# Distinct associations between body mass index and polyunsaturated fatty acids in dementia with Lewy Bodies and Alzheimer’s disease

**Authors:** Nicolás Castellanos-Perilla, Miguel Germán Borda, Joyce Ruifen Chong, Diego Alejandro Tovar-Rios, Alberto Jaramillo-Jimenez, Rolf K Berge, George E. Barreto, Dag Aarsland, Audun Osland Vik-M

PMC · DOI: 10.1016/j.jnha.2026.100810 · The Journal of Nutrition, Health & Aging · 2026-02-21

## TL;DR

This study found that body mass index is linked to specific fatty acid changes in dementia with Lewy bodies but not in Alzheimer's disease.

## Contribution

The study reveals distinct metabolic associations between BMI and PUFA in dementia subtypes, offering insights for personalized nutrition.

## Key findings

- DLB patients showed positive BMI associations with downstream omega-6 PUFAs like GLA, AA, and adrenic acid.
- BMI in DLB was linked to increased desaturase and elongase activity, indicating higher fatty acid turnover.
- No significant BMI-PUFA associations were found in Alzheimer's disease patients.

## Abstract

We aimed to assess the association between body mass index and polyunsaturated fatty acids to determine potential links and metabolic differences between Alzheimer's disease and dementia with Lewy bodies.

We performed a cross-sectional study of enrolment data with 133 patients with mild AD (n = 75) and DLB (n = 58) from a Norwegian cohort study. We used linear regression models adjusting for age, sex, and diagnosis to explore the association between PUFA concentrations and BMI estimates.

In DLB patients, BMI was positively associated with downstream omega-6 PUFA, including gamma-linolenic acid (GLA; β = 0.285, p = 0.012), arachidonic acid (AA; β = 0.320, p = 0.005), and adrenic acid (β = 0.303, p = 0.005). BMI was also related to increased Δ6-desaturase n-6 activity (β = 0.383, p = 0.002) and Δ6-desaturase n-3 activity (β = 0.335, p = 0.011), along with reduced elongase n-6 (β = –0.396, p = 0.002) and elongase n-3 (β = –0.376, p = 0.004), suggesting increased fatty acid turnover. No significant associations were found in the AD group.

BMI in DLB patients was positively associated with elevated downstream omega-6 metabolites and desaturase and elongase activity, compatible with higher fatty‑acid turnover and systemic inflammatory state hypothesized in DLB. These findings highlight the distinct metabolic alterations across dementia subtypes that are relevant for personalized nutritional strategies in dementia care.

## Linked entities

- **Chemicals:** gamma-linolenic acid (PubChem CID 5280933), arachidonic acid (PubChem CID 444899), adrenic acid (PubChem CID 5497181)
- **Diseases:** Alzheimer's disease (MONDO:0004975), dementia with Lewy bodies (MONDO:0007488)

## Full-text entities

- **Genes:** FADS1 (fatty acid desaturase 1) [NCBI Gene 3992] {aka D5D, FADS6, FADSD5, LLCDL1, TU12}, SNCA (synuclein alpha) [NCBI Gene 6622] {aka NACP, PARK1, PARK4, PD1}, FADS2 (fatty acid desaturase 2) [NCBI Gene 9415] {aka D6D, DES6, FADSD6, LLCDL2, SLL0262, TU13}, SLC6A3 (solute carrier family 6 member 3) [NCBI Gene 6531] {aka DAT, DAT1, PKDYS, PKDYS1}
- **Diseases:** frailty (MESH:D000073496), Stroke (MESH:D020521), delirium (MESH:D003693), psychiatric (MESH:D001523), AD (MESH:D000544), DLB (MESH:D020961), alpha-synucleinopathies (MESH:D000080874), chronic inflammation (MESH:D007249), neurodegeneration (MESH:D019636), Parkinson's disease (MESH:D010300), cognitive decline (MESH:D003072), Dementia (MESH:D003704), bipolar (MESH:D001714), psychotic disorder (MESH:D011618), neuropsychiatric (MESH:C000631768), malnutrition (MESH:D044342), terminal illness (MESH:D007153)
- **Chemicals:** 18:3n-3 (MESH:D017962), omega-6 PUFA (MESH:D043371), EPA (MESH:D015118), AA (MESH:D016718), 20:3n-6 (MESH:D015126), LA (MESH:D019787), 22:5n-3 (MESH:C026219), adrenic acid (MESH:C011395), 18:4n-3 (MESH:C062895), reactive oxygen species (MESH:D017382), Lipid (MESH:D008055), DHA (MESH:D004281), Fatty acids (MESH:D005227), 18:3n-6 (MESH:D017965), 20:5n-3 (-), PUFA (MESH:D005231)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12945632/full.md

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12945632/full.md

## References

29 references — full list in the complete paper: https://tomesphere.com/paper/PMC12945632/full.md

---
Source: https://tomesphere.com/paper/PMC12945632