PMID- 36009365 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20230308 IS - 2227-9059 (Print) IS - 2227-9059 (Electronic) IS - 2227-9059 (Linking) VI - 10 IP - 8 DP - 2022 Jul 28 TI - Relationship between the Soluble F11 Receptor and Annexin A5 in African Americans Patients with Type-2 Diabetes Mellitus. LID - 10.3390/biomedicines10081818 [doi] LID - 1818 AB - Type 2 diabetes mellitus (T2DM) is characterized by endothelial dysfunction, increased thrombogenicity, and inflammation. The soluble human F11 receptor (sF11R) and annexin A5 (ANXA5) play crucial roles in inflammatory thrombosis and atherosclerosis. We examined the relationship between circulating sF11R and ANXA5 and their impact on endothelial function. The study included 125 patients with T2DM. Plasma levels of sF11R and ANXA5 were quantified by ELISA. Microvascular function was assessed using the vascular reactivity index (VRI). Large artery stiffness was assessed by carotid-femoral pulse wave velocity (PWV). Carotid intima-media thickness (CIMT) was assessed by B-mode ultrasound imaging. The mean age of patients in the study was 59.7 +/- 7.8 years, 78% had hypertension, 76% had dyslipidemia, and 12% had CKD. sF11R correlated positively with ANXA5 levels (beta = 0.250, p = 0.005), and correlated inversely with VRI and total nitic oxide (NO), (beta = -0.201, p = 0.024; beta = -0.357, p = 0.0001, respectively). Multivariate regression analysis revealed that sF11R was independently associated with ANXA5 in the total population and in patients with HbA1c > 6.5% (beta = 0.366, p = 0.007; beta = 0.425, p = 0.0001, respectively). sF11R and ANXA5 were not associated with vascular outcome, suggesting that they may not be reliable markers of vascular dysfunction in diabetes. The clinical significance of sF11R/ANXA5 association in diabetes warrants further investigation in a larger population. FAU - Adedayo, Ajibola AU - Adedayo A AD - Department of Medicine, Downstate Medical Center, State University of New York, 450 Clarkson Ave., Brooklyn, New York, NY 11203, USA. FAU - Eluwole, Ayobami AU - Eluwole A AD - Department of Medicine, Downstate Medical Center, State University of New York, 450 Clarkson Ave., Brooklyn, New York, NY 11203, USA. FAU - Tedla, Fasika AU - Tedla F AD - Department of Medicine, Downstate Medical Center, State University of New York, 450 Clarkson Ave., Brooklyn, New York, NY 11203, USA. FAU - Kremer, Arye AU - Kremer A AD - Department of Medicine, Downstate Medical Center, State University of New York, 450 Clarkson Ave., Brooklyn, New York, NY 11203, USA. FAU - Khan, Muhammad AU - Khan M AD - Department of Medicine, Downstate Medical Center, State University of New York, 450 Clarkson Ave., Brooklyn, New York, NY 11203, USA. FAU - Mastrogiovanni, Nicole AU - Mastrogiovanni N AUID- ORCID: 0000-0001-7333-9572 AD - Department of Medicine, Downstate Medical Center, State University of New York, 450 Clarkson Ave., Brooklyn, New York, NY 11203, USA. FAU - Rosenberg, Carl AU - Rosenberg C AD - Department of Epidemiology and Biostatistics, School of Public Health, SUNY Downstate Health Sciences University, 450 Clarkson Ave., Brooklyn, New York, NY 11203, USA. FAU - Dreizen, Paul AU - Dreizen P AD - Department of Medicine, Downstate Medical Center, State University of New York, 450 Clarkson Ave., Brooklyn, New York, NY 11203, USA. FAU - La Rosa, John AU - La Rosa J AD - Department of Medicine, Downstate Medical Center, State University of New York, 450 Clarkson Ave., Brooklyn, New York, NY 11203, USA. FAU - Salciccioli, Louis AU - Salciccioli L AD - Department of Medicine, Downstate Medical Center, State University of New York, 450 Clarkson Ave., Brooklyn, New York, NY 11203, USA. FAU - Boutjdir, Mohamed AU - Boutjdir M AD - Department of Medicine, Downstate Medical Center, State University of New York, 450 Clarkson Ave., Brooklyn, New York, NY 11203, USA. FAU - Banerji, Mary Ann AU - Banerji MA AD - Department of Medicine, Downstate Medical Center, State University of New York, 450 Clarkson Ave., Brooklyn, New York, NY 11203, USA. FAU - Brown, Clinton AU - Brown C AD - Department of Medicine, Downstate Medical Center, State University of New York, 450 Clarkson Ave., Brooklyn, New York, NY 11203, USA. FAU - Lazar, Jason AU - Lazar J AUID- ORCID: 0000-0002-8548-7932 AD - Department of Medicine, Downstate Medical Center, State University of New York, 450 Clarkson Ave., Brooklyn, New York, NY 11203, USA. FAU - Salifu, Moro AU - Salifu M AD - Department of Medicine, Downstate Medical Center, State University of New York, 450 Clarkson Ave., Brooklyn, New York, NY 11203, USA. FAU - Bakillah, Ahmed AU - Bakillah A AUID- ORCID: 0000-0001-5434-1976 AD - Department of Medicine, Downstate Medical Center, State University of New York, 450 Clarkson Ave., Brooklyn, New York, NY 11203, USA. AD - King Abdullah International Medical Research Center (KAIMRC), King Saud bin Abdulaziz University for Health Sciences (KSAU-HS), Ministry of National Guard Health Affairs, Al Ahsa 31982, Saudi Arabia. LA - eng GR - ECRIP, 2015-2016/The New York State Department of Health/ PT - Journal Article DEP - 20220728 PL - Switzerland TA - Biomedicines JT - Biomedicines JID - 101691304 PMC - PMC9405000 OTO - NOTNLM OT - F11R OT - annexins OT - artery stiffness OT - biomarkers OT - cardiovascular disease OT - diabetes OT - endothelium function OT - vascular complications OT - vascular reactivity index COIS- The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, or in the decision to publish the results. EDAT- 2022/08/27 06:00 MHDA- 2022/08/27 06:01 PMCR- 2022/07/28 CRDT- 2022/08/26 01:05 PHST- 2022/04/25 00:00 [received] PHST- 2022/06/10 00:00 [revised] PHST- 2022/06/15 00:00 [accepted] PHST- 2022/08/26 01:05 [entrez] PHST- 2022/08/27 06:00 [pubmed] PHST- 2022/08/27 06:01 [medline] PHST- 2022/07/28 00:00 [pmc-release] AID - biomedicines10081818 [pii] AID - biomedicines-10-01818 [pii] AID - 10.3390/biomedicines10081818 [doi] PST - epublish SO - Biomedicines. 2022 Jul 28;10(8):1818. doi: 10.3390/biomedicines10081818.