Rapid Detection of Lithium Concentrations in Oral Fluid

Author:

Granger Douglas A.12,Parkin Georgia M.13,Buspavanich Pichit4,Findeisen Peter5,Rietschel Marcella6,McCarthy Michael J.78,Thomas Elizabeth A.19

Affiliation:

1. Institute for Interdisciplinary Salivary Bioscience Research, University of California Irvine, California;

2. Johns Hopkins University School of Medicine, Baltimore, Maryland;

3. Department of Neurosciences, University of California San Diego, California;

4. Charité - Universitätsmedizin Berlin, Department of Psychiatry and Psychotherapy, Research Unit Gender in Medicine, Institute of Sexology and Sexual Medicine, Berlin, Germany;

5. MVZ Laboratory Limbach, Heidelberg, Germany;

6. Department of Genetic Epidemiology in Psychiatry, Central Institute of Mental Health Faculty of Medicine, Mannheim, University of Heidelberg, Mannheim, Germany;

7. Department of Psychiatry, University of California San Diego, California;

8. Veterans Affairs San Diego Healthcare System, San Diego, California; and

9. Department of Epidemiology, University of California Irvine, California.

Abstract

Background: Lithium medication is considered to be the first-line treatment for bipolar disorder as a monotherapy, and for treatment-resistant depression with lithium augmentation. However, because of potential toxicity, lithium levels must be monitored frequently. Recent studies have demonstrated a significant correlation between lithium levels measured in serum and those detected in oral fluid, suggesting that oral fluid analysis may represent an easy, noninvasive means to monitor lithium levels. The aim of this study was to evaluate the analytical performance of rapid assays for lithium measurements in oral fluid. Methods: Levels of lithium in oral fluid from psychiatric patients (n = 108 in total) taking lithium medications were quantified using 2 rapid techniques: an automated clinical chemistry analyzer and a novel, commercially available colorimetric lithium assay. These results were compared with those obtained using inductively coupled plasma optical emission spectrometry (ICP-OES). Results: The mean and median oral fluid lithium levels in this cohort were 1.43–1.61 mM and 1.32–1.52 mM, respectively, depending on the method, with the overall range, across all methods, being 0.213–4.42 mM. Linear regression analysis showed excellent agreement between the oral fluid values measured using ICP-OES and the colorimetric method (r2 value = 0.926; P < 0.0001; slope = 1.084 ± 0.038). Similarly, excellent agreement was observed between ICP-OES and the automated method (r2 = 0.872; P < 0.0001; slope = 1.019 ± 0.057). Conclusions: These results demonstrate that lithium levels in oral fluid can be rapidly and reliably quantified using colorimetric approaches. These findings may facilitate the development of point-of-care lithium monitoring systems for use in oral fluid.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Pharmacology (medical),Pharmacology

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