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Comparison of daily glucose excursion by continuous glucose monitoring between type 2 diabetic patients receiving biphasic insulin aspart 30 or biphasic human insulin 30

Aims/Introduction:  Biphasic insulin aspart 30 (BIAsp 30) has an earlier and stronger peak effect with a similar duration of action to biphasic human insulin 30 (BHI 30). However, direct comparison of daily glucose excursion during treatment with these two types of insulin has not been carried out....

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Autores principales: Ohta, Akio, Suwa, Tomoko, Sada, Yoshiyuki, Kato, Hiroyuki, Koganei, Rieko, Asai, Shikou, Katabami, Takuyuki, Tanaka, Yasushi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4019310/
https://www.ncbi.nlm.nih.gov/pubmed/24843521
http://dx.doi.org/10.1111/j.2040-1124.2011.00123.x
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author Ohta, Akio
Suwa, Tomoko
Sada, Yoshiyuki
Kato, Hiroyuki
Koganei, Rieko
Asai, Shikou
Katabami, Takuyuki
Tanaka, Yasushi
author_facet Ohta, Akio
Suwa, Tomoko
Sada, Yoshiyuki
Kato, Hiroyuki
Koganei, Rieko
Asai, Shikou
Katabami, Takuyuki
Tanaka, Yasushi
author_sort Ohta, Akio
collection PubMed
description Aims/Introduction:  Biphasic insulin aspart 30 (BIAsp 30) has an earlier and stronger peak effect with a similar duration of action to biphasic human insulin 30 (BHI 30). However, direct comparison of daily glucose excursion during treatment with these two types of insulin has not been carried out. Materials and Methods:  We carried out continuous glucose monitoring (CGM) and evaluated the 48‐h glucose profile during twice‐daily injections of BIAsp 30 or BHI 30 at the same dosage in 12 hospitalized patients with type 2 diabetes who participated in a randomized cross‐over trial. Results:  The 48‐h average glucose level and mean amplitude of glucose excursion (MAGE) were lower during BIAsp 30 treatment than with BHI 30. The average glucose level during 2–3 h after breakfast and 2–4 h after dinner, and the incremental postprandial glucose from just before to 4 h after dinner were lower with BIAsp 30 treatment than with BHI 30. Furthermore, BIAsp 30 treatment reduced the SD from 30 min before to 4 h after breakfast and lunch compared with BHI 30. The average glucose level and SD during the 30 min before each meal and during the night were not different between the two insulin preparations, and hypoglycemia was not observed with either treatment. Conclusions:  Twice‐daily BIAsp 30 reduced the 48‐h average glucose and MAGE, the postprandial glucose (after breakfast and dinner), and the SD of glucose excursion (after breakfast and lunch) compared with the same dosage of BHI 30, without causing hypoglycemia or deterioration of glycemic control before meals and at night. This trial was registered with UMIN (no. UMIN000005129). (J Diabetes Invest, doi: 10.1111/j.2040‐1124.2011.00123.x, 2011)
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spelling pubmed-40193102014-05-19 Comparison of daily glucose excursion by continuous glucose monitoring between type 2 diabetic patients receiving biphasic insulin aspart 30 or biphasic human insulin 30 Ohta, Akio Suwa, Tomoko Sada, Yoshiyuki Kato, Hiroyuki Koganei, Rieko Asai, Shikou Katabami, Takuyuki Tanaka, Yasushi J Diabetes Investig Articles Aims/Introduction:  Biphasic insulin aspart 30 (BIAsp 30) has an earlier and stronger peak effect with a similar duration of action to biphasic human insulin 30 (BHI 30). However, direct comparison of daily glucose excursion during treatment with these two types of insulin has not been carried out. Materials and Methods:  We carried out continuous glucose monitoring (CGM) and evaluated the 48‐h glucose profile during twice‐daily injections of BIAsp 30 or BHI 30 at the same dosage in 12 hospitalized patients with type 2 diabetes who participated in a randomized cross‐over trial. Results:  The 48‐h average glucose level and mean amplitude of glucose excursion (MAGE) were lower during BIAsp 30 treatment than with BHI 30. The average glucose level during 2–3 h after breakfast and 2–4 h after dinner, and the incremental postprandial glucose from just before to 4 h after dinner were lower with BIAsp 30 treatment than with BHI 30. Furthermore, BIAsp 30 treatment reduced the SD from 30 min before to 4 h after breakfast and lunch compared with BHI 30. The average glucose level and SD during the 30 min before each meal and during the night were not different between the two insulin preparations, and hypoglycemia was not observed with either treatment. Conclusions:  Twice‐daily BIAsp 30 reduced the 48‐h average glucose and MAGE, the postprandial glucose (after breakfast and dinner), and the SD of glucose excursion (after breakfast and lunch) compared with the same dosage of BHI 30, without causing hypoglycemia or deterioration of glycemic control before meals and at night. This trial was registered with UMIN (no. UMIN000005129). (J Diabetes Invest, doi: 10.1111/j.2040‐1124.2011.00123.x, 2011) Blackwell Publishing Ltd 2011-05-10 2011-10-07 /pmc/articles/PMC4019310/ /pubmed/24843521 http://dx.doi.org/10.1111/j.2040-1124.2011.00123.x Text en © 2011 Asian Association for the Study of Diabetes and Blackwell Publishing Asia Pty Ltd
spellingShingle Articles
Ohta, Akio
Suwa, Tomoko
Sada, Yoshiyuki
Kato, Hiroyuki
Koganei, Rieko
Asai, Shikou
Katabami, Takuyuki
Tanaka, Yasushi
Comparison of daily glucose excursion by continuous glucose monitoring between type 2 diabetic patients receiving biphasic insulin aspart 30 or biphasic human insulin 30
title Comparison of daily glucose excursion by continuous glucose monitoring between type 2 diabetic patients receiving biphasic insulin aspart 30 or biphasic human insulin 30
title_full Comparison of daily glucose excursion by continuous glucose monitoring between type 2 diabetic patients receiving biphasic insulin aspart 30 or biphasic human insulin 30
title_fullStr Comparison of daily glucose excursion by continuous glucose monitoring between type 2 diabetic patients receiving biphasic insulin aspart 30 or biphasic human insulin 30
title_full_unstemmed Comparison of daily glucose excursion by continuous glucose monitoring between type 2 diabetic patients receiving biphasic insulin aspart 30 or biphasic human insulin 30
title_short Comparison of daily glucose excursion by continuous glucose monitoring between type 2 diabetic patients receiving biphasic insulin aspart 30 or biphasic human insulin 30
title_sort comparison of daily glucose excursion by continuous glucose monitoring between type 2 diabetic patients receiving biphasic insulin aspart 30 or biphasic human insulin 30
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4019310/
https://www.ncbi.nlm.nih.gov/pubmed/24843521
http://dx.doi.org/10.1111/j.2040-1124.2011.00123.x
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