# Soluble SORL1 in cerebrospinal fluid as a marker for functional impact of rare SORL1 variants

**Authors:** Matthijs W. J. de Waal, Sven J. van der Lee, Melanie Lunding, Lynn Boonkamp, Nolan Barrett, Giulia Monti, Anne Mette G. Jensen, Christian B. Vaegter, Jan Raska, Sona Cesnarikova, Jiri Sedmik, Calvin Trieu, Marjan M. Weiss, Rosalina van Spaendonk, Lisa Vermunt, Georgii Ozhegov, Niccolo Tesi, Marc Hulsman, Dovile Januliene, Arne Moller, Dasa Bohaciakova, Wiesje M. van der Flier, Olav M. Andersen, Charlotte E. Teunissen, Henne Holstege

PMC · DOI: 10.1002/alz.71042 · 2026-02-13

## TL;DR

This study shows that lower levels of soluble SORL1 in cerebrospinal fluid may indicate harmful genetic changes in SORL1, a protein linked to Alzheimer's disease.

## Contribution

The study introduces CSF-sSORL1 as a potential biomarker for the functional impact of rare SORL1 genetic variants.

## Key findings

- sSORL1 concentrations were significantly lower in carriers of protein-truncating and damaging missense SORL1 variants.
- CSF-sSORL1 levels correlated with tau pathology in Alzheimer's disease but not with Aβ42 levels.
- sSORL1 levels represent an in vivo biomarker of SORL1 function.

## Abstract

The sortilin‐related receptor (SORL1) directs APP and Aβ trafficking within the retromer pathway. Cleavage at the cell surface releases soluble SORL1 (sSORL1) into cerebrospinal fluid (CSF). We examined whether CSF‐sSORL1 can serve as an in vivo marker of genetically impaired SORL1.

CSF‐sSORL1 was quantified by enzyme‐linked immunosorbent assay (ELISA) in 218 participants: 90 carriers of SORL1 variants, 78 SORL1‐wildtype (WT) AD patients, and 50 SORL1‐WT controls.

sSORL1 concentrations were significantly lower in carriers of protein‐truncating and damaging missense variants. In SORL1‐WT patients, CSF‐sSORL1 correlated with pTau181 but not with Aβ42 among AD patients, and did not differ between patients and controls.

These findings suggest that impaired SORL1 trafficking reduces receptor delivery to the cell surface and thereby decreases sSORL1 shedding, supporting its potential use as a pathway‐specific biomarker.

Enzyme‐linked immunosorbent assay (ELISA) enables quantitative measurement of soluble sortilin‐related receptor (sSORL1) in cerebrospinal fluid (CSF).sSORL1 levels are reduced in CSF from carriers of a pathogenic SORL1 variant.CSF‐sSORL1 levels correlate with tau pathology in Alzheimer's disease.sSORL1 levels represent an in vivo biomarker of SORL1 function.

Enzyme‐linked immunosorbent assay (ELISA) enables quantitative measurement of soluble sortilin‐related receptor (sSORL1) in cerebrospinal fluid (CSF).

sSORL1 levels are reduced in CSF from carriers of a pathogenic SORL1 variant.

CSF‐sSORL1 levels correlate with tau pathology in Alzheimer's disease.

sSORL1 levels represent an in vivo biomarker of SORL1 function.

## Linked entities

- **Genes:** SORL1 (sortilin related receptor 1) [NCBI Gene 6653]
- **Proteins:** SORL1 (sortilin related receptor 1), APP (amyloid beta precursor protein), ab (abrupt)
- **Diseases:** Alzheimer's disease (MONDO:0004975)

## Full-text entities

- **Genes:** APP (amyloid beta precursor protein) [NCBI Gene 351] {aka AAA, ABETA, ABPP, AD1, APPI, CTFgamma}, MAPT (microtubule associated protein tau) [NCBI Gene 4137] {aka DDPAC, FTD1, FTDP-17, MAPTL, MSTD, MTBT1}, SORL1 (sortilin related receptor 1) [NCBI Gene 6653] {aka C11orf32, LR11, LRP9, SORLA, SorLA-1, gp250}
- **Diseases:** AD (MESH:D000544)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12902900/full.md

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Source: https://tomesphere.com/paper/PMC12902900