# Biochemical urine analysis of atorvastatin and rosuvastatin by LC-MS: a pilot study of an objective method to assess non-adherence

**Authors:** Maximilian Brockmeyer, Nadja Chernyak, Daniel Dröge, Hanna Wessel, Claudio Parco, Alexander Hoss, Kris G. Vargas, Yingfeng Lin, Annette Rickert, Stefanie Ritz, Andrea Icks, Malte Kelm, Georg Wolff, Oliver Temme

PMC · DOI: 10.1186/s12872-025-05475-0 · BMC Cardiovascular Disorders · 2026-01-09

## TL;DR

This study explores using urine tests to check if patients are taking their statin medications as prescribed, focusing on atorvastatin and rosuvastatin.

## Contribution

The study introduces a new method using LC-MS urine analysis to objectively assess adherence to high-potency statins.

## Key findings

- LC-MS urine analysis detected statin levels in most volunteers within one day of intake.
- After seven days, atorvastatin was undetectable in all volunteers, and rosuvastatin in 90%.
- Non-adherence was found to be low in the patient population studied.

## Abstract

Non-adherence to statins represents a contributing factor for poor attainment of low-density lipoprotein cholesterol treatment goals in secondary prevention of coronary artery disease (CAD). We aimed to establish urine analysis by liquid chromatography/mass spectrometry (LC-MS) as a method for objective measurement of non-adherence to high-potency statins. Additionally, we sought to apply the method to a population of ambulatory CAD patients at a German heart center in a cross-sectional pilot study.

Volunteers provided urine samples one, two, three, and seven days after intake of a single dose of atorvastatin and/or rosuvastatin. Additionally, urine samples from ambulatory CAD patients on prescription of atorvastatin or rosuvastatin were obtained. All urine samples were analyzed by LC-MS for concentrations of atorvastatin or rosuvastatin. Lower limits of detection were determined on spiked urine samples to define cut-off values (COVs) for the detection of statins (atorvastatin 1.40 ng/mL, rosuvastatin 1.00 ng/mL). Non-adherence was defined as a measurement of the respective statin below the COV.

On day one, in volunteers’ (n = 16, 37.3 ± 6 years, 81.3% male) urine samples, concentrations were above COV in 92.3% (atorvastatin, n = 13) and 90% (rosuvastatin, n = 10). After seven days, atorvastatin could not be detected in all 13 volunteers (100%) and rosuvastatin in nine of ten volunteers (90.0%),

LC-MS analysis of urine is a feasible method for direct testing of adherence to high-potency statins within a one-week time-window. In the investigated population of ambulatory patients with CAD, non-adherence to statins was found in a considerably low range.

ClinicalTrials.gov ID NCT05814692, first registered 20,230,403.

The online version contains supplementary material available at 10.1186/s12872-025-05475-0.

## Linked entities

- **Chemicals:** atorvastatin (PubChem CID 60823), rosuvastatin (PubChem CID 446157)
- **Diseases:** coronary artery disease (MONDO:0005010), CAD (MONDO:0005010)

## Full-text entities

- **Chemicals:** atorvastatin (MESH:D000069059), rosuvastatin (MESH:D000068718)

## Full text

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## Figures

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## References

2 references — full list in the complete paper: https://tomesphere.com/paper/PMC12836941/full.md

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Source: https://tomesphere.com/paper/PMC12836941