# Age-Related Glucose Intolerance Is Associated with Impaired Insulin Secretion in Community-Dwelling Japanese Adults: The Kumamoto Koshi Study

**Authors:** Kazuki Fukuda, Masaki Haneda, Naoto Kubota, Eiichi Araki, Kazuya Yamagata

PMC · DOI: 10.3390/biomedicines13020380 · Biomedicines · 2025-02-06

## TL;DR

This study finds that aging is linked to reduced insulin secretion, which may cause glucose intolerance in Japanese adults.

## Contribution

The study identifies impaired insulin secretion as a key factor in age-related glucose intolerance in Japanese individuals.

## Key findings

- Age was negatively correlated with insulin secretion indices like HOMA-β and the insulinogenic index.
- Multiple regression analysis confirmed age as a significant factor affecting insulin secretion.
- No significant correlation was found between age and insulin sensitivity indices like HOMA-IR or the Matsuda index.

## Abstract

Background/Objectives: Glucose tolerance progressively declines with age. However, the effects of aging on insulin secretion and insulin sensitivity in Japanese subjects are unclear. Methods: We conducted an oral glucose tolerance test (OGTT) in residents aged between 22 and 85 years in Koshi City, Kumamoto Prefecture, Japan, to clarify the characteristics of insulin secretion and insulin sensitivity in older adults. Participants were recruited using a flyer, and the OGTT was performed after an overnight fast (12–16 h) between 8:00 and 10:30 am. Results: HOMA-IR and the Matsuda index are indices of insulin action. No correlation of age with HOMA-IR or the Matsuda index was found, whereas HOMA-β, the insulinogenic index, and the disposition index, all indices of insulin secretion, were negatively correlated with age in all participants and in individuals with normal glucose tolerance. Multiple regression analysis showed that age was an explanatory factor for insulin secretion. Conclusions: Impaired insulin secretion may contribute to age-related glucose intolerance in Japanese individuals.

## Full-text entities

- **Genes:** INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}
- **Diseases:** Glucose Intolerance (MESH:D018149), Impaired Insulin Secretion (MESH:D007333)

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11852980/full.md

## References

40 references — full list in the complete paper: https://tomesphere.com/paper/PMC11852980/full.md

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Source: https://tomesphere.com/paper/PMC11852980