Cargando…

Linagliptin, when compared to placebo, improves CD34+ve endothelial progenitor cells in type 2 diabetes subjects with chronic kidney disease taking metformin and/or insulin: a randomized controlled trial

BACKGROUND: Endothelial Progenitor cells (EPCs) has been shown to be dysfunctional in both type 2 diabetes mellitus (T2DM) and chronic kidney disease (CKD) leading to poor regeneration of endothelium and renal perfusion. EPCs have been shown to be a robust cardiovascular disease (CVD) risk indicator...

Descripción completa

Detalles Bibliográficos
Autores principales: Awal, Hassan B., Nandula, Seshagiri Rao, Domingues, Cleyton C., Dore, Fiona J., Kundu, Nabanita, Brichacek, Beda, Fakhri, Mona, Elzarki, Adrian, Ahmadi, Neeki, Safai, Shauna, Fosso, Magan, Amdur, Richard L., Sen, Sabyasachi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7271387/
https://www.ncbi.nlm.nih.gov/pubmed/32493344
http://dx.doi.org/10.1186/s12933-020-01046-z
_version_ 1783542080553877504
author Awal, Hassan B.
Nandula, Seshagiri Rao
Domingues, Cleyton C.
Dore, Fiona J.
Kundu, Nabanita
Brichacek, Beda
Fakhri, Mona
Elzarki, Adrian
Ahmadi, Neeki
Safai, Shauna
Fosso, Magan
Amdur, Richard L.
Sen, Sabyasachi
author_facet Awal, Hassan B.
Nandula, Seshagiri Rao
Domingues, Cleyton C.
Dore, Fiona J.
Kundu, Nabanita
Brichacek, Beda
Fakhri, Mona
Elzarki, Adrian
Ahmadi, Neeki
Safai, Shauna
Fosso, Magan
Amdur, Richard L.
Sen, Sabyasachi
author_sort Awal, Hassan B.
collection PubMed
description BACKGROUND: Endothelial Progenitor cells (EPCs) has been shown to be dysfunctional in both type 2 diabetes mellitus (T2DM) and chronic kidney disease (CKD) leading to poor regeneration of endothelium and renal perfusion. EPCs have been shown to be a robust cardiovascular disease (CVD) risk indicator. Cellular mechanisms of DPP4 inhibitors such as linagliptin (LG) on CVD risk, in patients with T2DM with established CKD has not been established. Linagliptin, a DPP4 inhibitor when added to insulin, metformin or both may improve endothelial dysfunction in a diabetic kidney disease (DKD) population. METHODS: 31 subjects taking metformin and/or Insulin were enrolled in this 12 weeks, double blind, randomized placebo matched trial, with 5 mg LG compared to placebo. Type 2 diabetes subjects (30–70 years old), HbA1c of 6.5–10%, CKD Stage 1–3 were included. CD34+ cell number, migratory function, gene expression along with vascular parameters such as arterial stiffness, biochemistry, resting energy expenditure and body composition were measured. Data were collected at week 0, 6 and 12. A mixed model regression analysis was done with p value < 0.05 considered significant. RESULTS: A double positive CD34/CD184 cell count had a statistically significant increase (p < 0.02) as determined by flow cytometry in LG group where CD184 is SDF1a cell surface receptor. Though mRNA differences in CD34+ve was more pronounced CD34- cell mRNA analysis showed increase in antioxidants (superoxide dismutase 2 or SOD2, Catalase and Glutathione Peroxidase or GPX) and prominent endothelial markers (PECAM1, VEGF-A, vWF and NOS3). Arterial stiffness measures such as augmentation Index (AI) (p < 0.04) and pulse wave analysis (PWV) were improved (reduced in stiffness) in LG group. A reduction in LDL: HDL ratio was noted in treatment group (p < 0.04). Urinary exosome protein examining podocyte health (podocalyxin, Wilms tumor and nephrin) showed reduction or improvement. CONCLUSIONS: In DKD subjects, Linagliptin promotes an increase in CXCR4 expression on CD34 + progenitor cells with a concomitant improvement in vascular and renal parameters at 12 weeks. Trial Registration Number NCT02467478 Date of Registration: 06/08/2015
