The Relationship Between Plasma Osteoprotegerin and Endothelium-Dependent Arterial Dilation in Type 2 Diabetes

The Relationship Between Plasma Osteoprotegerin and Endothelium-Dependent Arterial Dilation in Type 2 Diabetes Guang-da Xiang , Lin Xu , Lin-shuang Zhao , Ling Yue and Jie Hou Department of Endocrinology, Wuhan General Hospital of Guangzhou Command, Wuhan, Hubei Province, China Address correspondenc...

Full description

Saved in:
Bibliographic Details
Published inDiabetes (New York, N.Y.) Vol. 55; no. 7; pp. 2126 - 2131
Main Authors Xiang, Guang-da, Xu, Lin, Zhao, Lin-shuang, Yue, Ling, Hou, Jie
Format Journal Article
LanguageEnglish
Published United States American Diabetes Association 01.07.2006
Subjects
Online AccessGet full text

Cover

Loading…
Abstract The Relationship Between Plasma Osteoprotegerin and Endothelium-Dependent Arterial Dilation in Type 2 Diabetes Guang-da Xiang , Lin Xu , Lin-shuang Zhao , Ling Yue and Jie Hou Department of Endocrinology, Wuhan General Hospital of Guangzhou Command, Wuhan, Hubei Province, China Address correspondence and reprint requests to Dr. Xiang Guang-da, Department of Endocrinology, Wuhan General Hospital of Guangzhou Command, Wuluo Road 627, Wuhan 430070, Hubei Province, P.R. China. E-mail: guangda64{at}hotmail.com Abstract Osteoprotegerin is a recently identified inhibitor of bone resorption. Recent studies indicate that osteoprotegerin also acts as an important regulatory molecule in the vasculature. The purpose of this study was to investigate the relationship between plasma osteoprotegerin levels and endothelium-dependent arterial dilation in type 2 diabetic patients. The study subjects included 40 newly diagnosed type 2 diabetic patients and 46 healthy subjects. All patients were given insulin therapy for 6 months. Plasma osteoprotegerin concentration was measured in duplicate by a sandwich enzyme-linked immunosorbent assay method, and high-resolution ultrasound was used to measure brachial artery diameter at rest, after reactive hyperemia, and after sublingual glyceryltrinitrate. The plasma osteoprotegerin level in patients before treatment was 3.36 ± 0.32 ng/l, which was significantly higher than that in control subjects (2.38 ± 0.25 ng/l, P < 0.001). After 6 months of treatment, osteoprotegerin levels decreased markedly (2.83 ± 0.34 ng/l, P < 0.001). Flow-mediated endothelium-dependent arterial dilation in patients before treatment was 3.21 ± 0.52%, which was significantly lower than that in control subjects (4.46 ± 0.56%, P < 0.01), and it improved markedly after 6 months of treatment (4.03 ± 0.49%, P < 0.01). In multivariate analysis, osteoprotegerin was significantly associated with endothelium-dependent arterial dilation, fasting blood glucose (FBG), HbA 1c (A1C), and ultrasensitive C-reactive protein (CRP) at baseline ( P < 0.01). The absolute changes in osteoprotegerin showed significant correlation with changes in endothelium-dependent arterial dilation, FBG, A1C, and CRP in diabetic patients during the course of treatment ( P < 0.01). This study shows that plasma osteoprotegerin levels are elevated in newly diagnosed diabetic patients and are significantly associated with endothelial function. Footnotes apo, apolipoprotein; CRP, C-reactive protein; FBG, fasting blood glucose; Lp(a), lipoprotein(a); RANKL, receptor activator of nuclear factor-κB ligand; UAER, urinary albumin excretion rate. The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked “advertisement” in accordance with 18 U.S.C. Section 1734 solely to indicate this fact Accepted March 27, 2006. Received February 19, 2006. DIABETES
AbstractList Osteoprotegerin is a recently identified inhibitor of bone resorption. Recent studies indicate that osteoprotegerin also acts as an important regulatory molecule in the vasculature. The purpose of this study was to investigate the relationship between plasma osteoprotegerin levels and endothelium-dependent arterial dilation in type 2 diabetic patients. The study subjects included 40 newly diagnosed type 2 diabetic patients and 46 healthy subjects. All patients were given insulin therapy for 6 months. Plasma osteoprotegerin concentration was measured in duplicate by a sandwich enzyme-linked immunosorbent assay method, and high-resolution ultrasound was used to measure brachial artery diameter at rest, after reactive hyperemia, and after sublingual glyceryltrinitrate. The plasma osteoprotegerin level in patients before treatment was 3.36 ± 0.32 ng/l, which was significantly higher than that in control subjects (2.38 ± 0.25 ng/l, P < 0.001). After 6 months of treatment, osteoprotegerin levels decreased markedly (2.83 ± 0.34 ng/l, P < 0.001). Flow-mediated endothelium-dependent arterial dilation in patients before treatment was 3.21 ± 0.52%, which was significantly lower than that in control subjects (4.46 ± 0.56%, P < 0.01), and it improved markedly after 6 months of treatment (4.03 ± 0.49%, P < 0.01). In multivariate analysis, osteoprotegerin was significantly associated with endothelium-dependent arterial dilation, fasting blood glucose (FBG), Hb[A.sub.1c] (A1C), and ultrasensitive C-reactive protein (CRP) at baseline (P < 0.01). The absolute changes in osteoprotegerin showed significant correlation with changes in endothelium-dependent arterial dilation, FBG, A1C, and CRP in diabetic patients during the course of treatment (P < 0.01). This study shows that plasma osteoprotegerin levels are elevated in newly diagnosed diabetic patients and are significantly associated with endothelial function.
