scholarly journals Immunoreactive Trypsinogen and Free Carnitine Changes on Newborn Screening after Birth in Patients Who Develop Type 1 Diabetes

Nutrients ◽  
2021 ◽  
Vol 13 (10) ◽  
pp. 3669
Author(s):  
Jane Frances Grace Lustre Estrella ◽  
Veronica C. Wiley ◽  
David Simmons

Are free carnitine concentrations on newborn screening (NBS) 48–72 h after birth lower in patients who develop type 1 diabetes than in controls? A retrospective case-control study of patients with type 1 diabetes was conducted. NBS results of patients from a Sydney hospital were compared against matched controls from the same hospital (1:5). Multiple imputation was performed for estimating missing data (gestational age) using gender and birthweight. Conditional logistic regression was used to control for confounding and to generate parameter estimates (α = 0.05). The Hommel approach was used for post-hoc analyses. Results are reported as medians and interquartile ranges. A total of 159 patients were eligible (80 females). Antibodies were detectable in 86. Median age at diagnosis was 8 years. Free carnitine concentrations were lower in patients than controls (25.50 µmol/L;18.98–33.61 vs. 27.26; 21.22–34.86 respectively) (p = 0.018). Immunoreactive trypsinogen was higher in this group (20.24 µg/L;16.15–29–52 vs. 18.71; 13.96–26.92) (p = 0.045), which did not persist in the post-hoc analysis. Carnitine levels are lower and immunoreactive trypsinogen might be higher, within 2–3 days of birth and years before development of type 1 diabetes as compared to controls, although the differences were well within reference ranges and provide insight into the pathogenesis into neonatal onset of type 1 diabetes development rather than use as a diagnostic tool. Given trypsinogen’s use for evaluation of new-onset type 1 diabetes, larger studies are warranted.

2021 ◽  
Author(s):  
Essi Laajala ◽  
Ubaid Ullah ◽  
Toni Grönroos ◽  
Omid Rasool ◽  
Viivi Halla-aho ◽  
...  

Distinct DNA methylation patterns have recently been observed to precede type 1 diabetes in whole blood collected from young children. Our aim was to determine, whether perinatal DNA methylation could be associated with later progression to type 1 diabetes. Reduced representation bisulfite sequencing (RRBS) analysis was performed on umbilical cord blood samples collected within the Type 1 Diabetes Prediction and Prevention (DIPP) study. Children later diagnosed with type 1 diabetes and/or testing positive for multiple islet autoantibodies (N=43) were compared to control individuals (N=79), who remained autoantibody-negative throughout the DIPP follow-up until 15 years of age. Potential confounding factors related to the pregnancy and the mother were included in the analysis. No differences in the cord blood methylation patterns were observed between these cases and controls.


2001 ◽  
Vol 53 (7) ◽  
pp. 603-605 ◽  
Author(s):  
Stefan Johansson ◽  
Benedicte A. Lie ◽  
Erik Thorsby ◽  
Dag E. Undlien

2004 ◽  
Vol 5 (1) ◽  
pp. 36-40 ◽  
Author(s):  
P Eerligh ◽  
B P C Koeleman ◽  
F Dudbridge ◽  
G Jan Bruining ◽  
B O Roep ◽  
...  

2003 ◽  
Vol 5 (6) ◽  
pp. 1017-1021 ◽  
Author(s):  
Robert F. Vogt ◽  
Nancy Meredith ◽  
L. Omar Henderson ◽  
W. Harry Hannon

Diabetes Care ◽  
2019 ◽  
Vol 42 (2) ◽  
pp. 200-207 ◽  
Author(s):  
Seth A. Sharp ◽  
Stephen S. Rich ◽  
Andrew R. Wood ◽  
Samuel E. Jones ◽  
Robin N. Beaumont ◽  
...  

2017 ◽  
Vol 50 (01) ◽  
pp. 44-49 ◽  
Author(s):  
Angela Hommel ◽  
Florian Haupt ◽  
Petrina Delivani ◽  
Christiane Winkler ◽  
Marina Stopsack ◽  
...  

AbstractAn increased risk for type 1 diabetes can be identified using genetic and immune markers. The Freder1k study introduces genetic testing for type 1 diabetes risk within the context of the newborn screening in order to identify newborns with a high risk to develop type 1 diabetes for follow-up testing of early stage type 1 diabetes and for primary prevention trials. Consent for research-based genetic testing of type 1 diabetes risk is obtained with newborn screening. Increased risk is assessed using three single nucleotide polymorphisms for HLA DRB1*03 (DR3), HLA DRB1*04 (DR4), HLA DQB1*0302 (DQ8) alleles, and defined as 1. an HLA DR3/DR4-DQ8 or DR4-DQ8/DR4-DQ8 genotype or 2. an HLA DR4-DQ8 haplotype and a first-degree family history of type 1 diabetes. Families of infants with increased risk are asked to participate in follow-up visits at infant age 6 months, 2 years, and 4 years for autoantibody testing and early diagnosis of type 1 diabetes. After 8 months, the screening rate has reached 181 per week, with 63% coverage of newborns within Freder1k-clinics and 24% of all registered births in Saxony. Of 4178 screened, 2.6% were identified to have an increased risk, and around 80% of eligible infants were recruited to follow-up. Psychological assessment of eligible families is ongoing with none of 31 families demonstrating signs of excessive burden associated with knowledge of type 1 diabetes risk. This pilot study has shown that it is feasible to perform genetic risk testing for childhood disease within the context of newborn screening programs.


2019 ◽  
Vol 26 (1) ◽  
Author(s):  
V. Venetsanaki ◽  
A. Boutis ◽  
A. Chrisoulidou ◽  
P. Papakotoulas

Cancer immunotherapy has been one of the highlights in the advancement of cancer care. Certain immune checkpoint inhibitors bind to PD-1 on T cells and mediate an antitumour immune response. Given that immune checkpoint inhibitors are becoming part of standard care, a new class of adverse events—immune-related adverse events—has emerged.  Among them is endocrine toxicity, most commonly targeting the thyroid, pituitary, or adrenal glands. New-onset diabetes mellitus has been reported in fewer than 1% of patients. We present a patient with type 1 diabetes mellitus secondary to immunotherapy, together with an overview of the associated literature. Patients who develop type 1 diabetes mellitus experience a rapid course, and diabetic ketoacidosis is commonly the presenting symptom. Insulin is currently the treatment of choice; oral antidiabetics or corticosteroids do not assist in management. Several predictive factors are under investigation, but physician awareness and prompt management are key to a positive outcome.


2018 ◽  
Vol 42 (5) ◽  
pp. S47
Author(s):  
Rémi Rabasa-Lhoret ◽  
Thomas R. Pieber ◽  
John B. Buse ◽  
Ludger Rose ◽  
Anders Gorst-Rasmussen ◽  
...  

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