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Skin odor signatures may shift with age
Investigators linked distinct odor patterns to life stage, sex, and skin microbes, while limited longitudinal evidence leaves their clinical utility uncertain.
To review evidence on skin volatile organic compounds (VOCs) and how odor profiles vary with age, sex, and other biological factors.
Approach:
Search and selection: The narrative review used systematic searches of PubMed/MEDLINE, Scopus, and Web of Science through May 2026. Of 487 records identified, 55 studies were included.
Evidence assessment: Studies were assessed using five criteria covering sample size, analytical validation, confounding control, study design, and reporting. Median sample size was 35; 38% were rated high quality, 41% moderate, and 21% low.
Key Findings:
Fatty acids were the most abundant chemical class; 3-methyl-2-hexenoic acid was identified as a characteristic axillary odorant.
Infant profiles were dominated by acidic VOCs, including acetic and propionic acids, and lacked androgen-related compounds typical of adult axillary odor. Evidence was limited to four small studies.
During puberty, androgen-mediated apocrine gland activation coincided with steroid VOCs, including androstenone and androstanol, and increased branched-chain fatty acids. These findings came from cross-sectional comparisons.
Sex-related differences were reported consistently in 10 of 11 adequately sized studies comparing male and female profiles. Androstenone was detected in 65%–80% of males and 10%–25% of females; female profiles also varied with menstrual cycle phase.
In older populations, 2-nonenal was reported as a characteristic odorant, with concentrations increasing after age 40 alongside changes in lipid peroxidation products. The proposed oxidative mechanism has not been directly established experimentally.
Skin microorganisms were associated with conversion of glandular secretions into VOCs: Corynebacterium with 3-methyl-2-hexenoic acid and other fatty acids, Staphylococcus with aldehydes and alcohols, and Cutibacterium acnes with propionic acid and other VOCs.
Disease-detection studies, including those involving diabetes and melanoma, were preliminary; most had fewer than 50 participants, cross-sectional designs, and no independent validation.
Interpretation:
The review describes age- and sex-associated patterns in skin odor and identifies glandular secretions and microbial metabolism as complementary contributors. The authors state that clinical applications remain preliminary and require further validation.
Limitations:
Most studies were cross-sectional; only 14% enrolled more than 100 participants, and 26% controlled for at least three potential confounders.
Only 14% used authentic chemical standards for definitive VOC identification.
The evidence had limited ethnic representation and substantial variation in sampling and analytical methods, with insufficient longitudinal data.
The review included only English-language literature; heterogeneity prevented meta-analysis, and quality assessment did not use a validated risk-of-bias instrument.
Conclusion:
The authors called for standardized analytical protocols, longitudinal studies, normative reference data, and rigorous validation before odor-based approaches move toward clinical use.
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