Chromosomal Radiosensitivity in Sjögren’s Syndrome with and Without Concomitant Malignancy

Connective tissue diseases have long been hypothesized to confer increased radiosensitivity and radiotherapy-related toxicity, although findings vary between disease entities. In a previous institutional study, we found increased radiosensitivity in patients suffering from systemic lupus erythematosus (SLE), primarily in patients with concomitant malignancy. We therefore investigated Sjögren’s syndrome, an autoimmune disease for which evidence has been limited. Ex vivo chromosomal radiosensitivity was assessed in 45 patients with Sjögren’s syndrome (27 non-oncological, 18 oncological) by three-color fluorescence in situ hybridization after 2 Gy irradiation of G0 peripheral blood lymphocytes. Results were compared with 211 healthy controls, 129 breast cancer patients, and the previously characterized SLE cohorts (37 non-oncological, 33 oncological). Demographic, clinical, serological, and treatment-related associations were explored in 31 deeply phenotyped patients. Radiosensitivity was significantly increased in non-oncological Sjögren patients (0.527 breaks per metaphase (B/M)) compared with healthy controls (0.411 B/M; p < 0.001) and non-oncological SLE patients (0.404 B/M; p = 0.001), and it remained similarly elevated in oncological Sjögren patients (0.527 B/M), whereas in SLE increased radiosensitivity was predominantly associated with concomitant malignancy. High-grade anti-SSB positivity was associated with increased radiosensitivity in the unadjusted analysis (p = 0.016), but did not withstand correction for multiple testing (q = 0.124). Sjögren’s syndrome is associated with increased ex vivo chromosomal radiosensitivity, with no further apparent increase in patients with concomitant malignancy. This pattern differs from SLE and may suggest a stronger contribution of disease-associated factors. High-grade anti-SSB positivity may represent a relevant serological signal in relation to radiosensitivity, but requires validation in larger cohorts. These findings support closer consideration of individual radiosensitivity in Sjögren’s syndrome and highlight the need for prospective studies integrating ex vivo radiosensitivity with radiotherapy-related toxicity and treatment outcomes in this patient population.

Authors

Institutions

Publication Details

Journal
Cells
Published
2026-10-13
DOI
https://doi.org/10.3390/cells15201855
Primary Topic
Effects of Radiation Exposure
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Chromosomal Radiosensitivity in Sjögren’s Syndrome with and Without Concomitant Malignancy

Hans Geinitz, Jochen Wacker, Luitpold Valentin Distel, Stefanie Corradini et al.
Cells
Effects of Radiation Exposure
article

Chromosomal Radiosensitivity in Sjögren’s Syndrome with and Without Concomitant Malignancy

Hans Geinitz, Jochen Wacker, Luitpold Valentin Distel, Stefanie Corradini, Georg Schett, Lukas Kuhlmann, Elena Strljic, Hannah Schenker
article en

Abstract

Connective tissue diseases have long been hypothesized to confer increased radiosensitivity and radiotherapy-related toxicity, although findings vary between disease entities. In a previous institutional study, we found increased radiosensitivity in patients suffering from systemic lupus erythematosus (SLE), primarily in patients with concomitant malignancy. We therefore investigated Sjögren’s syndrome, an autoimmune disease for which evidence has been limited. Ex vivo chromosomal radiosensitivity was assessed in 45 patients with Sjögren’s syndrome (27 non-oncological, 18 oncological) by three-color fluorescence in situ hybridization after 2 Gy irradiation of G0 peripheral blood lymphocytes. Results were compared with 211 healthy controls, 129 breast cancer patients, and the previously characterized SLE cohorts (37 non-oncological, 33 oncological). Demographic, clinical, serological, and treatment-related associations were explored in 31 deeply phenotyped patients. Radiosensitivity was significantly increased in non-oncological Sjögren patients (0.527 breaks per metaphase (B/M)) compared with healthy controls (0.411 B/M; p < 0.001) and non-oncological SLE patients (0.404 B/M; p = 0.001), and it remained similarly elevated in oncological Sjögren patients (0.527 B/M), whereas in SLE increased radiosensitivity was predominantly associated with concomitant malignancy. High-grade anti-SSB positivity was associated with increased radiosensitivity in the unadjusted analysis (p = 0.016), but did not withstand correction for multiple testing (q = 0.124). Sjögren’s syndrome is associated with increased ex vivo chromosomal radiosensitivity, with no further apparent increase in patients with concomitant malignancy. This pattern differs from SLE and may suggest a stronger contribution of disease-associated factors. High-grade anti-SSB positivity may represent a relevant serological signal in relation to radiosensitivity, but requires validation in larger cohorts. These findings support closer consideration of individual radiosensitivity in Sjögren’s syndrome and highlight the need for prospective studies integrating ex vivo radiosensitivity with radiotherapy-related toxicity and treatment outcomes in this patient population.

CellsVol. 15(20)
Johannes Kepler University of Linz (AT), Friedrich-Alexander-Universität Erlangen-Nürnberg (DE), Universitätsklinikum Erlangen (DE), Ordensklinikum Linz Barmherzige Schwestern (AT), Comprehensive Cancer Center Erlangen (DE)
Openalex Percentile: Top 13%
Effects of Radiation Exposure
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.