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Screening for celiac disease among patients with chronic kidney disease
Idris Sahin1, Lokman Eminbeyli, Safak Andic
1Nephrology Division, Department of Internal Medicine, Turgut Ozal Medical Center, Inonu University School of Medicine, Malatya, Turkey. sahinidris@hotmail.com
Insights
This study found a higher prevalence of celiac disease (CD) in patients with chronic kidney disease (CKD). Screening for CD in CKD patients may be beneficial for early diagnosis and management.
Area of Science:
- Nephrology
- Gastroenterology
- Immunology
Background:
- Celiac disease (CD) is a known risk factor for chronic kidney disease (CKD).
- The prevalence of CD in CKD patients remains understudied.
- Understanding this association is crucial for comprehensive patient care.
Purpose of the Study:
- To determine the prevalence of celiac disease (CD) among patients diagnosed with chronic kidney disease (CKD).
- To investigate the clinical and laboratory characteristics of CKD patients with CD.
Main Methods:
- Screened 292 CKD patients (eGFR <60 mL/min) for anti-endomysial IgA (EMA) antibodies.
- Patients with positive EMA underwent upper gastrointestinal endoscopy and intestinal biopsy for CD confirmation.
- Histopathological examination of biopsy specimens confirmed CD diagnosis.
Main Results:
- The prevalence of CD in the CKD cohort was 2.39% (7 out of 292 patients).
- CD was more frequent in females (3.1%) than males (1.85%).
- Gastrointestinal symptoms and laboratory parameters did not significantly differ between CD and non-CD patients.
Conclusions:
- This study indicates an increased frequency of celiac disease in patients with chronic kidney disease.
- Routine screening for CD in the CKD population is recommended for improved patient outcomes.
Aim:
Celiac disease (CD) is considered to be a risk factor for chronic kidney disease (CKD) but there is no study determining the prevalence of CD, among patients with CKD. We aim to determine the prevalence of CD in patients with CKD.
Materials And Methods:
Anti-endomysial IgA (EMA) antibody was screened in patients with CKD (glomerular filtration rate <60 mL/min). Patients who were EMA positive underwent upper gastrointestinal system endoscopy and intestinal biopsy for confirmation of definite diagnosis for CD.
Results:
Two hundred and ninety-two patients (161 males, mean age was 47.3 ± 16.3 years) with CKD were included. The EMA testing was positive in 10 patients (6F/4M). Of these, eight underwent upper gastrointestinal endoscopy and biopsies, two of them rejected endoscopy. Biopsy specimen of one of the patients was not appropriate for histopathological examination. Specimens of remaining cases (4F/3M) were compatible with CD on histopathological examination. The EMA-positive CKD patients were 3.42% (1/29 cases) and frequency of CD was 2.39% (1/42 cases). Frequency of CD was 3.1% in females and 1.85% in males. Female/male ratio was 1.67. We did not find statistically significant difference between two groups according to age and gender. Apparent chronic gastrointestinal symptoms such as abdominal pain, distension, constipation, dyspepsia, and diarrhea were absent in patients diagnosed with CD. Differences between some laboratory parameters (such as complete blood count, albumin, calcium, phosphate, total cholesterol, ferritin, parathormone) of CD and non-CD patients were not significant statistically.
Conclusion:
Our results showed increased frequency of CD among patients with CKD and screening for CD in CKD population can be helpful.
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