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Soluble Biomarkers of Osteoporosis and Osteoarthritis, from Pathway Mapping to Clinical Trials: An Update
Serum biomarkers of osteoarticular diseases have been in the limelight of current clinical research trends. Laboratory validation of defined and candidate biomarkers for both osteoarthritis and osteoporosis is of key importance for future decisional algorithms in the diagnosis, monitoring, and progn...
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Published in: | Clinical interventions in aging 2020-01, Vol.15, p.501-518 |
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description | Serum biomarkers of osteoarticular diseases have been in the limelight of current clinical research trends. Laboratory validation of defined and candidate biomarkers for both osteoarthritis and osteoporosis is of key importance for future decisional algorithms in the diagnosis, monitoring, and prognosis of these diseases. The current guidelines recommend the use of collagen degradation remnants, eg, CTX-I and CTX-II, in the complementary diagnosis of both osteoporosis and osteoarthritis. Besides the collagen degradation markers, enzymes that regulate bone and articular metabolism are useful in the clinical evaluation of osteoarticular pathologies. Along these, several other recommended and new nominee molecules have been recently studied. Wnts and Wnt-related molecules have a cardinal role in the bone-joint homeostasis, making them a promising target not only for pharmaceutical modulation, but also to be considered as soluble biomarkers. Sclerostin and dickkopf, two inhibitor molecules of the Wnt/β-catenin signaling, might have a dual role in the assessment of the clinical manifestations of the osteoarticular unit. In osteoarthritis, besides fragments of collagen type II many pathway-related molecules have been studied and proposed for biomarker validation. The most serious limitation is that a significant proportion of studies lack statistical power due to the reduced number of cases enrolled. Serum biomarkers of bone and joint turnover markers represent an encouraging possibility for the diagnosis and prognosis of osteoarticular diseases, although further studies and laboratory validations should be carried out as to solely rely on them. |
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Laboratory validation of defined and candidate biomarkers for both osteoarthritis and osteoporosis is of key importance for future decisional algorithms in the diagnosis, monitoring, and prognosis of these diseases. The current guidelines recommend the use of collagen degradation remnants, eg, CTX-I and CTX-II, in the complementary diagnosis of both osteoporosis and osteoarthritis. Besides the collagen degradation markers, enzymes that regulate bone and articular metabolism are useful in the clinical evaluation of osteoarticular pathologies. Along these, several other recommended and new nominee molecules have been recently studied. Wnts and Wnt-related molecules have a cardinal role in the bone-joint homeostasis, making them a promising target not only for pharmaceutical modulation, but also to be considered as soluble biomarkers. Sclerostin and dickkopf, two inhibitor molecules of the Wnt/β-catenin signaling, might have a dual role in the assessment of the clinical manifestations of the osteoarticular unit. In osteoarthritis, besides fragments of collagen type II many pathway-related molecules have been studied and proposed for biomarker validation. The most serious limitation is that a significant proportion of studies lack statistical power due to the reduced number of cases enrolled. Serum biomarkers of bone and joint turnover markers represent an encouraging possibility for the diagnosis and prognosis of osteoarticular diseases, although further studies and laboratory validations should be carried out as to solely rely on them.</description><identifier>ISSN: 1178-1998</identifier><identifier>ISSN: 1176-9092</identifier><identifier>EISSN: 1178-1998</identifier><identifier>DOI: 10.2147/CIA.S242288</identifier><identifier>PMID: 32308378</identifier><language>eng</language><publisher>New Zealand: Dove Medical Press Limited</publisher><subject>Age ; Alendronate ; Algorithms ; Arthritis ; Biological markers ; Biomarkers ; Circadian rhythm ; Clinical trials ; Collagen ; Cytokines ; Disease ; Diseases ; Enzymes ; Fractures ; Gender ; Homeostasis ; Hyperthyroidism ; Intervention ; Medical research ; Metabolism ; Osteoarthritis ; Osteoporosis ; Phosphatase ; Physiological aspects ; Power (Philosophy) ; Prognosis ; Review ; Womens health</subject><ispartof>Clinical interventions in aging, 2020-01, Vol.15, p.501-518</ispartof><rights>2020 Nagy et al.</rights><rights>COPYRIGHT 2020 Dove Medical Press Limited</rights><rights>2020. 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Laboratory validation of defined and candidate biomarkers for both osteoarthritis and osteoporosis is of key importance for future decisional algorithms in the diagnosis, monitoring, and prognosis of these diseases. The current guidelines recommend the use of collagen degradation remnants, eg, CTX-I and CTX-II, in the complementary diagnosis of both osteoporosis and osteoarthritis. Besides the collagen degradation markers, enzymes that regulate bone and articular metabolism are useful in the clinical evaluation of osteoarticular pathologies. Along these, several other recommended and new nominee molecules have been recently studied. Wnts and Wnt-related molecules have a cardinal role in the bone-joint homeostasis, making them a promising target not only for pharmaceutical modulation, but also to be considered as soluble biomarkers. Sclerostin and dickkopf, two inhibitor molecules of the Wnt/β-catenin signaling, might have a dual role in the assessment of the clinical manifestations of the osteoarticular unit. In osteoarthritis, besides fragments of collagen type II many pathway-related molecules have been studied and proposed for biomarker validation. The most serious limitation is that a significant proportion of studies lack statistical power due to the reduced number of cases enrolled. Serum biomarkers of bone and joint turnover markers represent an encouraging possibility for the diagnosis and prognosis of osteoarticular diseases, although further studies and laboratory validations should be carried out as to solely rely on them.