# Psychological Burden in Relapsing-Remitting Multiple Sclerosis: Sociodemographic and Clinical Determinants of Persistent Anxiety and Depression over a Six-Month Follow-Up

**Authors:** María Lourdes Bermello López, Emilio Rubén Pego Pérez, Eva Gómez Fernández, María del Rosario Marín Arnés, Mercedes Fernández Vázquez, María Irene Núñez Hernández, Emilio Gutiérrez García

PMC · DOI: 10.3390/nursrep16020039 · Nursing Reports · 2026-01-26

## TL;DR

This study tracks anxiety and depression in multiple sclerosis patients over six months, finding that these conditions persist and are linked to factors like income and autoimmune comorbidities.

## Contribution

The study identifies sociodemographic and clinical predictors of persistent anxiety and depression in RRMS patients over a six-month period.

## Key findings

- Anxiety and depression scores remained stable over six months, but specific symptoms like pessimism worsened.
- Lower income and employment status were significantly associated with higher psychological distress.
- Baseline psychological scores strongly predicted future anxiety and depression levels.

## Abstract

Background/Objectives: Multiple sclerosis (MS) is a chronic neurological disease characterized by demyelination, inflammation, and autoimmunity, leading to progressive physical and psychological impairments. Anxiety and depression are among the most prevalent neuropsychiatric comorbidities in MS, significantly impacting patients’ quality of life (QoL). This study aimed to assess the evolution of anxiety and depression in individuals with relapsing-remitting multiple sclerosis (RRMS) over a six-month follow-up period, identify associated factors, and explore potential predictors of these psychological conditions. Methods: A prospective observational study was conducted with 35 RRMS patients diagnosed at the Lucus Augusti University Hospital between January 2023 and March 2025. Psychological symptoms were assessed at baseline, after 3 months, and after 6 months using the Goldberg Anxiety and Depression Scale (GADS), the Beck Depression Inventory (BDI), and the Beck Anxiety Inventory (BAI). Data were analyzed using non-parametric tests to account for the small sample size and non-normal distribution of variables. Results: Anxiety and depression were prevalent and persistent in the study population, with no significant changes in mean scores over time (p > 0.05). However, specific symptoms, such as pessimism and loss of pleasure, showed worsening trends, while sadness and guilt remained stable. Sociodemographic factors, including lower income and employment status, were significantly associated with higher anxiety and depression scores (p < 0.05). Additionally, clinical factors such as autoimmune comorbidities and a history of mononucleosis were linked to higher depressive symptoms. Baseline anxiety and depression scores emerged as strong predictors of future levels (p < 0.01), emphasizing the importance of early assessments. Conclusions: Anxiety and depression are prevalent and persistent in RRMS patients, with specific symptoms fluctuating over time. Sociodemographic and clinical factors play a significant role in psychological outcomes, highlighting the need for integrated care models that address both physical and psychosocial aspects of MS. Early psychological assessments and targeted interventions are critical for improving QoL and mitigating the long-term burden of mental health challenges in RRMS.

## Linked entities

- **Diseases:** multiple sclerosis (MONDO:0005301), relapsing-remitting multiple sclerosis (MONDO:0005314)

## Full-text entities

- **Genes:** NEFL (neurofilament light chain) [NCBI Gene 4747] {aka CMT1F, CMT2E, CMTDIG, NF-L, NF68, NFL}
- **Diseases:** Anxiety disorders (MESH:D001008), inability to (MESH:C564980), neuropsychological deficits (MESH:D009461), MDD (MESH:D003865), Fatigue (MESH:D005221), neurological disease (MESH:D020271), mononucleosis (MESH:D007244), autoimmune (MESH:D001327), mood disorders (MESH:D019964), suicidal ideation (MESH:D001072), Anxiety (MESH:D001007), schizophrenia (MESH:D012559), neuroinflammation (MESH:D000090862), muscle weakness (MESH:D018908), sensory disturbances (MESH:D012678), irritability (MESH:D001523), substance use disorders (MESH:D019966), Sensory and visual impairments (MESH:D014786), pain (MESH:D010146), anhedonia (MESH:D059445), sleep disorders (MESH:D012893), loss (MESH:D016388), Epstein-Barr virus infection (MESH:D020031), inflammation (MESH:D007249), autoimmune, and neurodegenerative disease (MESH:D019636), injury to (MESH:D014947), axonal damage (MESH:D001480), neurological disability (MESH:D009069), BDI (MESH:D057767), cognitive disability (MESH:D003072), pallor (MESH:D010167), MS (MESH:D009103), bipolar disorder (MESH:D001714), paresthesia (MESH:D010292), Depression (MESH:D003866), RRMS (MESH:D020529), dizziness (MESH:D004244), hypoesthesia (MESH:D006987), COVID-19 (MESH:D000086382), neuropsychiatric comorbidities (MESH:C000631768), diplopia (MESH:D004172), demyelination (MESH:D003711), facial flushing (MESH:D005483)
- **Chemicals:** alemtuzumab (MESH:D000074323), ponesimod (MESH:C550169), alcohol (MESH:D000438), natalizumab (MESH:D000069442), cladribine (MESH:D017338), fingolimod (MESH:D000068876), Ocrelizumab (MESH:C533411), ublituximab (MESH:C000619007), Pilates (-)
- **Species:** Nicotiana tabacum (American tobacco, species) [taxon 4097], Homo sapiens (human, species) [taxon 9606], human gammaherpesvirus 4 (Epstein Barr virus, no rank) [taxon 10376]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12942824/full.md

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12942824/full.md

## References

78 references — full list in the complete paper: https://tomesphere.com/paper/PMC12942824/full.md

---
Source: https://tomesphere.com/paper/PMC12942824