Human evolution and osteoporosis-related spinal fractures.

The field of evolutionary medicine examines the possibility that some diseases are the result of trade-offs made in human evolution. Spinal fractures are the most common osteoporosis-related fracture in humans, but are not observed in apes, even in cases of severe osteopenia. In humans, the developm...

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Autores principales: Meghan M Cotter, David A Loomis, Scott W Simpson, Bruce Latimer, Christopher J Hernandez
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Publicado: Public Library of Science (PLoS) 2011
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Acceso en línea:https://doaj.org/article/0333f72248274073b99b566c678aa8f6
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spelling oai:doaj.org-article:0333f72248274073b99b566c678aa8f62021-11-18T07:36:12ZHuman evolution and osteoporosis-related spinal fractures.1932-620310.1371/journal.pone.0026658https://doaj.org/article/0333f72248274073b99b566c678aa8f62011-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22028933/pdf/?tool=EBIhttps://doaj.org/toc/1932-6203The field of evolutionary medicine examines the possibility that some diseases are the result of trade-offs made in human evolution. Spinal fractures are the most common osteoporosis-related fracture in humans, but are not observed in apes, even in cases of severe osteopenia. In humans, the development of osteoporosis is influenced by peak bone mass and strength in early adulthood as well as age-related bone loss. Here, we examine the structural differences in the vertebral bodies (the portion of the vertebra most commonly involved in osteoporosis-related fractures) between humans and apes before age-related bone loss occurs. Vertebrae from young adult humans and chimpanzees, gorillas, orangutans, and gibbons (T8 vertebrae, n = 8-14 per species, male and female, humans: 20-40 years of age) were examined to determine bone strength (using finite element models), bone morphology (external shape), and trabecular microarchitecture (micro-computed tomography). The vertebrae of young adult humans are not as strong as those from apes after accounting for body mass (p<0.01). Human vertebrae are larger in size (volume, cross-sectional area, height) than in apes with a similar body mass. Young adult human vertebrae have significantly lower trabecular bone volume fraction (0.26±0.04 in humans and 0.37±0.07 in apes, mean ± SD, p<0.01) and thinner vertebral shells than apes (after accounting for body mass, p<0.01). Since human vertebrae are more porous and weaker than those in apes in young adulthood (after accounting for bone mass), even modest amounts of age-related bone loss may lead to vertebral fracture in humans, while in apes, larger amounts of bone loss would be required before a vertebral fracture becomes likely. We present arguments that differences in vertebral bone size and shape associated with reduced bone strength in humans is linked to evolutionary adaptations associated with bipedalism.Meghan M CotterDavid A LoomisScott W SimpsonBruce LatimerChristopher J HernandezPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 6, Iss 10, p e26658 (2011)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Meghan M Cotter
David A Loomis
Scott W Simpson
Bruce Latimer
Christopher J Hernandez
Human evolution and osteoporosis-related spinal fractures.
description The field of evolutionary medicine examines the possibility that some diseases are the result of trade-offs made in human evolution. Spinal fractures are the most common osteoporosis-related fracture in humans, but are not observed in apes, even in cases of severe osteopenia. In humans, the development of osteoporosis is influenced by peak bone mass and strength in early adulthood as well as age-related bone loss. Here, we examine the structural differences in the vertebral bodies (the portion of the vertebra most commonly involved in osteoporosis-related fractures) between humans and apes before age-related bone loss occurs. Vertebrae from young adult humans and chimpanzees, gorillas, orangutans, and gibbons (T8 vertebrae, n = 8-14 per species, male and female, humans: 20-40 years of age) were examined to determine bone strength (using finite element models), bone morphology (external shape), and trabecular microarchitecture (micro-computed tomography). The vertebrae of young adult humans are not as strong as those from apes after accounting for body mass (p<0.01). Human vertebrae are larger in size (volume, cross-sectional area, height) than in apes with a similar body mass. Young adult human vertebrae have significantly lower trabecular bone volume fraction (0.26±0.04 in humans and 0.37±0.07 in apes, mean ± SD, p<0.01) and thinner vertebral shells than apes (after accounting for body mass, p<0.01). Since human vertebrae are more porous and weaker than those in apes in young adulthood (after accounting for bone mass), even modest amounts of age-related bone loss may lead to vertebral fracture in humans, while in apes, larger amounts of bone loss would be required before a vertebral fracture becomes likely. We present arguments that differences in vertebral bone size and shape associated with reduced bone strength in humans is linked to evolutionary adaptations associated with bipedalism.
format article
author Meghan M Cotter
David A Loomis
Scott W Simpson
Bruce Latimer
Christopher J Hernandez
author_facet Meghan M Cotter
David A Loomis
Scott W Simpson
Bruce Latimer
Christopher J Hernandez
author_sort Meghan M Cotter
title Human evolution and osteoporosis-related spinal fractures.
title_short Human evolution and osteoporosis-related spinal fractures.
title_full Human evolution and osteoporosis-related spinal fractures.
title_fullStr Human evolution and osteoporosis-related spinal fractures.
title_full_unstemmed Human evolution and osteoporosis-related spinal fractures.
title_sort human evolution and osteoporosis-related spinal fractures.
publisher Public Library of Science (PLoS)
publishDate 2011
url https://doaj.org/article/0333f72248274073b99b566c678aa8f6
work_keys_str_mv AT meghanmcotter humanevolutionandosteoporosisrelatedspinalfractures
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AT scottwsimpson humanevolutionandosteoporosisrelatedspinalfractures
AT brucelatimer humanevolutionandosteoporosisrelatedspinalfractures
AT christopherjhernandez humanevolutionandosteoporosisrelatedspinalfractures
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