## Classification and Epidemiology of Chronic Gastritis **Key Point:** Helicobacter pylori (Type B) gastritis is the most common cause of chronic gastritis worldwide, accounting for ~90% of cases in developing countries including India. ### Types of Chronic Gastritis | Type | Cause | Pathology | Prevalence | | --- | --- | --- | --- | | **Type A (Autoimmune)** | Autoimmune destruction | Fundic gland atrophy, parietal cell loss | 5–10% | | **Type B (H. pylori)** | *Helicobacter pylori* infection | Antral inflammation → intestinal metaplasia | **80–90%** | | **Type C (Chemical)** | Bile reflux, NSAIDs | Foveolar hyperplasia, minimal inflammation | 5–10% | | **Type AB (Mixed)** | H. pylori + autoimmune | Combined features | Rare | **High-Yield:** Although the clinical presentation (parietal cell loss, intestinal metaplasia) superficially resembles Type A autoimmune gastritis, Type B (H. pylori) is far more common globally and in India. The question stem does not explicitly state antiparietal antibodies, which would be diagnostic of Type A. ### Pathogenesis of H. pylori Gastritis 1. **Colonization** — H. pylori adheres to gastric mucosa via flagella and adhesins 2. **Chronic inflammation** — triggers Th1/Th17 response → IL-6, TNF-α, IL-8 3. **Mucosal damage** — neutrophil infiltration → epithelial erosion 4. **Intestinal metaplasia** — chronic injury → replacement of gastric mucosa with intestinal-type epithelium 5. **Atrophy** — progressive loss of glandular cells (including parietal cells) **Clinical Pearl:** H. pylori is a Class I carcinogen (WHO). Chronic infection increases risk of intestinal-type gastric adenocarcinoma and MALT lymphoma. Eradication therapy is recommended even in asymptomatic carriers in high-prevalence regions. ### Distinguishing Type A from Type B Gastritis | Feature | Type A (Autoimmune) | Type B (H. pylori) | | --- | --- | --- | | **Serology** | Anti-parietal, anti-intrinsic factor antibodies | H. pylori IgG/IgM positive | | **Location** | Fundus and body | Antrum > fundus | | **Achlorhydria** | Early and severe | Late (if atrophy develops) | | **Prevalence** | Rare in India | Very common | | **Intestinal metaplasia** | Less common | Common | **Mnemonic:** **HAP** = **H**. pylori, **A**ntrum (primary site), **P**revalent (most common cause of gastritis globally). **Warning:** Do not confuse prevalence with pathology. Both Type A and Type B can cause parietal cell loss and intestinal metaplasia; the distinction lies in etiology and serology. In an Indian patient without explicit mention of autoimmune markers, Type B is statistically most likely.
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