Javascript must be enabled to continue!
SAT-413 Does Dipeptidyl Peptidase-4 Inhibitor Exacerbate Graves’ Disease?
View through CrossRef
Abstract
Abstract: [Background] Dipeptidyl peptidase-4 (DPP-4) is expressed as CD26 on the surface of immune cells including T cells, suggesting that inhibition of DPP-4 may affect the immune system (1). Actually, DPP-4 inhibitor (DPP-4i)-induced polyarthritis and bullous pemphigoid have been reported (2, 3). It has also been reported that the prevalence of Hashimoto’s thyroiditis was significantly higher in patients on DPP-4i treatment (4). However, relationships between DPP-4i and Graves’ disease has been unclear. [Methods] To investigate the impact of DPP-4i administration on the activity of Graves’ disease, we conducted a multicenter observational trial that included patients with both Graves’ disease and type 2 diabetes mellitus who were administered an oral hypoglycemic agent (OHA) including DPP-4i from December in 2009 to April in 2018. Patients who had systemic diseases affecting thyroid function and those who underwent thyroidectomy or radioiodine treatment within 6 months before or after OHA administration were excluded. Exacerbation of Graves’ disease was defined as an increase in antithyroid drug dose within 6 months after OHA administration. The trial was approved by the institutional review board of Hokkaido University Hospital. [Results] Eighty-three patients were enrolled in the study, and they were divided into an exacerbation group (n = 18) and a non-exacerbation group (n = 65). Comparing baseline characteristics, the percentage of DPP-4i administration was higher in the exacerbation group (83.3%) than in the non-exacerbation group (32.3%) (p = 0.0001). Mean age was also significantly higher in the exacerbation group (p = 0.04), and the duration of Graves’ disease was significantly shorter (p = 0.01). Multivariate logistic regression analysis using factors extracted by comparing baseline characteristics demonstrated a significant association between DPP-4i administration and Graves’ disease exacerbation (odds ratio 5.62, 95% confidence interval 1.16–27.0, p = 0.02). [Conclusion] The current study suggests that DPP-4i administration is associated with exacerbation of Graves’ disease.
Reference: (1) Morimoto C et al., Immunol Rev. 1998 Feb;161:55–70. (2) Yokota K et al., Intern Med. 2012;51(15):2041–4. (3) Yoshiji S et al. J Diabetes Investig. 2018 Mar;9(2):445–447. (4) Kridin K et al. Immunol Res. 2018 Jun;66(3):425–430.
Title: SAT-413 Does Dipeptidyl Peptidase-4 Inhibitor Exacerbate Graves’ Disease?
Description:
Abstract
Abstract: [Background] Dipeptidyl peptidase-4 (DPP-4) is expressed as CD26 on the surface of immune cells including T cells, suggesting that inhibition of DPP-4 may affect the immune system (1).
Actually, DPP-4 inhibitor (DPP-4i)-induced polyarthritis and bullous pemphigoid have been reported (2, 3).
It has also been reported that the prevalence of Hashimoto’s thyroiditis was significantly higher in patients on DPP-4i treatment (4).
However, relationships between DPP-4i and Graves’ disease has been unclear.
[Methods] To investigate the impact of DPP-4i administration on the activity of Graves’ disease, we conducted a multicenter observational trial that included patients with both Graves’ disease and type 2 diabetes mellitus who were administered an oral hypoglycemic agent (OHA) including DPP-4i from December in 2009 to April in 2018.
Patients who had systemic diseases affecting thyroid function and those who underwent thyroidectomy or radioiodine treatment within 6 months before or after OHA administration were excluded.
Exacerbation of Graves’ disease was defined as an increase in antithyroid drug dose within 6 months after OHA administration.
The trial was approved by the institutional review board of Hokkaido University Hospital.
[Results] Eighty-three patients were enrolled in the study, and they were divided into an exacerbation group (n = 18) and a non-exacerbation group (n = 65).
Comparing baseline characteristics, the percentage of DPP-4i administration was higher in the exacerbation group (83.
3%) than in the non-exacerbation group (32.