Osteoprotegerin is a recently identified inhibitor of bone resorption. Recent studies indicate that osteoprotegerin also acts as an important regulatory molecule in the vasculature. The purpose of this study was to investigate the relationship between plasma osteoprotegerin levels and endothelium-dependent arterial dilation in type 2 diabetic patients. The study subjects included 40 newly diagnosed type 2 diabetic patients and 46 healthy subjects. All patients were given insulin therapy for 6 months. Plasma osteoprotegerin concentration was measured in duplicate by a sandwich enzyme-linked immunosorbent assay method, and high-resolution ultrasound was used to measure brachial artery diameter at rest, after reactive hyperemia, and after sublingual glyceryltrinitrate. The plasma osteoprotegerin level in patients before treatment was 3.36 ± 0.32 ng/l, which was significantly higher than that in control subjects (2.38 ± 0.25 ng/l, P < 0.001). After 6 months of treatment, osteoprotegerin levels decreased markedly (2.83 ± 0.34 ng/l, P < 0.001). Flow-mediated endothelium-dependent arterial dilation in patients before treatment was 3.21 ± 0.52%, which was significantly lower than that in control subjects (4.46 ± 0.56%, P < 0.01), and it improved markedly after 6 months of treatment (4.03 ± 0.49%, P < 0.01). In multivariate analysis, osteoprotegerin was significantly associated with endothelium-dependent arterial dilation, fasting blood glucose (FBG), HbA1c (A1C), and ultrasensitive C-reactive protein (CRP) at baseline (P < 0.01). The absolute changes in osteoprotegerin showed significant correlation with changes in endothelium-dependent arterial dilation, FBG, A1C, and CRP in diabetic patients during the course of treatment (P < 0.01). This study shows that plasma osteoprotegerin levels are elevated in newly diagnosed diabetic patients and are significantly associated with endothelial function.
Osteoprotegerin is a recently identified inhibitor of bone resorption. Recent studies indicate that osteoprotegerin also acts as an important regulatory molecule in the vasculature. The purpose of this study was to investigate the relationship between plasma osteoprotegerin levels and endothelium-dependent arterial dilation in type 2 diabetic patients. The study subjects included 40 newly diagnosed type 2 diabetic patients and 46 healthy subjects. All patients were given insulin therapy for 6 months. Plasma osteoprotegerin concentration was measured in duplicate by a sandwich enzyme-linked immunosorbent assay method, and high-resolution ultrasound was used to measure brachial artery diameter at rest, after reactive hyperemia, and after sublingual glyceryltrinitrate. The plasma osteoprotegerin level in patients before treatment was 3.36 +/- 0.32 ng/l, which was significantly higher than that in control subjects (2.38 +/- 0.25 ng/l, P < 0.001). After 6 months of treatment, osteoprotegerin levels decreased markedly (2.83 +/- 0.34 ng/l, P < 0.001). Flow-mediated endothelium-dependent arterial dilation in patients before treatment was 3.21 +/- 0.52%, which was significantly lower than that in control subjects (4.46 +/- 0.56%, P < 0.01), and it improved markedly after 6 months of treatment (4.03 +/- 0.49%, P < 0.01). In multivariate analysis, osteoprotegerin was significantly associated with endothelium-dependent arterial dilation, fasting blood glucose (FBG), HbA(1c) (A1C), and ultrasensitive C-reactive protein (CRP) at baseline (P < 0.01). The absolute changes in osteoprotegerin showed significant correlation with changes in endothelium-dependent arterial dilation, FBG, A1C, and CRP in diabetic patients during the course of treatment (P < 0.01). This study shows that plasma osteoprotegerin levels are elevated in newly diagnosed diabetic patients and are significantly associated with endothelial function.Osteoprotegerin is a recently identified inhibitor of bone resorption. Recent studies indicate that osteoprotegerin also acts as an important regulatory molecule in the vasculature. The purpose of this study was to investigate the relationship between plasma osteoprotegerin levels and endothelium-dependent arterial dilation in type 2 diabetic patients. The study subjects included 40 newly diagnosed type 2 diabetic patients and 46 healthy subjects. All patients were given insulin therapy for 6 months. Plasma osteoprotegerin concentration was measured in duplicate by a sandwich enzyme-linked immunosorbent assay method, and high-resolution ultrasound was used to measure brachial artery diameter at rest, after reactive hyperemia, and after sublingual glyceryltrinitrate. The plasma osteoprotegerin level in patients before treatment was 3.36 +/- 0.32 ng/l, which was significantly higher than that in control subjects (2.38 +/- 0.25 ng/l, P < 0.001). After 6 months of treatment, osteoprotegerin levels decreased markedly (2.83 +/- 0.34 ng/l, P < 0.001). Flow-mediated endothelium-dependent arterial dilation in patients before treatment was 3.21 +/- 0.52%, which was significantly lower than that in control subjects (4.46 +/- 0.56%, P < 0.01), and it improved markedly after 6 months of treatment (4.03 +/- 0.49%, P < 0.01). In multivariate analysis, osteoprotegerin was significantly associated with endothelium-dependent arterial dilation, fasting blood glucose (FBG), HbA(1c) (A1C), and ultrasensitive C-reactive protein (CRP) at baseline (P < 0.01). The absolute changes in osteoprotegerin showed significant correlation with changes in endothelium-dependent arterial dilation, FBG, A1C, and CRP in diabetic patients during the course of treatment (P < 0.01). This study shows that plasma osteoprotegerin levels are elevated in newly diagnosed diabetic patients and are significantly associated with endothelial function.
