Loading…

LRP5, Bone Density, and Mechanical Stress: A Case Report and Literature Review

The Wnt-β-catenin pathway receptor, low-density lipoprotein receptor-related protein 5 (LRP5), is a known regulator of bone mineral density. It has been hypothesized that specific human polymorphisms in impact bone density, in part, by altering the anabolic response of bone to mechanical loading. Al...

Full description

Saved in:
Bibliographic Details
Published in:Frontiers in endocrinology (Lausanne) 2019-03, Vol.10, p.184
Main Authors: Norwitz, Nicholas G, Mota, Adrian Soto, Misra, Madhusmita, Ackerman, Kathryn E
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c429t-b934e8e8ae0a95b5f7c01280689acc5e7cb0e28a16743a97780c9449fa58c8033
cites cdi_FETCH-LOGICAL-c429t-b934e8e8ae0a95b5f7c01280689acc5e7cb0e28a16743a97780c9449fa58c8033
container_end_page
container_issue
container_start_page 184
container_title Frontiers in endocrinology (Lausanne)
container_volume 10
creator Norwitz, Nicholas G
Mota, Adrian Soto
Misra, Madhusmita
Ackerman, Kathryn E
description The Wnt-β-catenin pathway receptor, low-density lipoprotein receptor-related protein 5 (LRP5), is a known regulator of bone mineral density. It has been hypothesized that specific human polymorphisms in impact bone density, in part, by altering the anabolic response of bone to mechanical loading. Although experiments in animal models support this hypothesis, there is limited evidence that polymorphisms can alter the anabolic response of bone to mechanical loading in humans. Herein, we report a young male who harbors a rare missense mutation (A745V) and who provides potential proof of principle for this mechanotransduction hypothesis for low bone density. The subject had no history of fractures until age 18, a year into a career in competitive distance running. As he continued to run over the following 2 years, his mileage threshold to fracture steadily and rapidly decreased until he was diagnosed with severe osteoporosis (lumbar spine BMD Z-score of -3.2). By contextualizing this case within the existing and mechanical stress literature, we speculate that this represents the first documented case of an individual in whom a genetic mutation altered the anabolic response of bone to mechanical stress in a manner sufficient to contribute to osteoporosis.
doi_str_mv 10.3389/fendo.2019.00184
format article
fullrecord <record><control><sourceid>pubmed_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_f78502f1fcd341c6be2deb31acdcda40</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_f78502f1fcd341c6be2deb31acdcda40</doaj_id><sourcerecordid>30972028</sourcerecordid><originalsourceid>FETCH-LOGICAL-c429t-b934e8e8ae0a95b5f7c01280689acc5e7cb0e28a16743a97780c9449fa58c8033</originalsourceid><addsrcrecordid>eNpVkctOwzAQRS0EAgTds0L5gLaMH0lsFkilPKXyUIG1NXEmNFWbVHYK4u9JW0DUm7Fm5p5ZHMZOOPSl1OasoCqv-wK46QNwrXbYIU8S1RPSiN1__wPWCWEK7VPtrtH77ECCSQUIfcgeR-PnuBtd1hVFV1SFsvnqRljl0QO5CValw1n00ngK4TwaREMMFI1pUftmvTQqG_LYLP2q-1HS5zHbK3AWqPNTj9jbzfXr8K43erq9Hw5GPaeEaXqZkYo0aSRAE2dxkTrgQkOiDToXU-oyIKGRJ6mSaNJUgzNKmQJj7TRIecTuN9y8xqld-HKO_svWWNp1o_bvFn1TuhnZItUxiIIXLpeKuyQjkVMmObrc5aigZV1sWItlNqfcUdV4nG1BtydVObHv9YdNlJIpVy0ANgDn6xA8FX9ZDnalyq5V2ZUqu1bVRk7_3_wL_IqR35T5j-k</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>LRP5, Bone Density, and Mechanical Stress: A Case Report and Literature Review</title><source>Open Access: PubMed Central</source><creator>Norwitz, Nicholas G ; Mota, Adrian Soto ; Misra, Madhusmita ; Ackerman, Kathryn E</creator><creatorcontrib>Norwitz, Nicholas G ; Mota, Adrian Soto ; Misra, Madhusmita ; Ackerman, Kathryn E</creatorcontrib><description>The Wnt-β-catenin pathway receptor, low-density lipoprotein receptor-related protein 5 (LRP5), is a known regulator of bone mineral density. It has been hypothesized that specific human polymorphisms in impact bone density, in part, by altering the anabolic response of bone to mechanical loading. Although experiments in animal models support this hypothesis, there is limited evidence that polymorphisms can alter the anabolic response of bone to mechanical loading in humans. Herein, we report a young male who harbors a rare missense mutation (A745V) and who provides potential proof