Analysis of LCT-13910 genotypes and bone mineral density in ancient skeletal materials

PLoS One. 2018 Apr 30;13(4):e0194966. doi: 10.1371/journal.pone.0194966. eCollection 2018.

Abstract

The relation of LCT-13910 genotypes and bone mineral density (BMD) has been the subject of modern-day human population studies, giving inconsistent results. In the present study we analyze for the first time a relation of LCT-13910 genotypes and BMD in historical skeletal individuals. Ancient population might be a model for testing this association due to elimination of non-natural factors affecting bone density. Among 22 medieval individuals from Sanok churchyard (South-Eastern Poland; dated from XIV to XVII c. AD) we identified 4 individuals with osteoporosis (mean BMD = 0.468 g/cm2, SD = 0.090), 10 individuals with osteopenia (mean BMD = 0.531 g/cm2, SD = 0.066) and 8 individuals with normal BMD values (mean BMD = 0,642 g/cm2, SD = 0.060). Analyses of BMD and LCT-13910 genotypes revealed that mean BMD was the highest (0.583 g/cm2, SD = 0.065) in the individuals with lactose tolerance genotypes (TT and CT). We also found possible association of lower BMD at the radius and CC genotypes due to higher but not statistically significant frequency of osteoporosis in the lactose intolerant group (p = 0.60). Statistically significant correlation was found between BMD and females aged 20-35 years, with tendency to reduce BMD with age (p = 0.02).

Publication types

  • Historical Article
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Anthropology
  • Bone Density / genetics*
  • Bone and Bones / metabolism*
  • Bone and Bones / pathology
  • Female
  • Genetic Markers
  • Genotype
  • History, 15th Century
  • History, 16th Century
  • History, 17th Century
  • History, Medieval
  • Humans
  • Lactase-Phlorizin Hydrolase / genetics
  • Lactose Intolerance / genetics*
  • Male
  • Middle Aged
  • Minichromosome Maintenance Complex Component 6 / genetics*
  • Poland
  • Polymorphism, Single Nucleotide*
  • Young Adult

Substances

  • Genetic Markers
  • Lactase-Phlorizin Hydrolase
  • MCM6 protein, human
  • Minichromosome Maintenance Complex Component 6

Grants and funding

This work was supported by grant project awarded by Uniwersytet Jagielloński w Krakowie [DS/MND/WBiNoZ/IZ/37/2015 to B.M]. The funder had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.