Literature DB >> 34059720

A randomized controlled trial of two diets enriched with protein or fat in patients with type 2 diabetes treated with dapagliflozin.

Yasuhiro Watanabe1, Daisuke Suzuki2, Nobuichi Kuribayashi3, Daigaku Uchida4, Mitsutoshi Kato5, Hiroshi Ohashi6, Daiji Nagayama7, Takashi Yamaguchi1, Masahiro Ohira1, Atsuhito Saiki1, Ichiro Tatsuno8,9.   

Abstract

Sodium-glucose cotranspsorter-2 (SGLT2) inhibitors (SGLT2i) involve loss of skeletal muscle mass, potentially leading to inadequate HbA1c reduction in type 2 diabetes (T2DM), since muscle mass is related to insulin sensitivity. The benefit of protein-enriched diet for improving HbA1c in SGLT2i-treated T2DM patients remains unclear. We conducted a multicenter, double-blind, randomized, controlled, investigator-initiated clinical trial. 130 T2DM patients treated with dapagliflozin (5 mg) were randomized to isoenergic protein-rich formula diet (P-FD) or fat-rich FD (F-FD) (1:1 allocation) to replace one of three meals/day for 24 weeks. Primary outcome was change in HbA1c. Secondary outcomes were changes in serum insulin, body composition and other metabolic parameters. Although HbA1c decreased significantly in both groups [mean (95% confidence interval) - 0.7% (- 0.9 to - 0.5) in P-FD, - 0.6% (- 0.8 to - 0.5) in F-FD], change in HbA1c was not significantly different between the two groups (P = 0.4474). Fasting insulin and body fat mass decreased, while HDL-cholesterol increased significantly in P-FD, and these changes were significantly greater compared with F-FD (all, P < 0.05). In T2DM treated with dapagliflozin, protein-enriched diet does not contribute to HbA1c reduction, although it decreases serum insulin and body fat mass, and increases HDL-cholesterol compared with fat-enriched diet with identical calories and carbohydrate ratio.

Entities:  

Year:  2021        PMID: 34059720     DOI: 10.1038/s41598-021-90879-z

Source DB:  PubMed          Journal:  Sci Rep        ISSN: 2045-2322            Impact factor:   4.379


  34 in total

1.  Dapagliflozin maintains glycaemic control while reducing weight and body fat mass over 2 years in patients with type 2 diabetes mellitus inadequately controlled on metformin.

Authors:  J Bolinder; Ö Ljunggren; L Johansson; J Wilding; A M Langkilde; C D Sjöström; J Sugg; S Parikh
Journal:  Diabetes Obes Metab       Date:  2013-08-29       Impact factor: 6.577

2.  Evaluation of the effects of dapagliflozin, a sodium-glucose co-transporter-2 inhibitor, on hepatic steatosis and fibrosis using transient elastography in patients with type 2 diabetes and non-alcoholic fatty liver disease.

Authors:  Masanori Shimizu; Kunihiro Suzuki; Kanako Kato; Teruo Jojima; Toshie Iijima; Toshimitsu Murohisa; Makoto Iijima; Hidehiro Takekawa; Isao Usui; Hideyuki Hiraishi; Yoshimasa Aso
Journal:  Diabetes Obes Metab       Date:  2018-10-02       Impact factor: 6.577

3.  Effects of dapagliflozin on body weight, total fat mass, and regional adipose tissue distribution in patients with type 2 diabetes mellitus with inadequate glycemic control on metformin.

Authors:  Jan Bolinder; Östen Ljunggren; Joel Kullberg; Lars Johansson; John Wilding; Anna Maria Langkilde; Jennifer Sugg; Shamik Parikh
Journal:  J Clin Endocrinol Metab       Date:  2012-01-11       Impact factor: 5.958

4.  Relative muscle mass is inversely associated with insulin resistance and prediabetes. Findings from the third National Health and Nutrition Examination Survey.

Authors:  Preethi Srikanthan; Arun S Karlamangla
Journal:  J Clin Endocrinol Metab       Date:  2011-07-21       Impact factor: 5.958

Review 5.  MECHANISMS IN ENDOCRINOLOGY: SGLT2 inhibitors: clinical benefits by restoration of normal diurnal metabolism?

Authors:  Russell L Esterline; Allan Vaag; Jan Oscarsson; Jiten Vora
Journal:  Eur J Endocrinol       Date:  2018-01-25       Impact factor: 6.664

6.  Comparative study of the effects of ipragliflozin and sitagliptin on multiple metabolic variables in Japanese patients with type 2 diabetes: A multicentre, randomized, prospective, open-label, active-controlled study.

Authors:  Yuya Tsurutani; Kazuki Nakai; Kosuke Inoue; Kosuke Azuma; Sei Mukai; Seitaro Maruyama; Takashi Iizuka; Yoko Matsuzawa; Jun Saito; Masao Omura; Tetsuo Nishikawa
Journal:  Diabetes Obes Metab       Date:  2018-07-04       Impact factor: 6.577

7.  Luseogliflozin reduces epicardial fat accumulation in patients with type 2 diabetes: a pilot study.

Authors:  Ryotaro Bouchi; Masahiro Terashima; Yuriko Sasahara; Masahiro Asakawa; Tatsuya Fukuda; Takato Takeuchi; Yujiro Nakano; Masanori Murakami; Isao Minami; Hajime Izumiyama; Koshi Hashimoto; Takanobu Yoshimoto; Yoshihiro Ogawa
Journal:  Cardiovasc Diabetol       Date:  2017-03-03       Impact factor: 9.951

8.  Sodium-glucose cotransporter 2 inhibitor-induced changes in body composition and simultaneous changes in metabolic profile: 52-week prospective LIGHT (Luseogliflozin: the Components of Weight Loss in Japanese Patients with Type 2 Diabetes Mellitus) Study.

Authors:  Takashi Sasaki; Masahiro Sugawara; Masahiro Fukuda
Journal:  J Diabetes Investig       Date:  2018-05-16       Impact factor: 4.232

9.  Sodium-glucose cotransport inhibition with dapagliflozin in type 2 diabetes.

Authors:  James F List; Vincent Woo; Enrique Morales; Weihua Tang; Fred T Fiedorek
Journal:  Diabetes Care       Date:  2008-12-29       Impact factor: 17.152

10.  Sodium-Glucose Cotransporter 2 (SGLT2) Inhibitor Increases Circulating Zinc-Α2-Glycoprotein Levels in Patients with Type 2 Diabetes.

Authors:  Xin Liao; Xuemei Wang; Haopeng Li; Ling Li; Guohao Zhang; Mengliu Yang; Lei Yuan; Hua Liu; Gangyi Yang; Lin Gao
Journal:  Sci Rep       Date:  2016-09-09       Impact factor: 4.379

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