Affiliations 

  • 1 Endocrine Department, Dubai Hospital, Dubai Health Authority, Dubai, United Arab Emirates. Electronic address: mhassanein148@hotmail.com
  • 2 Internal Medicine Department, Head Division of Endocrinology, Rafic Hariri University Hospital, Bir Hassan, Jinah, POB: 5244, 2833-7401, Beirut, Lebanon. Electronic address: akramechtay2@gmail.com
  • 3 Department of Internal Medicine, CHU Setif, 19000, Algeria. Electronic address: rmalekdz@gmail.com
  • 4 Department of Diabetes and Endocrinology, University of KwaZulu Natal, Durban, South Africa. Electronic address: momars@telkomsa.net
  • 5 Department of Endocrinology, Prince Aly Khan Hospital, Mumbai, India. Electronic address: drshehla@rediffmail.com
  • 6 Novo Nordisk A/S, Vandtaarnsvej 114, DK 2860, Søborg, Denmark. Electronic address: muek@novonordisk.com
  • 7 Novo Nordisk A/S, Vandtaarnsvej 114, DK 2860, Søborg, Denmark. Electronic address: kdka@novonordisk.com
  • 8 UKM Medical Centre, National University of Malaysia, Jalan Yaacob Latif, Bandar Tun Razal, Cheras Kuala Lumpur, Malaysia. Electronic address: dr.nor.azmi@gmail.com
Diabetes Res Clin Pract, 2018 Jan;135:218-226.
PMID: 29183844 DOI: 10.1016/j.diabres.2017.11.027

Abstract

AIMS: To compare the efficacy and safety of insulin degludec/insulin aspart (IDegAsp) and biphasic insulin aspart 30 (BIAsp 30) before, during and after Ramadan in patients with type 2 diabetes mellitus (T2DM) who fasted during Ramadan.

METHODS: In this multinational, randomised, treat-to-target trial, patients with T2DM who intended to fast and were on basal, pre- or self-mixed insulin ± oral antidiabetic drugs for ≥90 days were randomised (1:1) to IDegAsp twice daily (BID) or BIAsp 30 BID. Treatment period included pre-Ramadan treatment initiation (with insulin titration for 8-20 weeks), Ramadan (4 weeks) and post-Ramadan (4 weeks). Insulin doses were reduced by 30-50% for the pre-dawn meal (suhur) on the first day of Ramadan, and readjusted to the pre-Ramadan levels at the end of Ramadan. Hypoglycaemia was analysed as overall (severe or plasma glucose <3.1 mmol/L [56 mg/dL]), nocturnal (00:01-05:59) or severe (requiring assistance of another person).

RESULTS: During the treatment period, IDegAsp (n = 131) had significantly lower overall and nocturnal hypoglycaemia rates with similar glycaemic efficacy, versus BIAsp 30 (n = 132). During Ramadan, despite achieving significantly lower pre-iftar (meal at sunset) self-measured plasma glucose (estimated treatment difference: -0.54 mmol/L [-1.02; -0.07]95% CI, p = .0247; post hoc) with similar overall glycaemic efficacy, IDegAsp showed significantly lower overall and nocturnal hypoglycaemia rates versus BIAsp 30.

CONCLUSIONS: IDegAsp is a suitable therapeutic agent for patients who need insulin for sustained glucose control before, during and after Ramadan fasting, with a significantly lower risk of hypoglycaemia, versus BIAsp 30, an existing premixed insulin analogue.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

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