Association of osteocalcin, osteoprotegerin, and osteopontin with cardiovascular disease and retinopathy in type 2 diabetes.


Journal

Diabetes/metabolism research and reviews
ISSN: 1520-7560
Titre abrégé: Diabetes Metab Res Rev
Pays: England
ID NLM: 100883450

Informations de publication

Date de publication:
Jul 2023
Historique:
revised: 02 12 2022
received: 25 08 2022
accepted: 26 02 2023
medline: 10 7 2023
pubmed: 8 3 2023
entrez: 7 3 2023
Statut: ppublish

Résumé

Novel biomarkers of vascular disease in diabetes could help identify new mechanistic pathways. Osteocalcin, osteoprotegerin, and osteopontin are key molecules involved in bone and vascular calcification processes, both of which are compromised in diabetes. We aimed to evaluate possible associations of osteocalcin, osteoprotegerin, and osteopontin with cardiovascular disease (CVD) and diabetic retinopathy (DR) among people with type 2 diabetes (T2D). Osteocalcin, osteoprotegerin, and osteopontin concentrations were measured at enrolment in 848 participants with T2D from the Sapienza University Mortality and Morbidity Event Rate (SUMMER) Study (ClinicalTrials.gov: NCT02311244). Logistic regression models and propensity score matching were used to assess possible associations of osteocalcin, osteoprotegerin, and osteopontin with a history of CVD and with evidence of any grade of DR adjusting for confounders. Previous CVD was reported in 139 (16.4%) participants, while 144 (17.0%) had DR. After adjusting for possible confounders, osteocalcin but not osteoprotegerin or osteopontin concentrations were associated with a history of CVD (Odds Ratio [OR] and 95% CI for one standard deviation (SD) increase in osteocalcin concentrations (natural log): 1.35 (1.06-1.72), p = 0.014). Associations with prevalent DR were seen for osteoprotegerin (OR for one SD increase in osteoprotegerin concentrations (natural log): 1.25 (1.01-1.55), p = 0.047) and osteopontin (OR for one SD increase in osteopontin concentrations (natural log): 1.25 (1.02-1.53), p = 0.022), but not osteocalcin. In T2D, higher serum osteocalcin concentrations are associated with macrovascular complications and higher osteoprotegerin and osteopontin concentrations with microvascular complications, suggesting that these osteokines might be involved in pathways directly related to vascular disease.

Sections du résumé

BACKGROUND BACKGROUND
Novel biomarkers of vascular disease in diabetes could help identify new mechanistic pathways. Osteocalcin, osteoprotegerin, and osteopontin are key molecules involved in bone and vascular calcification processes, both of which are compromised in diabetes. We aimed to evaluate possible associations of osteocalcin, osteoprotegerin, and osteopontin with cardiovascular disease (CVD) and diabetic retinopathy (DR) among people with type 2 diabetes (T2D).
MATERIALS AND METHODS METHODS
Osteocalcin, osteoprotegerin, and osteopontin concentrations were measured at enrolment in 848 participants with T2D from the Sapienza University Mortality and Morbidity Event Rate (SUMMER) Study (ClinicalTrials.gov: NCT02311244). Logistic regression models and propensity score matching were used to assess possible associations of osteocalcin, osteoprotegerin, and osteopontin with a history of CVD and with evidence of any grade of DR adjusting for confounders.
RESULTS RESULTS
Previous CVD was reported in 139 (16.4%) participants, while 144 (17.0%) had DR. After adjusting for possible confounders, osteocalcin but not osteoprotegerin or osteopontin concentrations were associated with a history of CVD (Odds Ratio [OR] and 95% CI for one standard deviation (SD) increase in osteocalcin concentrations (natural log): 1.35 (1.06-1.72), p = 0.014). Associations with prevalent DR were seen for osteoprotegerin (OR for one SD increase in osteoprotegerin concentrations (natural log): 1.25 (1.01-1.55), p = 0.047) and osteopontin (OR for one SD increase in osteopontin concentrations (natural log): 1.25 (1.02-1.53), p = 0.022), but not osteocalcin.
CONCLUSIONS CONCLUSIONS
In T2D, higher serum osteocalcin concentrations are associated with macrovascular complications and higher osteoprotegerin and osteopontin concentrations with microvascular complications, suggesting that these osteokines might be involved in pathways directly related to vascular disease.

Identifiants

pubmed: 36880127
doi: 10.1002/dmrr.3632
doi:

Substances chimiques

Osteopontin 106441-73-0
Osteocalcin 104982-03-8
Biomarkers 0

Banques de données

ClinicalTrials.gov
['NCT02311244']

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e3632

Subventions

Organisme : Sapienza Università di Roma
Organisme : Ministero della Salute
Organisme : European Foundation for the Study of Diabetes
Organisme : Fondazione Diabete Ricerca
Organisme : National Institute for Health Research

Investigateurs

Federica Alberico (F)
Elena Alessi (E)
Francesco Bagella (F)
Ilaria Barchetta (I)
Silvia Carletti (S)
Tiziana Filardi (T)
Giulia Leanza (G)
Giacomo Marini (G)
Pamela Piscitelli (P)
Federica Sentinelli (F)

Informations de copyright

© 2023 The Authors. Diabetes/Metabolism Research and Reviews published by John Wiley & Sons Ltd.

Références

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Auteurs

Ernesto Maddaloni (E)

Sapienza University of Rome, Rome, Italy.
Diabetes Trials Unit, OCDEM, University of Oxford, Oxford, UK.

Lucia Coraggio (L)

Sapienza University of Rome, Rome, Italy.

Rocco Amendolara (R)

Sapienza University of Rome, Rome, Italy.

Marco G Baroni (MG)

University of L'Aquila, Rome, Italy.

Maria G Cavallo (MG)

Sapienza University of Rome, Rome, Italy.

Massimiliano Copetti (M)

Fondazione IRCCS Casa Sollievo della Sofferenza, San Giovanni Rotondo, Rome, Italy.

Efisio Cossu (E)

Cagliari University Hospital, Cagliari, Italy.

Paola D'Angelo (P)

Sandro Pertini Hospital, Rome, Italy.

Luca D'Onofrio (L)

Sapienza University of Rome, Rome, Italy.

Salvatore De Cosmo (S)

Fondazione IRCCS Casa Sollievo della Sofferenza, San Giovanni Rotondo, Rome, Italy.

Frida Leonetti (F)

Sapienza University of Rome, Rome, Italy.

Susanna Morano (S)

Sapienza University of Rome, Rome, Italy.

Lelio Morviducci (L)

Santo Spirito Hospital, Rome, Italy.

Nicola Napoli (N)

Campus Bio-Medico University, Rome, Italy.

Sabrina Prudente (S)

Fondazione IRCCS Casa Sollievo della Sofferenza, San Giovanni Rotondo, Rome, Italy.

Giuseppe Pugliese (G)

Sapienza University of Rome, Rome, Italy.

Kyoungmin Park (K)

Joslin Diabetes Center, Harvard Medical School, Boston, Massachusetts, USA.

Rury R Holman (RR)

Diabetes Trials Unit, OCDEM, University of Oxford, Oxford, UK.

Vincenzo Trischitta (V)

Sapienza University of Rome, Rome, Italy.
Fondazione IRCCS Casa Sollievo della Sofferenza, San Giovanni Rotondo, Rome, Italy.

Raffaella Buzzetti (R)

Sapienza University of Rome, Rome, Italy.

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