format Online
Article
Text
id pubmed-7271387
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-72713872020-06-08 Linagliptin, when compared to placebo, improves CD34+ve endothelial progenitor cells in type 2 diabetes subjects with chronic kidney disease taking metformin and/or insulin: a randomized controlled trial Awal, Hassan B. Nandula, Seshagiri Rao Domingues, Cleyton C. Dore, Fiona J. Kundu, Nabanita Brichacek, Beda Fakhri, Mona Elzarki, Adrian Ahmadi, Neeki Safai, Shauna Fosso, Magan Amdur, Richard L. Sen, Sabyasachi Cardiovasc Diabetol Original Investigation BACKGROUND: Endothelial Progenitor cells (EPCs) has been shown to be dysfunctional in both type 2 diabetes mellitus (T2DM) and chronic kidney disease (CKD) leading to poor regeneration of endothelium and renal perfusion. EPCs have been shown to be a robust cardiovascular disease (CVD) risk indicator. Cellular mechanisms of DPP4 inhibitors such as linagliptin (LG) on CVD risk, in patients with T2DM with established CKD has not been established. Linagliptin, a DPP4 inhibitor when added to insulin, metformin or both may improve endothelial dysfunction in a diabetic kidney disease (DKD) population. METHODS: 31 subjects taking metformin and/or Insulin were enrolled in this 12 weeks, double blind, randomized placebo matched trial, with 5 mg LG compared to placebo. Type 2 diabetes subjects (30–70 years old), HbA1c of 6.5–10%, CKD Stage 1–3 were included. CD34+ cell number, migratory function, gene expression along with vascular parameters such as arterial stiffness, biochemistry, resting energy expenditure and body composition were measured. Data were collected at week 0, 6 and 12. A mixed model regression analysis was done with p value < 0.05 considered significant. RESULTS: A double positive CD34/CD184 cell count had a statistically significant increase (p < 0.02) as determined by flow cytometry in LG group where CD184 is SDF1a cell surface receptor. Though mRNA differences in CD34+ve was more pronounced CD34- cell mRNA analysis showed increase in antioxidants (superoxide dismutase 2 or SOD2, Catalase and Glutathione Peroxidase or GPX) and prominent endothelial markers (PECAM1, VEGF-A, vWF and NOS3). Arterial stiffness measures such as augmentation Index (AI) (p < 0.04) and pulse wave analysis (PWV) were improved (reduced in stiffness) in LG group. A reduction in LDL: HDL ratio was noted in treatment group (p < 0.04). Urinary exosome protein examining podocyte health (podocalyxin, Wilms tumor and nephrin) showed reduction or improvement. CONCLUSIONS: In DKD subjects, Linagliptin promotes an increase in CXCR4 expression on CD34 + progenitor cells with a concomitant improvement in vascular and renal parameters at 12 weeks. Trial Registration Number NCT02467478 Date of Registration: 06/08/2015 BioMed Central 2020-06-03 /pmc/articles/PMC7271387/ /pubmed/32493344 http://dx.doi.org/10.1186/s12933-020-01046-z Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Original Investigation
Awal, Hassan B.
Nandula, Seshagiri Rao
Domingues, Cleyton C.
Dore, Fiona J.
Kundu, Nabanita
Brichacek, Beda
Fakhri, Mona
Elzarki, Adrian
Ahmadi, Neeki
Safai, Shauna
Fosso, Magan
Amdur, Richard L.
