Development and validation of an LC-MSMS method to quantify creatinine from dried blood spots
•Creatinine can be accurately measured from dried blood spots (DBS) using LC-MSMS.•DBS creatinine measurements were not significantly affected by varying hematocrit or blood spot volume.•DBS analysis of creatinine has the potential to improve access to CKD screening. Screening for chronic kidney dis...
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Veröffentlicht in: | Journal of mass spectrometry and advances in the clinical lab 2024-04, Vol.32, p.50-59 |
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Zusammenfassung: | •Creatinine can be accurately measured from dried blood spots (DBS) using LC-MSMS.•DBS creatinine measurements were not significantly affected by varying hematocrit or blood spot volume.•DBS analysis of creatinine has the potential to improve access to CKD screening.
Screening for chronic kidney disease relies on accurate and precise creatinine measurements. Traditionally, creatinine is measured in serum or plasma using high-throughput chemistry analyzers. However, dried blood spots (DBS) can also be utilized to improve testing access.
Samples were obtained from a 6 mm DBS punch, which was reconstituted in water before undergoing an acetonitrile crash. The resulting supernatant was diluted using an 80:20 acetonitrile: water before injection. Creatinine was identified using an isocratic gradient, and detected using an API 4000 triple quadrupole mass analyzer. Quantification relied on matrix-matched calibrators, with values harmonized to the Roche Cobas enzymatic assay. Validation studies assessing method performance included precision, linearity, accuracy, method comparison, stability, interference, and matrix effects.
The LC-MSMS assay was linear from 0.3 to 20 mg/dL (y = 1.02x-0.11; R2 = 0.996). Precision ranged from 5.2 to 8.1 % using matrix-matched controls (n = 4) that spanned the analytical measurement range. LC-MSMS results corresponded to the enzymatic assay (Roche) with a fitted line equation of y = 0.956x–0.07 (R2 = 0.995; n = 173). The Siemens and Roche enzymatic assays demonstrated higher accuracy in correlating to the DBS creatinine concentration (n = 40 paired venous/DBS collections) compared to the Beckman Jaffe assay (-2.5 % and −0.8 % versus −6.3 % and −4.1 %, respectively) or the iSTAT (-28.4 % and −27.1 %, respectively). Accuracy was unaffected by hematocrit, blood spot volume, excess IgG or IgA, or hypertriglyceridemia. No matrix effects were observed, and both extraction and processing efficiency were robust.
Ambient stability extended to at least 10 days, and exposure to extreme temperature did not affect the creatinine results.
We successfully developed an accurate and precise LC-MSMS method for quantifying creatinine in DBS. |
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ISSN: | 2667-145X 2667-1468 2667-145X |
DOI: | 10.1016/j.jmsacl.2024.03.001 |