A 2-year calorie restriction intervention may reduce glycomic biological age biomarkers – a pilot study
In this pilot study, a subset of CALERIE Phase 2 (No. NCT00427193, registered 25th Jan 2007) participants ( n = 26) were evaluated for the effects of 2 years of 25% calorie restriction (CR) on N-glycosylation of IgG, plasma, and complement C3, as well as IgG-based biological age (GlycAge). Plasma s...
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| Vydáno v: | npj aging Ročník 11; číslo 1; s. 71 |
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| Hlavní autoři: | , , , , , , , , , , , , , , , , , , , |
| Médium: | Journal Article |
| Jazyk: | angličtina |
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London
Nature Publishing Group UK
01.08.2025
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| ISSN: | 2731-6068, 2731-6068, 2056-3973 |
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| Abstract | In this pilot study, a subset of CALERIE Phase 2 (No. NCT00427193, registered 25th Jan 2007) participants (
n
= 26) were evaluated for the effects of 2 years of 25% calorie restriction (CR) on N-glycosylation of IgG, plasma, and complement C3, as well as IgG-based biological age (GlycAge). Plasma samples were collected at baseline (BL), 12 (12mo), and 24 months (24mo). IgG galactosylation was higher at 24mo compared to BL (
p
= 0.051) and increased from 12mo to 24mo (
p
= 0.016); GlycAge decreased over the same period (
p
= 0.027). GlycAge was positively associated with TNF-α (
p
= 0.030) and ICAM-1 (
p
= 0.017). Between BL and 24mo, plasma high-branched glycans declined (
p
= 0.013), bisecting GlcNAcs increased in both plasma (
p
< 0.001) and IgG (
p
= 0.01), complement C3 protein (
p
< 0.001), C3-Man9 (
p
< 0.001), and C3-Man9Glc1C3 (
p
= 0.046) were reduced. The absence of a control group warrants cautious interpretation. |
|---|---|
| AbstractList | In this pilot study, a subset of CALERIE Phase 2 (No. NCT00427193, registered 25th Jan 2007) participants (n = 26) were evaluated for the effects of 2 years of 25% calorie restriction (CR) on N-glycosylation of IgG, plasma, and complement C3, as well as IgG-based biological age (GlycAge). Plasma samples were collected at baseline (BL), 12 (12mo), and 24 months (24mo). IgG galactosylation was higher at 24mo compared to BL (p = 0.051) and increased from 12mo to 24mo (p = 0.016); GlycAge decreased over the same period (p = 0.027). GlycAge was positively associated with TNF-α (p = 0.030) and ICAM-1 (p = 0.017). Between BL and 24mo, plasma high-branched glycans declined (p = 0.013), bisecting GlcNAcs increased in both plasma (p < 0.001) and IgG (p = 0.01), complement C3 protein (p < 0.001), C3-Man9 (p < 0.001), and C3-Man9Glc1C3 (p = 0.046) were reduced. The absence of a control group warrants cautious interpretation. In this pilot study, a subset of CALERIE Phase 2 (No. NCT00427193, registered 25th Jan 2007) participants (n = 26) were evaluated for the effects of 2 years of 25% calorie restriction (CR) on N-glycosylation of IgG, plasma, and complement C3, as well as IgG-based biological age (GlycAge). Plasma samples were collected at baseline (BL), 12 (12mo), and 24 months (24mo). IgG galactosylation was higher at 24mo compared to BL (p = 0.051) and increased from 12mo to 24mo (p = 0.016); GlycAge decreased over the same period (p = 0.027). GlycAge was positively associated with TNF-α (p = 0.030) and ICAM-1 (p = 0.017). Between BL and 24mo, plasma high-branched glycans declined (p = 0.013), bisecting GlcNAcs increased in both plasma (p < 0.001) and IgG (p = 0.01), complement C3 protein (p < 0.001), C3-Man9 (p < 0.001), and C3-Man9Glc1C3 (p = 0.046) were reduced. The absence of a control group warrants cautious interpretation.In this pilot study, a subset of CALERIE Phase 2 (No. NCT00427193, registered 25th Jan 2007) participants (n = 26) were evaluated for the effects of 2 years of 25% calorie restriction (CR) on N-glycosylation of IgG, plasma, and complement C3, as well as IgG-based biological age (GlycAge). Plasma samples were collected at baseline (BL), 12 (12mo), and 24 months (24mo). IgG galactosylation was higher at 24mo compared to BL (p = 0.051) and increased from 12mo to 24mo (p = 0.016); GlycAge decreased over the same period (p = 0.027). GlycAge was positively associated with TNF-α (p = 0.030) and ICAM-1 (p = 0.017). Between BL and 24mo, plasma high-branched glycans declined (p = 0.013), bisecting GlcNAcs increased in both plasma (p < 0.001) and IgG (p = 0.01), complement C3 protein (p < 0.001), C3-Man9 (p < 0.001), and C3-Man9Glc1C3 (p = 0.046) were reduced. The absence of a control group warrants cautious interpretation. In this pilot study, a subset of CALERIE Phase 2 (No. NCT00427193, registered 25th Jan 2007) participants ( n = 26) were evaluated for the effects of 2 years of 25% calorie restriction (CR) on N-glycosylation of IgG, plasma, and complement C3, as well as IgG-based biological age (GlycAge). Plasma samples were collected at baseline (BL), 12 (12mo), and 24 months (24mo). IgG galactosylation was higher at 24mo compared to BL ( p = 0.051) and increased from 12mo to 24mo ( p = 0.016); GlycAge decreased over the same period ( p = 0.027). GlycAge was positively associated with TNF-α ( p = 0.030) and ICAM-1 ( p = 0.017). Between BL and 24mo, plasma high-branched glycans declined ( p = 0.013), bisecting GlcNAcs increased in both plasma ( p < 0.001) and IgG ( p = 0.01), complement C3 protein ( p < 0.001), C3-Man9 ( p < 0.001), and C3-Man9Glc1C3 ( p = 0.046) were reduced. The absence of a control group warrants cautious interpretation. |