of principle for this mechanotransduction hypothesis for low bone density. The subject had no history of fractures until age 18, a year into a career in competitive distance running. As he continued to run over the following 2 years, his mileage threshold to fracture steadily and rapidly decreased until he was diagnosed with severe osteoporosis (lumbar spine BMD Z-score of -3.2). By contextualizing this case within the existing and mechanical stress literature, we speculate that this represents the first documented case of an individual in whom a genetic mutation altered the anabolic response of bone to mechanical stress in a manner sufficient to contribute to osteoporosis.</description><identifier>ISSN: 1664-2392</identifier><identifier>EISSN: 1664-2392</identifier><identifier>DOI: 10.3389/fendo.2019.00184</identifier><identifier>PMID: 30972028</identifier><language>eng</language><publisher>Switzerland: Frontiers Media S.A</publisher><subject>bone mineral density ; Endocrinology ; LRP5 ; mechanical stress ; osteoporosis ; Wnt-β-catenin signaling</subject><ispartof>Frontiers in endocrinology (Lausanne), 2019-03, Vol.10, p.184</ispartof><rights>Copyright © 2019 Norwitz, Mota, Misra and Ackerman. 2019 Norwitz, Mota, Misra and Ackerman</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c429t-b934e8e8ae0a95b5f7c01280689acc5e7cb0e28a16743a97780c9449fa58c8033</citedby><cites>FETCH-LOGICAL-c429t-b934e8e8ae0a95b5f7c01280689acc5e7cb0e28a16743a97780c9449fa58c8033</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6443714/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6443714/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30972028$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Norwitz, Nicholas G</creatorcontrib><creatorcontrib>Mota, Adrian Soto</creatorcontrib><creatorcontrib>Misra, Madhusmita</creatorcontrib><creatorcontrib>Ackerman, Kathryn E</creatorcontrib><title>LRP5, Bone Density, and Mechanical Stress: A Case Report and Literature Review</title><title>Frontiers in endocrinology (Lausanne)</title><addtitle>Front Endocrinol (Lausanne)</addtitle><description>The Wnt-β-catenin pathway receptor, low-density lipoprotein receptor-related protein 5 (LRP5), is a known regulator of bone mineral density. It has been hypothesized that specific human polymorphisms in impact bone density, in part, by altering the anabolic response of bone to mechanical loading. Although experiments in animal models support this hypothesis, there is limited evidence that polymorphisms can alter the anabolic response of bone to mechanical loading in humans. Herein, we report a young male who harbors a rare missense mutation (A745V) and who provides potential proof of principle for this mechanotransduction hypothesis for low bone density. The subject had no history of fractures until age 18, a year into a career in competitive distance running. As he continued to run over the following 2 years, his mileage threshold to fracture steadily and rapidly decreased until he was diagnosed with severe osteoporosis (lumbar spine BMD Z-score of -3.2). By contextualizing this case within the existing and mechanical stress literature, we speculate that this represents the first documented case of an individual in whom a genetic mutation altered the anabolic response of bone to mechanical stress in a manner sufficient to contribute to osteoporosis.</description><subject>bone mineral density</subject><subject>Endocrinology</subject><subject>LRP5</subject><subject>mechanical stress</subject><subject>osteoporosis</subject><subject>Wnt-β-catenin signaling</subject><issn>1664-2392</issn><issn>1664-2392</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNpVkctOwzAQRS0EAgTds0L5gLaMH0lsFkilPKXyUIG1NXEmNFWbVHYK4u9JW0DUm7Fm5p5ZHMZOOPSl1OasoCqv-wK46QNwrXbYIU8S1RPSiN1__wPWCWEK7VPtrtH77ECCSQUIfcgeR-PnuBtd1hVFV1SFsvnqRljl0QO5CValw1n00ngK4TwaREMMFI1pUftmvTQqG_LYLP2q-1HS5zHbK3AWqPNTj9jbzfXr8K43erq9Hw5GPaeEaXqZkYo0aSRAE2dxkTrgQkOiDToXU-oyIKGRJ6mSaNJUgzNKmQJj7TRIecTuN9y8xqld-HKO_svWWNp1o_bvFn1TuhnZItUxiIIXLpeKuyQjkVMmObrc5aigZV1sWItlNqfcUdV4nG1BtydVObHv9YdNlJIpVy0ANgDn6xA8FX9ZDnalyq5V2ZUqu1bVRk7_3_wL_IqR35T5j-k</recordid><startdate>20190326</startdate><enddate>20190326</enddate><creator>Norwitz, Nicholas