Elevated Serum Growth Differentiation Factor 15 Levels as a Potential Biomarker of the Efficacy of Imeglimin in Individuals With Type 2 Diabetes Mellitus: An Exploratory Study

The aim of the present study was to conduct a prospective observational study to explore the effects of imeglimin on systemic energy metabolism/body composition and to identify potential mitochondria-related biomarkers of the efficacy of the drug in clinical settings. In this prospective observation...

Full description

Saved in:
Bibliographic Details
Published inJournal of clinical medicine research Vol. 16; no. 10; pp. 503 - 508
Main Authors Wada, Naoki, Murakami, Takaaki, Fauzi, Muhammad, Sakaki, Kentaro, Oshima, Shinobu, Shimada, Yoshihito, Asai, Kanae, Oshima, Ayako, Nomura, Satoko, Joo, Erina, Mori, Michiko, Fujiwara, Ryoko, Shide, Kenichiro, Wada, Keiko, Yabe, Daisuke, Inagaki, Nobuya, Harada, Norio
Format Journal Article
LanguageEnglish
Published Canada Elmer Press 01.10.2024
Subjects
Online AccessGet full text
ISSN1918-3003
1918-3011
DOI10.14740/jocmr6031

Cover

Abstract The aim of the present study was to conduct a prospective observational study to explore the effects of imeglimin on systemic energy metabolism/body composition and to identify potential mitochondria-related biomarkers of the efficacy of the drug in clinical settings. In this prospective observational study, 16 participants with type 2 diabetes mellitus in the diabetes clinic of Kyoto University Hospital were enrolled. Individuals were started on imeglimin as monotherapy or add-on therapy. After 3 months under imeglimin treatment, there was no significant change in basal metabolism or body composition. However, serum levels of growth differentiation factor 15 (GDF15) were higher while those of serum fibroblast growth factor 21 and urine 8-hydroxy-2'-deoxyguanosine were not changed. Additional examination revealed that imeglimin induces GDF15 protein release from human hepatocytes. Three-month imeglimin treatment increased serum GDF15 levels in clinical type 2 diabetes mellitus patients along with little change in basal metabolism or body composition, suggesting GDF15 as a potential marker for the efficacy of imeglimin.
AbstractList The aim of the present study was to conduct a prospective observational study to explore the effects of imeglimin on systemic energy metabolism/body composition and to identify potential mitochondria-related biomarkers of the efficacy of the drug in clinical settings.BackgroundThe aim of the present study was to conduct a prospective observational study to explore the effects of imeglimin on systemic energy metabolism/body composition and to identify potential mitochondria-related biomarkers of the efficacy of the drug in clinical settings.In this prospective observational study, 16 participants with type 2 diabetes mellitus in the diabetes clinic of Kyoto University Hospital were enrolled. Individuals were started on imeglimin as monotherapy or add-on therapy.MethodsIn this prospective observational study, 16 participants with type 2 diabetes mellitus in the diabetes clinic of Kyoto University Hospital were enrolled. Individuals were started on imeglimin as monotherapy or add-on therapy.After 3 months under imeglimin treatment, there was no significant change in basal metabolism or body composition. However, serum levels of growth differentiation factor 15 (GDF15) were higher while those of serum fibroblast growth factor 21 and urine 8-hydroxy-2'-deoxyguanosine were not changed. Additional in vitro examination revealed that imeglimin induces GDF15 protein release from human hepatocytes.ResultsAfter 3 months under imeglimin treatment, there was no significant change in basal metabolism or body composition. However, serum levels of growth differentiation factor 15 (GDF15) were higher while those of serum fibroblast growth factor 21 and urine 8-hydroxy-2'-deoxyguanosine were not changed. Additional in vitro examination revealed that imeglimin induces GDF15 protein release from human hepatocytes.Three-month imeglimin treatment increased serum GDF15 levels in clinical type 2 diabetes mellitus patients along with little change in basal metabolism or body composition, suggesting GDF15 as a potential marker for the efficacy of imeglimin.ConclusionsThree-month imeglimin treatment increased serum GDF15 levels in clinical type 2 diabetes mellitus patients along with little change in basal metabolism or body composition, suggesting GDF15 as a potential marker for the efficacy of imeglimin.