Osteoprotegerin is a recently identified inhibitor of bone resorption. Recent studies indicate that osteoprotegerin also acts as an important regulatory molecule in the vasculature. The purpose of this study was to investigate the relationship between plasma osteoprotegerin levels and endothelium-dependent arterial dilation in type 2 diabetic patients. The study subjects included 40 newly diagnosed type 2 diabetic patients and 46 healthy subjects. All patients were given insulin therapy for 6 months. Plasma osteoprotegerin concentration was measured in duplicate by a sandwich enzyme-linked immunosorbent assay method, and high-resolution ultrasound was used to measure brachial artery diameter at rest, after reactive hyperemia, and after sublingual glyceryltrinitrate. The plasma osteoprotegerin level in patients before treatment was 3.36 +/- 0.32 ng/l, which was significantly higher than that in control subjects (2.38 +/- 0.25 ng/l, P < 0.001). After 6 months of treatment, osteoprotegerin levels decreased markedly (2.83 +/- 0.34 ng/l, P < 0.001). Flow-mediated endothelium-dependent arterial dilation in patients before treatment was 3.21 +/- 0.52%, which was significantly lower than that in control subjects (4.46 +/- 0.56%, P < 0.01), and it improved markedly after 6 months of treatment (4.03 +/- 0.49%, P < 0.01). In multivariate analysis, osteoprotegerin was significantly associated with endothelium-dependent arterial dilation, fasting blood glucose (FBG), HbA(1c) (A1C), and ultrasensitive C-reactive protein (CRP) at baseline (P < 0.01). The absolute changes in osteoprotegerin showed significant correlation with changes in endothelium-dependent arterial dilation, FBG, A1C, and CRP in diabetic patients during the course of treatment (P < 0.01). This study shows that plasma osteoprotegerin levels are elevated in newly diagnosed diabetic patients and are significantly associated with endothelial function.
The Relationship Between Plasma Osteoprotegerin and Endothelium-Dependent Arterial Dilation in Type 2 Diabetes Guang-da Xiang , Lin Xu , Lin-shuang Zhao , Ling Yue and Jie Hou Department of Endocrinology, Wuhan General Hospital of Guangzhou Command, Wuhan, Hubei Province, China Address correspondence and reprint requests to Dr. Xiang Guang-da, Department of Endocrinology, Wuhan General Hospital of Guangzhou Command, Wuluo Road 627, Wuhan 430070, Hubei Province, P.R. China. E-mail: guangda64{at}hotmail.com Abstract Osteoprotegerin is a recently identified inhibitor of bone resorption. Recent studies indicate that osteoprotegerin also acts as an important regulatory molecule in the vasculature. The purpose of this study was to investigate the relationship between plasma osteoprotegerin levels and endothelium-dependent arterial dilation in type 2 diabetic patients. The study subjects included 40 newly diagnosed type 2 diabetic patients and 46 healthy subjects. All patients were given insulin therapy for 6 months. Plasma osteoprotegerin concentration was measured in duplicate by a sandwich enzyme-linked immunosorbent assay method, and high-resolution ultrasound was used to measure brachial artery diameter at rest, after reactive hyperemia, and after sublingual glyceryltrinitrate. The plasma osteoprotegerin level in patients before treatment was 3.36 ± 0.32 ng/l, which was significantly higher than that in control subjects (2.38 ± 0.25 ng/l, P < 0.001). After 6 months of treatment, osteoprotegerin levels decreased markedly (2.83 ± 0.34 ng/l, P < 0.001). Flow-mediated endothelium-dependent arterial dilation in patients before treatment was 3.21 ± 0.52%, which was significantly lower than that in control subjects (4.46 ± 0.56%, P < 0.01), and it improved markedly after 6 months of treatment (4.03 ± 0.49%, P < 0.01). In multivariate analysis, osteoprotegerin was significantly associated with endothelium-dependent arterial dilation, fasting blood glucose (FBG), HbA 1c (A1C), and ultrasensitive C-reactive protein (CRP) at baseline ( P < 0.01). The absolute changes in osteoprotegerin showed significant correlation with changes in endothelium-dependent arterial dilation, FBG, A1C, and CRP in diabetic patients during the course of treatment ( P < 0.01). This study shows that plasma osteoprotegerin levels are elevated in newly diagnosed diabetic patients and are significantly associated with endothelial function. Footnotes apo, apolipoprotein; CRP, C-reactive protein; FBG, fasting blood glucose; Lp(a), lipoprotein(a); RANKL, receptor activator of nuclear factor-κB ligand; UAER, urinary albumin excretion rate. The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked “advertisement” in accordance with 18 U.S.C. Section 1734 solely to indicate this fact Accepted March 27, 2006. Received February 19, 2006. DIABETES
Osteoprotegerin is a recently identified inhibitor of bone resorption. Recent studies indicate that osteoprotegerin also acts as an important regulatory molecule in the vasculature. The purpose of this study was to investigate the relationship between plasma osteoprotegerin levels and endothelium-dependent arterial dilation in type 2 diabetic patients. The study subjects included 40 newly diagnosed type 2 diabetic patients and 46 healthy subjects. All patients were given insulin therapy for 6 months. Plasma osteoprotegerin concentration was measured in duplicate by a sandwich enzyme-linked immunosorbent assay method, and high-resolution ultrasound was used to measure brachial artery diameter at rest, after reactive hyperemia, and after sublingual glyceryltrinitrate. The plasma osteoprotegerin level in patients before treatment was 3.36 [+ or -] 0.32 ng/l, which was significantly higher than that in control subjects (2.38 [+ or -] 0.25 ng/l, P < 0.001). After 6 months of treatment, osteoprotegerin levels decreased markedly (2.83 [+ or -] 0.34 ng/l, P < 0.001). Flow-mediated endothelium-dependent arterial dilation in patients before treatment was 3.21 [+ or -] 0.52%, which was significantly lower than that in control subjects (4.46 [+ or -] 0.56%, P < 0.01), and it improved markedly after 6 months of treatment (4.03 [+ or -] 0.49%, P < 0.01). In multivariate analysis, osteoprotegerin was significantly associated with endothelium-dependent arterial dilation, fasting blood glucose (FBG), Hb[A.sub.1c] (A1C), and ultrasensitive C-reactive protein (CRP) at baseline (P < 0.01). The absolute changes in osteoprotegerin showed significant correlation with changes in endothelium-dependent arterial dilation, FBG, A1C, and CRP in diabetic patients during the course of treatment (P < 0.01). This study shows that plasma osteoprotegerin levels are elevated in newly diagnosed diabetic patients and are significantly associated with endothelial function.