| ArticleNumber | 71 |
| Author | Šimunović, Jelena Kraus, William E. Pribić, Tea Lewis, Nathan E. Huffman, Kim M. Đerek, Lovorka Krishnan, Sridevi Das, Sai Krupa Pieper, Carl Belsky, Daniel W. Banskota, Nirad Štambuk, Tamara Das, Jayanta K. Deriš, Helena Frkatović-Hodžić, Azra Racette, Susan B. Kraus, Virginia B. Ferrucci, Luigi Orenduff, Melissa Lauc, Gordan |
| Author_xml | – sequence: 1 givenname: Tea surname: Pribić fullname: Pribić, Tea organization: Genos Ltd, Glycoscience Research Laboratory – sequence: 2 givenname: Jayanta K. surname: Das fullname: Das, Jayanta K. organization: Longitudinal Studies Section, Translation Gerontology Branch, National Institute on Aging, National Institutes of Health – sequence: 3 givenname: Lovorka surname: Đerek fullname: Đerek, Lovorka organization: Clinical Department for Laboratory Diagnostics, University Hospital Dubrava – sequence: 4 givenname: Daniel W. surname: Belsky fullname: Belsky, Daniel W. organization: Robert N Butler Columbia Aging Center and Department of Epidemiology, Columbia University Mailman School of Public Health – sequence: 5 givenname: Melissa surname: Orenduff fullname: Orenduff, Melissa organization: Duke Molecular Physiology Institute and Department of Medicine, Duke University School of Medicine – sequence: 6 givenname: Kim M. surname: Huffman fullname: Huffman, Kim M. organization: Duke Molecular Physiology Institute and Department of Medicine, Duke University School of Medicine – sequence: 7 givenname: William E. surname: Kraus fullname: Kraus, William E. organization: Duke Molecular Physiology Institute and Department of Medicine, Duke University School of Medicine – sequence: 8 givenname: Helena surname: Deriš fullname: Deriš, Helena organization: Genos Ltd, Glycoscience Research Laboratory – sequence: 9 givenname: Jelena surname: Šimunović fullname: Šimunović, Jelena organization: Genos Ltd, Glycoscience Research Laboratory – sequence: 10 givenname: Tamara surname: Štambuk fullname: Štambuk, Tamara organization: Genos Ltd, Glycoscience Research Laboratory – sequence: 11 givenname: Azra surname: Frkatović-Hodžić fullname: Frkatović-Hodžić, Azra organization: Genos Ltd, Glycoscience Research Laboratory – sequence: 12 givenname: Virginia B. surname: Kraus fullname: Kraus, Virginia B. organization: Duke Molecular Physiology Institute and Department of Medicine, Duke University School of Medicine – sequence: 13 givenname: Sai Krupa surname: Das fullname: Das, Sai Krupa organization: Jean Mayer, USDA, Human Nutrition Research Center on Aging at Tufts University – sequence: 14 givenname: Susan B. surname: Racette fullname: Racette, Susan B. organization: College of Health Solutions, Arizona State University – sequence: 15 givenname: Nirad surname: Banskota fullname: Banskota, Nirad organization: Computational Biology and Genomics Core, National Institute on Aging, National Institutes of Health – sequence: 16 givenname: Luigi surname: Ferrucci fullname: Ferrucci, Luigi organization: Longitudinal Studies Section, Translation Gerontology Branch, National Institute on Aging, National Institutes of Health – sequence: 17 givenname: Carl surname: Pieper fullname: Pieper, Carl organization: Division of Biostatistics, Department of Biostatistics and Bioinformatics, Duke University School of Medicine – sequence: 18 givenname: Nathan E. surname: Lewis fullname: Lewis, Nathan E. organization: Departments of Pediatrics and Bioengineering, University of California – sequence: 19 givenname: Gordan surname: Lauc fullname: Lauc, Gordan organization: Genos Ltd, Glycoscience Research Laboratory, Faculty of Pharmacy and Biochemistry, University of Zagreb – sequence: 20 givenname: Sridevi surname: Krishnan fullname: Krishnan, Sridevi email: skrishnan@arizona.edu organization: School of Nutritional Sciences and Wellness, BIO5, University of Arizona |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/40750782$$D View this record in MEDLINE/PubMed |
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| Title | A 2-year calorie restriction intervention may reduce glycomic biological age biomarkers – a pilot study |
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