# Does Serum Anti-tissue Transglutaminase Level Predict Duodenal Histopathology and Clinical Manifestations of Celiac Disease in Adults?

**Authors:** Reza Gholamrezaei, Atefeh Vaezi, Fatemeh Maghool, Nahid Jamali, Mohammad Hassan Emami

PMC · DOI: 10.34172/mejdd.2025.429 · Middle East Journal of Digestive Diseases · 2025-07-30

## TL;DR

This study examines how well anti-tissue transglutaminase (anti-tTG) levels predict the severity of celiac disease in adults based on symptoms and intestinal damage.

## Contribution

The study provides new evidence on the correlation between anti-tTG levels and histopathological severity in adult celiac disease patients.

## Key findings

- Higher anti-tTG levels were significantly associated with more severe Marsh classification (e.g., Marsh III).
- Anti-tTG levels showed moderate diagnostic accuracy for advanced intestinal damage (AUC of 0.733).
- Symptoms like diarrhea, arthralgia, and osteoporosis correlated with higher anti-tTG levels.

## Abstract

Celiac disease (CD) is an autoimmune disorder triggered by gluten ingestion. This study aimed to evaluate the correlation between anti-tTG antibodies and histopathology, as classified by the Marsh system, and clinical manifestations.

This retrospective cross-sectional study analyzed the records of 346 patients with confirmed CD from 2010 to 2021. Anti-tTG levels, clinical manifestations, body mass index (BMI), and pathological results were reviewed.

This study included 346 patients (mean age 26.5±16.6 years; 56.4% female). Most patients (53.2%) had atypical CD, and normal BMI was prevalent (57.1%). Common symptoms included anxiety (70.2%), fatigue/weakness (64.2%), borborygmi (53.2%), abdominal pain (51.2%), and bloating (46.8%). Disease severity analysis revealed 75.1% had Marsh III, while 15.9% had normal/Marsh I and 9.0% had Marsh II. Anti-tTG levels were significantly higher in advanced Marsh classes (Marsh III: 169.27±180.17 vs. normal/Marsh I: 70.94±116.45, P<0.001) and in typical CD (180.44±216.22) compared to atypical CD (126.20±121.72, P=0.005). Diarrhea, arthralgia, and osteoporosis/osteomalacia showed significant correlations with anti-tTG levels (P<0.05). ROC analysis for anti-tTG in diagnosing Marsh II or higher yielded an AUC of 0.733.

Anti-tTG demonstrated moderate diagnostic accuracy for advanced duodenal damage, highlighting its utility as a biomarker in CD. Larger studies are needed to validate these findings further.

## Linked entities

- **Diseases:** celiac disease (MONDO:0005130), osteoporosis (MONDO:0005298), osteomalacia (MONDO:0001068)

## Full-text entities

- **Genes:** CD79A (CD79a molecule) [NCBI Gene 973] {aka IGA, IGAlpha, MB-1, MB1}, TGM2 (transglutaminase 2) [NCBI Gene 7052] {aka G(h), TG(C), TGC, hTG2, tTG}
- **Diseases:** IgA deficiency (MESH:D017098), anemia (MESH:D000740), decreased libido (MESH:D009123), headache (MESH:D006261), steatorrhea (MESH:D045602), fractures (MESH:D050723), Bone pain (MESH:D010146), malabsorption (MESH:D008286), hematuria (MESH:D006417), growth impairment (MESH:D006130), polyneuropathy (MESH:D011115), weakness (MESH:D018908), abortion (MESH:D000026), infertility (MESH:D007246), Arthralgia (MESH:D018771), abdominal pain (MESH:D015746), weight loss (MESH:D015431), juvenile idiopathic arthritis (MESH:D001171), edema (MESH:D004487), Osteoporosis (MESH:D010024), anxiety (MESH:D001007), Osteomalacia (MESH:D010018), lymphadenopathy (MESH:D008206), enamel defects (MESH:D000094602), IBS-D (MESH:D043183), duodenal damage (MESH:D004378), autoimmune disorder (MESH:D001327), NLR (MESH:D064726), Abdominal discomfort (MESH:D000007), depression (MESH:D003866), obese (MESH:D009765), mucosal damage (MESH:D052016), villous atrophy (MESH:C564019), fatigue (MESH:D005221), delayed puberty (MESH:D011628), Diarrhea (MESH:D003967), overweight (MESH:D050177), vitamin D deficiency (MESH:D014808), hypo/hyperthyroidism (MESH:D006980), constipation (MESH:D003248), autoimmune enteropathy (MESH:C538273), Marsh II (MESH:D008288), bloating (MESH:C535647), dyspepsia (MESH:D004415), chronic fatigue (MESH:D015673), crypt hyperplasia (MESH:D006965), mucosal lymphocytosis (MESH:D008218), CD (MESH:D002446), tissue damage (MESH:D017695)
- **Chemicals:** vitamin D (MESH:D014807), phosphate (MESH:D010710), calcium (MESH:D002118)
- **Species:** Homo sapiens (human, species) [taxon 9606]

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## References

29 references — full list in the complete paper: https://tomesphere.com/paper/PMC12958312/full.md

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Source: https://tomesphere.com/paper/PMC12958312