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Home capillary sampling and screening for type 1 diabetes, celiac disease, and autoimmune thyroid disease in a Swedish general pediatric population: the TRIAD study.
Naredi Scherman, Maria; Lind, Alexander; Hamdan, Samia; Lundgren, Markus; Svensson, Johan; Pociot, Flemming; Agardh, Daniel.
Afiliación
  • Naredi Scherman M; Department of Clinical Sciences Malmö, Lund University, Malmö, Sweden.
  • Lind A; Department of Pediatrics, Skåne University Hospital, Malmö, Sweden.
  • Hamdan S; Department of Clinical Sciences Malmö, Lund University, Malmö, Sweden.
  • Lundgren M; Department of Clinical Sciences Malmö, Lund University, Malmö, Sweden.
  • Svensson J; Department of Clinical Sciences Malmö, Lund University, Malmö, Sweden.
  • Pociot F; Department of Pediatrics, Kristianstad Central Hospital, Kristianstad, Sweden.
  • Agardh D; Department of Clinical Sciences Malmö, Lund University, Malmö, Sweden.
Front Pediatr ; 12: 1386513, 2024.
Article en En | MEDLINE | ID: mdl-38699153
ABSTRACT

Objective:

To screen a general pediatric population for type 1 diabetes (T1D), celiac disease (CD), and autoimmune thyroid disease (AITD) after home capillary sampling.

Methods:

Swedish schoolchildren between 6-9 years and 13-16 years of age were invited to screening by taking a capillary sample at home. Samples were returned by mail and assessed for autoantibodies associated with T1D, CD, and AITD. Persistently autoantibody-positive children were referred for clinical follow-up.

Results:

Of 19,593 invited, 3,527 (18.0%) consented to participate and 2,315/3,527 (65.6%) returned a blood sample of sufficient volume. Hemolysis occurred in 830/2,301 (36.1%) samples. After exclusion of 42 children with previously known T1D, CD, or AITD, and two autoantibody-positive children who declined a confirmatory sample, 2,271/19,593 (11.6%) were included. 211/2,271 (9.3%) had persistent autoantibodies 60/2,271 (2.6%) with T1D autoantibodies, 61/2,271 (2.7%) with CD autoantibodies, and 99/2,271 (4.4%) with AITD autoantibodies; 9/2,271 (0.4%) were autoantibody positive for ≥1 disease. After clinical follow-up, 3/2,271 (0.1%) were diagnosed with T1D, 26/2,271 (1.1%) with CD, and 6/2,271 (0.3%) with AITD. Children with a first-degree relative (FDR) with T1D, CD, and/or AITD, had higher occurrence of autoantibodies compared to children without an FDR (63/344, 18.3%, vs. 148/1,810, 8.2%) (p < 0.0001, OR 2.52, 95% CI 1.83-3.47), and higher occurrence of screening-detected diagnosis (14/344, 4.1%, vs. 21/1,810, 1.2%) (p < 0.0001, OR 3.61, 95% CI 1.82-7.18). Half of these children screened positive for another disease than the FDR.

Conclusion:

Screening for T1D, CD, and AITD by home capillary sampling in a Swedish general pediatric population detected autoimmunity in 9.3% and undiagnosed disease in 1.5%.
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Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Front Pediatr Año: 2024 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Front Pediatr Año: 2024 Tipo del documento: Article