Increased Serum Sclerostin Levels in Patients With Active Acromegaly

Abstract Context Bone mineral density is normal in acromegalic patients and the cause of increased fracture risk that characterizes active acromegaly is unknown. Objective This study compared serum sclerostin levels between patients with active acromegaly and healthy individuals. Design, Setting, an...

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Veröffentlicht in:The journal of clinical endocrinology and metabolism 2020-03, Vol.105 (3), p.920-924
Hauptverfasser: Pekkolay, Zafer, Kılınç, Faruk, Gozel, Nevzat, Önalan, Ebru, Tuzcu, Alpaslan Kemal
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container_issue 3
container_start_page 920
container_title The journal of clinical endocrinology and metabolism
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creator Pekkolay, Zafer
Kılınç, Faruk
Gozel, Nevzat
Önalan, Ebru
Tuzcu, Alpaslan Kemal
description Abstract Context Bone mineral density is normal in acromegalic patients and the cause of increased fracture risk that characterizes active acromegaly is unknown. Objective This study compared serum sclerostin levels between patients with active acromegaly and healthy individuals. Design, Setting, and Participants The serum sclerostin levels of patients with active acromegaly were compared with those of healthy volunteers in a cross-sectional study. The mean age of the 30 acromegaly patients (male/female: 14/16) was 47.26 ± 12.52 years (range, 18–64 years) and that of the healthy volunteers (male/female: 17/13) was 44.56 ± 10.74 years (range, 19–62 years). IGF-1 and GH levels were measured using an electrochemiluminescence method, and serum sclerostin levels using an ELISA. The Mann-Whitney U test was used to compare sclerostin levels between the 2 groups. The correlations of sclerostin level with IGF-1 and GH were determined using Spearman’s test. Results The 2 groups did not differ in age or sex (P > 0.05). The median GH and IGF-1 levels in the patient group were 2.49 ng/mL (range, 0.22–70.00 ng/mL) (interquartile range [IQR], 1.3–4.52) and 338.5 ng/mL (range, 147–911 ng/mL) (IQR, 250–426), respectively. The median GH and IGF-1 levels in the control group were 0.95 ng/mL (range, 0.3-2.3) and 144 ng/mL (range, 98–198), respectively. The median sclerostin level was 29.95 ng/mL (range, 7.5–78.1 ng/mL) (IQR, 14.37–37.47) in the acromegaly group and 22.44 ng/mL (range, 8.45–36.44 ng/mL) (IQR, 13.71–27.52) in the control group (P 
doi_str_mv 10.1210/clinem/dgz254
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Objective This study compared serum sclerostin levels between patients with active acromegaly and healthy individuals. Design, Setting, and Participants The serum sclerostin levels of patients with active acromegaly were compared with those of healthy volunteers in a cross-sectional study. The mean age of the 30 acromegaly patients (male/female: 14/16) was 47.26 ± 12.52 years (range, 18–64 years) and that of the healthy volunteers (male/female: 17/13) was 44.56 ± 10.74 years (range, 19–62 years). IGF-1 and GH levels were measured using an electrochemiluminescence method, and serum sclerostin levels using an ELISA. The Mann-Whitney U test was used to compare sclerostin levels between the 2 groups. The correlations of sclerostin level with IGF-1 and GH were determined using Spearman’s test. Results The 2 groups did not differ in age or sex (P &gt; 0.05). The median GH and IGF-1 levels in the patient group were 2.49 ng/mL (range, 0.22–70.00 ng/mL) (interquartile range [IQR], 1.3–4.52) and 338.5 ng/mL (range, 147–911 ng/mL) (IQR, 250–426), respectively. The median GH and IGF-1 levels in the control group were 0.95 ng/mL (range, 0.3-2.3) and 144 ng/mL (range, 98–198), respectively. The median sclerostin level was 29.95 ng/mL (range, 7.5–78.1 ng/mL) (IQR, 14.37–37.47) in the acromegaly group and 22.44 ng/mL (range, 8.45–36.44 ng/mL) (IQR, 13.71–27.52) in the control group (P &lt; 0.05). There was a moderate positive correlation between the sclerostin and IGF-1 levels (rho = 0.54; P &lt; 0.01), and between the sclerostin and GH levels (rho = 0.41; P &lt; 0.05). Conclusions High sclerostin levels may contribute to the increased fracture risk seen in patients with acromegaly.