Sen, Sabyasachi
Linagliptin, when compared to placebo, improves CD34+ve endothelial progenitor cells in type 2 diabetes subjects with chronic kidney disease taking metformin and/or insulin: a randomized controlled trial
title Linagliptin, when compared to placebo, improves CD34+ve endothelial progenitor cells in type 2 diabetes subjects with chronic kidney disease taking metformin and/or insulin: a randomized controlled trial
title_full Linagliptin, when compared to placebo, improves CD34+ve endothelial progenitor cells in type 2 diabetes subjects with chronic kidney disease taking metformin and/or insulin: a randomized controlled trial
title_fullStr Linagliptin, when compared to placebo, improves CD34+ve endothelial progenitor cells in type 2 diabetes subjects with chronic kidney disease taking metformin and/or insulin: a randomized controlled trial
title_full_unstemmed Linagliptin, when compared to placebo, improves CD34+ve endothelial progenitor cells in type 2 diabetes subjects with chronic kidney disease taking metformin and/or insulin: a randomized controlled trial
title_short Linagliptin, when compared to placebo, improves CD34+ve endothelial progenitor cells in type 2 diabetes subjects with chronic kidney disease taking metformin and/or insulin: a randomized controlled trial
title_sort linagliptin, when compared to placebo, improves cd34+ve endothelial progenitor cells in type 2 diabetes subjects with chronic kidney disease taking metformin and/or insulin: a randomized controlled trial
topic Original Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7271387/
https://www.ncbi.nlm.nih.gov/pubmed/32493344
http://dx.doi.org/10.1186/s12933-020-01046-z
work_keys_str_mv AT awalhassanb linagliptinwhencomparedtoplaceboimprovescd34veendothelialprogenitorcellsintype2diabetessubjectswithchronickidneydiseasetakingmetforminandorinsulinarandomizedcontrolledtrial
AT nandulaseshagirirao linagliptinwhencomparedtoplaceboimprovescd34veendothelialprogenitorcellsintype2diabetessubjectswithchronickidneydiseasetakingmetforminandorinsulinarandomizedcontrolledtrial
AT dominguescleytonc linagliptinwhencomparedtoplaceboimprovescd34veendothelialprogenitorcellsintype2diabetessubjectswithchronickidneydiseasetakingmetforminandorinsulinarandomizedcontrolledtrial
AT dorefionaj linagliptinwhencomparedtoplaceboimprovescd34veendothelialprogenitorcellsintype2diabetessubjectswithchronickidneydiseasetakingmetforminandorinsulinarandomizedcontrolledtrial
AT kundunabanita linagliptinwhencomparedtoplaceboimprovescd34veendothelialprogenitorcellsintype2diabetessubjectswithchronickidneydiseasetakingmetforminandorinsulinarandomizedcontrolledtrial
AT brichacekbeda linagliptinwhencomparedtoplaceboimprovescd34veendothelialprogenitorcellsintype2diabetessubjectswithchronickidneydiseasetakingmetforminandorinsulinarandomizedcontrolledtrial
AT fakhrimona linagliptinwhencomparedtoplaceboimprovescd34veendothelialprogenitorcellsintype2diabetessubjectswithchronickidneydiseasetakingmetforminandorinsulinarandomizedcontrolledtrial
AT elzarkiadrian linagliptinwhencomparedtoplaceboimprovescd34veendothelialprogenitorcellsintype2diabetessubjectswithchronickidneydiseasetakingmetforminandorinsulinarandomizedcontrolledtrial
AT ahmadineeki linagliptinwhencomparedtoplaceboimprovescd34veendothelialprogenitorcellsintype2diabetessubjectswithchronickidneydiseasetakingmetforminandorinsulinarandomizedcontrolledtrial
AT safaishauna linagliptinwhencomparedtoplaceboimprovescd34veendothelialprogenitorcellsintype2diabetessubjectswithchronickidneydiseasetakingmetforminandorinsulinarandomizedcontrolledtrial
AT fossomagan linagliptinwhencomparedtoplaceboimprovescd34veendothelialprogenitorcellsintype2diabetessubjectswithchronickidneydiseasetakingmetforminandorinsulinarandomizedcontrolledtrial
AT amdurrichardl linagliptinwhencomparedtoplaceboimprovescd34veendothelialprogenitorcellsintype2diabetessubjectswithchronickidneydiseasetakingmetforminandorinsulinarandomizedcontrolledtrial
AT sensabyasachi linagliptinwhencomparedtoplaceboimprovescd34veendothelialprogenitorcellsintype2diabetessubjectswithchronickidneydiseasetakingmetforminandorinsulinarandomizedcontrolledtrial