The aim of the present study was to conduct a prospective observational study to explore the effects of imeglimin on systemic energy metabolism/body composition and to identify potential mitochondria-related biomarkers of the efficacy of the drug in clinical settings. In this prospective observational study, 16 participants with type 2 diabetes mellitus in the diabetes clinic of Kyoto University Hospital were enrolled. Individuals were started on imeglimin as monotherapy or add-on therapy. After 3 months under imeglimin treatment, there was no significant change in basal metabolism or body composition. However, serum levels of growth differentiation factor 15 (GDF15) were higher while those of serum fibroblast growth factor 21 and urine 8-hydroxy-2'-deoxyguanosine were not changed. Additional examination revealed that imeglimin induces GDF15 protein release from human hepatocytes. Three-month imeglimin treatment increased serum GDF15 levels in clinical type 2 diabetes mellitus patients along with little change in basal metabolism or body composition, suggesting GDF15 as a potential marker for the efficacy of imeglimin.
Author Murakami, Takaaki
Nomura, Satoko
Mori, Michiko
Fujiwara, Ryoko
Fauzi, Muhammad
Joo, Erina
Shide, Kenichiro
Inagaki, Nobuya
Wada, Keiko
Harada, Norio
Oshima, Ayako
Sakaki, Kentaro
Asai, Kanae
Shimada, Yoshihito
Yabe, Daisuke
Wada, Naoki
Oshima, Shinobu
AuthorAffiliation c Medical Research Institute Kitano Hospital, PIIF Tazuke-Kofukai, Osaka, Japan
d Department of Endocrinology and Metabolism, School of Medical Sciences, University of Fukui, Japan
a Department of Diabetes, Endocrinology, and Nutrition, Graduate School of Medicine, Kyoto University, Kyoto, Japan
b Department of Metabolism and Clinical Nutrition, Kyoto University Hospital, Kyoto, Japan
e These authors contributed equally to this work
AuthorAffiliation_xml – name: b Department of Metabolism and Clinical Nutrition, Kyoto University Hospital, Kyoto, Japan
– name: a Department of Diabetes, Endocrinology, and Nutrition, Graduate School of Medicine, Kyoto University, Kyoto, Japan
– name: e These authors contributed equally to this work
– name: d Department of Endocrinology and Metabolism, School of Medical Sciences, University of Fukui, Japan
– name: c Medical Research Institute Kitano Hospital, PIIF Tazuke-Kofukai, Osaka, Japan
Author_xml – sequence: 1
  givenname: Naoki
  surname: Wada
  fullname: Wada, Naoki
– sequence: 2
  givenname: Takaaki
  orcidid: 0000-0003-3844-1138
  surname: Murakami
  fullname: Murakami, Takaaki
– sequence: 3
  givenname: Muhammad
  surname: Fauzi
  fullname: Fauzi, Muhammad
– sequence: 4
  givenname: Kentaro
  surname: Sakaki
  fullname: Sakaki, Kentaro
– sequence: 5
  givenname: Shinobu
  surname: Oshima
  fullname: Oshima, Shinobu
– sequence: 6
  givenname: Yoshihito
  surname: Shimada