</description><identifier>ISSN: 0021-972X</identifier><identifier>EISSN: 1945-7197</identifier><identifier>DOI: 10.1210/clinem/dgz254</identifier><identifier>PMID: 31821453</identifier><language>eng</language><publisher>US: Oxford University Press</publisher><subject>Acromegaly ; Bone mineral density ; Care and treatment ; Cellular proteins ; Development and progression ; Fractures ; Gene expression ; Genetic aspects ; Health aspects ; Insulin-like growth factor I ; Osteoporosis ; SOST protein</subject><ispartof>The journal of clinical endocrinology and metabolism, 2020-03, Vol.105 (3), p.920-924</ispartof><rights>Endocrine Society 2019. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com 2019</rights><rights>Copyright © Oxford University Press 2015</rights><rights>Endocrine Society 2019. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.</rights><rights>COPYRIGHT 2020 Oxford University Press</rights><rights>Endocrine Society 2019. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5024-a92fd84ce985553b6d27d60bc90a238ecabe547737a572cabbb2900df88778153</citedby><cites>FETCH-LOGICAL-c5024-a92fd84ce985553b6d27d60bc90a238ecabe547737a572cabbb2900df88778153</cites><orcidid>0000-0002-5323-2257</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/2431027385?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>314,780,784,21388,21389,27924,27925,33530,33531,33744,33745,43659,43805,64385,64387,64389,72469,73123,73128,73129,73131</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31821453$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pekkolay, Zafer</creatorcontrib><creatorcontrib>Kılınç, Faruk</creatorcontrib><creatorcontrib>Gozel, Nevzat</creatorcontrib><creatorcontrib>Önalan, Ebru</creatorcontrib><creatorcontrib>Tuzcu, Alpaslan Kemal</creatorcontrib><title>Increased Serum Sclerostin Levels in Patients With Active Acromegaly</title><title>The journal of clinical endocrinology and metabolism</title><addtitle>J Clin Endocrinol Metab</addtitle><description>Abstract Context Bone mineral density is normal in acromegalic patients and the cause of increased fracture risk that characterizes active acromegaly is unknown. Objective This study compared serum sclerostin levels between patients with active acromegaly and healthy individuals. Design, Setting, and Participants The serum sclerostin levels of patients with active acromegaly were compared with those of healthy volunteers in a cross-sectional study. The mean age of the 30 acromegaly patients (male/female: 14/16) was 47.26 ± 12.52 years (range, 18–64 years) and that of the healthy volunteers (male/female: 17/13) was 44.56 ± 10.74 years (range, 19–62 years). IGF-1 and GH levels were measured using an electrochemiluminescence method, and serum sclerostin levels using an ELISA. The Mann-Whitney U test was used to compare sclerostin levels between the 2 groups. The correlations of sclerostin level with IGF-1 and GH were determined using Spearman’s test. Results The 2 groups did not differ in age or sex (P &gt; 0.05). The median GH and IGF-1 levels in the patient group were 2.49 ng/mL (range, 0.22–70.00 ng/mL) (interquartile range [IQR], 1.3–4.52) and 338.5 ng/mL (range, 147–911 ng/mL) (IQR, 250–426), respectively. The median GH and IGF-1 levels in the control group were 0.95 ng/mL (range, 0.3-2.3) and 144 ng/mL (range, 98–198), respectively. The median sclerostin level was 29.95 ng/mL (range, 7.5–78.1 ng/mL) (IQR, 14.37–37.47) in the acromegaly group and 22.44 ng/mL (range, 8.45–36.44 ng/mL) (IQR, 13.71–27.52) in the control group (P &lt; 0.05). There was a moderate positive correlation between the sclerostin and IGF-1 levels (rho = 0.54; P &lt; 0.01), and between the sclerostin and GH levels (rho = 0.41; P &lt; 0.05). Conclusions High sclerostin levels may contribute to the increased fracture risk seen in patients with acromegaly.</description><subject>Acromegaly</subject><subject>Bone mineral density</subject><subject>Care and treatment</subject><subject>Cellular proteins</subject><subject>Development and progression</subject><subject>Fractures</subject><subject>Gene expression</subject><subject>Genetic aspects</subject><subject>Health aspects</subject><subject>Insulin-like growth factor I</subject><subject>Osteoporosis</subject><subject>SOST