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Efficacy and safety of canagliflozin in patients with type 2 diabetes mellitus living in hot climates.
John, Mathew; Cerdas, Sonia; Violante, Rafael; Deerochanawong, Chaicharn; Hassanein, Mohamed; Slee, April; Canovatchel, William; Hamilton, Gill.
Afiliação
  • John M; Providence Endocrine & Diabetes Specialty Centre, Trivandrum, Kerala, India. drmathewjohn@yahoo.com.
  • Cerdas S; Hospital Cima, Centro de Investigacíon Clínica San Agustín, San José, Costa Rica.
  • Violante R; Centro de Estudios de Investigacíon Metabólicos y Cardiovasculares S.C., Tampico, Mexico.
  • Deerochanawong C; Rajavithi Hospital, Rangsit Medical School, Bangkok, Thailand.
  • Hassanein M; Dubai Hospital, Dubai Health Authority, Dubai, United Arab Emirates.
  • Slee A; Axio Research, Seattle, WA, USA.
  • Canovatchel W; Janssen Global Services, LLC, Raritan, NJ, USA.
  • Hamilton G; Janssen-Cilag Ltd, High Wycombe, UK.
Int J Clin Pract ; 70(9): 775-85, 2016 Sep.
Article em En | MEDLINE | ID: mdl-27600862
ABSTRACT

AIMS:

Patients with type 2 diabetes mellitus (T2DM) have increased risk of adverse events (AEs; e.g. dehydration, hypoglycaemia) in hot weather. This analysis assessed the efficacy and safety of canagliflozin, a sodium glucose co-transporter 2 (SGLT2) inhibitor, in patients with T2DM who live in hot climates.

METHODS:

This post hoc analysis evaluated patients with T2DM using pooled data from four 26-week, placebo-controlled studies (N=2,313) and data from a 104-week, active-controlled study (add-on to metformin vs glimepiride; N=1,450). Changes in HbA1c, fasting plasma glucose (FPG), body weight and blood pressure (BP) were assessed in subsets of patients living in hot climates (pooled, placebo-controlled studies, n=611; active-controlled study, n=307) and those living in other climates (i.e. other climate subset; pooled, placebo-controlled studies, n=1,702; active-controlled study, n=1,143). Safety was assessed based on AE reports.

RESULTS:

Canagliflozin 100 and 300 mg lowered HbA1c, FPG, body weight and BP vs placebo over 26 weeks and glimepiride over 104 weeks in the hot climate subsets. Canagliflozin was generally well tolerated in the hot climate subsets, with a higher incidence of AEs related to the mechanism of SGLT2 inhibition (i.e. genital mycotic infections). Volume depletion-related AEs were low across groups.

CONCLUSION:

Canagliflozin improved glycaemic control, lowered body weight and BP, and was generally well tolerated in patients with T2DM living in hot climates compared with placebo over 26 weeks or glimepiride over 104 weeks. CLINICAL TRIALS REGISTRATION ClinicalTrials.gov NCT01081834, NCT01106677, NCT01106625, NCT01106690, NCT00968812.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Diabetes Mellitus Tipo 2 / Canagliflozina / Hipoglicemiantes Tipo de estudo: Clinical_trials Limite: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Int J Clin Pract Assunto da revista: MEDICINA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Índia

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Diabetes Mellitus Tipo 2 / Canagliflozina / Hipoglicemiantes Tipo de estudo: Clinical_trials Limite: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Int J Clin Pract Assunto da revista: MEDICINA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Índia