Evaluation of the effect of tofogliflozin on the tissue characteristics of the carotid wall-a sub-analysis of the UTOPIA trial.
Adult
Aged
Benzhydryl Compounds
/ adverse effects
Carotid Arteries
/ diagnostic imaging
Carotid Artery Diseases
/ diagnostic imaging
Carotid Intima-Media Thickness
Diabetes Mellitus, Type 2
/ diagnosis
Female
Glucosides
/ adverse effects
Humans
Japan
Male
Middle Aged
Plaque, Atherosclerotic
Prospective Studies
Sodium-Glucose Transporter 2 Inhibitors
/ adverse effects
Time Factors
Treatment Outcome
Atherosclerosis
Carotid artery
Diabetes
SGLT2 inhibitor
Tissue characteristics
Tofogliflozin
Journal
Cardiovascular diabetology
ISSN: 1475-2840
Titre abrégé: Cardiovasc Diabetol
Pays: England
ID NLM: 101147637
Informations de publication
Date de publication:
05 02 2022
05 02 2022
Historique:
received:
17
11
2021
accepted:
25
01
2022
entrez:
6
2
2022
pubmed:
7
2
2022
medline:
1
3
2022
Statut:
epublish
Résumé
Since sodium-glucose cotransporter 2 (SGLT2) inhibitors have a pleiotropic antiatherogenic effect, they are expected to attenuate the progression of atherosclerosis. However, whether SGLT2 inhibitors affect the tissue characteristics of the human arterial wall remains unclear. This study aimed to evaluate the effects of tofogliflozin, a selective SGLT2 inhibitor, on the tissue characteristics of the human arterial wall in type 2 diabetes (T2DM) patients without apparent cardiovascular disease (CVD). The present study was a post hoc analysis based on data obtained from the Using Tofogliflozin for Possible Better Intervention against Atherosclerosis for Type 2 Diabetes Patients (UTOPIA) trial, which was a multicenter prospective, randomized, open-label, blinded-endpoint study conducted to evaluate the efficacy of tofogliflozin in preventing the progression of atherosclerosis in patients with T2DM. We evaluated the longitudinal change in the ultrasonic tissue characteristics of the carotid wall using gray-scale median (GSM), an established index of ultrasonic tissue characteristics. The right and left intima-medial areas were delineated, and the GSM values were evaluated (right GSM-CCA and left GSM-CCA). The average values of the right and left carotid arteries were defined as "mean GSM-CCA value." In a mixed-effects model for repeated measures, mean GSM-CCA, along with the right and left GSM-CCA values, did not significantly change in either the tofogliflozin (n = 168) or conventional treatment group (n = 169). In addition, the tofogliflozin and conventional treatment groups did not significantly differ regarding the change of the mean GSM-CCA (mean difference [95% CI] - 1.24[- 3.87, 1.38], P = 0.35), along with the right (mean difference [95% CI] - 2.33[- 5.70, 1.05], P = 0.18) and the left GSM-CCA (mean difference [95% CI] - 0.29 [- 3.53, 2.95], P = 0.86) values. Similar findings were obtained even after adjusting for traditional cardiovascular risk factors and/or the administration of drugs at baseline. The tissue characteristics of the carotid arterial wall did not change in either the tofogliflozin or conventional treatment group during the 104-week treatment period, and there was no significant difference between the treatment groups. Clinical trial registration UMIN000017607 ( https://www.umin.ac.jp/icdr/index.html ).
Sections du résumé
BACKGROUND
Since sodium-glucose cotransporter 2 (SGLT2) inhibitors have a pleiotropic antiatherogenic effect, they are expected to attenuate the progression of atherosclerosis. However, whether SGLT2 inhibitors affect the tissue characteristics of the human arterial wall remains unclear. This study aimed to evaluate the effects of tofogliflozin, a selective SGLT2 inhibitor, on the tissue characteristics of the human arterial wall in type 2 diabetes (T2DM) patients without apparent cardiovascular disease (CVD).
METHODS
The present study was a post hoc analysis based on data obtained from the Using Tofogliflozin for Possible Better Intervention against Atherosclerosis for Type 2 Diabetes Patients (UTOPIA) trial, which was a multicenter prospective, randomized, open-label, blinded-endpoint study conducted to evaluate the efficacy of tofogliflozin in preventing the progression of atherosclerosis in patients with T2DM. We evaluated the longitudinal change in the ultrasonic tissue characteristics of the carotid wall using gray-scale median (GSM), an established index of ultrasonic tissue characteristics. The right and left intima-medial areas were delineated, and the GSM values were evaluated (right GSM-CCA and left GSM-CCA). The average values of the right and left carotid arteries were defined as "mean GSM-CCA value."
