# Sex-Related Differences in the Diagnosis and Evolution of Parietal Cell Antibody-Positive Autoimmune Gastritis: A Large Single-Center Retrospective Cohort Study

**Authors:** Esteban Fuentes-Valenzuela, Santiago Blanco, Sergio Escribano Cruz, Javier Parra Villanueva, Almudena Calvache Rodríguez, Ariadna Gil Diaz, María del Carmen López-Martín, Itziar Rubio de la Plaza, Irene Chivato Martín-Falquina, Beatriz Rodríguez-Batllori Aran, Raquel Latorre Martínez, Luis Alonso Castillo Herrera, Daniel Alcalde Rodríguez, Karina Guzmán López, Alicia Bejerano Domínguez

PMC · DOI: 10.3390/diagnostics16030387 · Diagnostics · 2026-01-26

## TL;DR

This study finds that women diagnosed with autoimmune gastritis are more likely to have certain conditions like iron deficiency anemia and autoimmune hypothyroidism, but the disease progression is similar between sexes.

## Contribution

The study provides new insights into sex-related differences in autoimmune gastritis diagnosis and evolution using a large single-center cohort.

## Key findings

- Females with autoimmune gastritis were more likely to have iron deficiency anemia, dyspepsia, and autoimmune hypothyroidism.
- Males were more likely to have vitamin B12 deficiency compared to females.
- No significant differences were observed in disease progression between the sexes.

## Abstract

Background/Objectives: Autoimmune gastritis (AIG) is more common in females, although studies assessing the differences between females and males are scarce. Therefore, this retrospective observational study aimed to assess differences at diagnosis and the evolution of the full spectrum of AIG between females and males. Methods: A large retrospective single-center cohort study was performed. Two cohorts were included: patients newly diagnosed with AIG with positive parietal cell antibodies between June 2013 and June 2023, and those who underwent at least one follow-up endoscopy, constituted the second cohort. Both cohorts were categorized by sex. Results: A total of four hundred twenty-six patients were included. Three hundred seventeen were females (74.4%) and 109 males, with a median age of 53.5 years (IQR 44.7–65.3). Females were more likely to be non-smokers (71.5%, 226 patients versus 57.8%, 63 patients; p = 0.01), higher prevalence of autoimmune hypothyroidism (72 females, 22.7% versus nine males, 8.3%; p = 0.001), dyspepsia (130 individuals, 41% versus 28 individuals, 25.7%; p = 0.004), and iron deficiency anemia (100 females, 31.6% versus 18 males, 16.5%; p = 0.002), while vitamin B12 deficiency was higher amongst males (22, 21.6% versus 36; 11.6%; p = 0.012). Histological and endoscopic stages were similar at the diagnosis. The logistic regression identified iron deficiency anemia (OR 2.9; 95% CI 1.47–5.72; p = 0.002), dyspepsia (OR 2.3; 95% CI 1.28–3.9; p = 0.005), lower ferritin levels (OR 0.99; 95% CI 0.98–0.99; p < 0.001), and autoimmune hypothyroidism (OR 2.7; 95% CI 1.24–5.8, p = 0.012) associated with females at diagnosis. No significant differences were observed regarding progression to a worse stage (47 females, 39.1% versus 9 males, 28.1%; p = 0.26). Conclusions: In conclusion, this large retrospective study showed some differences in clinical factors associated with AIG, although the evolution was similar. Clinicians should be particularly vigilant for the diagnosis of AIG in female patients with iron deficiency anemia, dyspeptic symptoms, and autoimmune hypothyroidism.

## Linked entities

- **Diseases:** autoimmune gastritis (MONDO:0031014), iron deficiency anemia (MONDO:0001356), vitamin B12 deficiency (MONDO:0020696)

## Full-text entities

- **Diseases:** iron deficiency anemia (MESH:D018798), autoimmune hypothyroidism (MESH:C562768), dyspeptic symptoms (MESH:D012816), AIG (MESH:D005756), vitamin B12 deficiency (MESH:D014806), dyspepsia (MESH:D004415)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

21 references — full list in the complete paper: https://tomesphere.com/paper/PMC12897096/full.md

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Source: https://tomesphere.com/paper/PMC12897096