TY - JOUR
T1 - Pregnancy-Related Bone Mineral and Microarchitecture Changes in Women Aged 30 to 45 Years
AU - Ó Breasail, Mícheál
AU - Prentice, Ann
AU - Ward, Kate
N1 - Funding Information:
The authors acknowledge the contribution of the study participants; Jenny Woolston of MRC Elsie Widdowson Laboratory, who helped with ethical application and study setup; Drs Catherine Aiken and Jeremy Brockelsby for local oversight; Julie Holgate and Sue Tiplady of the Rosie Hospital (Cambridge University Hospital) for study recruitment; Darren Cole of MRC Elsie Widdowson Laboratory for database creation and pQCT cleaning tool design; and Millie Parsons of MRC Lifecourse Epidemiology Unit for statistical advice. This research was conducted under the Medical Research Council Program Grant Code U105960371.
Funding Information:
The authors acknowledge the contribution of the study participants; Jenny Woolston of MRC Elsie Widdowson Laboratory, who helped with ethical application and study setup; Drs Catherine Aiken and Jeremy Brockelsby for local oversight; Julie Holgate and Sue Tiplady of the Rosie Hospital (Cambridge University Hospital) for study recruitment; Darren Cole of MRC Elsie Widdowson Laboratory for database creation and pQCT cleaning tool design; and Millie Parsons of MRC Lifecourse Epidemiology Unit for statistical advice. This research was conducted under the Medical Research Council Program Grant Code U105960371. Authors' roles: Study design: MOB, KW, and AP. Study conduct: MOB and KW. Data collection: MOB. Data analysis: MOB and KW. Data interpretation: MOB, KW, and AP. Drafting manuscript: MOB, KW, and AP. Revising manuscript content: MOB, KW, and AP. Approving final version of manuscript: MOB, KW, and AP. MOB takes responsibility for the integrity of the data analysis.
Publisher Copyright:
© 2020 Crown copyright. Journal of Bone and Mineral Research published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research (ASBMR). This article is published with the permission of the Controller of HMSO and the Queen's Printer for Scotland.
PY - 2020/7
Y1 - 2020/7
N2 - At birth, the neonatal skeleton contains 20 to 30 g calcium (Ca). It is hypothesized maternal bone mineral may be mobilized to support fetal skeletal development, although evidence of pregnancy-induced mineral mobilization is limited. We recruited healthy pregnant (n = 53) and non-pregnant non-lactating (NPNL; n = 37) women aged 30 to 45 years (mean age 35.4 ± 3.8 years) and obtained peripheral quantitative computed tomography (pQCT) and high-resolution pQCT (HR-pQCT) scans from the tibia and radius at 14 to 16 and 34 to 36 weeks of pregnancy, with a similar scan interval for NPNL. Multiple linear regression models were used to assess group differences in change between baseline and follow-up; differences are expressed as standard deviation scores (SDS) ± SEM. Decreases in volumetric bone mineral density (vBMD) outcomes were found in both groups; however, pregnancy-related decreases for pQCT total and trabecular vBMD were −0.65 ± 0.22 SDS and −0.50 ± 0.23 SDS greater (p <.05). HR-pQCT total and cortical vBMD decreased compared with NPNL by −0.49 ± 0.24 SDS and −0.67 ± 0.23 SDS, respectively; trabecular vBMD decreased in both groups to a similar magnitude. Pregnancy-related changes in bone microarchitecture significantly exceeded NPNL change for trabecular number (0.47 ± 0.23 SDS), trabecular separation (−0.54 ± 0.24 SDS), cortical thickness (−1.01 ± 0.21 SDS), and cortical perimeter (0.78 ± 0.23 SDS). At the proximal radius, cortical vBMD and endosteal circumference increased by 0.50 ± 0.23 SDS and 0.46 ± 0.23 SDS, respectively, compared with NPNL, whereas cortical thickness decreased −0.50 ± 0.22 SDS. Pregnancy-related decreases in total and compartment-specific vBMD exceed age-related change at the distal tibia. Changes at the radius were only evident with pQCT at the cortical-rich proximal site and suggest endosteal resorption. Although the magnitude of these pregnancy-related changes in the appendicular skeleton are small, if they reflect global changes across the skeleton at large, they may contribute substantially to the Ca requirements of the fetus.
AB - At birth, the neonatal skeleton contains 20 to 30 g calcium (Ca). It is hypothesized maternal bone mineral may be mobilized to support fetal skeletal development, although evidence of pregnancy-induced mineral mobilization is limited. We recruited healthy pregnant (n = 53) and non-pregnant non-lactating (NPNL; n = 37) women aged 30 to 45 years (mean age 35.4 ± 3.8 years) and obtained peripheral quantitative computed tomography (pQCT) and high-resolution pQCT (HR-pQCT) scans from the tibia and radius at 14 to 16 and 34 to 36 weeks of pregnancy, with a similar scan interval for NPNL. Multiple linear regression models were used to assess group differences in change between baseline and follow-up; differences are expressed as standard deviation scores (SDS) ± SEM. Decreases in volumetric bone mineral density (vBMD) outcomes were found in both groups; however, pregnancy-related decreases for pQCT total and trabecular vBMD were −0.65 ± 0.22 SDS and −0.50 ± 0.23 SDS greater (p <.05). HR-pQCT total and cortical vBMD decreased compared with NPNL by −0.49 ± 0.24 SDS and −0.67 ± 0.23 SDS, respectively; trabecular vBMD decreased in both groups to a similar magnitude. Pregnancy-related changes in bone microarchitecture significantly exceeded NPNL change for trabecular number (0.47 ± 0.23 SDS), trabecular separation (−0.54 ± 0.24 SDS), cortical thickness (−1.01 ± 0.21 SDS), and cortical perimeter (0.78 ± 0.23 SDS). At the proximal radius, cortical vBMD and endosteal circumference increased by 0.50 ± 0.23 SDS and 0.46 ± 0.23 SDS, respectively, compared with NPNL, whereas cortical thickness decreased −0.50 ± 0.22 SDS. Pregnancy-related decreases in total and compartment-specific vBMD exceed age-related change at the distal tibia. Changes at the radius were only evident with pQCT at the cortical-rich proximal site and suggest endosteal resorption. Although the magnitude of these pregnancy-related changes in the appendicular skeleton are small, if they reflect global changes across the skeleton at large, they may contribute substantially to the Ca requirements of the fetus.
KW - AGING
KW - ANALYSIS/QUANTITATION OF BONE
KW - BONE QCT/μCT
KW - EPIDEMIOLOGY
KW - GENERAL POPULATION STUDIES
UR - https://www.scopus.com/pages/publications/85082968168
U2 - 10.1002/jbmr.3998
DO - 10.1002/jbmr.3998
M3 - Article
C2 - 32119748
AN - SCOPUS:85082968168
SN - 0884-0431
VL - 35
SP - 1253
EP - 1262
JO - Journal of Bone and Mineral Research
JF - Journal of Bone and Mineral Research
IS - 7
ER -