Audience Professional
Author Guang-da Xiang
Jie Hou
Lin-shuang Zhao
Lin Xu
Ling Yue
Author_xml – sequence: 1
  givenname: Guang-da
  surname: Xiang
  fullname: Xiang, Guang-da
  organization: Department of Endocrinology, Wuhan General Hospital of Guangzhou Command, Wuhan, Hubei Province, China
– sequence: 2
  givenname: Lin
  surname: Xu
  fullname: Xu, Lin
  organization: Department of Endocrinology, Wuhan General Hospital of Guangzhou Command, Wuhan, Hubei Province, China
– sequence: 3
  givenname: Lin-shuang
  surname: Zhao
  fullname: Zhao, Lin-shuang
  organization: Department of Endocrinology, Wuhan General Hospital of Guangzhou Command, Wuhan, Hubei Province, China
– sequence: 4
  givenname: Ling
  surname: Yue
  fullname: Yue, Ling
  organization: Department of Endocrinology, Wuhan General Hospital of Guangzhou Command, Wuhan, Hubei Province, China
– sequence: 5
  givenname: Jie
  surname: Hou
  fullname: Hou, Jie
  organization: Department of Endocrinology, Wuhan General Hospital of Guangzhou Command, Wuhan, Hubei Province, China
BackLink https://www.ncbi.nlm.nih.gov/pubmed/16804084$$D View this record in MEDLINE/PubMed
BookMark eNptkt9r2zAQx8XoWNNuD_sHhtnDYAy3-mHJ8mOWdt0gkDEy2JuQrXOiIsupJdP1v6_SZC0Z4R4kjs8d37v7nqET33tA6D3BF5Sx8tLUWOSYMvIKTUjFqpzR8s8JmmBMaE7KqjxFZyHcYoxFijfolAiJCyyLCfLLNWS_wOloex_WdpN9hXgP4LOfTodOZ4sQod8MfYQVDNZn2pvs2ps-rsHZscuvYAPegI_ZdIiJ0C67srt2WcKXDxvIaErpGiKEt-h1q12Ad_v3HP3-dr2cfc_ni5sfs-k8b3glYk4NrnXJDWskmFpgTdu6bYQUBhMhaiI5x1xDW8m6NCUxuiCas4pRYnArSsrO0add36T8boQQVWdDA85pD_0YlJBcclbIBH78D7ztx8EnbYoSUUiOKU9QvoNW2oGyvu3joJsVeBi0S6dobUpPSSELSThmib84wqcw0NnmaMHng4LERPgbV3oMQcmb-SGbH2Ob3rl0IpXWOFsc8h_2E451B0ZtBtvp4UH980ACLndAM_QhDNCqxsanAybV1imC1dZlausytXXZi9zniuemR9gvO3ZtV-t7O4Ayey-8fDhXZVo3FewRl8_dkA
CODEN DIAEAZ
CitedBy_id crossref_primary_10_1002_dmrr_731
crossref_primary_10_1016_j_atherosclerosis_2014_04_036
crossref_primary_10_1093_cvr_cvw025
crossref_primary_10_1016_j_jdiacomp_2015_01_001
crossref_primary_10_1016_j_metabol_2017_09_008
crossref_primary_10_1159_000508978
crossref_primary_10_1111_j_1440_1681_2009_05210_x
crossref_primary_10_1016_j_diabres_2008_07_014
crossref_primary_10_1007_s12020_016_1121_4
crossref_primary_10_1038_nrendo_2009_266
crossref_primary_10_1111_j_1365_2265_2007_03099_x
crossref_primary_10_1161_JAHA_118_009012
crossref_primary_10_1177_1479164112440815
crossref_primary_10_1016_j_atherosclerosis_2008_09_033
crossref_primary_10_1016_j_amjcard_2011_09_043
crossref_primary_10_1186_s13073_024_01336_1
crossref_primary_10_1002_jcla_23886
crossref_primary_10_1038_s42255_022_00671_0
crossref_primary_10_1161_STROKEAHA_111_619288
crossref_primary_10_2337_db18_1055
crossref_primary_10_1016_j_atherosclerosis_2014_10_013
crossref_primary_10_1155_2013_182060
crossref_primary_10_1111_j_1464_5491_2009_02683_x
crossref_primary_10_1016_j_metabol_2009_09_019
crossref_primary_10_1177_0961203313517151
crossref_primary_10_1038_oby_2010_193
crossref_primary_10_1186_s12933_017_0581_z
crossref_primary_10_1097_HJH_0b013e32834c1e95
crossref_primary_10_1016_j_diabres_2010_09_028
crossref_primary_10_1111_cen_12312
crossref_primary_10_17116_terarkh201789491_94
crossref_primary_10_1111_j_1365_2265_2007_03159_x
crossref_primary_10_1016_j_obmed_2025_100596
crossref_primary_10_1016_j_vph_2008_11_003
crossref_primary_10_1002_dmrr_1109
crossref_primary_10_1007_s00125_008_1123_8
crossref_primary_10_1016_j_thromres_2010_09_003
crossref_primary_10_4236_ojemd_2013_35033
crossref_primary_10_1902_jop_2009_090510
crossref_primary_10_1016_j_jjcc_2012_05_010
crossref_primary_10_1016_j_diabres_2006_09_008
crossref_primary_10_1111_dom_15306
crossref_primary_10_1007_BF03347065
crossref_primary_10_1007_s12020_013_0095_8
crossref_primary_10_1016_j_acvd_2015_01_015
crossref_primary_10_1097_MED_0b013e3280d5f7e9
crossref_primary_10_1093_ndt_gfp301
crossref_primary_10_1155_2015_564934
crossref_primary_10_3109_07853890_2012_727019
crossref_primary_10_1038_mt_2016_160
crossref_primary_10_1097_QAI_0000000000000725
crossref_primary_10_1530_EJE_10_0875
crossref_primary_10_1007_s12020_014_0443_3
crossref_primary_10_1126_sciadv_abe6903
crossref_primary_10_3109_00365513_2011_570868
crossref_primary_10_1080_14397595_2018_1500736
crossref_primary_10_1530_EJE_09_0421
crossref_primary_10_1016_j_ijcard_2011_09_036
crossref_primary_10_1177_1479164116678158
