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Hepatocyte growth factor is a potential biomarker for osteoproliferation and osteoporosis in ankylosing spondylitis

Summary We explored relations between serum hepatocyte growth factor (HGF), disease activity, osteoproliferation, and bone mineral density (BMD) in ankylosing spondylitis (AS), in comparison with healthy controls. HGF was increased especially in male AS patients and smokers and associated with both...

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Published in:Osteoporosis international 2019-02, Vol.30 (2), p.441-449
Main Authors: Torres, L., Klingberg, E., Nurkkala, M., Carlsten, H., Forsblad-d’Elia, H.
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Nurkkala, M.
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Forsblad-d’Elia, H.
description Summary We explored relations between serum hepatocyte growth factor (HGF), disease activity, osteoproliferation, and bone mineral density (BMD) in ankylosing spondylitis (AS), in comparison with healthy controls. HGF was increased especially in male AS patients and smokers and associated with both lower BMD and more chronic radiographic changes in the spine. Introduction Ankylosing spondylitis (AS) is characterized by both osteoproliferation and increased bone loss. Biomarkers are requested to predict the processes. The aims of this study were to compare serum levels of hepatocyte growth factor (HGF), matrix metalloproteinase-3 (MMP-3), and vascular endothelial growth factor (VEGF) in AS patients with healthy controls (HC) and to explore the associations with disease activity, osteoproliferation, and bone mineral density (BMD). Methods Serum from AS patients (modified NY-criteria) and HC was analyzed for HGF, MMP-3, and VEGF with ELISA. Disease activity parameters were collected. Osteoproliferation was assessed with modified Stoke Ankylosing Spondylitis Spine Score (mSASSS) and BMD was measured in femoral neck. Results Totally, 204 AS patients and 80 sex and age matched HC were included. Serum HGF was higher in the AS patients compared with the HC, whereas serum MMP-3 and VEGF were not. Serum HGF was also higher in smokers and in the male AS patients positively correlated with age, BASMI, and mSASSS, and negatively correlated with BMD. The biomarkers were all positively associated with ESR, CRP, and WBC. In multiple linear regression analysis serum HGF remained associated with higher mSASSS and lower BMD, after adjusting for age, sex, CRP, smoking, and body mass index. Conclusions Serum HGF was increased in male AS patients and associated with higher mSASSS and lower BMD. In addition, serum HGF was positively associated with risk factors for osteoproliferation such as age, CRP and smoking. HGF could be a potential biomarker of importance for the bone metabolism in AS. Trial registration NCT00858819.
doi_str_mv 10.1007/s00198-018-4721-4
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HGF was increased especially in male AS patients and smokers and associated with both lower BMD and more chronic radiographic changes in the spine. Introduction Ankylosing spondylitis (AS) is characterized by both osteoproliferation and increased bone loss. Biomarkers are requested to predict the processes. The aims of this study were to compare serum levels of hepatocyte growth factor (HGF), matrix metalloproteinase-3 (MMP-3), and vascular endothelial growth factor (VEGF) in AS patients with healthy controls (HC) and to explore the associations with disease activity, osteoproliferation, and bone mineral density (BMD). Methods Serum from AS patients (modified NY-criteria) and HC was analyzed for HGF, MMP-3, and VEGF with ELISA. Disease activity parameters were collected. Osteoproliferation was assessed with modified Stoke Ankylosing Spondylitis Spine Score (mSASSS) and BMD was measured in femoral neck. Results Totally, 204 AS patients and 80 sex and age matched HC were included. Serum HGF was higher in the AS patients compared with the HC, whereas serum MMP-3 and VEGF were not. Serum HGF was also higher in smokers and in the male AS patients positively correlated with age, BASMI, and mSASSS, and negatively correlated with BMD. The biomarkers were all positively associated with ESR, CRP, and WBC. In multiple linear regression analysis serum HGF remained associated with higher mSASSS and lower BMD, after adjusting for age, sex, CRP, smoking, and body mass index. Conclusions Serum HGF was increased in male AS patients and associated with higher mSASSS and lower BMD. In addition, serum HGF was positively associated with risk factors for osteoproliferation such as age, CRP and smoking. HGF could be a potential biomarker of importance for the bone metabolism in AS. 