G</creator><creator>Mota, Adrian Soto</creator><creator>Misra, Madhusmita</creator><creator>Ackerman, Kathryn E</creator><general>Frontiers Media S.A</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20190326</creationdate><title>LRP5, Bone Density, and Mechanical Stress: A Case Report and Literature Review</title><author>Norwitz, Nicholas G ; Mota, Adrian Soto ; Misra, Madhusmita ; Ackerman, Kathryn E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c429t-b934e8e8ae0a95b5f7c01280689acc5e7cb0e28a16743a97780c9449fa58c8033</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>bone mineral density</topic><topic>Endocrinology</topic><topic>LRP5</topic><topic>mechanical stress</topic><topic>osteoporosis</topic><topic>Wnt-β-catenin signaling</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Norwitz, Nicholas G</creatorcontrib><creatorcontrib>Mota, Adrian Soto</creatorcontrib><creatorcontrib>Misra, Madhusmita</creatorcontrib><creatorcontrib>Ackerman, Kathryn E</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Frontiers in endocrinology (Lausanne)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Norwitz, Nicholas G</au><au>Mota, Adrian Soto</au><au>Misra, Madhusmita</au><au>Ackerman, Kathryn E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>LRP5, Bone Density, and Mechanical Stress: A Case Report and Literature Review</atitle><jtitle>Frontiers in endocrinology (Lausanne)</jtitle><addtitle>Front Endocrinol (Lausanne)</addtitle><date>2019-03-26</date><risdate>2019</risdate><volume>10</volume><spage>184</spage><pages>184-</pages><issn>1664-2392</issn><eissn>1664-2392</eissn><abstract>The Wnt-β-catenin pathway receptor, low-density lipoprotein receptor-related protein 5 (LRP5), is a known regulator of bone mineral density. It has been hypothesized that specific human polymorphisms in impact bone density, in part, by altering the anabolic response of bone to mechanical loading. Although experiments in animal models support this hypothesis, there is limited evidence that polymorphisms can alter the anabolic response of bone to mechanical loading in humans. Herein, we report a young male who harbors a rare missense mutation (A745V) and who provides potential proof of principle for this mechanotransduction hypothesis for low bone density. The subject had no history of fractures until age 18, a year into a career in competitive distance running. As he continued to run over the following 2 years, his mileage threshold to fracture steadily and rapidly decreased until he was diagnosed with severe osteoporosis (lumbar spine BMD Z-score of -3.2). By contextualizing this case within the existing and mechanical stress literature, we speculate that this represents the first documented case of an individual in whom a genetic mutation altered the anabolic response of bone to mechanical stress in a manner sufficient to contribute to osteoporosis.</abstract><cop>Switzerland</cop><pub>Frontiers Media S.A</pub><pmid>30972028</pmid><doi>10.3389/fendo.2019.00184</doi><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1664-2392
ispartof Frontiers in endocrinology (Lausanne), 2019-03, Vol.10, p.184
issn 1664-2392
1664-2392
language eng
recordid cdi_doaj_primary_oai_doaj_org_article_f78502f1fcd341c6be2deb31acdcda40
source Open Access: PubMed Central
subjects bone mineral density
Endocrinology
LRP5
mechanical stress
osteoporosis
Wnt-β-catenin signaling
title LRP5, Bone Density, and Mechanical Stress: A Case Report and Literature Review
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T17%3A17%3A52IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-pubmed_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=LRP5,%20Bone%20Density,%20and%20Mechanical%20Stress:%20A%20Case%20Report%20and%20Literature%20Review&rft.jtitle=Frontiers%20in%20endocrinology%20(Lausanne)&rft.au=Norwitz,%20Nicholas%20G&rft.date=2019-03-26&rft.volume=10&rft.spage=184&rft.pages=184-&rft.issn=1664-2392&rft.eissn=1664-2392&rft_id=info:doi/10.3389/fendo.2019.00184&rft_dat=%3Cpubmed_doaj_%3E30972028%3C/pubmed_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c429t-b934e8e8ae0a95b5f7c01280689acc5e7cb0e28a16743a97780c9449fa58c8033%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/30972028&rfr_iscdi=true