TY - JOUR
T1 - Coexisiting type 1 diabetes and celiac disease is associated with lower Hba1c when compared to type 1 diabetes alone
T2 - data from the Australasian Diabetes Data Network (ADDN) registry
AU - James, Steven
AU - Perry, Lin
AU - Lowe, Julia
AU - Donaghue, Kim C.
AU - Pham-Short, Anna
AU - Craig, Maria E.
AU - Ambler, Geoff
AU - Anderson, Kym
AU - Andrikopoulos, Sof
AU - Batch, Jenny
AU - Brown, Justin
AU - Cameron, Fergus
AU - Colman, Peter G.
AU - Conwell, Louise
AU - Cotterill, Andrew
AU - Couper, Jennifer
AU - Davis, Elizabeth
AU - de Bock, Martin
AU - Fairchild, Jan
AU - Fegan, Gerry
AU - Fourlanos, Spiros
AU - Glastras, Sarah
AU - Goss, Peter
AU - Gray, Leonie
AU - Hamblin, Peter Shane
AU - Hofman, Paul
AU - Holmes-Walker, Dianne Jane
AU - Huynh, Tony
AU - Isaacs, Sonia
AU - Jefferies, Craig
AU - Johnson, Stephanie
AU - Jones, Tim
AU - Kao, Jeff
AU - King, Bruce R.
AU - Lafferty, Antony
AU - Martin, Michelle
AU - McCrossin, Robert
AU - Neville, Kris
AU - Pascoe, Mark
AU - Paul, Ryan
AU - Peña, Alexia
AU - Phillips, Liza
AU - Price, Darrell
AU - Rodda, Christine
AU - Simmons, David
AU - Sinnott, Richard
AU - Smart, Carmel
AU - Stone, Monique
AU - Stranks, Steve
AU - Tham, Elaine
AU - Waddell, Barbara
AU - Ward, Glenn
AU - Wheeler, Ben
AU - Woodhead, Helen
AU - Zimmermann, Anthony
AU - the ADDN Study Group
N1 - Funding Information:
Open Access funding enabled and organized by CAUL and its Member Institutions. Maria E. Craig was supported by a NHMRC practitioner fellowship (APP1136735).
Funding Information:
This research was conducted as part of the Australasian Diabetes Data Network (ADDN), which is supported by the Australian Type 1 Diabetes Clinical Research Network, led by the Juvenile Diabetes Research Foundation (JDRF) Australia, the recipient of Australian Government funding from the Australian Research Council (through a Special Research Initiative) and the Department of Health and Ageing. We are grateful to the children and young people with diabetes and their families who contribute to ADDN and to members of the ADDN Study Group who provided the data and reviewed the manuscript.
Publisher Copyright:
© 2023, The Author(s).
PY - 2023/11
Y1 - 2023/11
N2 - Aim: To compare HbA1c and clinical outcomes in adolescents and young adults with type 1 diabetes (T1D), with or without celiac disease (CD). Methods: Longitudinal data were extracted from ADDN, a prospective clinical diabetes registry. Inclusion criteria were T1D (with or without CD), ≥ 1 HbA1c measurement, age 16–25 years and diabetes duration ≥ 1 year at last measurement. Multivariable Generalised Estimated Equation models were used for longitudinal analysis of variables associated with HbA1c. Results: Across all measurements, those with coexisting T1D and CD had lower HbA1c when compared to those with T1D alone (8.5 ± 1.5% (69.4 ± 16.8 mmol/mol) vs. 8.7 ± 1.8% (71.4 ± 19.8 mmol/mol); p < 0.001); lower HbA1c was associated with shorter diabetes duration (B = − 0.06; 95% CI − 0.07 to − 0.05; p < 0.001), male sex (B = − 0.24; − 0.36 to − 0.11; p < 0.001), insulin pump therapy use (B = − 0.46; -0.58 to -0.34; p < 0.001), coexistence of T1D and CD (B = − 0.48 to − 0.07; p = 0.01), blood pressure (B = − 0.16; − 0.23 to − 0.09; p < 0.001) and body mass index (B = -0.03; − 0.02 to − 0.04; p = 0.01) in the normal range. At last measurement, 11.7% of the total population had a HbA1c < 7.0% (53.0 mmol/mol). Conclusions: Across all measurements, coexisting T1D and CD is associated with lower HbA1c when compared to T1D alone. However, HbA1c is above target in both groups.
AB - Aim: To compare HbA1c and clinical outcomes in adolescents and young adults with type 1 diabetes (T1D), with or without celiac disease (CD). Methods: Longitudinal data were extracted from ADDN, a prospective clinical diabetes registry. Inclusion criteria were T1D (with or without CD), ≥ 1 HbA1c measurement, age 16–25 years and diabetes duration ≥ 1 year at last measurement. Multivariable Generalised Estimated Equation models were used for longitudinal analysis of variables associated with HbA1c. Results: Across all measurements, those with coexisting T1D and CD had lower HbA1c when compared to those with T1D alone (8.5 ± 1.5% (69.4 ± 16.8 mmol/mol) vs. 8.7 ± 1.8% (71.4 ± 19.8 mmol/mol); p < 0.001); lower HbA1c was associated with shorter diabetes duration (B = − 0.06; 95% CI − 0.07 to − 0.05; p < 0.001), male sex (B = − 0.24; − 0.36 to − 0.11; p < 0.001), insulin pump therapy use (B = − 0.46; -0.58 to -0.34; p < 0.001), coexistence of T1D and CD (B = − 0.48 to − 0.07; p = 0.01), blood pressure (B = − 0.16; − 0.23 to − 0.09; p < 0.001) and body mass index (B = -0.03; − 0.02 to − 0.04; p = 0.01) in the normal range. At last measurement, 11.7% of the total population had a HbA1c < 7.0% (53.0 mmol/mol). Conclusions: Across all measurements, coexisting T1D and CD is associated with lower HbA1c when compared to T1D alone. However, HbA1c is above target in both groups.
KW - Adolescent
KW - Celiac disease
KW - HbA1c
KW - Insulin pump therapy
KW - Type 1 diabetes
KW - Young adult
UR - http://www.scopus.com/inward/record.url?scp=85162672970&partnerID=8YFLogxK
U2 - 10.1007/s00592-023-02113-z
DO - 10.1007/s00592-023-02113-z
M3 - Article
C2 - 37338603
AN - SCOPUS:85162672970
SN - 0940-5429
VL - 60
SP - 1471
EP - 1477
JO - Acta Diabetologica
JF - Acta Diabetologica
IS - 11
ER -