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HGF was increased especially in male AS patients and smokers and associated with both lower BMD and more chronic radiographic changes in the spine. Introduction Ankylosing spondylitis (AS) is characterized by both osteoproliferation and increased bone loss. Biomarkers are requested to predict the processes. The aims of this study were to compare serum levels of hepatocyte growth factor (HGF), matrix metalloproteinase-3 (MMP-3), and vascular endothelial growth factor (VEGF) in AS patients with healthy controls (HC) and to explore the associations with disease activity, osteoproliferation, and bone mineral density (BMD). Methods Serum from AS patients (modified NY-criteria) and HC was analyzed for HGF, MMP-3, and VEGF with ELISA. Disease activity parameters were collected. Osteoproliferation was assessed with modified Stoke Ankylosing Spondylitis Spine Score (mSASSS) and BMD was measured in femoral neck. Results Totally, 204 AS patients and 80 sex and age matched HC were included. Serum HGF was higher in the AS patients compared with the HC, whereas serum MMP-3 and VEGF were not. Serum HGF was also higher in smokers and in the male AS patients positively correlated with age, BASMI, and mSASSS, and negatively correlated with BMD. The biomarkers were all positively associated with ESR, CRP, and WBC. In multiple linear regression analysis serum HGF remained associated with higher mSASSS and lower BMD, after adjusting for age, sex, CRP, smoking, and body mass index. Conclusions Serum HGF was increased in male AS patients and associated with higher mSASSS and lower BMD. In addition, serum HGF was positively associated with risk factors for osteoproliferation such as age, CRP and smoking. HGF could be a potential biomarker of importance for the bone metabolism in AS. 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Public Health</subject><subject>Metalloproteinase</subject><subject>Middle Aged</subject><subject>Original</subject><subject>Original Article</subject><subject>Orthopedics</subject><subject>Osteogenesis - physiology</subject><subject>Osteoporosis</subject><subject>Osteoporosis - diagnosis</subject><subject>Osteoporosis - etiology</subject><subject>Osteoporosis - physiopathology</subject><subject>Osteoproliferation</subject><subject>repair</subject><subject>Reumatologi och inflammation</subject><subject>rheumatoid-arthritis</subject><subject>Rheumatology</subject><subject>Rheumatology and Autoimmunity</subject><subject>Risk factors</subject><subject>serum</subject><subject>Serum levels</subject><subject>Severity of Illness Index</subject><subject>Smoking</subject><subject>Spine</subject><subject>Spondylitis</subject><subject>Spondylitis, Ankylosing - blood</subject><subject>Spondylitis, Ankylosing - complications</subject><subject>Spondylitis, Ankylosing - pathology</subject><subject>Spondylitis, Ankylosing - physiopathology</subject><subject>Stromelysin 1</subject><subject>structural damage</subject><subject>synovitis</subject><subject>teoporosis</subject><subject>tissue inhibitors</subject><subject>Vascular endothelial growth factor</subject><subject>Vascular endothelial growth factor (VEGF)</subject><subject>Vascular Endothelial Growth Factor A - blood</subject><issn>0937-941X</issn><issn>1433-2965</issn><issn>1433-2965</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp9ksFu1DAQhi0EotvCA3BBkbhwCXhsx44vSFWhFKkSF0DcLMfrpG6zcbCdVvv2zGqXQpHgZHnm-8eemZ-QF0DfAKXqbaYUdFtTaGuhGNTiEVmB4LxmWjaPyYpqrmot4PsROc75mqJGa_WUHHHKqWQMViRf-NmW6LbFV0OKd-Wq6q0rMVUhV7aaY_FTCXasuhA3Nt34VPWYjLn4OKc4ht4nW0KcKjutD-GYYkZ12MVutiNepqHKc5zW2zGUkJ-RJ70ds39-OE_I1_MPX84u6svPHz-dnV7WrhGy1Ez4jmundMdoA8qunbRWOskFFWvvAFplO7DQO9fpTlvV8kYy5awGJVsr-Qmp93XznZ-XzswpYAtbE20wwzIbDA2Lyd6wloLk_-Xfh2-nJqbBLJvFQNMqCci_2_MIb_za4aSSHR_IHmamcGWGeGukEJozhgVeHwqk-GPxuZhNyM6Po518XLJh2CMHpmiD6Ku_0Ou4pAnHt6OU5LjYFinYUw5XkJPv7z8D1OwsY_aWMWgZs7OMEah5-WcX94pfHkGAHcaCqWnw6ffT_676E_oQ0ME</recordid><startdate>20190201</startdate><enddate>20190201</enddate><creator>Torres, L.