Evidence map›Paper›PMID 42118256›Full record

ArticleDiabetologia2026

Nocturnal fat oxidation is lower in older individuals with overweight/obesity, including those with type 2 diabetes, and is associated with fasting triglyceride levels.

Soraya S de Kam, Jeroen H P M van der Velde, Anna Veelen, Johanna A Jörgensen, Joris Hoeks, Patrick Schrauwen

Abstract readComparative Study
In one paragraph

Article in Diabetologia, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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

What it found

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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

1 citing paper in PubMed.

  1. Review
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.

Soraya S de KamDepartment of Nutrition and Movement Sciences, Maastricht University Medical Center+, Maastricht, the Netherlands.ORCID http://orcid.org/0009-0009-5040-6117
Jeroen H P M van der VeldeDepartment of Clinical Epidemiology, Leiden University Medical Center, Leiden, the Netherlands.ORCID http://orcid.org/0000-0002-2904-4598
Anna VeelenDepartment of Nutrition and Movement Sciences, Maastricht University Medical Center+, Maastricht, the Netherlands.ORCID http://orcid.org/0000-0002-5846-4444
Johanna A JörgensenDepartment of Nutrition and Movement Sciences, Maastricht University Medical Center+, Maastricht, the Netherlands.ORCID http://orcid.org/0009-0009-6404-1956
Joris HoeksDepartment of Nutrition and Movement Sciences, Maastricht University Medical Center+, Maastricht, the Netherlands. j.hoeks@maastrichtuniversity.nl.ORCID http://orcid.org/0000-0002-0265-0870
Patrick SchrauwenDepartment of Clinical Epidemiology, Leiden University Medical Center, Leiden, the Netherlands. patrick.schrauwen@ddz.de.ORCID http://orcid.org/0000-0002-0973-847X

Funding

CIHR TNC-174963Diabetes Fonds 2019.11.101Health-Holland LSHM20107ZonMw 459001021
6 · The paper itself

Abstract

aims/hypothesisWe previously showed that nocturnal fat oxidation is reduced in older individuals with overweight/obesity and impaired glucose tolerance and insulin sensitivity compared with young lean individuals. Here, we compared nocturnal energy expenditure and substrate oxidation across groups varying in age, body composition and metabolic status to unravel factors underlying variations in nocturnal substrate metabolism.

methodsData were collected from 18 previously conducted human clinical studies (N=187), all performed under conditions of energy balance with similar diet composition and meal timing. Individuals were categorised into four groups: young lean (YL); older lean (OL); older with overweight/obesity (OBE); and older with overweight/obesity and type 2 diabetes (T2D). Nocturnal energy expenditure and substrate oxidation were determined by whole-room indirect calorimetry, body composition was assessed by air-displacement plethysmography or dual energy x-ray absorptiometry, and glucose, insulin, HOMA-IR, NEFA and triglycerides were measured from fasted blood samples. Group comparisons for nocturnal energy expenditure and substrate oxidation were performed using Kruskal-Wallis tests, and over time using linear mixed models including group × time interactions, with Bonferroni correction applied to both analyses. Multivariate linear regression analysis was applied to identify whether age, sex, HOMA-IR, fasting NEFA, fasting triglycerides, fat mass and fat-free mass were independent factors of nocturnal energy expenditure and substrate oxidation.

resultsNocturnal energy expenditure, adjusted for fat-free mass, was higher in OBE compared with YL and OL (p<0.01 for both); it was also higher in T2D compared with OL (p<0.01). Nocturnal fat oxidation, expressed as a percentage of energy expenditure, was lower in OBE (median: 46.28%, IQR: 37.74-53.05) and T2D (median: 46.48%, IQR: 41.05-53.65) compared with YL (median: 52.95%, IQR: 47.82-57.61; p<0.01 for both) and OL (median: 55.21%, IQR: 54.15-58.89; p<0.01 for both). Standardised linear regression models revealed that fasting triglycerides were positively associated with nocturnal respiratory exchange ratio (β=0.337; 95% CI 0.165, 0.508) and nocturnal carbohydrate oxidation (% of energy expenditure; β=0.337; 95% CI 0.166, 0.509), and inversely associated with nocturnal fat oxidation (% of energy expenditure; β=-0.352; 95% CI -0.520, -0.813). CONCLUSIONS/

interpretationNocturnal fat oxidation (% of energy expenditure) is diminished in older individuals with overweight/obesity, irrespective of diabetes status. No differences in nocturnal energy expenditure (adjusted for fat-free mass) or substrate oxidation were observed between young and older lean individuals, suggesting that age per se may not strongly influence nocturnal substrate metabolism. Fasting triglyceride level was the strongest associated factor of nocturnal substrate oxidation.

Indexed as

Circadian RhythmDiabetes Mellitus, Type 2ObesityOverweightTriglyceridesAbsorptiometry, PhotonAdolescentAdultAgedAge FactorsBlood GlucoseBody CompositionCalorimetry, IndirectClinical Trials as TopicEnergy MetabolismFastingBlood GlucoseTriglyceridesEnergy expenditureIndirect calorimetryMetabolic flexibilityNocturnal fat oxidationObesitySubstrate metabolismType 2 diabetes

Identifiers

PMID42118256
PMCPMC13310229

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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.