crossref_primary_10_2337_dc07_1771
crossref_primary_10_1016_j_metabol_2010_04_011
crossref_primary_10_1016_j_cca_2008_03_004
crossref_primary_10_1016_j_jdiacomp_2021_108073
crossref_primary_10_1177_0004563214533669
crossref_primary_10_1016_j_metabol_2010_10_001
crossref_primary_10_4103_tmj_tmj_51_19
crossref_primary_10_1016_j_atherosclerosis_2008_10_024
crossref_primary_10_1007_s10741_021_10153_2
crossref_primary_10_1007_s10354_011_0022_7
crossref_primary_10_1007_s11745_014_3950_3
crossref_primary_10_1038_ajh_2010_38
crossref_primary_10_1177_1358863X10367537
crossref_primary_10_1016_j_jdiacomp_2009_04_003
crossref_primary_10_1007_s12020_012_9624_0
crossref_primary_10_1210_endocr_bqaa003
crossref_primary_10_1530_EJE_10_0720
Cites_doi 10.1016/j.jacc.2004.06.076
10.1007/s00125-003-1060-5
10.2337/diacare.29.01.06.dc05-1422
10.1016/S0014-5793(02)02872-7
10.1530/eje.0.1490039
10.1161/hq1201.100229
10.1007/s00223-003-0011-y
10.1210/jc.2002-020775
10.1074/jbc.273.23.14363
10.1161/01.CIR.0000127957.43874.BB
10.2337/diacare.28.9.2176
10.1016/S0140-6736(01)05494-0
10.1042/CS20040255
10.1210/jc.86.2.631
10.1161/hq1001.097102
10.1210/jc.2005-0562
10.1084/jem.192.4.463
10.1161/01.CIR.0000031524.49139.29
10.1111/j.1365-2265.2005.02390.x
10.1101/gad.12.9.1260
10.2337/diacare.27.3.801
10.1016/S0092-8674(00)80209-3
10.1161/01.ATV.0000051384.43104.FC
10.1074/jbc.C000290200
ContentType Journal Article
Copyright COPYRIGHT 2006 American Diabetes Association
COPYRIGHT 2006 American Diabetes Association
Copyright American Diabetes Association Jul 2006
Copyright_xml – notice: COPYRIGHT 2006 American Diabetes Association
– notice: COPYRIGHT 2006 American Diabetes Association
– notice: Copyright American Diabetes Association Jul 2006
DBID AAYXX
CITATION
CGR
CUY
CVF
ECM
EIF
NPM
8GL
3V.
7RV
7X7
7XB
88E
88I
8AF
8AO
8C1
8FE
8FH
8FI
8FJ
8FK
8G5
ABUWG
AFKRA
AZQEC
BBNVY
BEC
BENPR
BHPHI
CCPQU
DWQXO
FYUFA
GHDGH
GNUQQ
GUQSH
HCIFZ
K9-
K9.
KB0
LK8
M0R
M0S
M1P
M2O
M2P
M7P
MBDVC
NAPCQ
PHGZM
PHGZT
PJZUB
PKEHL
PPXIY
PQEST
PQGLB
PQQKQ
PQUKI
PRINS
Q9U
S0X
7X8
DOI 10.2337/db06-0231
DatabaseName CrossRef
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
Gale In Context: High School
ProQuest Central (Corporate)
Nursing & Allied Health Database
Health & Medical Collection
ProQuest Central (purchase pre-March 2016)
Medical Database (Alumni Edition)
Science Database (Alumni Edition)
STEM Database
ProQuest Pharma Collection
Public Health Database
ProQuest SciTech Collection
ProQuest Natural Science Journals
ProQuest Hospital Collection
Hospital Premium Collection (Alumni Edition)
ProQuest Central (Alumni) (purchase pre-March 2016)
ProQuest Research Library
ProQuest Central (Alumni)
ProQuest Central UK/Ireland
ProQuest Central Essentials
Biological Science Collection
eLibrary
ProQuest Central
Natural Science Collection
ProQuest One Community College
ProQuest Central
Health Research Premium Collection
Health Research Premium Collection (Alumni)
ProQuest Central Student
ProQuest Research Library
SciTech Premium Collection
Consumer Health Database (Alumni Edition)
ProQuest Health & Medical Complete (Alumni)
Nursing & Allied Health Database (Alumni Edition)
Biological Sciences
Consumer Health Database
ProQuest Health & Medical Collection
Medical Database
Research Library
Science Database
Biological Science Database
Research Library (Corporate)
Nursing & Allied Health Premium
ProQuest Central Premium
ProQuest One Academic
ProQuest Health & Medical Research Collection
ProQuest One Academic Middle East (New)
ProQuest One Health & Nursing
ProQuest One Academic Eastern Edition (DO NOT USE)
ProQuest One Applied & Life Sciences
ProQuest One Academic
ProQuest One Academic UKI Edition
ProQuest Central China
ProQuest Central Basic
SIRS Editorial
MEDLINE - Academic
DatabaseTitle CrossRef
MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
Research Library Prep
ProQuest Central Student
ProQuest Central Essentials
elibrary
ProQuest AP Science
SciTech Premium Collection
ProQuest Central China
ProQuest One Applied & Life Sciences
Health Research Premium Collection
Natural Science Collection
Health & Medical Research Collection
Biological Science Collection
ProQuest Central (New)
ProQuest Medical Library (Alumni)
ProQuest Science Journals (Alumni Edition)
ProQuest Biological Science Collection
ProQuest Family Health