protein</subject><issn>0021-972X</issn><issn>1945-7197</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNqFkU1P3DAQhi3UCraUI9cqUi-9BPwZJ8cV_QBppSLRqr1ZjjNhTZ14azsg-utrlAUEoqp8mLH1zDvjeRE6JPiIUIKPjbMjDMfd5R8q-A5akIaLUpJGvkILjCkpG0l_7qE3MV5hTDgXbBftMVJTktMF-ng2mgA6QldcQJiG4sI4CD4mOxYruAYXi5yd62RhTLH4YdO6WJpkryGH4Ae41O72LXrdaxfhYBv30ffPn76dnJarr1_OTpar0ghMeakb2nc1N9DUQgjWVh2VXYVb02BNWQ1GtyC4lExqIWm-tS1tMO76upayJoLtow-z7ib43xPEpAYbDTinR_BTVJRR3hBMRJXR98_QKz-FMU-nKGcEU8lq8UjlX4CyY-9T0OZOVC0rTgWpsCSZOnqByqeDwRo_Qm_z-5OCci7IG4oxQK82wQ463CqC1Z1ranZNza5l_t122KkdoHug723KAJmBG-8ShPjLTTcQ1Bq0S-t_im6X5afNf_r_BQVnsLg</recordid><startdate>20200301</startdate><enddate>20200301</enddate><creator>Pekkolay, Zafer</creator><creator>Kılınç, Faruk</creator><creator>Gozel, Nevzat</creator><creator>Önalan, Ebru</creator><creator>Tuzcu, Alpaslan Kemal</creator><general>Oxford University Press</general><general>Copyright Oxford University Press</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QP</scope><scope>7T5</scope><scope>7TM</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</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>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-5323-2257</orcidid></search><sort><creationdate>20200301</creationdate><title>Increased Serum Sclerostin Levels in Patients With Active Acromegaly</title><author>Pekkolay, Zafer ; Kılınç, Faruk ; Gozel, Nevzat ; Önalan, Ebru ; Tuzcu, Alpaslan Kemal</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5024-a92fd84ce985553b6d27d60bc90a238ecabe547737a572cabbb2900df88778153</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Acromegaly</topic><topic>Bone mineral density</topic><topic>Care and treatment</topic><topic>Cellular proteins</topic><topic>Development and progression</topic><topic>Fractures</topic><topic>Gene expression</topic><topic>Genetic aspects</topic><topic>Health aspects</topic><topic>Insulin-like growth factor I</topic><topic>Osteoporosis</topic><topic>SOST protein</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pekkolay, Zafer</creatorcontrib><creatorcontrib>Kılınç, Faruk</creatorcontrib><creatorcontrib>Gozel, Nevzat</creatorcontrib><creatorcontrib>Önalan, Ebru</creatorcontrib><creatorcontrib>Tuzcu, Alpaslan Kemal</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium &amp; 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Objective This study compared serum sclerostin levels between patients with active acromegaly and healthy individuals. Design, Setting, and Participants The serum sclerostin levels of patients with active acromegaly were compared with those of healthy volunteers in a cross-sectional study. The mean age of the 30 acromegaly patients (male/female: 14/16) was 47.26 ± 12.52 years (range, 18–64 years) and that of the healthy volunteers (male/female: 17/13) was 44.56 ± 10.74 years (range, 19–62 years). IGF-1 and GH levels were measured using an electrochemiluminescence method, and serum sclerostin levels using an ELISA. The Mann-Whitney U test was used to compare sclerostin levels between the 2 groups. The correlations of sclerostin level with IGF-1 and GH were determined using Spearman’s test. Results The 2 groups did not differ in age or sex (P &gt; 0.05). The median GH and IGF-1 levels in the patient group were 2.49 ng/mL (range, 0.22–70.00 ng/mL) (interquartile range [IQR], 1.3–4.52) and 338.5 ng/mL (range, 147–911 ng/mL) (IQR, 250–426), respectively. The median GH and IGF-1 levels in the control group were 0.95 ng/mL (range, 0.3-2.3) and 144 ng/mL (range, 98–198), respectively. The median sclerostin level was 29.95 ng/mL (range, 7.5–78.1 ng/mL) (IQR, 14.37–37.47) in the acromegaly group and 22.44 ng/mL (range, 8.45–36.44 ng/mL) (IQR, 13.71–27.52) in the control group (P &lt; 0.05). There was a moderate positive correlation between the sclerostin and IGF-1 levels (rho = 0.54; P &lt; 0.01), and between the sclerostin and GH levels (rho = 0.41; P &lt; 0.05). Conclusions High sclerostin levels may contribute to the increased fracture risk seen in patients with acromegaly.</abstract><cop>US</cop><pub>Oxford University Press</pub><pmid>31821453</pmid><doi>10.1210/clinem/dgz254</doi><tpages>5</tpages><orcidid>https://orcid.org/0000-0002-5323-2257</orcidid><oa>free_for_read</oa></addata></record>
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subjects Acromegaly
Bone mineral density
Care and treatment
Cellular proteins
Development and progression
Fractures
Gene expression
Genetic aspects
Health aspects
Insulin-like growth factor I
Osteoporosis
SOST protein
title Increased Serum Sclerostin Levels in Patients With Active Acromegaly
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