# Temporal Dietary Patterns and Frailty in Korean Older Adults: Evening-Skewed and Morning–Evening Eating Patterns Associated with Frailty Risk

**Authors:** Han Byul Jang, Sarang Jeong, Min-Ju Kim, Hyun-Joung Lim, Kyung Eun Lee

PMC · DOI: 10.3390/nu18040701 · Nutrients · 2026-02-22

## TL;DR

Eating more in the evening or both morning and evening is linked to higher frailty risk in older adults compared to balanced eating patterns.

## Contribution

Identifies specific temporal dietary patterns associated with frailty risk in older adults using a large national dataset.

## Key findings

- Evening-skewed eating patterns increase frailty risk by 48% compared to balanced patterns.
- Morning–evening eating patterns increase frailty risk by 43% compared to balanced patterns.
- Late-night eating offsets the benefits of higher total energy intake, increasing frailty risk.

## Abstract

Background: Meal timing has emerged as a potential determinant of healthy aging; however, evidence linking temporal dietary patterns (TDPs) with frailty remains limited. We aimed to identify distinct TDPs among older adults and examine their associations with frailty and its components. Methods: In this cross-sectional study, 4184 adults aged ≥ 65 years from the Korea National Health and Nutrition Examination Survey (2016–2018) were analyzed. Temporal energy-intake trajectories from 24 h recalls were clustered using dynamic time warping-based kernel k-means. Frailty was defined using a modified Fried phenotype, and diet quality was assessed employing the Healthy Eating Index. Survey-weighted logistic regression and mediation analyses were performed. Results: Five distinct patterns were identified as follows: balanced (n = 1665, 38.8%), steady (n = 735, 17.8%), midday (n = 737, 18.0%), evening (n = 627, 15.2%), and morning–evening (n = 420, 10.2%). Among these, the evening-skewed (characterized by a disproportionate concentration of energy intake in the late evening; adjusted odds ratio [OR] = 1.48, 95% confidence interval [CI] = 1.03–2.10) and morning–evening (characterized by higher energy intake in both the morning and evening; OR = 1.43, 95% CI = 1.01–2.03) patterns were associated with higher frailty risk than the balanced pattern. Mediation analysis showed that higher total energy intake had a protective role in the evening-skewed pattern; however, this benefit was offset by the adverse impact of late-night eating, resulting in increased frailty risk. In the morning–evening pattern, both a direct association with frailty and an indirect pathway mediated by lower energy intake and poorer diet quality contributed to the increased frailty risk. Conclusions: Older adults with evening-skewed or morning–evening TDPs had greater frailty risk than those with balanced eating patterns. Optimizing meal timing—by reducing late-day energy loading and ensuring adequate overall intake and dietary quality—may represent a feasible chrono-nutrition strategy for frailty prevention.

## Linked entities

- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, LEP (leptin) [NCBI Gene 3952] {aka LEPD, OB, OBS}
- **Diseases:** inflammation (MESH:D007249), Sarcopenia (MESH:D055948), injury to (MESH:D014947), metabolic syndrome (MESH:D024821), undernutrition (MESH:D044342), micronutrient deficiencies (MESH:D007153), HEI (MESH:D000088102), pain (MESH:D010146), impaired sleep quality (MESH:D012893), Weakness (MESH:D018908), impaired immune function (MESH:D007154), weight loss (MESH:D015431), anxiety (MESH:D001007), insulin resistance (MESH:D007333), sleep fragmentation (MESH:D012892), depression (MESH:D003866), obesity (MESH:D009765), circadian misalignment (MESH:D017760), impaired muscle function (MESH:D009135), fatigue (MESH:D005221), metabolic, and social deficits (MESH:D009461), TDP (MESH:C536956), Frailty (MESH:D000073496), Chewing difficulty (MESH:D051346)
- **Chemicals:** fat (MESH:D005223), EQ-5D-5L (-), melatonin (MESH:D008550), sugars (MESH:D000073893), sodium (MESH:D012964), amino acid (MESH:D000596), cortisol (MESH:D006854), carbohydrate (MESH:D002241), lipid (MESH:D008055), alcohol (MESH:D000438), glucose (MESH:D005947)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

57 references — full list in the complete paper: https://tomesphere.com/paper/PMC12943149/full.md

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Source: https://tomesphere.com/paper/PMC12943149