Evidence map›Paper›PMID 39656321›Full record

ArticleBiogerontology2024

Associations between dietary carotenoid and biological age acceleration: insights from NHANES 2009-2018.

Xinyun Chen, Chunying He, Wenhui Yu, Liang Ma, Shenju Gou, Ping Fu

Abstract read
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In one paragraph

Article in Biogerontology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Xinyun Chen *Department of Health Management, Health Management Center, General Practice Center, West China Hospital, Sichuan University, Chengdu, 610041, China.
Chunying He *Department of Nephrology, Institute of Kidney Diseases, West China Hospital, Sichuan University, 37 Guoxue Alley, Chengdu, 610041, China.
Wenhui YuDepartment of Nephrology, Institute of Kidney Diseases, West China Hospital, Sichuan University, 37 Guoxue Alley, Chengdu, 610041, China.
Liang MaDepartment of Nephrology, Institute of Kidney Diseases, West China Hospital, Sichuan University, 37 Guoxue Alley, Chengdu, 610041, China.
Shenju GouDepartment of Nephrology, Institute of Kidney Diseases, West China Hospital, Sichuan University, 37 Guoxue Alley, Chengdu, 610041, China. goushenju@scu.edu.cn.
Ping FuDepartment of Nephrology, Institute of Kidney Diseases, West China Hospital, Sichuan University, 37 Guoxue Alley, Chengdu, 610041, China.

Funding

1.3.5 project for disciplines of excellence from West China Hospital of Sichuan University ZYGD23015Sichuan Provincial Science and Technology Support Program No.2020JDRC0022
6 · The paper itself

Abstract

Carotenoids are naturally occurring pigments found in plants and certain microorganisms. Some carotenoids act as precursors to vitamin A, which is essential for various health aspects, including vision, immune function, and skin health. Carotenoids, including α-carotene, β-carotene, β-cryptoxanthin, lycopene, lutein and zeaxanthin, are known to reduce the risk of age-related diseases and promote healthy aging. This study examines the relationship between dietary carotenoid levels and biological age. This study utilized data from the National Health and Nutrition Examination Survey (NHANES) from 2009 to 2018, and 19,280 participants were included. The Phenotypic Age (PhenoAge) was used to measure biological age, and the Klemera-Doubal Method (KDM) was employed in sensitivity analyses. Biological age acceleration was determined by calculating the residuals of PhenoAge or KDM after regressing them against chronological age. Weighted multivariate linear and logistic regressions were conducted to examine the relationship between carotenoids and biological age acceleration. Additionally, restricted cubic spline regression, subgroup analysis, interaction analysis, and sensitivity analyses were employed for further examination. Both linear regression and logistic regression analyses indicated that participants with higher carotenoid intake exhibited lower rates of phenotypic age acceleration, with α-carotene, β-carotene, β-cryptoxanthin, lutein and zeaxanthin, and lycopene all demonstrating protective effects. Restricted cubic spline regression indicates non-linear associations between carotenoid levels and phenotypic age acceleration. Subgroup analyses revealed that younger participants, females, and individuals with hypertension or diabetes benefited more from higher carotenoid intake. Sensitivity analyses further confirmed the robustness of inverse relationship. The WQS analysis identifies β-carotene and β-cryptoxanthin as the most influential compounds. Higher dietary intake of carotenoids is associated with reduced biological age acceleration, underscoring their protective role against aging. Further longitudinal studies are needed to establish causal relationships and explore the underlying mechanisms of carotenoid benefits on aging.

Indexed as

AgingCarotenoidsDietNutrition SurveysAdultAgedFemaleHumansMaleMiddle AgedUnited StatesCarotenoidsBiological ageCarotenoidsNHANESPhenotypic age

Identifiers

PMID39656321

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.