ProQuest One Academic Eastern Edition
ProQuest Hospital Collection
Health Research Premium Collection (Alumni)
Biological Science Database
ProQuest Hospital Collection (Alumni)
Nursing & Allied Health Premium
ProQuest Health & Medical Complete
ProQuest One Academic UKI Edition
ProQuest Nursing & Allied Health Source (Alumni)
ProQuest One Academic
ProQuest One Academic (New)
ProQuest One Academic Middle East (New)
SIRS Editorial
ProQuest Health & Medical Complete (Alumni)
ProQuest Central (Alumni Edition)
ProQuest One Community College
ProQuest One Health & Nursing
Research Library (Alumni Edition)
ProQuest Natural Science Collection
ProQuest Pharma Collection
ProQuest Family Health (Alumni Edition)
ProQuest Central
ProQuest Health & Medical Research Collection
Health and Medicine Complete (Alumni Edition)
ProQuest Central Korea
ProQuest Research Library
ProQuest Public Health
ProQuest Central Basic
ProQuest Science Journals
ProQuest Nursing & Allied Health Source
ProQuest SciTech Collection
ProQuest Medical Library
ProQuest Central (Alumni)
MEDLINE - Academic
DatabaseTitleList
CrossRef
MEDLINE - Academic
MEDLINE


Research Library Prep
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
– sequence: 2
  dbid: EIF
  name: MEDLINE
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search
  sourceTypes: Index Database
– sequence: 3
  dbid: BENPR
  name: ProQuest Central
  url: https://www.proquest.com/central
  sourceTypes: Aggregation Database
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
EISSN 1939-327X
EndPage 2131
ExternalDocumentID 1081557061
A148481503
16804084
10_2337_db06_0231
diabetes_55_7_2126
Genre Journal Article
Comparative Study
GroupedDBID -
08R
0R
1AW
29F
2WC
3V.
4.4
53G
55
5GY
5RE
5RS
5VS
7RV
7X7
88E
88I
8AF
8AO
8C1
8F7
8FE
8FH
8FI
8FJ
8G5
8GL
8R4
8R5
AAQQT
AAWTL
AAYEP
AAYJJ
ABFLS
ABOCM
ABPTK
ABUWG
ACDCL
ACGOD
ACPRK
ADACO
ADBBV
ADBIT
AENEX
AFFNX
AFKRA
AHMBA
ALMA_UNASSIGNED_HOLDINGS
AZQEC
BAWUL
BBAFP
BBNVY
BCR
BCU
BEC
BENPR
BES
BHPHI
BKEYQ
BKNYI
BLC
BPHCQ
BVXVI
C1A
CS3
DIK
DU5
DWQXO
E3Z
EBS
EDB
EJD
EX3
F5P
FRP
FYUFA
GICCO
GJ
GNUQQ
GUQSH
GX1
H13
HCIFZ
HZ
IAG
IAO
IEA
IHR
INH
INR
IOF
IPO
J5H
K-O
K9-
KM
KQ8
L7B
LK8
M0R
M1P
M2O
M2P
M2Q
M5
M7P
MBDVC
O0-
O9-
OB3
OBH
OK1
OVD
P2P
PADUT
PCD
PEA
PQEST
PQQKQ
PQUKI
PRINS
PROAC
PSQYO
Q2X
RHF
RHI
RPM
S0X
SJFOW
SJN
SV3
TDI
WH7
WOQ
WOW
X7M
XZ
ZA5
ZGI
ZY1
---
.55
.GJ
.XZ
08P
0R~
18M
354
6PF
AAFWJ
AAKAS
AAYOK
AAYXX
ACGFO
ADGHP
ADZCM
AEGXH
AERZD
AIAGR
AIZAD
ALIPV
BTFSW
CCPQU
CITATION
EMOBN
HMCUK
HZ~
ITC
K2M
M5~
N4W
NAPCQ
OHH
PHGZM
PHGZT
TEORI
TR2
UKHRP
VVN
W8F
YFH
YHG
YOC
~KM
1CY
AFHIN
AI.
CGR
CUY
CVF
ECM
EIF
H~9
MVM
NPM
O5R
O5S
PKN
VH1
XOL
YQJ
ZXP
PMFND
7XB
8FK
K9.
PJZUB
PKEHL
PPXIY
PQGLB
Q9U
7X8
ID FETCH-LOGICAL-c596t-2d0ba75d3c8edb60a2fbfc686d0166b185505aef98b7d71da41a539321d0f6723
IEDL.DBID 7X7
ISSN 0012-1797
IngestDate Fri Jul 11 08:22:21 EDT 2025
Fri Jul 25 19:29:21 EDT 2025
Fri Jun 13 00:43:24 EDT 2025
Tue Jun 10 21:38:30 EDT 2025
Fri Jun 27 05:00:40 EDT 2025
Tue Jun 10 19:02:20 EDT 2025
Wed Feb 19 01:46:13 EST 2025
Thu Apr 24 22:59:00 EDT 2025
Tue Jul 01 04:24:03 EDT 2025
Fri Jan 15 19:45:48 EST 2021
IsDoiOpenAccess false
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 7
Language English
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c596t-2d0ba75d3c8edb60a2fbfc686d0166b185505aef98b7d71da41a539321d0f6723
Notes ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 14
content type line 23
OpenAccessLink https://diabetesjournals.org/diabetes/article-pdf/55/7/2126/383483/zdb00706002126.pdf
PMID 16804084
PQID 216485025
PQPubID 34443
PageCount 6
ParticipantIDs gale_infotracgeneralonefile_A148481503
proquest_journals_216485025
pubmed_primary_16804084
crossref_citationtrail_10_2337_db06_0231
crossref_primary_10_2337_db06_0231
gale_incontextcollege_GICCO_A148481503
highwire_diabetes_diabetes_55_7_2126
proquest_miscellaneous_68585348
gale_infotracacademiconefile_A148481503
gale_incontextgauss_8GL_A148481503
ProviderPackageCode RHF
RHI
CITATION
AAYXX
PublicationCentury 2000
PublicationDate 20060701
2006-07-01
2006-Jul
PublicationDateYYYYMMDD 2006-07-01
PublicationDate_xml – month: 07
  year: 2006
  text: 20060701
  day: 01
PublicationDecade 2000
PublicationPlace United States
PublicationPlace_xml – name: United States
– name: New York
PublicationTitle Diabetes (New York, N.Y.)