  fullname: Shimada, Yoshihito
– sequence: 7
  givenname: Kanae
  surname: Asai
  fullname: Asai, Kanae
– sequence: 8
  givenname: Ayako
  surname: Oshima
  fullname: Oshima, Ayako
– sequence: 9
  givenname: Satoko
  surname: Nomura
  fullname: Nomura, Satoko
– sequence: 10
  givenname: Erina
  surname: Joo
  fullname: Joo, Erina
– sequence: 11
  givenname: Michiko
  surname: Mori
  fullname: Mori, Michiko
– sequence: 12
  givenname: Ryoko
  surname: Fujiwara
  fullname: Fujiwara, Ryoko
– sequence: 13
  givenname: Kenichiro
  surname: Shide
  fullname: Shide, Kenichiro
– sequence: 14
  givenname: Keiko
  surname: Wada
  fullname: Wada, Keiko
– sequence: 15
  givenname: Daisuke
  orcidid: 0000-0002-5334-7687
  surname: Yabe
  fullname: Yabe, Daisuke
– sequence: 16
  givenname: Nobuya
  orcidid: 0000-0001-8261-2593
  surname: Inagaki
  fullname: Inagaki, Nobuya
– sequence: 17
  givenname: Norio
  orcidid: 0000-0001-8720-1013
  surname: Harada
  fullname: Harada, Norio
BackLink https://www.ncbi.nlm.nih.gov/pubmed/39544328$$D View this record in MEDLINE/PubMed
BookMark eNpVUttuEzEQtVARLaUvfACaR4QU8G13HV5QKWmJFARSi3hcOd5x47Jrp7Y3sF_FL2LaEoE1GnvkM-foaOYpOfDBIyHPGX3NZCPpm5tghlhTwR6RIzZnaiYoYwf7NxWH5CSlG1qOEExR9YQcinklpeDqiPxa9LjTGTu4xDgOcBHDj7yBD85ajOiz09kFD-fa5BCBVbDCHfYJdAn4EvIdpIf3Lgw6fscIwULeICysdUab6U-9HPC6d4PzUGLpO7dz3agLyTdXpK6mLQIvinqNGRN8wr53eUxv4dTD4ue2D1EX7Qku89hNz8hjW1rx5OE-Jl_PF1dnH2erzxfLs9PVzAjF86zrlFS1VqwyyGuptGq47JDaWlqF85JMUxlpcN1wYyW3c12SFGtqJasbKo7Ju3ve7bgesDPFZ9R9u42u-JzaoF37_493m_Y67FrGqqqpqCwMLx8YYrgdMeV2cMkUc9pjGFMrGFeKN5LzAn3xr9he5e-YCuDVPcDEkFJEu4cw2t6tQbtfA_EbDsyoAQ
ContentType Journal Article
Copyright Copyright 2024, Wada et al.
Copyright 2024, Wada et al. 2024
Copyright_xml – notice: Copyright 2024, Wada et al.
– notice: Copyright 2024, Wada et al. 2024
DBID AAYXX
CITATION
NPM
7X8
5PM
DOI 10.14740/jocmr6031
DatabaseName CrossRef
PubMed
MEDLINE - Academic
PubMed Central (Full Participant titles)
DatabaseTitle CrossRef
PubMed
MEDLINE - Academic
DatabaseTitleList MEDLINE - Academic
PubMed
Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
DocumentTitleAlternate Elevated GDF15 in Treatment With Imeglimin
EISSN 1918-3011
EndPage 508
ExternalDocumentID PMC11557504
39544328
10_14740_jocmr6031
Genre Journal Article
GroupedDBID 53G
5VS
AAYXX
ADBBV
ADRAZ
ALMA_UNASSIGNED_HOLDINGS
AOIJS
BAWUL
CITATION
DIK
E3Z
EBS
EJD
F5P
H13
HYE
KQ8
M48
O5R
O5S
OK1
PGMZT
RNS
RPM
TR2
GROUPED_DOAJ
NPM
7X8
5PM
ID FETCH-LOGICAL-c382t-dd8486a815ce2648a8724de0f64f8e94f8c75c4ceb72cf42f9a42f43b0f416703
IEDL.DBID M48
ISSN 1918-3003
IngestDate Thu Aug 21 18:30:19 EDT 2025
Fri Jul 11 03:33:27 EDT 2025
Thu Jan 02 22:24:02 EST 2025
Tue Jul 01 01:04:21 EDT 2025
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed false
IsScholarly true
Issue 10
Keywords Imeglimin
GDF15
Diabetes mellitus
Language English
License Copyright 2024, Wada et al.
