The biorhythm of human skeletal growth.
Identifieur interne : 000269 ( PubMed/Corpus ); précédent : 000268; suivant : 000270The biorhythm of human skeletal growth.
Auteurs : Patrick Mahoney ; Justyna J. Miszkiewicz ; Simon Chapple ; Mona Le Luyer ; Stephen H. Schlecht ; Tahlia J. Stewart ; Richard A. Griffiths ; Chris Deter ; Debbie Guatelli-SteinbergSource :
- Journal of anatomy [ 1469-7580 ] ; 2017.
Abstract
Evidence of a periodic biorhythm is retained in tooth enamel in the form of Retzius lines. The periodicity of Retzius lines (RP) correlates with body mass and the scheduling of life history events when compared between some mammalian species. The correlation has led to the development of the inter-specific Havers-Halberg oscillation (HHO) hypothesis, which holds great potential for studying aspects of a fossil species biology from teeth. Yet, our understanding of if, or how, the HHO relates to human skeletal growth is limited. The goal here is to explore associations between the biorhythm and two hard tissues that form at different times during human ontogeny, within the context of the HHO. First, we investigate the relationship of RP to permanent molar enamel thickness and the underlying daily rate that ameloblasts secrete enamel during childhood. Following this, we develop preliminary research conducted on small samples of adult human bone by testing associations between RP, adult femoral length (as a proxy for attained adult stature) and cortical osteocyte lacunae density (as a proxy for the rate of osteocyte proliferation). Results reveal RP is positively correlated with enamel thickness, negatively correlated with femoral length, but weakly associated with the rate of enamel secretion and osteocyte proliferation. These new data imply that a slower biorhythm predicts thicker enamel for children but shorter stature for adults. Our results develop the intra-specific HHO hypothesis suggesting that there is a common underlying systemic biorhythm that has a role in the final products of human enamel and bone growth.
DOI: 10.1111/joa.12709
PubMed: 29023695
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Miszkiewicz</name><affiliation><nlm:affiliation>Skeletal Biology and Forensic Anthropology Research Group, School of Archaeology and Anthropology, Australian National University, Canberra, ACT, Australia.</nlm:affiliation></affiliation></author><author><name sortKey="Chapple, Simon" sort="Chapple, Simon" uniqKey="Chapple S" first="Simon" last="Chapple">Simon Chapple</name><affiliation><nlm:affiliation>Human Osteology Lab, Skeletal Biology Research Centre, School of Anthropology and Conservation, University of Kent, Canterbury, UK.</nlm:affiliation></affiliation></author><author><name sortKey="Le Luyer, Mona" sort="Le Luyer, Mona" uniqKey="Le Luyer M" first="Mona" last="Le Luyer">Mona Le Luyer</name><affiliation><nlm:affiliation>Human Osteology Lab, Skeletal Biology Research Centre, School of Anthropology and Conservation, University of Kent, Canterbury, UK.</nlm:affiliation></affiliation></author><author><name sortKey="Schlecht, Stephen H" sort="Schlecht, Stephen H" uniqKey="Schlecht S" first="Stephen H" last="Schlecht">Stephen H. Schlecht</name><affiliation><nlm:affiliation>Department of Orthopaedic Surgery, University of Michigan, Ann Arbor, MI, USA.</nlm:affiliation></affiliation></author><author><name sortKey="Stewart, Tahlia J" sort="Stewart, Tahlia J" uniqKey="Stewart T" first="Tahlia J" last="Stewart">Tahlia J. Stewart</name><affiliation><nlm:affiliation>Skeletal Biology and Forensic Anthropology Research Group, School of Archaeology and Anthropology, Australian National University, Canberra, ACT, Australia.</nlm:affiliation></affiliation></author><author><name sortKey="Griffiths, Richard A" sort="Griffiths, Richard A" uniqKey="Griffiths R" first="Richard A" last="Griffiths">Richard A. 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Miszkiewicz</name><affiliation><nlm:affiliation>Skeletal Biology and Forensic Anthropology Research Group, School of Archaeology and Anthropology, Australian National University, Canberra, ACT, Australia.</nlm:affiliation></affiliation></author><author><name sortKey="Chapple, Simon" sort="Chapple, Simon" uniqKey="Chapple S" first="Simon" last="Chapple">Simon Chapple</name><affiliation><nlm:affiliation>Human Osteology Lab, Skeletal Biology Research Centre, School of Anthropology and Conservation, University of Kent, Canterbury, UK.</nlm:affiliation></affiliation></author><author><name sortKey="Le Luyer, Mona" sort="Le Luyer, Mona" uniqKey="Le Luyer M" first="Mona" last="Le Luyer">Mona Le Luyer</name><affiliation><nlm:affiliation>Human Osteology Lab, Skeletal Biology Research Centre, School of Anthropology and Conservation, University of Kent, Canterbury, UK.</nlm:affiliation></affiliation></author><author><name sortKey="Schlecht, Stephen H" sort="Schlecht, Stephen H" uniqKey="Schlecht S" first="Stephen H" last="Schlecht">Stephen H. Schlecht</name><affiliation><nlm:affiliation>Department of Orthopaedic Surgery, University of Michigan, Ann Arbor, MI, USA.