# MOGAD: A Shifting Landscape—From Pathogenesis to Personalised Management, Global Perspectives and Latin American Insights

**Authors:** Ethel Ciampi

PMC · DOI: 10.3390/biomedicines13102344 · Biomedicines · 2025-09-25

## TL;DR

This review explores MOGAD, a distinct autoimmune disorder, covering its causes, diagnosis, treatment, and regional differences, especially in Latin America.

## Contribution

The paper provides a comprehensive synthesis of MOGAD's evolving landscape, emphasizing global and regional insights.

## Key findings

- MOGAD is distinct from MS and AQP4+NMOSD in clinical and immunopathological features.
- Emerging biomarkers and longitudinal MOG-IgG assessments have prognostic value.
- Latin America shows unique clinical phenotypes and challenges in diagnosis and treatment access.

## Abstract

Myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) has emerged as a distinct autoimmune demyelinating disorder, characterised by clinical, radiological, and immunopathological features that differentiate it from Multiple Sclerosis (MS) and AQP4+ neuromyelitis optica spectrum disorder (AQP4+NMOSD). This review provides a comprehensive synthesis of the evolving landscape of MOGAD, from its immunopathogenesis and diagnostic criteria to treatment strategies and global epidemiological insights. We explore the role of MOG-IgG antibodies in disease mechanisms, the utility of emerging biomarkers, and the prognostic value of tools like clinical scores or longitudinal MOG-IgG assessment. Special attention is given to regional disparities, with a focus on Latin America, highlighting diagnostic delays, access inequities, and unique clinical phenotypes. We also examine the limitations of current evidence, including gaps in long-term longitudinal follow-up and variability in diagnostic testing. Finally, we discuss global collaborative efforts and clinical trials that are shaping the future of personalised care in MOGAD. As the field advances, integrating biomarker-driven monitoring, equitable access to therapies, and regionally adapted guidelines will be essential to improving outcomes for patients worldwide.

## Linked entities

- **Diseases:** Multiple Sclerosis (MONDO:0005301)

## Full-text entities

- **Genes:** MOG (myelin oligodendrocyte glycoprotein) [NCBI Gene 4340] {aka BTN6, BTNL11, MOGIG2, NRCLP7}, AQP4 (aquaporin 4) [NCBI Gene 361] {aka MIWC, MLC4, WCH4, hAQP4}
- **Diseases:** MS (MESH:D009103), neuromyelitis optica spectrum disorder (MESH:D009471), MOGAD (MESH:D003711)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12561739/full.md

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12561739/full.md

## References

120 references — full list in the complete paper: https://tomesphere.com/paper/PMC12561739/full.md

---
Source: https://tomesphere.com/paper/PMC12561739