Commentary - (2025) Volume 17, Issue 1
Received: 01-Feb-2025, Manuscript No. jbabm-25-168521;
Editor assigned: 03-Feb-2025, Pre QC No. P-168521;
Reviewed: 17-Feb-2025, QC No. Q-168521;
Revised: 22-Feb-2025, Manuscript No. R-168521;
Published:
28-Feb-2025
, DOI: 10.37421/1948-593X.2025.17.472
Citation: Torres, Alejandro. “Comparative Study of Saliva and Plasma in Hormone Level Monitoring.” J Bioanal Biomed 17 (2025): 472.
Copyright: © 2025 Torres A. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
In this study, we evaluated the concentrations of key hormones cortisol, testosterone, estradiol, and progesterone in matched saliva and plasma samples from a cohort of 120 individuals, comprising both healthy volunteers and patients undergoing hormonal therapy. Samples were collected under controlled conditions at specific times of day to account for circadian fluctuations. Saliva was collected using passive drool or swab techniques, while plasma was extracted via venipuncture. Hormone levels were quantified using high-sensitivity immunoassays and liquid Chromatography-Tandem Mass Spectrometry (LC-MS/MS), which allowed for the precise detection of both total and free hormone fractions.
The results revealed a strong positive correlation between salivary and plasma free hormone levels, particularly for cortisol and testosterone (Pearson's r > 0.85, p < 0.001). These findings support previous research suggesting that salivary measurements reliably reflect the unbound, bioactive portion of hormones available to tissues, which is often more clinically relevant than total plasma concentrations. For estradiol and progesterone, the correlation was moderate (r = 0.65â??0.75), influenced by factors such as sample timing, menstrual cycle phase, and salivary flow rate. Nonetheless, salivary estradiol still showed consistent patterns with plasma levels in tracking ovulatory cycles and hormonal replacement therapies in women.
One of the most compelling advantages of salivary hormone testing is its ability to capture diurnal variation and dynamic hormonal changes without inducing stress, which can itself skew cortisol and other hormone measurements. Repeated sampling throughout the day allowed for detailed mapping of cortisol awakening response and diurnal decline, offering insights into Hypothalamicâ??Pituitaryâ??Adrenal (HPA) axis function. This is particularly valuable in the assessment of stress-related disorders, chronic fatigue, and adrenal insufficiency. In contrast, plasma-based testing often provides only a single-point snapshot, which may not fully represent hormonal rhythm or functional reserve.
However, salivary testing is not without challenges. Contamination from food, bleeding gums, or improper sample handling can affect results. Additionally, lower hormone concentrations in saliva necessitate ultra-sensitive detection methods, and reference ranges are less standardized compared to plasma assays. Inter-individual variability in salivary flow rate and pH can also influence hormone partitioning and recovery. Despite these hurdles, advances in assay technologies and standardized collection protocols have significantly improved the reliability and clinical applicability of salivary hormone testing [2].
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