</creator><creator>Klingberg, E.</creator><creator>Nurkkala, M.</creator><creator>Carlsten, H.</creator><creator>Forsblad-d’Elia, H.</creator><general>Springer London</general><general>Springer Nature B.V</general><scope>C6C</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QP</scope><scope>7RV</scope><scope>7TS</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>ADHXS</scope><scope>ADTPV</scope><scope>AOWAS</scope><scope>D8T</scope><scope>D93</scope><scope>ZZAVC</scope><scope>F1U</scope><orcidid>https://orcid.org/0000-0001-6858-6413</orcidid></search><sort><creationdate>20190201</creationdate><title>Hepatocyte growth factor is a potential biomarker for osteoproliferation and osteoporosis in ankylosing spondylitis</title><author>Torres, L. ; Klingberg, E. ; Nurkkala, M. ; Carlsten, H. ; Forsblad-d’Elia, H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c546t-24eb39c79b20517adc6aa6c63404dec1187ab1a1fccb9b9a7835627ca91768a63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Absorptiometry, Photon - methods</topic><topic>Adult</topic><topic>Age</topic><topic>Aging - blood</topic><topic>Ankylosing spondylitis</topic><topic>Biomarkers</topic><topic>Biomarkers - blood</topic><topic>Body mass index</topic><topic>Bone density</topic><topic>Bone Density - physiology</topic><topic>Bone loss</topic><topic>Bone mineral density</topic><topic>Bone turnover</topic><topic>Case-Control Studies</topic><topic>disease-activity</topic><topic>Endocrinology</topic><topic>Endocrinology and Diabetes</topic><topic>Endokrinologi och diabetes</topic><topic>Enzyme-linked immunosorbent assay</topic><topic>factor hgf</topic><topic>Female</topic><topic>Femur</topic><topic>Femur Neck - physiopathology</topic><topic>Hepatocyte growth factor</topic><topic>Hepatocyte growth factor (HGF)</topic><topic>Hepatocyte Growth Factor - blood</topic><topic>Humans</topic><topic>Male</topic><topic>Matrix metalloproteinase</topic><topic>Matrix Metalloproteinase 3 - blood</topic><topic>Matrix metalloproteinase-3 (MMP-3)</topic><topic>matrix metalloproteinases</topic><topic>matrix-metalloproteinase-3</topic><topic>Medicine</topic><topic>Medicine &amp; Public Health</topic><topic>Metalloproteinase</topic><topic>Middle Aged</topic><topic>Original</topic><topic>Original Article</topic><topic>Orthopedics</topic><topic>Osteogenesis - physiology</topic><topic>Osteoporosis</topic><topic>Osteoporosis - diagnosis</topic><topic>Osteoporosis - etiology</topic><topic>Osteoporosis - physiopathology</topic><topic>Osteoproliferation</topic><topic>repair</topic><topic>Reumatologi och inflammation</topic><topic>rheumatoid-arthritis</topic><topic>Rheumatology</topic><topic>Rheumatology and Autoimmunity</topic><topic>Risk factors</topic><topic>serum</topic><topic>Serum levels</topic><topic>Severity of Illness Index</topic><topic>Smoking</topic><topic>Spine</topic><topic>Spondylitis</topic><topic>Spondylitis, Ankylosing - blood</topic><topic>Spondylitis, Ankylosing - complications</topic><topic>Spondylitis, Ankylosing - pathology</topic><topic>Spondylitis, Ankylosing - physiopathology</topic><topic>Stromelysin 1</topic><topic>structural damage</topic><topic>synovitis</topic><topic>teoporosis</topic><topic>tissue inhibitors</topic><topic>Vascular endothelial growth factor</topic><topic>Vascular endothelial growth factor (VEGF)</topic><topic>Vascular Endothelial Growth Factor A - blood</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Torres, L.</creatorcontrib><creatorcontrib>Klingberg, E.</creatorcontrib><creatorcontrib>Nurkkala, M.</creatorcontrib><creatorcontrib>Carlsten, H.</creatorcontrib><creatorcontrib>Forsblad-d’Elia, H.</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium &amp; 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Allied Health Database (Alumni Edition)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>SWEPUB Umeå universitet full text</collection><collection>SwePub</collection><collection>SwePub Articles</collection><collection>SWEPUB Freely available online</collection><collection>SWEPUB Umeå universitet</collection><collection>SwePub Articles full text</collection><collection>SWEPUB Göteborgs universitet</collection><jtitle>Osteoporosis international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Torres, L.</au><au>Klingberg, E.</au><au>Nurkkala, M.</au><au>Carlsten, H.