</description><subject>Age</subject><subject>Alendronate</subject><subject>Algorithms</subject><subject>Arthritis</subject><subject>Biological markers</subject><subject>Biomarkers</subject><subject>Circadian rhythm</subject><subject>Clinical trials</subject><subject>Collagen</subject><subject>Cytokines</subject><subject>Disease</subject><subject>Diseases</subject><subject>Enzymes</subject><subject>Fractures</subject><subject>Gender</subject><subject>Homeostasis</subject><subject>Hyperthyroidism</subject><subject>Intervention</subject><subject>Medical research</subject><subject>Metabolism</subject><subject>Osteoarthritis</subject><subject>Osteoporosis</subject><subject>Phosphatase</subject><subject>Physiological aspects</subject><subject>Power (Philosophy)</subject><subject>Prognosis</subject><subject>Review</subject><subject>Womens health</subject><issn>1178-1998</issn><issn>1176-9092</issn><issn>1178-1998</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqNktuLEzEYxQdR3HX1yXcJCL5oa24zmfgg1OKlsLLC7j6HXDup08mYpMr-92Zt3bYgrOQh4eR8v-RLTlU9R3CKEWVv54vZ9BJTjNv2QXWKEGsniPP24cH6pHqS0grCumE1flydEExgS1h7WvnL0G9Ub8EHH9YyfrcxgeDARco2jCGG5BOQg9kKMuYu-uzTG-BiWINvMne_5A34KsfRD0uQA5j3fvBa9uAqetmnd2A2gOvRyGyfVo9cUeyz3XxWXX_6eDX_Mjm_-LyYz84nmiGSJ6pVRklONDFUNpA5RLThlDAIeUsh1842tdGKQI2gxlQq12KqIFNWwlJHzqrFlmuCXIkx-tLWjQjSiz9CiEtR-vC6twIzSkmrGLJYUU45l46RxkJkCWPW0MJ6v2WNG7W2RtshR9kfQY93Bt-JZfgpGKoxI7eXebkDxPBjY1MWq7CJQ-lfYMIhRxBjvHctZbmVH1woML32SYtZgxvMKSb3uUjd8Iax4pr-w1WGsWuvw2CdL_oR9j8L9ie8OijorOxzl0qKsg9DOibfY9wTX2-NugQuRevuXhhBcZtxUTIudhkv7heHn3Ln_Rtq8hsVSfLW</recordid><startdate>20200101</startdate><enddate>20200101</enddate><creator>Nagy, Előd Ernő</creator><creator>Nagy-Finna, Csilla</creator><creator>Popoviciu, Horațiu</creator><creator>Kovács, Béla</creator><general>Dove Medical Press Limited</general><general>Taylor & Francis Ltd</general><general>Dove</general><general>Dove Medical Press</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7XB</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>KB0</scope><scope>M2O</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0003-3881-8636</orcidid><orcidid>https://orcid.org/0000-0001-5215-6152</orcidid><orcidid>https://orcid.org/0000-0002-2503-5555</orcidid></search><sort><creationdate>20200101</creationdate><title>Soluble Biomarkers of Osteoporosis and Osteoarthritis, from Pathway Mapping to Clinical Trials: An Update</title><author>Nagy, Előd Ernő ; 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Laboratory validation of defined and candidate biomarkers for both osteoarthritis and osteoporosis is of key importance for future decisional algorithms in the diagnosis, monitoring, and prognosis of these diseases. The current guidelines recommend the use of collagen degradation remnants, eg, CTX-I and CTX-II, in the complementary diagnosis of both osteoporosis and osteoarthritis. Besides the collagen degradation markers, enzymes that regulate bone and articular metabolism are useful in the clinical evaluation of osteoarticular pathologies. Along these, several other recommended and new nominee molecules have been recently studied. Wnts and Wnt-related molecules have a cardinal role in the bone-joint homeostasis, making them a promising target not only for pharmaceutical modulation, but also to be considered as soluble biomarkers. Sclerostin and dickkopf, two inhibitor molecules of the Wnt/β-catenin signaling, might have a dual role in the assessment of the clinical manifestations of the osteoarticular unit. In osteoarthritis, besides fragments of collagen type II many pathway-related molecules have been studied and proposed for biomarker validation. The most serious limitation is that a significant proportion of studies lack statistical power due to the reduced number of cases enrolled. Serum biomarkers of bone and joint turnover markers represent an encouraging possibility for the diagnosis and prognosis of osteoarticular diseases, although further studies and laboratory validations should be carried out as to solely rely on them.</abstract><cop>New Zealand</cop><pub>Dove Medical Press Limited</pub><pmid>32308378</pmid><doi>10.2147/CIA.S242288</doi><tpages>18</tpages><orcidid>https://orcid.org/0000-0003-3881-8636</orcidid><orcidid>https://orcid.org/0000-0001-5215-6152</orcidid><orcidid>https://orcid.org/0000-0002-2503-5555</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Age Alendronate Algorithms Arthritis Biological markers Biomarkers Circadian rhythm Clinical trials Collagen Cytokines Disease Diseases Enzymes Fractures Gender Homeostasis Hyperthyroidism Intervention Medical research Metabolism Osteoarthritis Osteoporosis Phosphatase Physiological aspects Power (Philosophy) Prognosis Review Womens health |
title | Soluble Biomarkers of Osteoporosis and Osteoarthritis, from Pathway Mapping to Clinical Trials: An Update |
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