Development and Validation of a Tool for Assessing Adherence to Gluten-Free Diet in Patients With Celiac Disease

被引:0
|
作者
Mehtab, Wajiha [1 ,2 ]
Malhotra, Anita [3 ]
Upadhyay, Ashish [4 ]
Singh, Namrata [1 ]
Agarwal, Ashish [5 ]
Chauhan, Ashish [6 ]
Mehta, Shubham [1 ]
Ahmed, Anam [1 ]
Singh, Alka [1 ]
Sreenivas, V. [4 ]
Siddhu, Anupa [2 ]
Ahuja, Vineet [1 ]
Makharia, Govind K. [1 ]
机构
[1] All India Inst Med Sci, Dept Gastroenterol & Human Nutr, New Delhi, India
[2] Univ Delhi, Dept Home Sci, New Delhi, India
[3] Univ Delhi, Lakshmibai Coll, Dept Home Sci, New Delhi, India
[4] All India Inst Med Sci, Dept Biostat, New Delhi, India
[5] All India Inst Med Sci, Dept Gastroenterol, Jodhpur, India
[6] Indira Gandhi Med Coll, Dept Gastroenterol, Shimla, India
来源
AMERICAN JOURNAL OF GASTROENTEROLOGY | 2024年 / 119卷 / 12期
关键词
monitoring; standard dietary evaluation; celiac disease adherence test; anti-tissue transglutaminase antibody; gluten immunogenic peptide; compliance;
D O I
10.14309/ajg.0000000000002911
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
INTRODUCTION:Life-long adherence to gluten-free diet (GFD) and its assessment is essential for patients with celiac disease (CeD). We have developed and validated a tool for assessing adherence to GFD which can be used by both physicians and dietitians. METHODS:Phase 1: Development, content validation, and assessment of reliability of tool. Phase 2: Validation of tool against standard dietary evaluation (SDE) (gold standard), immunoglobulin A - anti-tissue transglutaminase antibodies (IgA anti-tTG Ab), and gluten immunogenic peptides in urine. Overall, 380 biopsy-confirmed patients with CeD (derivation cohort: n = 100 [phase 1], n = 210 [phase 2] and independent validation cohort, n = 70) were recruited. RESULTS:Of an initial 90-point questionnaire, 84 items (Celiac Disease: Compliance Assessment Test [CD-CAT.v1]) were retained after content validation and pilot testing. In phase 1, upon administering CD-CAT.v1 on 100 patients, a comprehensive 35-item tool (CD-CAT.v2; alpha = 0.86) was obtained after removing items with low test-retest reliability and item-rest correlation values. In phase 2, upon administering CD-CAT.v2 on 210 patients, 22 items were removed having low correlation values (R < 0.4) with SDE. Finally, a 13-item tool (CD-CAT.v3; alpha = 0.84) was obtained with high criterion validity with SDE (r = 0.806, P < 0.001), moderate convergent validity with celiac disease adherence test (r = 0.602, P = 0.007), and moderate to weak correlation with urine gluten immunogenic peptides (r = 0.46, P = 0.001) and IgA anti-tTG Ab (r = 0.39, P = 0.008), respectively. The final 13-item tool also strongly correlated with SDE (r = 0.78, P < 0.001) in an independent validation cohort of 70 patients with CeD. Principal component analysis identified 3 relevant subscales with a cumulative variance of 62%. The sensitivity and specificity of CD-CAT.v3 were 80% and 91%, respectively, with an area under curve of 0.905 with SDE. The obtained cutoff score of <19 from the receiver operating characteristic curve was further categorized as 13 = excellent, 14-18 = very good, 19-28 = average, and >28 = poor adherence to GFD. DISCUSSION:CD-CAT is a new and rapid tool for monitoring dietary adherence to GFD with high sensitivity and specificity, which can be administered by both physicians and dietitians.
引用
收藏
页码:2501 / 2509
页数:9
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