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14 - Preliminary Protocol to Identify Parturitions Lines in Acellular Cementum

from Part II - Protocols

Published online by Cambridge University Press:  20 January 2022

Stephan Naji
Affiliation:
New York University
William Rendu
Affiliation:
University of Bordeaux (CNRS)
Lionel Gourichon
Affiliation:
Université de Nice, Sophia Antipolis
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Summary

Dental tissues have the unique property of recording their development history as histological growth markers. Animal studies have shown that many stress events (birth, weaning, infections) can generate a chemical signature. Enamel and dentin offer a retrospective view of significant events occurring in growth but are limited in time to the end of the permanent dentition growth and development. Recent improvements in cementum histological analysis offer new perspectives for analyzing stressors and life history events throughout life. This chapter tests the hypothesis that pregnancy may disrupt acellular cementum (AC) deposits visible in the mineralized matrix, using light microscopy, Raman spectrometry, and scanning electron microscopy equipped with an EDS probe. Two human samples with known age at pregnancies demonstrated that accentuated AC increments can be identified and precisely matched to these events. In both samples, these AC variations were the most outstanding optically and chemically. This is notable since such a method’s ultimate purpose is to identify fertility events in archaeological samples blindly.

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Chapter
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Publisher: Cambridge University Press
Print publication year: 2022

