Published online Jul 19, 2026. doi: 10.5498/wjp.120249
Revised: May 12, 2026
Accepted: May 27, 2026
Published online: July 19, 2026
Processing time: 99 Days and 16.2 Hours
Sjögren’s syndrome (SS) is a common systemic autoimmune disease that predominantly affects women, and typically manifests with lymphocytic infiltration of exocrine glands with wide-ranging extra glandular organ involvement. Depression and anxiety, two of the most common psychological disorders (PD) reported in patients with SS, remain undervalued on clinical practice. There are however limited, and conflicting data on the specific risk factors for PDs in SS which might be linked to severity of organ involvement, with respect to type distribution.
To evaluate the occurrence and risk factors of PDs in patients with SS and inves
This retrospective study comprised a total of 286 patients with SS who met the diagnostic criteria for SS at the Department of Rheumatology and Immunology of our hospital between January 1, 2019 and December 1, 2024. Psychological status was assessed using the Hamilton Depression Rating Scale (HAMD) and Hamilton Anxiety Rating Scale (HAMA), and patients were divided into the PD group (156 cases) and non-PD group (130 cases). Risk factors were analyzed with the help of logistic regression, while Pearson correlation analysis was applied to assess association with organ involvement.
Out of 286 SS patients, PDs were found in 156 patients (54.5%), including pure depression in 58 cases (20.3%), pure anxiety in 38 cases (13.3%) and depression-anxiety comorbidity, 60 cases (21.0%). PD group had higher HAMD scores (14.7 ± 6.2) and HAMA scores (12.3 ± 5.8) than without PD group respectively (all P < 0.001). Patients with PDs had more severe clinical manifestations, higher dry mouth visual analogue scale (VAS) scores (7.2 ± 1.8 vs 5.4 ± 2.1), dry eye VAS scores (6.9 ± 2.0 vs 5.1 ± 2.3) and joint pain incidence (78.27% vs 61.54%), inflammatory markers including erythrocyte sedimentation rate (42.3 ± 18.7 mm/hour vs 35.6 ± 16.17 mm/hour), C-reactive protein (8.93 ± 12.37 mg/L vs 5.68 ± 8.25 mg/L), anti-SSA/Ro52 antibody positivity rate (82.1% vs 69.2%), complement component 3 levels (85 ± 23 mg/L vs 94 ± 21 mg/L), more severe organ involvement with higher EULAR SS Disease Activity Index (ESSDAI) scores (12.4 ± 8.6 vs 7.8 ± 5.9), and significantly increased incidence of interstitial lung disease (18.5% vs 13.8%), peripheral neuropathy (16.8% vs 7.8%), and arthritis (56.4% vs 38.5%) (all P < 0.05). Multivariate analysis showed that female gender [odds ratio (OR) = 2.34], disease duration ≥ 5 years (OR = 1.89), ESSDAI ≥ 12 points (OR = 2.67), interstitial lung disease (OR = 2.15), and peripheral neuropathy (OR = 3.42) were independent risk factors. The severity of PDs was positively correlated with number of organs involved (r = 0.425), disease activity (r = 0.378), and disease duration (r = 0.589), and negatively correlated with quality of life (r = -0.656, all P < 0.001).
PDs are common in SS, predominantly as anxiety and depression. Female sex, long disease duration, high disease activity and involvement of particular organs remain key risk factors for PDs. The severity of organ involvement strongly correlates with the degrees of PDs, indicating that might be beneficial for psychologic health screening and total count administration in SS patients leading to better prognosis and quality of life.
Core Tip: Psychological disorders are Sjögren’s syndrome (SS), patient subjective stress inventory more than half of the studied population. Higher disease activity, longer disease duration and multi-organ involvement (especially interstitial lung disease and peripheral neuropathy) are closely tied with depression and anxiety. Quality of life correlates negatively, whereas psychological severity correlates positively with inflammatory markers. Independent risk factors included female sex and EULAR SS Disease Activity Index ≥ 12. These results demonstrate the two-way interaction between immune-mediated inflammation and mental health, indicating that regular psychological assessment alongside integrated multidisciplinary management of SS patients is warranted.