TY - JOUR
T1 - Characterizing and Evaluating Diurnal Salivary Uric Acid Across Pregnancy Among Healthy Women
AU - Riis, Jenna L.
AU - Cook, Stephanie H.
AU - Letourneau, Nicole
AU - Campbell, Tavis
AU - Granger, Douglas A.
AU - Giesbrecht, Gerald F.
N1 - Funding Information:
Grant support for this work was provided by the Canadian Institutes of Health Research (201003MOP-219205) and The Alberta Centre for Child, Family & Community Research (100415TOP). SC is supported by several private and public grants. In particular, she is supported by the National Heart, Lung, and Blood Institute (R25HL105446-11; PI: Boutjdir) and the National Institute on Drug Abuse (R01 DA052426-01A1; PI: Bennet). The sponsors had no role in the study design, data collection, analysis and interpretation, writing of the report, or the decision to submit the article for publication.
Funding Information:
The authors gratefully acknowledge the participants of the Fetal Programming Study and Melinda van Sloten for assistance with biosample collection. We are extremely grateful to all the families who took part in this study and the whole APrON team (APrONstudy.ca), investigators, research assistants, graduate and undergraduate students, volunteers, clerical staff and mangers. This cohort was established by an interdisciplinary team grant from Alberta Innovates Health Solutions (formally the Alberta Heritage Foundation for Medical Research), Alberta Innovates Interdisciplinary Team Grant, and the Alberta Children’s Hospital Foundation. Additional funding from the Canadian Institutes of Health Research and The Alberta Centre for Child, Family & Community Research enabled the establishment of the Fetal Programming sub-cohort and the collection and analysis of the data presented in this manuscript. The authors thank Salimetrics LLC for the donation of salivary assay kits, Kaitlin Smith, Hillary Piccerillo, Tatum Stauffer, and Andrew Huang at the Institute for Interdisciplinary Salivary Bioscience Research for coordinating and conducting the biospecimen assay work, and Portia Shea for assistance with data analysis.
Funding Information:
The authors gratefully acknowledge the participants of the Fetal Programming Study and Melinda van Sloten for assistance with biosample collection. We are extremely grateful to all the families who took part in this study and the whole APrON team (APrONstudy.ca), investigators, research assistants, graduate and undergraduate students, volunteers, clerical staff and mangers. This cohort was established by an interdisciplinary team grant from Alberta Innovates Health Solutions (formally the Alberta Heritage Foundation for Medical Research), Alberta Innovates Interdisciplinary Team Grant, and the Alberta Children’s Hospital Foundation. Additional funding from the Canadian Institutes of Health Research and The Alberta Centre for Child, Family & Community Research enabled the establishment of the Fetal Programming sub-cohort and the collection and analysis of the data presented in this manuscript. The authors thank Salimetrics LLC for the donation of salivary assay kits, Kaitlin Smith, Hillary Piccerillo, Tatum Stauffer, and Andrew Huang at the Institute for Interdisciplinary Salivary Bioscience Research for coordinating and conducting the biospecimen assay work, and Portia Shea for assistance with data analysis.
Publisher Copyright:
Copyright © 2022 Riis, Cook, Letourneau, Campbell, Granger and Giesbrecht.
PY - 2022/3/18
Y1 - 2022/3/18
N2 - Uric acid levels during pregnancy have been examined as a potential indicator of risk for gestational diabetes mellites, hypertension, and related adverse birth outcomes. However, evidence supporting the utility of serum uric acid levels in predicting poor maternal and fetal health has been mixed. The lack of consistent findings may be due to limitations inherent in serum-based biomeasure evaluations, such as minimal repeated assessments and variability in the timing of these assessments. To address these gaps, we examined repeated measurements of diurnal salivary uric acid (sUA) levels in a sample of 44 healthy women across early-mid and late pregnancy. We assessed potential covariates and confounds of sUA levels and diurnal trajectories, as well as associations between maternal weight gain and blood pressure during pregnancy and sUA concentrations. Using multilevel linear models, we found sUA increased across pregnancy and displayed a robust diurnal pattern with the highest concentrations at waking, a steep decline in the early morning, and decreasing levels across the day. Maternal pre-pregnancy BMI, age, prior-night sleep duration, and fetal sex were associated with sUA levels and/or diurnal slopes. Maternal blood pressure and gestational weight gain also showed significant associations with sUA levels across pregnancy. Our results expand upon those found with serum UA measurements. Further, they demonstrate the feasibility of using at-home, minimally-invasive saliva sampling procedures to track UA levels across pregnancy with potential applications for the long-term monitoring of maternal cardiometabolic risk.
AB - Uric acid levels during pregnancy have been examined as a potential indicator of risk for gestational diabetes mellites, hypertension, and related adverse birth outcomes. However, evidence supporting the utility of serum uric acid levels in predicting poor maternal and fetal health has been mixed. The lack of consistent findings may be due to limitations inherent in serum-based biomeasure evaluations, such as minimal repeated assessments and variability in the timing of these assessments. To address these gaps, we examined repeated measurements of diurnal salivary uric acid (sUA) levels in a sample of 44 healthy women across early-mid and late pregnancy. We assessed potential covariates and confounds of sUA levels and diurnal trajectories, as well as associations between maternal weight gain and blood pressure during pregnancy and sUA concentrations. Using multilevel linear models, we found sUA increased across pregnancy and displayed a robust diurnal pattern with the highest concentrations at waking, a steep decline in the early morning, and decreasing levels across the day. Maternal pre-pregnancy BMI, age, prior-night sleep duration, and fetal sex were associated with sUA levels and/or diurnal slopes. Maternal blood pressure and gestational weight gain also showed significant associations with sUA levels across pregnancy. Our results expand upon those found with serum UA measurements. Further, they demonstrate the feasibility of using at-home, minimally-invasive saliva sampling procedures to track UA levels across pregnancy with potential applications for the long-term monitoring of maternal cardiometabolic risk.
KW - APrON study
KW - blood pressure (BP)
KW - body mass index - BMI
KW - diurnal pattern
KW - pregnancy
KW - saliva
KW - uric acid (UA)
UR - http://www.scopus.com/inward/record.url?scp=85128183181&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85128183181&partnerID=8YFLogxK
U2 - 10.3389/fendo.2022.813564
DO - 10.3389/fendo.2022.813564
M3 - Article
C2 - 35370953
AN - SCOPUS:85128183181
SN - 1664-2392
VL - 13
JO - Frontiers in Endocrinology
JF - Frontiers in Endocrinology
M1 - 813564
ER -