PublicationTitleAlternate Diabetes
PublicationYear 2006
Publisher American Diabetes Association
Publisher_xml – name: American Diabetes Association
References 2022031209315287400_R19
2022031209315287400_R17
2022031209315287400_R18
2022031209315287400_R11
2022031209315287400_R12
2022031209315287400_R10
2022031209315287400_R15
2022031209315287400_R16
2022031209315287400_R13
2022031209315287400_R14
2022031209315287400_R8
2022031209315287400_R9
2022031209315287400_R6
2022031209315287400_R7
2022031209315287400_R4
2022031209315287400_R5
2022031209315287400_R2
2022031209315287400_R3
2022031209315287400_R22
2022031209315287400_R23
2022031209315287400_R20
2022031209315287400_R21
2022031209315287400_R24
2022031209315287400_R25
2022031209315287400_R1
References_xml – ident: 2022031209315287400_R19
  doi: 10.1016/j.jacc.2004.06.076
– ident: 2022031209315287400_R12
  doi: 10.1007/s00125-003-1060-5
– ident: 2022031209315287400_R23
  doi: 10.2337/diacare.29.01.06.dc05-1422
– ident: 2022031209315287400_R4
  doi: 10.1016/S0014-5793(02)02872-7
– ident: 2022031209315287400_R8
  doi: 10.1530/eje.0.1490039
– ident: 2022031209315287400_R2
  doi: 10.1161/hq1201.100229
– ident: 2022031209315287400_R14
  doi: 10.1007/s00223-003-0011-y
– ident: 2022031209315287400_R7
  doi: 10.1210/jc.2002-020775
– ident: 2022031209315287400_R15
  doi: 10.1074/jbc.273.23.14363
– ident: 2022031209315287400_R16
  doi: 10.1161/01.CIR.0000127957.43874.BB
– ident: 2022031209315287400_R9
  doi: 10.2337/diacare.28.9.2176
– ident: 2022031209315287400_R21
  doi: 10.1016/S0140-6736(01)05494-0
– ident: 2022031209315287400_R22
  doi: 10.1042/CS20040255
– ident: 2022031209315287400_R10
  doi: 10.1210/jc.86.2.631
– ident: 2022031209315287400_R18
  doi: 10.1161/hq1001.097102
– ident: 2022031209315287400_R25
  doi: 10.1210/jc.2005-0562
– ident: 2022031209315287400_R17
  doi: 10.1084/jem.192.4.463
– ident: 2022031209315287400_R6
  doi: 10.1161/01.CIR.0000031524.49139.29
– ident: 2022031209315287400_R20
  doi: 10.1111/j.1365-2265.2005.02390.x
– ident: 2022031209315287400_R3
  doi: 10.1101/gad.12.9.1260
– ident: 2022031209315287400_R13
  doi: 10.2337/diacare.27.3.801
– ident: 2022031209315287400_R1
  doi: 10.1016/S0092-8674(00)80209-3
– ident: 2022031209315287400_R24
– ident: 2022031209315287400_R11
  doi: 10.1161/01.ATV.0000051384.43104.FC
– ident: 2022031209315287400_R5
  doi: 10.1074/jbc.C000290200
SSID ssj0006060
Score 2.1668644
Snippet The Relationship Between Plasma Osteoprotegerin and Endothelium-Dependent Arterial Dilation in Type 2 Diabetes Guang-da Xiang , Lin Xu , Lin-shuang Zhao , Ling...
Osteoprotegerin is a recently identified inhibitor of bone resorption. Recent studies indicate that osteoprotegerin also acts as an important regulatory...
