# Heritability and shared environmental effects of brain diseases in 12,040 extended families

**Authors:** Janna I. R. Dijkstra, Marc Hulsman, Lisa Waterink, Henne Holstege, Charlotte E. Teunissen, Wouter F. L. Christiaansen, Bryan A. de Jong, Peter Kochunov, Brian Donohue, Marissa D. Zwan, Anouk den Braber, Lisa Vermunt, Sven J. van der Lee

PMC · DOI: 10.1038/s44400-025-00030-2 · Npj Dementia · 2025-11-03

## TL;DR

This study analyzed genetic and shared environmental influences on brain diseases in over 12,000 families, finding strong genetic contributions and some shared environmental effects.

## Contribution

The study provides novel heritability and shared environmental effect estimates for nine common brain diseases using a large family-based dataset.

## Key findings

- Alzheimer’s disease showed the highest heritability at 73%.
- Shared environmental effects were significant for Alzheimer’s and vascular dementia.
- Multiple sclerosis had the lowest heritability at 10%.

## Abstract

Brain diseases have complex patterns of genetic and environmental risk factors, and better understanding of these risks is required for more effective prevention strategies. Participants of the Dutch Brain Research Registry provided detailed information on family structure and occurrence of brain diseases. A total of 12,040 participants (73% female, aged 64.9 ± 11 years) provided information on 101,379 family members (53% female, aged 62 ± 25 years). We estimated heritability (h2) of the nine most common brain diseases using polygenic modeling in SOLAR and assessed variations in h2 through bootstrapping; Alzheimer’s disease (AD) (h2 = 73, range 53–86, Pfdr < 0.001), ALS (h2 = 72, range 10–98, Pfdr = 0.030), frontotemporal dementia (FTD) (h2 = 48, range 0–97, Pfdr = 0.132), vascular dementia (VaD) (h2 = 41, range 7–64, P = 0.003), Lewy Body dementia (h2 = 34, range 0–58, P = 0.132), iCVA (h2 = 27, 6–59, Pfdr = 0.013), hCVA (h2 = 29, 8–57, Pfdr = 0.007), Parkinson’s disease (PD) (h2 = 38, 6–66, Pfdr = 0.013), and multiple sclerosis (h2 = 10, 10–97, Pfdr < 0.001). Shared environmental effects could be estimated for AD (c2 = 5.8%, Pfdr = 0.011), VaD (c2 = 9.0%, Pfdr = 0.021), FTD (c2 = 9.7%, Pfdr = 0.33), iCVA (c2 = 15.9%, Pfdr < 0.001), hCVA (c2 = 14.9%, Pfdr = 0.005), and PD (c2 = 7.5%, Pfdr = 0.25). These findings underscore the significance of genetic contribution to most brain diseases and the important role of shared environments in AD and vascular-related conditions, highlighting initiatives to mitigate modifiable risk factors.

## Linked entities

- **Diseases:** Alzheimer’s disease (MONDO:0004975), ALS (MONDO:0004976), frontotemporal dementia (MONDO:0010857), vascular dementia (MONDO:0004648), Lewy Body dementia (MONDO:0007488), Parkinson’s disease (MONDO:0005180), multiple sclerosis (MONDO:0005301)

## Full-text entities

- **Diseases:** Brain diseases (MESH:D001927), ALS (MESH:D008113), FTD (MESH:D057180), multiple sclerosis (MESH:D009103), Lewy Body dementia (MESH:D020961), AD (MESH:D000544), VaD (MESH:D015140), PD (MESH:D010300)

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12583135/full.md

## References

8 references — full list in the complete paper: https://tomesphere.com/paper/PMC12583135/full.md

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Source: https://tomesphere.com/paper/PMC12583135