White matter microstructure differences in obstructive sleep apnea severity groups assessed by diffusion tensor metrics and biophysical modeling
Obstructive sleep apnea (OSA) is a complex condition characterized by repeated episodes of upper airway collapse during sleep, leading to chronic intermittent hypoxia. Diffusion magnetic resonance imaging (dMRI) techniques offer sensitivity to white matter (WM) microstructure changes. 150 individuals from a community-based study underwent one-night nocturnal polysomnography (NPSG), cognitive assessments, and brain structural MRI. Gaussian and non-Gaussian diffusion signal changes in WM tracts were quantified with diffusion tensor metrics as (DTI) and Diffusion Kurtosis Imaging (DKI), respectively. While changes in WM microstructure were assessed in terms of Standard Model metrics. The genu of the corpus callosum (GCC) demonstrated negative correlations between AHI3A and FA (p < 0.01), AD (p < 0.05), f (SMI-based axonal water fraction) (p < 0.05), and p2 (p < 0.05) (SMI-based extra-axonal water), alongside positive correlations with RD (p < 0.05). The right cingulum showed negative associations with FA (p < 0.01), RK (p < 0.01), f (p < 0.01) and $${p}^{2}$$(p < 0.01). Subjects without OSA showed higher values in FA (p = 0.001), AD (p = 0.01), f (p = 0.03), and $${p}^{2}$$ (p = 0.0006) in the GCC and cingulum. The strongest differences between severity groups were observed between AHI3A(0–5/h) and AHI3A(> 30/h), particularly in the GCC FA (p = 0.001), RD (p = 0.008), and RK (p = 0.02), and the cingulum f (p ≤ 0.01). Decreases in AD, RK, and FA, and increased RD with increasing OSA severity suggest demyelination and axonal loss. This contrasts with f, a direct measurement for axonal density, which was lower in the OSA group, demonstrating that OSA affects the WM microstructure. Future studies should include longitudinal evaluations to assess the effects of disease duration, and the clinical significance of changes in dMRI metrics over time.
Authors
- Shayna Pehel
- Jaime Ramos‐Cejudo (ORCID: https://orcid.org/0000-0002-0993-9909)
- Sara Badía
- Ivana Rosenzweig (ORCID: https://orcid.org/0000-0003-2152-9694)
- Sharon L. Naismith (ORCID: https://orcid.org/0000-0001-9076-2778)
- Ankit Parekh (ORCID: https://orcid.org/0000-0002-5396-0553)
- Xiaotong Song (ORCID: https://orcid.org/0009-0001-3561-5852)
- Tovia Jacobs
- Moses Gonzalez
- Gabriela Silva-Albornoz
- Luisa F Figueredo
- Esther M Blessing
- Naomi L. Gaggi
- D. Rapoport
- O. Bubu
- J. Gills
- A. Mullins
- Korey Kam
- Dmitry S. Novikov
- Jenny Chen
- Indu Ayappa
- Els Fieremans
- Ricardo S. Osorio
- Andrew W. Varga
Institutions
- Nathan Kline Institute for Psychiatric Research (US)
- The University of Sydney (AU)
- Allen Institute for Brain Science (US)
- University of Kentucky (US)
- King's College London (GB)
- Hospital de Sant Pau (ES)
- International Neuromodulation Society (US)
- Monash University (AU)
- New York University (US)
- Penn State Milton S. Hershey Medical Center (US)
- Icahn School of Medicine at Mount Sinai (US)
Publication Details
- Journal
- Scientific Reports
- Published
- 2026-03-04
- DOI
- https://doi.org/10.1038/s41598-026-39162-7
- Primary Topic
- Obstructive Sleep Apnea Research
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Alzheimer's Association
- BrightFocus Foundation
- American Academy of Sleep Medicine Foundation
- National Institutes of Health
- National Institute on Aging