This article is distributed under the terms of the Creative Commons Attribution Non-Commercial 4.0 International License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c382t-dd8486a815ce2648a8724de0f64f8e94f8c75c4ceb72cf42f9a42f43b0f416703
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ORCID 0000-0001-8261-2593
0000-0001-8720-1013
0000-0002-5334-7687
0000-0003-3844-1138
OpenAccessLink http://journals.scholarsportal.info/openUrl.xqy?doi=10.14740/jocmr6031
PMID 39544328
PQID 3128827422
PQPubID 23479
PageCount 6
ParticipantIDs pubmedcentral_primary_oai_pubmedcentral_nih_gov_11557504
proquest_miscellaneous_3128827422
pubmed_primary_39544328
crossref_primary_10_14740_jocmr6031
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2024-10-01
PublicationDateYYYYMMDD 2024-10-01
PublicationDate_xml – month: 10
  year: 2024
  text: 2024-10-01
  day: 01
PublicationDecade 2020
PublicationPlace Canada
PublicationPlace_xml – name: Canada
PublicationTitle Journal of clinical medicine research
PublicationTitleAlternate J Clin Med Res
PublicationYear 2024
Publisher Elmer Press
Publisher_xml – name: Elmer Press
SSID ssj0000331808
Score 2.276352
Snippet The aim of the present study was to conduct a prospective observational study to explore the effects of imeglimin on systemic energy metabolism/body...
SourceID pubmedcentral
proquest
pubmed
crossref
SourceType Open Access Repository
Aggregation Database
Index Database
StartPage 503
SubjectTerms Short Communication
Title Elevated Serum Growth Differentiation Factor 15 Levels as a Potential Biomarker of the Efficacy of Imeglimin in Individuals With Type 2 Diabetes Mellitus: An Exploratory Study
URI https://www.ncbi.nlm.nih.gov/pubmed/39544328
https://www.proquest.com/docview/3128827422
https://pubmed.ncbi.nlm.nih.gov/PMC11557504
Volume 16
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV3db9MwED-NISFeJr5XPqab4DUos53EQZqmAe02RBEPVOwtchx7q9Qm0KSI_lX8i9wlabUCD0iWpSR2EuV357uTL_cDeJUoF0YiiQISIBGo1OaBdqEJtCH9c3HijeVAcfwpPp-oD5fR5Q6s-Tv7D1j_M7RjPqnJYvb65_fVCSn8MSu8SlRIs-x8wXTJt-A2WaSYg7Bx7-a3K7IkyW3J6Sg60YGkE32l0u3p27bpL4fzz7zJG4ZodA_2eg8STzvI78OOKx_AnXG_R_4Qfg1n7gd5kAXSOrCc4xkF2s01vu-ZUJoOCxy1RDt4FOFHzhuq0VDDz1XTDpnh22k159SdBVYeyUvEIRebMHbFxxdzdzVjPjCkdrH5p6vGr1N6FMe2KLBPtqlxzEU_m2X9Bk9L7JL-2r195CTG1SOYjIZf3p0HPS1DYKUWTVAUWunY6KPIOs6PMzoRqnChj5XXLqXOJpFV1uWJsF4JnxrqlMxDz9iE8jHsllXp9gFVHqeEgcitlyQnIheFNNYXiVcuztNoAC_XgGTfuuobGUctDFu2gW0Ah2usMlIO3vEwpauWdSbJ-mrejBYDeNJht7mPTLn0n9AD0FuobgZw4e3tK-X0ui3ATV50xGXxn_7X6z2Du4I8oS4D8DnsNoule0GeTJMftGL6G_bN9hk
linkProvider Scholars Portal
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Elevated+Serum+Growth+Differentiation+Factor+15+Levels+as+a+Potential+Biomarker+of+the+Efficacy+of+Imeglimin+in+Individuals+With+Type+2+Diabetes+Mellitus%3A+An+Exploratory+Study&rft.jtitle=Journal+of+clinical+medicine+research&rft.au=Wada%2C+Naoki&rft.au=Murakami%2C+Takaaki&rft.au=Fauzi%2C+Muhammad&rft.au=Sakaki%2C+Kentaro&rft.date=2024-10-01&rft.issn=1918-3003&rft.eissn=1918-3011&rft.volume=16&rft.issue=10&rft.spage=503&rft.epage=508&rft_id=info:doi/10.14740%2Fjocmr6031&rft.externalDBID=n%2Fa&rft.externalDocID=10_14740_jocmr6031
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1918-3003&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1918-3003&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1918-3003&client=summon