RESULTS
In a mixed-effects model for repeated measures, mean GSM-CCA, along with the right and left GSM-CCA values, did not significantly change in either the tofogliflozin (n = 168) or conventional treatment group (n = 169). In addition, the tofogliflozin and conventional treatment groups did not significantly differ regarding the change of the mean GSM-CCA (mean difference [95% CI] - 1.24[- 3.87, 1.38], P = 0.35), along with the right (mean difference [95% CI] - 2.33[- 5.70, 1.05], P = 0.18) and the left GSM-CCA (mean difference [95% CI] - 0.29 [- 3.53, 2.95], P = 0.86) values. Similar findings were obtained even after adjusting for traditional cardiovascular risk factors and/or the administration of drugs at baseline.
CONCLUSIONS
The tissue characteristics of the carotid arterial wall did not change in either the tofogliflozin or conventional treatment group during the 104-week treatment period, and there was no significant difference between the treatment groups. Clinical trial registration UMIN000017607 ( https://www.umin.ac.jp/icdr/index.html ).
Identifiants
pubmed: 35123483
doi: 10.1186/s12933-022-01451-6
pii: 10.1186/s12933-022-01451-6
pmc: PMC8817596
doi:
Substances chimiques
Benzhydryl Compounds
0
Glucosides
0
Sodium-Glucose Transporter 2 Inhibitors
0
6-((4-ethylphenyl)methyl)-3',4',5',6'-tetrahydro-6'-(hydroxymethyl)spiro(isobenzofuran-1(3H),2'-(2H)pyran)-3',4',5'-triol
P8DD8KX4O4
Banques de données
UMIN-CTR
['UMIN000017607']
Types de publication
Journal Article
Multicenter Study
Randomized Controlled Trial
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
19Informations de copyright
© 2022. The Author(s).
Références
Endocrine. 2009 Jun;35(3):365-70
pubmed: 19277910
Cardiovasc Diabetol. 2018 Apr 9;17(1):52
pubmed: 29631585
AJNR Am J Neuroradiol. 2019 Oct;40(10):1731-1737
pubmed: 31558503
Circulation. 2001 Jul 3;104(1):68-73
pubmed: 11435340
Ann Med. 2017 May;49(3):206-216
pubmed: 27763781
N Engl J Med. 2017 Aug 17;377(7):644-657
pubmed: 28605608
Heart. 2011 Sep;97(17):1397-402
pubmed: 21653220
Stroke. 2000 Sep;31(9):2189-96
pubmed: 10978050
Cerebrovasc Dis. 2009;27(4):322-7
pubmed: 19218797
Circulation. 2001 Feb 20;103(7):926-33
pubmed: 11181465
Diabetes Ther. 2018 Feb;9(1):317-329
pubmed: 29330812
Stroke. 2006 Sep;37(9):2420-7
pubmed: 16888250
Cardiovasc Diabetol. 2021 May 4;20(1):95
pubmed: 33947398
Cardiovasc Diabetol. 2014 Oct 26;13:148
pubmed: 25344694
J Med Ultrason (2001). 2009 Dec;36(4):219-26
pubmed: 27277444
Atherosclerosis. 2010 Nov;213(1):8-20
pubmed: 20494361
J Intern Med. 1991 Mar;229(3):225-31
pubmed: 2007840
Diabetologia. 2017 Feb;60(2):364-376
pubmed: 27866224
Diabetes Ther. 2017 Oct;8(5):999-1013
pubmed: 28864997
J Clin Endocrinol Metab. 2014 Aug;99(8):2754-62
pubmed: 24712565
Atherosclerosis. 2009 Jun;204(2):612-8
pubmed: 19200993
Cardiovasc Diabetol. 2020 Jul 9;19(1):110
pubmed: 32646498
Eur Heart J. 2007 Sep;28(18):2243-8
pubmed: 17681956
Circulation. 2000 Aug 29;102(9):959-64
pubmed: 10961958
Expert Rev Cardiovasc Ther. 2011 Oct;9(10):1315-30
pubmed: 21985544
J Diabetes Complications. 2014 Jul-Aug;28(4):523-7
pubmed: 24746439
Am J Hypertens. 2006 Dec;19(12):1206-12
pubmed: 17161764
Cardiovasc Diabetol. 2018 Jul 26;17(1):106
pubmed: 30049285
Cardiovasc Diabetol. 2018 Feb 05;17(1):24
pubmed: 29402270
Atherosclerosis. 2005 Dec;183(2):369-71
pubmed: 16162349
N Engl J Med. 2015 Nov 26;373(22):2117-28
pubmed: 26378978
Atherosclerosis. 2007 Jan;190(1):187-93
pubmed: 16494881
Stroke. 1997 Mar;28(3):518-25
pubmed: 9056605
Medicine (Baltimore). 2021 Nov 12;100(45):e27638
pubmed: 34766565
Diabetes Care. 1998 Jun;21(6):1004-7
pubmed: 9614622
AJNR Am J Neuroradiol. 2008 May;29(5):875-82
pubmed: 18272562
Stroke. 2001 Sep;32(9):1960-5
pubmed: 11546881
Am J Epidemiol. 1991 Aug 1;134(3):250-6
pubmed: 1877584
Eur J Vasc Endovasc Surg. 1997 Dec;14(6):439-45
pubmed: 9467517