3%) (p = 0.
0001).
Mean age was also significantly higher in the exacerbation group (p = 0.
04), and the duration of Graves’ disease was significantly shorter (p = 0.
01).
Multivariate logistic regression analysis using factors extracted by comparing baseline characteristics demonstrated a significant association between DPP-4i administration and Graves’ disease exacerbation (odds ratio 5.
62, 95% confidence interval 1.
16–27.
0, p = 0.
02).
[Conclusion] The current study suggests that DPP-4i administration is associated with exacerbation of Graves’ disease.
Reference: (1) Morimoto C et al.
, Immunol Rev.
1998 Feb;161:55–70.
(2) Yokota K et al.
, Intern Med.
2012;51(15):2041–4.
(3) Yoshiji S et al.
J Diabetes Investig.
2018 Mar;9(2):445–447.
(4) Kridin K et al.
Immunol Res.
2018 Jun;66(3):425–430.
Related Results
Dynamics of total volume of pancreatic α‐ and β ‐cells under the influence sulfonylureas and their combination with dipeptidyl peptidase‐4 inhibitors
Dynamics of total volume of pancreatic α‐ and β ‐cells under the influence sulfonylureas and their combination with dipeptidyl peptidase‐4 inhibitors
AbstractObjectiveSulfonylureas and dipeptidyl peptidase‐4 inhibitors have a multidirectional effect on pancreatic cells. We aimed to evaluate the effects of these drugs on β‐ and α...
Dreipassen – en magisk genstand?
Dreipassen – en magisk genstand?
The trefoil – a magical object?In 1997, a trefoil was found in a cremation pit at Bilstrup near Skive in Viborg county. The other grave goods, comprising fragments of arm rings and...
The Gender-Specific Effect of Subcutaneous and Visceral Adipose Tissues on Cardiometabolic Risk in a Chinese Population
The Gender-Specific Effect of Subcutaneous and Visceral Adipose Tissues on Cardiometabolic Risk in a Chinese Population
Abstract
BackgroundPrevious studies demonstrated that visceral adipose tissue (VAT) contributed to increased risks for multiple cardiometabolic factors. However, the effect...
Evaluation of the catalytic specificity, biochemical properties, and milk clotting abilities of an aspartic peptidase from Rhizomucor miehei
Evaluation of the catalytic specificity, biochemical properties, and milk clotting abilities of an aspartic peptidase from Rhizomucor miehei
Abstract
In this study, we detail the specificity of an aspartic peptidase from Rhizomucor miehei and evaluate the effects of this peptidase on clotting milk using t...
Growth hormone and insulin-like growth factor 1 affect the severity of Graves’ disease
Growth hormone and insulin-like growth factor 1 affect the severity of Graves’ disease
Summary
Graves’ disease, the most common form of hyperthyroidism in iodine-replete countries, is associated with the presence of immunoglobulins G (IgGs) that are responsible for t...
Robert Graves and the White Goddess, 1940–1985; Robert Graves: Life on the Edge; Robert Graves: Collected Writings on Poetry
Robert Graves and the White Goddess, 1940–1985; Robert Graves: Life on the Edge; Robert Graves: Collected Writings on Poetry
This chapter evaluates three publications regarding Robert Graves. For any biographer of Graves the problem is to reconcile two beings: the old-fashioned, chivalrous Englishman and...
Dipeptidyl Peptidase‐4 Inhibition Potentiates Stimulated Growth Hormone Secretion and Vasodilation in Women
Dipeptidyl Peptidase‐4 Inhibition Potentiates Stimulated Growth Hormone Secretion and Vasodilation in Women
Background
Diminished growth hormone (
GH
) is associated with impaired endothelial function and fibrinolysis.
...
Improving Local Search for Random 3-SAT Using Quantitative Configuration Checking
Improving Local Search for Random 3-SAT Using Quantitative Configuration Checking
Configuration Checking (CC) was proposed as a new diversification strategy for Stochastic Local Search (SLS) algorithm for solving Minimum Vertex Cover, and has been successfully u...

