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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 |
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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 |
format | article |
fullrecord | <record><control><sourceid>proquest_swepu</sourceid><recordid>TN_cdi_swepub_primary_oai_gup_ub_gu_se_280163</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2118312705</sourcerecordid><originalsourceid>FETCH-LOGICAL-c546t-24eb39c79b20517adc6aa6c63404dec1187ab1a1fccb9b9a7835627ca91768a63</originalsourceid><addsrcrecordid>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</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2117639978</pqid></control><display><type>article</type><title>Hepatocyte growth factor is a potential biomarker for osteoproliferation and osteoporosis in ankylosing spondylitis</title><source>Springer Nature</source><creator>Torres, L. ; Klingberg, E. ; Nurkkala, M. ; Carlsten, H. ; Forsblad-d’Elia, H.</creator><creatorcontrib>Torres, L. ; Klingberg, E. ; Nurkkala, M. ; Carlsten, H. ; Forsblad-d’Elia, H.</creatorcontrib><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.</description><identifier>ISSN: 0937-941X</identifier><identifier>ISSN: 1433-2965</identifier><identifier>EISSN: 1433-2965</identifier><identifier>DOI: 10.1007/s00198-018-4721-4</identifier><identifier>PMID: 30306221</identifier><language>eng</language><publisher>London: Springer London</publisher><subject>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</subject><ispartof>Osteoporosis international, 2019-02, Vol.30 (2), p.441-449</ispartof><rights>The Author(s) 2018</rights><rights>Osteoporosis International is a copyright of Springer, (2018). All Rights Reserved. © 2018. This work is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c546t-24eb39c79b20517adc6aa6c63404dec1187ab1a1fccb9b9a7835627ca91768a63</citedby><cites>FETCH-LOGICAL-c546t-24eb39c79b20517adc6aa6c63404dec1187ab1a1fccb9b9a7835627ca91768a63</cites><orcidid>0000-0001-6858-6413</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30306221$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-158761$$DView record from Swedish Publication Index$$Hfree_for_read</backlink><backlink>$$Uhttps://gup.ub.gu.se/publication/280163$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Torres, L.</creatorcontrib><creatorcontrib>Klingberg, E.</creatorcontrib><creatorcontrib>Nurkkala, M.</creatorcontrib><creatorcontrib>Carlsten, H.</creatorcontrib><creatorcontrib>Forsblad-d’Elia, H.</creatorcontrib><title>Hepatocyte growth factor is a potential biomarker for osteoproliferation and osteoporosis in ankylosing spondylitis</title><title>Osteoporosis international</title><addtitle>Osteoporos Int</addtitle><addtitle>Osteoporos Int</addtitle><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.</description><subject>Absorptiometry, Photon - methods</subject><subject>Adult</subject><subject>Age</subject><subject>Aging - blood</subject><subject>Ankylosing spondylitis</subject><subject>Biomarkers</subject><subject>Biomarkers - blood</subject><subject>Body mass index</subject><subject>Bone density</subject><subject>Bone Density - physiology</subject><subject>Bone loss</subject><subject>Bone mineral density</subject><subject>Bone turnover</subject><subject>Case-Control Studies</subject><subject>disease-activity</subject><subject>Endocrinology</subject><subject>Endocrinology and Diabetes</subject><subject>Endokrinologi och diabetes</subject><subject>Enzyme-linked immunosorbent assay</subject><subject>factor hgf</subject><subject>Female</subject><subject>Femur</subject><subject>Femur Neck - physiopathology</subject><subject>Hepatocyte growth factor</subject><subject>Hepatocyte growth factor (HGF)</subject><subject>Hepatocyte Growth Factor - blood</subject><subject>Humans</subject><subject>Male</subject><subject>Matrix metalloproteinase</subject><subject>Matrix Metalloproteinase 3 - blood</subject><subject>Matrix metalloproteinase-3 (MMP-3)</subject><subject>matrix metalloproteinases</subject><subject>matrix-metalloproteinase-3</subject><subject>Medicine</subject><subject>Medicine & 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 & 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 & Calcified Tissue Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Physical Education Index</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Nursing & 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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recordid | cdi_swepub_primary_oai_gup_ub_gu_se_280163 |
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 |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-01T23%3A14%3A44IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_swepu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Hepatocyte%20growth%20factor%20is%20a%20potential%20biomarker%20for%20osteoproliferation%20and%20osteoporosis%20in%20ankylosing%20spondylitis&rft.jtitle=Osteoporosis%20international&rft.au=Torres,%20L.&rft.date=2019-02-01&rft.volume=30&rft.issue=2&rft.spage=441&rft.epage=449&rft.pages=441-449&rft.issn=0937-941X&rft.eissn=1433-2965&rft_id=info:doi/10.1007/s00198-018-4721-4&rft_dat=%3Cproquest_swepu%3E2118312705%3C/proquest_swepu%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c546t-24eb39c79b20517adc6aa6c63404dec1187ab1a1fccb9b9a7835627ca91768a63%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2117639978&rft_id=info:pmid/30306221&rfr_iscdi=true |