SourceID proquest
gale
pubmed
crossref
highwire
SourceType Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 2126
SubjectTerms Adult
Arteries - physiopathology
Blood Glucose - metabolism
C-Reactive Protein - analysis
Care and treatment
Diabetes Mellitus, Type 2 - blood
Diabetes Mellitus, Type 2 - physiopathology
Endothelium, Vascular - physiopathology
Female
Glycated Hemoglobin A - analysis
Glycoproteins - blood
Humans
Male
Middle Aged
Osteoprotegerin
Receptors, Cytoplasmic and Nuclear - blood
Receptors, Tumor Necrosis Factor - blood
Reference Values
Risk factors
Type 2 diabetes
Vasodilation
Title The Relationship Between Plasma Osteoprotegerin and Endothelium-Dependent Arterial Dilation in Type 2 Diabetes
URI http://diabetes.diabetesjournals.org/content/55/7/2126.abstract
https://www.ncbi.nlm.nih.gov/pubmed/16804084
https://www.proquest.com/docview/216485025
https://www.proquest.com/docview/68585348
Volume 55
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV1La9wwEBZtAqWX0nfdtKkoIe3FxLZkyT6VZLNpKM2D0sDehB72diHxbuLd_98ZS3YwpL0YgwdZHo1HnzSjbwjZcwbjabaOS5OyGGs5xCYpk9iBPXFelTXrIrpn5-L0iv-Y5bOQm9OGtMreJ3aO2i0t7pEfZIDrixxm6G-r2xiLRmFwNVTQeEy2kbkMM7rkbFhvJYDN_QmUNEMWTumJhTLG5AF0EXNvWTqajnqn3DMF_xt1drPPyXPyLMBGeujH-QV5VDUvyZOzEBh_RRoYbjoktv1ZrOiRT8CilwCPbzS9gNFcdqQMczzwR3Xj6LRxeP7qerG5iY9DMdw1vqOzSnq88M1REMflKs1oyJ9pX5Ork-nvyWkcSinENi_FOs5cYrTMHbNF5YxIdFab2opCOIB8wqRIa5brqi4LI51Mneapzhlgu9QltZAZe0O2mmVTvSPU1rbMXFkj-IHVjjC2kpoznTIuKi55RL72GlU28IxjuYtrBesNVL5C5StUfkQ-D6IrT67xkNA-DotCsooGs2Gs31FR8H2TC3UInUDCmYRBa2PBud60rSq-_xwJfQlC9RJ6ZXU4hQDfhkRYI8n9keTc04A_JLjXG4zqN8zvb_JcSQX4QERkpzcmFfxEqwarjsin4Sn84Bi10U213LSqKxDAeBGRt94C71UlCnDBBX__35Z3yFO_bYQpxh_I1vpuU30EILU2u93vAtdiku6S7aPp-eWvv2s2HOc
linkProvider ProQuest
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1fT9swELdQkba9TPu_wDasibG9RCSx4yQP0wS0rIy2oAkk3oxjJ6USJN3SatqH2nfcXZwURWJ74y1STo5zPp_vfHe_I2TbpBhP07mbpD5zsZeDm3qJ5xqQJ86zJGd1RHc8EcNz_u0ivFgjf9paGEyrbHVirahNqfGOfDcAuz4O4YT-Mv_hYtMoDK62HTSsVBxnv3-Bx1Z9PurD8n4IgsPB2cHQbZoKuDpMxMINjJeqKDRMx5lJhaeCPM21iIUB40ekPgJ8hSrLkziNTOQbxX0VMrByfOPlIkKcA9D465yBJ9Mj6_uDyen3leoHb8DWvPgB4n5GFsooYCzaBaZgti_zOwdgewy02MT_tnPr8-7wCXncGKp0z0rWU7KWFc_Ig3ETin9OChAwukqlu5rN6b5N-aKnYJDfKHoC8lPWMBBTLDGkqjB0UBis-LqeLW_cftN-d4HfqPcB7c_scBTI0UGmAW0ydqoX5Pxe-PyS9IqyyF4TqnOdBCbJ0dwC_0qkOosUZ8pnXGQ84g751HJU6gbZHBtsXEvwcJD5EpkvkfkOeb8inVs4j7uIdnBZJMJjFJh_o-0djoT_OziRezAJhLjxGIzWJZyqZVXJ-OuoQ_SxIcpLmJVWTd0D_BtCb3UodzqUUws8fhfhdiswsr2iv30IQxlJsEiEQzZbYZKNZqrkah85ZGv1FlQKxolUkZXLStYtCRiPHfLKSuAtq0QMSj_mG_8deYs8HJ6NR3J0NDneJI_spRWmTL4hvcXPZfYWzLhF-q7ZPJRc3vd-_Qv1tljc
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV3db9QwDI-mIU28IL4pAxahMXiprm3SpH1AaOx2bOzzgUn3lqVJe5y0tQe9E-JP47_DbtpOlQZve6tUK21d27Fj-2dCtm2G-TRT-GkWMh9nOfhZkAa-BXniPE8L1mR0T07FwQX_Oo2na-RP1wuDZZWdTWwMta0MnpGPIvDrkxh26FHRVkWcjyefFj98HCCFidZumoaTkKP89y-I3uqPh2P41e-iaLL_be_AbwcM-CZOxdKPbJBpGVtmktxmItBRkRVGJMKCIySyEMG-Yp0XaZJJK0OreahjBh5PaINCSMQ8AOt_T7I4RBWT0z7WCyAucN0vYYQIoNKBGkWMyRGwB-t-WTjYCrsNoUMp_rfH2-x8k4fkQeuy0l0nY4_IWl4-JhsnbVL-CSlB1GhfVPd9vqCfXfEXPQfX_FrTM5CkqgGEmGGzIdWlpfulxd6vq_nq2h-3g3iX-IxGI-h47pajQI6hMo1oW7tTPyUXd8LlZ2S9rMr8BaGmMGlk0wIdL4i0RGZyqTnTIeMi55J75EPHUWVajHMctXGlINZB5itkvkLme-RtT7pwwB63Ee3gb1EIlFGizBl3mqPg-_bO1C68BILdBAxWGxLO9KquVfLleED0viUqKngro9sOCPg2BOEaUO4MKGcOgvw2wu1OYFR3WH9zEcdKKvBNhEc2O2FSrY2qVa9RHtnq74JxwYyRLvNqVatmOAHjiUeeOwm8YZVIwPwn_OV_V94iG6Cl6vjw9GiT3HenV1jp_IqsL3-u8tfgzy2zN43mUHJ516r6Fzf3W6s
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=The+relationship+between+plasma+osteoprotegerin+and+endothelium-dependent+arterial+dilation+in+type+2+diabetes&rft.jtitle=Diabetes+%28New+York%2C+N.Y.%29&rft.au=Xiang%2C+Guang-da&rft.au=Xu%2C+Lin&rft.au=Zhao%2C+Lin-shuang&rft.au=Yue%2C+Ling&rft.date=2006-07-01&rft.pub=American+Diabetes+Association&rft.issn=0012-1797&rft.volume=55&rft.issue=7&rft.spage=2126&rft_id=info:doi/10.2337%2Fdb06-0231&rft.externalDocID=A148481503
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0012-1797&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0012-1797&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0012-1797&client=summon