increase with age. However, further analysis is needed to conclude how lipophilic carotenoids may associate with lipid oxidation and cognitive impairment.

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Publication Details

Journal
Alzheimer s & Dementia
Published
2024-12-01
DOI
https://doi.org/10.1002/alz.087972
Citations
1
Primary Topic
Antioxidant Activity and Oxidative Stress
Type
article
Field-Weighted Citation Impact
0.22
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article

Exploring the Interplay between Carotenoids, Lipid Oxidation, and Cognitive Impairment in Aging

Maria Cristina Polidori, Joris Deelen, Irundika H.K. Dias, Helen R. Griffiths et al.
1 citations
Alzheimer s & Dementia
Antioxidant Activity and Oxidative Stress
0.22
article

Exploring the Interplay between Carotenoids, Lipid Oxidation, and Cognitive Impairment in Aging

Maria Cristina Polidori, Joris Deelen, Irundika H.K. Dias, Helen R. Griffiths, Lena Pickert, Sewa Abdullah, Alexander Thimm, Dumindri Abeysena
article en
1 citations

Abstract

Abstract Background Alzheimer's disease (AD) is a progressive neurodegenerative disorder characterised by cognitive decline, memory loss, and impaired daily functioning. As the global population ages, the prevalence of AD continues to rise, emphasising the urgent need for effective preventive and therapeutic strategies. Carotenoids, a group of naturally occurring pigments with antioxidant properties, have gained attention for their potential neuroprotective effects. Carotenoids interrupt the oxidative process by scavenging free radicals and quenching singlet oxygen, ultimately reducing lipid oxidation and preserving the integrity of lipids in biological systems. This project investigated the relationship between blood carotenoid levels, lipid oxidation and their impact on cognitive impairment. Method Serum samples were collected from 49 healthy individuals (17 male, 32 female) who are 65 years or older. Serum carotenoids (Retinol, Lutein, Zeaxanthin, Lycopene, Alpha‐Tocopherol, β‐Carotene) were analysed by reversed phase HPLC method using methanol/acetonitrile/water gradient. Method validation was performed to establish linearity, sensitivity, recovery, and accuracy. Lipid oxidation products (oxysterols and oxidised phospholipids) were analysed using targeted mass spectrometry methods developed in our laboratory. Cognitive functions were measured using Montreal Cognitive Assessment, Trail Making Tests, letter fluency, category fluency and CogState. Result HPLC assay for carotenoids assay showed a linear dynamic range (R2 > 0.94) of 0.01 µM‐20 µM for the six carotenoids that were tested. High intra‐ and inter‐day precision (CV < 9%) and high concentration accuracy (< 15% absolute error) were observed for the QC plasma samples. Correlation analyses did not show any relationship between cognitive status with serum carotenoids or oxysterols; 7‐ketocholesterol, 7β hydroxycholesterol and 25‐hydroxycholesterol and 27‐hydroxycholesterol). 27‐hydroxycholesterol was increased in individuals >80 years old. Conclusion Our data suggests some lipid oxidation products such as 27‐ hydroxycholesterol may increase with age. However, further analysis is needed to conclude how lipophilic carotenoids may associate with lipid oxidation and cognitive impairment.

Alzheimer s & DementiaVol. 20(S2)
Aston University (GB), Swansea University (GB), University Hospital Cologne (DE), Max Planck Institute for Biology of Ageing (DE)
Clean water and sanitation
Openalex Percentile: Top 50%
Antioxidant Activity and Oxidative Stress
0.22
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