</nlm:affiliation></affiliation></author><author><name sortKey="Stewart, Tahlia J" sort="Stewart, Tahlia J" uniqKey="Stewart T" first="Tahlia J" last="Stewart">Tahlia J. Stewart</name><affiliation><nlm:affiliation>Skeletal Biology and Forensic Anthropology Research Group, School of Archaeology and Anthropology, Australian National University, Canberra, ACT, Australia.</nlm:affiliation></affiliation></author><author><name sortKey="Griffiths, Richard A" sort="Griffiths, Richard A" uniqKey="Griffiths R" first="Richard A" last="Griffiths">Richard A. Griffiths</name><affiliation><nlm:affiliation>Durrell Institute of Conservation and Ecology, School of Anthropology and Conservation, University of Kent, Canterbury, UK.</nlm:affiliation></affiliation></author><author><name sortKey="Deter, Chris" sort="Deter, Chris" uniqKey="Deter C" first="Chris" last="Deter">Chris Deter</name><affiliation><nlm:affiliation>Human Osteology Lab, Skeletal Biology Research Centre, School of Anthropology and Conservation, University of Kent, Canterbury, UK.</nlm:affiliation></affiliation></author><author><name sortKey="Guatelli Steinberg, Debbie" sort="Guatelli Steinberg, Debbie" uniqKey="Guatelli Steinberg D" first="Debbie" last="Guatelli-Steinberg">Debbie Guatelli-Steinberg</name><affiliation><nlm:affiliation>Department of Anthropology, The Ohio State University, Columbus, OH, USA.</nlm:affiliation></affiliation></author></analytic><series><title level="j">Journal of anatomy</title><idno type="eISSN">1469-7580</idno><imprint><date when="2017" type="published">2017</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Evidence of a periodic biorhythm is retained in tooth enamel in the form of Retzius lines. The periodicity of Retzius lines (RP) correlates with body mass and the scheduling of life history events when compared between some mammalian species. The correlation has led to the development of the inter-specific Havers-Halberg oscillation (HHO) hypothesis, which holds great potential for studying aspects of a fossil species biology from teeth. Yet, our understanding of if, or how, the HHO relates to human skeletal growth is limited. The goal here is to explore associations between the biorhythm and two hard tissues that form at different times during human ontogeny, within the context of the HHO. First, we investigate the relationship of RP to permanent molar enamel thickness and the underlying daily rate that ameloblasts secrete enamel during childhood. Following this, we develop preliminary research conducted on small samples of adult human bone by testing associations between RP, adult femoral length (as a proxy for attained adult stature) and cortical osteocyte lacunae density (as a proxy for the rate of osteocyte proliferation). Results reveal RP is positively correlated with enamel thickness, negatively correlated with femoral length, but weakly associated with the rate of enamel secretion and osteocyte proliferation. These new data imply that a slower biorhythm predicts thicker enamel for children but shorter stature for adults. Our results develop the intra-specific HHO hypothesis suggesting that there is a common underlying systemic biorhythm that has a role in the final products of human enamel and bone growth.</div></front></TEI><pubmed><MedlineCitation Status="Publisher" Owner="NLM"><PMID Version="1">29023695</PMID><DateCreated><Year>2017</Year><Month>10</Month><Day>12</Day></DateCreated><DateRevised><Year>2017</Year><Month>10</Month><Day>21</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1469-7580</ISSN><JournalIssue CitedMedium="Internet"><PubDate><Year>2017</Year><Month>Oct</Month><Day>10</Day></PubDate></JournalIssue><Title>Journal of anatomy</Title><ISOAbbreviation>J. Anat.</ISOAbbreviation></Journal><ArticleTitle>The biorhythm of human skeletal growth.</ArticleTitle><ELocationID EIdType="doi" ValidYN="Y">10.1111/joa.12709</ELocationID><Abstract><AbstractText>Evidence of a periodic biorhythm is retained in tooth enamel in the form of Retzius lines. The periodicity of Retzius lines (RP) correlates with body mass and the scheduling of life history events when compared between some mammalian species. The correlation has led to the development of the inter-specific Havers-Halberg oscillation (HHO) hypothesis, which holds great potential for studying aspects of a fossil species biology from teeth. Yet, our understanding of if, or how, the HHO relates to human skeletal growth is limited. The goal here is to explore associations between the biorhythm and two hard tissues that form at different times during human ontogeny, within the context of the HHO. First, we investigate the relationship of RP to permanent molar enamel thickness and the underlying daily rate that ameloblasts secrete enamel during childhood. Following this, we develop preliminary research conducted on small samples of adult human bone by testing associations between RP, adult femoral length (as a proxy for attained adult stature) and cortical osteocyte lacunae density (as a proxy for the rate of osteocyte proliferation). Results reveal RP is positively correlated with enamel thickness, negatively correlated with femoral length, but weakly associated with the rate of enamel secretion and osteocyte proliferation. These new data imply that a slower biorhythm predicts thicker enamel for children but shorter stature for adults. Our results develop the intra-specific HHO hypothesis suggesting that there is a common underlying systemic biorhythm that has a role in the final products of human enamel and bone growth.