</au><au>Forsblad-d’Elia, H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hepatocyte growth factor is a potential biomarker for osteoproliferation and osteoporosis in ankylosing spondylitis</atitle><jtitle>Osteoporosis international</jtitle><stitle>Osteoporos Int</stitle><addtitle>Osteoporos Int</addtitle><date>2019-02-01</date><risdate>2019</risdate><volume>30</volume><issue>2</issue><spage>441</spage><epage>449</epage><pages>441-449</pages><issn>0937-941X</issn><issn>1433-2965</issn><eissn>1433-2965</eissn><abstract>Summary We explored relations between serum hepatocyte growth factor (HGF), disease activity, osteoproliferation, and bone mineral density (BMD) in ankylosing spondylitis (AS), in comparison with healthy controls. HGF was increased especially in male AS patients and smokers and associated with both lower BMD and more chronic radiographic changes in the spine. Introduction Ankylosing spondylitis (AS) is characterized by both osteoproliferation and increased bone loss. Biomarkers are requested to predict the processes. The aims of this study were to compare serum levels of hepatocyte growth factor (HGF), matrix metalloproteinase-3 (MMP-3), and vascular endothelial growth factor (VEGF) in AS patients with healthy controls (HC) and to explore the associations with disease activity, osteoproliferation, and bone mineral density (BMD). Methods Serum from AS patients (modified NY-criteria) and HC was analyzed for HGF, MMP-3, and VEGF with ELISA. Disease activity parameters were collected. Osteoproliferation was assessed with modified Stoke Ankylosing Spondylitis Spine Score (mSASSS) and BMD was measured in femoral neck. Results Totally, 204 AS patients and 80 sex and age matched HC were included. Serum HGF was higher in the AS patients compared with the HC, whereas serum MMP-3 and VEGF were not. Serum HGF was also higher in smokers and in the male AS patients positively correlated with age, BASMI, and mSASSS, and negatively correlated with BMD. The biomarkers were all positively associated with ESR, CRP, and WBC. In multiple linear regression analysis serum HGF remained associated with higher mSASSS and lower BMD, after adjusting for age, sex, CRP, smoking, and body mass index. Conclusions Serum HGF was increased in male AS patients and associated with higher mSASSS and lower BMD. In addition, serum HGF was positively associated with risk factors for osteoproliferation such as age, CRP and smoking. HGF could be a potential biomarker of importance for the bone metabolism in AS. Trial registration NCT00858819.</abstract><cop>London</cop><pub>Springer London</pub><pmid>30306221</pmid><doi>10.1007/s00198-018-4721-4</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0001-6858-6413</orcidid><oa>free_for_read</oa></addata></record>
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source Springer Nature
subjects Absorptiometry, Photon - methods
Adult
Age
Aging - blood
Ankylosing spondylitis
Biomarkers
Biomarkers - blood
Body mass index
Bone density
Bone Density - physiology
Bone loss
Bone mineral density
Bone turnover
Case-Control Studies
disease-activity
Endocrinology
Endocrinology and Diabetes
Endokrinologi och diabetes
Enzyme-linked immunosorbent assay
factor hgf
Female
Femur
Femur Neck - physiopathology
Hepatocyte growth factor
Hepatocyte growth factor (HGF)
Hepatocyte Growth Factor - blood
Humans
Male
Matrix metalloproteinase
Matrix Metalloproteinase 3 - blood
Matrix metalloproteinase-3 (MMP-3)
matrix metalloproteinases
matrix-metalloproteinase-3
Medicine
Medicine & Public Health
Metalloproteinase
Middle Aged
Original
Original Article
Orthopedics
Osteogenesis - physiology
Osteoporosis
Osteoporosis - diagnosis
Osteoporosis - etiology
Osteoporosis - physiopathology
Osteoproliferation
repair
Reumatologi och inflammation
rheumatoid-arthritis
Rheumatology
Rheumatology and Autoimmunity
Risk factors
serum
Serum levels
Severity of Illness Index
Smoking
Spine
Spondylitis
Spondylitis, Ankylosing - blood
Spondylitis, Ankylosing - complications
Spondylitis, Ankylosing - pathology
Spondylitis, Ankylosing - physiopathology
Stromelysin 1
structural damage
synovitis
teoporosis
tissue inhibitors
Vascular endothelial growth factor
Vascular endothelial growth factor (VEGF)
Vascular Endothelial Growth Factor A - blood
title Hepatocyte growth factor is a potential biomarker for osteoproliferation and osteoporosis in ankylosing spondylitis
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