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References

Alqahtani, S. J., Hector, M. P, and Liversidge, H. M. 2010. Brief communication: The London atlas of human tooth development and eruption. American Journal of Physical Anthropology 142(3): 481–90.CrossRefGoogle ScholarPubMed
Boyde, A., 1963. Estimation of age at death from young human skeletal remains from incremental lines in dental enamel. Third International Meeting in Forensic Immunology, Medicine, Pathology and Toxicology, London, 3646.Google Scholar
Buikstra, J. (2022). A brief history of cemental annuli research, with emphasis upon anthropological applications. In Naji, S., Gourichon, L., & Rendu, W., eds., Cementum in Anthropology: Back to the Root. Cambridge: Cambridge University Press, ch. 1.Google Scholar
Cool, S. M., Forwood, M. R, Campbell, P, and Bennett, M. B. 2002. Comparisons between bone and cementum compositions and the possible basis for their layered appearances. Bone 30(2): 386–92.Google Scholar
Blondiaux, J., Alduc-Le Bagousse, A., Niel, C., et al. 2006. Relevance of cement annulations to paleopathology. Paleopathology Newsletter 135: 415.Google Scholar
Cerrito, P., Bailey, S. E., Hu, B., et al. 2020. Parturitions, menopause and other physiological stressors are recorded in dental cementum microstructure. Scientific Reports 10(1): 110.CrossRefGoogle ScholarPubMed
Colard, T., Bertrand, B., Naji, S., Delannoy, Y., and Bécart, A.. 2015. Toward the adoption of cementochronology in forensic context. International Journal of Legal Medicine 129: 18.Google Scholar
Colard, T., Falgayrac, G., Bertrand, B., et al. 2016. New insights on the composition and the structure of the acellular extrinsic fiber cementum by Raman Analysis. PLoS ONE 11(12): e0167316.Google Scholar
Courbebaisse, M., and Souberbielle, J. C.. 2011. Phosphocalcic metabolism: Regulation and explorations. Nephrologie & Therapeutique 7(2): 118–38.Google Scholar
Dean, M. C. 1987. Growth layers and incremental markings in hard tissues: A review of the literature and some preliminary observations about enamel structure in Paranthropus boisei. Journal of Human Evolution 16: 157–72.Google Scholar
Dean, M. C. 2000. Incremental markings in enamel and dentine: What they can tell us about the way teeth grow. Development, Function and Evolution of Teeth, 119–30.Google Scholar
Dean, M. C., Le Cabec, A., Spiers, K., Zhang, Y., and Garrevoet, J.. 2018. Incremental distribution of strontium and zinc in great ape and fossil hominin cementum using synchrotron X-ray fluorescence mapping. Journal of the Royal Society Interface 15: 20170626.CrossRefGoogle ScholarPubMed
Falgayrac, G., et al. 2010. New method for Raman investigation of the orientation of collagen fibrils and crystallites in the Haversian system of bone. Applied Spectroscopy 64(7): 775–80.CrossRefGoogle ScholarPubMed
Ferreira, T., Kota, M., Bitdeli, C., and Eglinger, J.. 2015. Scripts: BAR 1.1.6 (Version 1.1.6). Zenodo. http://doi.org/10.5281/zenodo.28838Google Scholar
Giraud-Guille, M. M. 1988. Twisted plywood architecture of collagen fibrils in human compact bone osteons. Calcified Tissue International 42(3): 167–80.Google Scholar
Giraud-Guille, M. M., Besseau, L., and Martin, R.. 2003. Liquid crystalline assemblies of collagen in bone and in vitro systems. Journal of Biomechanics 36(10): 1571–9.CrossRefGoogle ScholarPubMed
Guatelli-Steinberg, D., Larsen, C. S., and Hutchsinson, D. L.. 2004. Prevalence and the duration of linear enamel hypoplasia: a comparative study of Neandertals and Inuit foragers. Journal of Human Evolution 47( 1–2): 6584.Google Scholar
Kagerer, P., and Grupe, G.. 2001. Age-at-death diagnosis and determination of life-history parameters by incremental lines in human dental cementum as an identification aid. Forensic Science International 118, 7582.CrossRefGoogle ScholarPubMed
Klevezal’, G. A. 1996. Recording Structures of Mammals: Determination of Age and Reconstruction of Life History. Rotterdam: A. A. Balkema Series.Google Scholar
Kovacs, C. S. 2005. Calcium and bone metabolism during pregnancy and lactation. Journal of Mammary Gland Biology and Neoplasia 10(2): 105–18.CrossRefGoogle ScholarPubMed
Kovacs, C. S. 2016. Maternal mineral and bone metabolism during pregnancy, lactation, and post-weaning recovery. Physiological Reviews 96(2): 449547.CrossRefGoogle ScholarPubMed
Kovacs, C. S. 2017. The skeleton is a storehouse of mineral that is plundered during lactation and (fully?) replenished afterwards. Journal of Bone and Mineral Research 32(4): 676–80.CrossRefGoogle ScholarPubMed
Lieberman, D. E. 1993. Life history variables preserved in dental cementum microstructure. Science 261(5125): 1162–64.Google Scholar
Mani-Caplazi, G., Hotz, G, Wittwer-Backofen, U., and Vach, W.. 2019. Measuring incremental line width and appearance in the tooth cementum of recent and archaeological human teeth to identify irregularities: First insights using a standardized protocol. International Journal of Paleopathology 27: 2437.Google Scholar
Naji, S., et al. 2016. Cementochronology, to cut or not to cut? International Journal of Paleopathology 15: 113–19.Google Scholar
Reid, D. J. and Dean, M. C. 2006. Variation in modern human enamel formation times. Journal of Human Evolution 50(3): 329–46.Google Scholar
Ristova, M., Talevska, M., and Stojanovska, Z.. 2018. Accurate age estimations from dental cementum and a childbirth indicator – A pilot study. Journal of Forensic Science & Criminology 6: 112.Google Scholar
Salari, P., and Abdollahi, M.. 2014. The influence of pregnancy and lactation on maternal bone health: A systematic review. Journal of Family & Reproductive Health 8(4): 135.Google Scholar
Schindelin, J., Arganda-Carreras, I., Frise, E, et al. 2012. Fiji: An open-source platform for biological-image analysis. Nature Methods 9(7): 676–82.CrossRefGoogle ScholarPubMed
Schwartz, G. T., Reid, D. J., Dean, M. C., and Zihlman, A. L.. 2006. A faithful record of stressful life events recorded in the dental developmental record of a juvenile gorilla. International Journal of Primatology 27: 1201–19.Google Scholar
Skinner, M., and Byra, C.. 2019. Signatures of stress: Pilot study of accentuated laminations in porcine enamel. American Journal of Physical Anthropology 169(4): 619–31.Google Scholar
Stock, S. R., et al. 2017. Cementum structure in beluga whale teeth. Acta Biomaterialia 48: 289–99.Google Scholar
Surarit, R., Krishnamra, N., and Seriwatanachai, D. 2016. Prolactin receptor and osteogenic induction of prolactin in human periodontal ligament fibroblasts. Cell Biology International 40(4): 419–27.Google Scholar
Wittwer-Backofen, U. 2012. Age estimation using tooth cementum annulation. In Forensic Microscopy for Skeletal Tissues. Bell, L. S (ed.). Totowa, NJ: Humana Press, 129–43.Google Scholar

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