# Vitamin Status and Risk of Age-Related Diseases Among Adult Residents of the Pearl River Delta Region

**Authors:** Yongze Zhao, Siqian Zheng, Bohan Wang, Wenhui Xiao, Ping He, Ying Bian

PMC · DOI: 10.3390/nu17101637 · 2025-05-10

## TL;DR

This study examines how vitamin levels in adults from the Pearl River Delta region relate to age-related diseases like hypertension and diabetes, finding complex associations that vary with age and vitamin type.

## Contribution

The study identifies specific vitamin thresholds and J-shaped relationships with age-related diseases, highlighting the need for personalized vitamin assessments in older adults.

## Key findings

- Blood concentrations of nine vitamins showed a right-skewed distribution among participants.
- A J-shaped relationship was observed between vitamin levels and age-related diseases, except for Vitamin A-HTN/T2DM showing Maximum Effective Concentration.
- The protective effect of vitamins against age-related diseases decreased with age, and higher levels of vitamins A and B1 correlated with increased hypertension risk in older adults.

## Abstract

Background: The Pearl River Delta (PRD) region in Guangdong, China, is urbanized and economically significant. Rapid development has shaped diverse dietary habits. In this densely populated area, there is an urgent need to assess vitamin status and its impact on age-related diseases. Methods: A total of 2646 participants (age: 50.92 ± 9.30 years; male: 64.06%) were recruited from the Pearl River Delta (PRD) region. Participants were included from 1 December 2020 to 30 November 2021. Three restricted cubic spline logistic models, interaction terms, and mediated effects analyses were used to assess the association between vitamin A, B, E, B1, B2, B3, B5, B6, and B9 between five age-related diseases: cerebrovascular disease (CVD), coronary heart disease (CHD), hypertension (HTN), dyslipidemia (DYS), and type 2 diabetes mellitus (T2DM). Results: Blood concentrations of nine vitamins showed a right-skewed distribution. Significant correlations were found between vitamin levels and age-related diseases across nine groups (p < 0.05). A J-shaped relationship was observed between vitamin levels and the risk of age-related diseases, except for the Vitamin A-HTN/T2DM, which showed Maximum Effective Concentration (MEC). Specific thresholds included: Vitamin A: 1080 ng/mL (DYS); Vitamin B1: 77 ng/mL (CVD), 75.5 ng/mL (HTN); Vitamin B5: 900 ng/mL (CVD), 600 ng/mL (HTN), 690 ng/mL (DYS); Vitamin B6: 82 ng/mL (CVD). The protective effect of vitamins against age-related diseases decreased with age, and higher levels of vitamins A and B1 correlated with increased hypertension risk in older adults (Pinteraction < 0.01). Low Body Resilience Index (BRI) and physical activity mediated the protective effects of vitamins A and B5 on HTN and DYS, while no mediating effects were found for smoking and alcohol consumption. Conclusions: The effectiveness of multivitamin supplementation in preventing cardiovascular, cerebrovascular, and metabolic diseases may be limited in healthy aging populations. Health professionals should consider patients’ physiological conditions and blood vitamin levels to avoid overdose. More interventional studies are needed to establish causal relationships.

## Linked entities

- **Diseases:** cerebrovascular disease (MONDO:0011057), coronary heart disease (MONDO:0005010), dyslipidemia (MONDO:0002525), type 2 diabetes mellitus (MONDO:0005148)

## Full-text entities

- **Diseases:** age (MESH:D019588), cardiovascular, cerebrovascular, and metabolic diseases (MESH:D002318), CVD (MESH:D002561), HTN (MESH:D006973), overdose (MESH:D062787), CHD (MESH:D003327), DYS (MESH:D050171), Age-Related Diseases (MESH:D010024), T2DM (MESH:D003924)
- **Chemicals:** Vitamin B6 (MESH:D025101), alcohol (MESH:D000438), Vitamin B1 (MESH:D013831), vitamins A and B1 (-), Vitamin A (MESH:D014801), Vitamin B5 (MESH:D010205)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12114280/full.md

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Source: https://tomesphere.com/paper/PMC12114280