Author |
Year |
Design |
Population |
Global Sample |
Results |
Conclusions |
Vajravelu et al. [42] |
2018 |
Cohort Study |
Individuals from United Kingdom primary care database |
9,180 patients diagnosed with T1DM between one and 35 years old with no previous diagnosis of CD |
CD was diagnosed in 196 T1DM patients (2%) during the study. A younger age at T1DM at diagnosis (HR 0.91 [95% CI 0.88-0.94]) and female sex (HR 3.19 [95% CI 1.39-7.34]) were associated with an increased risk of CD. |
The greater risk of developing CD was found in those who were diagnosed of T1DM at a younger age and in the female sex. Even though CD could develop in any age after T1DM, CD screening should be done in childhood and adulthood |
Paul et al. [45] |
2018 |
Prospective study |
Children and adolescents at the Bristol Royal Hospital in England |
2,035 children and adolescents with T1DM |
157 T1DM children with no clinical symptoms were diagnosed with CD. 53.5% had anti-tTG >10× ULN (normal <10 IU/mL) and 89% were from high-risk groups; all of this percentage had a positive histological evidence of small bowel enteropathy |
In children and adolescents, the levels of anti-tTG could be used as a noninvasive diagnostic method |
Laitinen et al. [46] |
2017 |
Cohort study |
Children and adolescents at the Tampere University Hospital, Finland |
520 children and adolescents between 0 and 17 years |
Children from the screening had less decreased growth (p = 0.016) and symptomatology (p < 0.001) at diagnosis than the children that were tested after they had symptoms. |
In the serological CD screening group, the patients were less affected by clinical symptoms and decreased growth than the ones diagnosed after clinical suspicions. Also, both groups showed signs of malabsorption and similar advanced intestine mucosal damage. Therefore, a screening for celiac disease should be done in every patient with T1DM. |
Unal et al. [47] |
2021 |
Retrospective study |
T1DM at the University of Health Sciences in Turkey |
779 T1DM patients |
The majority of CD cases (76.1%) were found at the diagnosis of T1DM and (21.7%) in the first five years, making together the 97.8% of cases diagnosed in the first five years of T1DM diagnosis; and the rest of the cases (2.2%) in the following years. However, the percentage of BPCD were just 6.9% at the time of the diagnosis. Additionally, in 23.3% cases, the positive autoantibodies spontaneously normalized without a GFD. |
A serological test for diagnosis and follow-up is recommended, instead of biopsy-required diagnosis of CD. Also, not initiating an immediate GFD therapy is suggested, especially in asymptomatic patients or with a mild value of autoantibodies test because it adds an additional burden in the diagnosed children and their families. |
Kaur et al. [48] |
2019 |
Randomized controlled trial |
Patients with T1DM from India |
320 patients with T1DM |
The number of hypoglycemic episodes per month declined in the patients under a GFD (3.5 episodes at the beginning of the study versus 2.3 episodes at the sixth month). Also, the HbA1c was reduced by 0.73% in the GFD patients and elevated in 0.99% in the normal diet. |
In patients with T1DM and CD, following a GFD could decrease the hypoglycemic episodes and could lead to an improved glycemic control. |