</AbstractText><CopyrightInformation>© 2017 Anatomical Society.</CopyrightInformation></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Mahoney</LastName><ForeName>Patrick</ForeName><Initials>P</Initials><Identifier Source="ORCID">http://orcid.org/0000-0002-2715-3096</Identifier><AffiliationInfo><Affiliation>Human Osteology Lab, Skeletal Biology Research Centre, School of Anthropology and Conservation, University of Kent, Canterbury, UK.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Miszkiewicz</LastName><ForeName>Justyna J</ForeName><Initials>JJ</Initials><AffiliationInfo><Affiliation>Skeletal Biology and Forensic Anthropology Research Group, School of Archaeology and Anthropology, Australian National University, Canberra, ACT, Australia.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Chapple</LastName><ForeName>Simon</ForeName><Initials>S</Initials><AffiliationInfo><Affiliation>Human Osteology Lab, Skeletal Biology Research Centre, School of Anthropology and Conservation, University of Kent, Canterbury, UK.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Le Luyer</LastName><ForeName>Mona</ForeName><Initials>M</Initials><AffiliationInfo><Affiliation>Human Osteology Lab, Skeletal Biology Research Centre, School of Anthropology and Conservation, University of Kent, Canterbury, UK.</Affiliation></AffiliationInfo><AffiliationInfo><Affiliation>De la Prehistoire à l'Actuel: Culture, Environment et Anthropologie (UMR 5199 PACEA), Université de Bordeaux, Pessac, France.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Schlecht</LastName><ForeName>Stephen H</ForeName><Initials>SH</Initials><AffiliationInfo><Affiliation>Department of Orthopaedic Surgery, University of Michigan, Ann Arbor, MI, USA.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Stewart</LastName><ForeName>Tahlia J</ForeName><Initials>TJ</Initials><AffiliationInfo><Affiliation>Skeletal Biology and Forensic Anthropology Research Group, School of Archaeology and Anthropology, Australian National University, Canberra, ACT, Australia.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Griffiths</LastName><ForeName>Richard A</ForeName><Initials>RA</Initials><AffiliationInfo><Affiliation>Durrell Institute of Conservation and Ecology, School of Anthropology and Conservation, University of Kent, Canterbury, UK.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Deter</LastName><ForeName>Chris</ForeName><Initials>C</Initials><AffiliationInfo><Affiliation>Human Osteology Lab, Skeletal Biology Research Centre, School of Anthropology and Conservation, University of Kent, Canterbury, UK.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Guatelli-Steinberg</LastName><ForeName>Debbie</ForeName><Initials>D</Initials><Identifier Source="ORCID">http://orcid.org/0000-0002-1345-5384</Identifier><AffiliationInfo><Affiliation>Department of Anthropology, The Ohio State University, Columbus, OH, USA.</Affiliation></AffiliationInfo></Author></AuthorList><Language>eng</Language><GrantList CompleteYN="Y"><Grant><GrantID>T32 DE007057</GrantID><Acronym>DE</Acronym><Agency>NIDCR NIH HHS</Agency><Country>United States</Country></Grant></GrantList><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2017</Year><Month>10</Month><Day>10</Day></ArticleDate></Article><MedlineJournalInfo><Country>England</Country><MedlineTA>J Anat</MedlineTA><NlmUniqueID>0137162</NlmUniqueID><ISSNLinking>0021-8782</ISSNLinking></MedlineJournalInfo><KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="N">Retzius line periodicity</Keyword><Keyword MajorTopicYN="N">daily enamel secretion rates</Keyword><Keyword MajorTopicYN="N">enamel thickness</Keyword><Keyword MajorTopicYN="N">osteocyte lacunar density</Keyword><Keyword MajorTopicYN="N">stature</Keyword></KeywordList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="accepted"><Year>2017</Year><Month>08</Month><Day>23</Day></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2017</Year><Month>10</Month><Day>13</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2017</Year><Month>10</Month><Day>13</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2017</Year><Month>10</Month><Day>13</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>aheadofprint</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">29023695</ArticleId><ArticleId IdType="doi">10.1111/joa.12709</ArticleId></ArticleIdList></PubmedData></pubmed></record>Pour manipuler ce document sous Unix (Dilib)
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