Home Low-dose oral methotrexate-induced crystalluria
Article Open Access

Low-dose oral methotrexate-induced crystalluria

  • Santiago A. Lojo-Rocamonde ORCID logo EMAIL logo and Susana B. Bravo-López
Published/Copyright: October 22, 2020

To the Editor,

A 56-year-old man with psoriatic arthritis was prescribed oral methotrexate (15 mg each week every Sunday at around 13:00 UTC). No other relevant medication was administered. After 42 h, a routine control analysis was performed without significant abnormal results. Solely and surprisingly, a large number of crystals were observed in the urine sample in the absence of risk factors of drug-induced precipitation or other causes of crystal nephropathy, except an acidic pH of 5.5, the primary cause (along with volume depletion) of drug precipitation [1]. A possible, yet remote, cause points to a high intake of cola drinks during several days preceding the drug administration [2], as the patient has explicitly acknowledged. The capture of the images took place within the 90 min after micturition, and the spectral data throughout the same morning. One urine collected 10 weeks before and other three analyzed 3, 6 days and 7 weeks later showed no abnormalities, as well as no symptoms during urination. The sequence of analysis was as follows:

  1. Ten weeks before (without treatment): Creatinine 71 µmol/L, eGFR(CKD-EPI) >90 mL/min/1.73 m2, albumin 46 g/L, urea 6.16 mmol/L, GGT 20 IU/L, sodium 144 mmol/L, potassium 4.6 mmol/L and erythrocyte count 4.52 × 1012/L. Normal urine (negative results for elemental analysis), specific gravity 1025 and pH 5.5 (“Clinitek Atlas” analyzer, “Multistix Pro-10LS” strips [Siemens Healthcare, Tarrytown, NY, USA]). No crystals.

  2. On the same day that urine cloudy sediment (case study): Creatinine 73 µmol/L, eGFR >90 mL/min/1.73 m2, albumin 47 g/L, urea 8.16 mmol/L, GGT 21 IU/L, sodium 141 mmol/L, potassium 4.3 mmol/L and erythrocyte count 4.49 × 1012/L. Normal urine (negative results for elemental analysis), specific gravity 1020 and pH 5.5.

  3. Three days after (continuing oral treatment): Normal urine (negative results for elemental analysis), specific gravity 1020 and pH 6.5. No crystals.

  4. Six days later (continuing oral treatment): Normal urine (negative results for elemental analysis), specific gravity 1025 and pH 6.5. No crystals.

The deposit was made up of a needle-shaped unit arranged in other three structures: (I) Toothpick-like elemental formation, (II) shell-like macle, (III) symmetric or asymmetric wheat-sheaf-like macle, and (IV) aggregates of the previous macles linked by the “isthmus/narrow” zone (Figure 1A). All these are strongly birefringent (Figure 1B, C). The basic shape of this polymorphic crystalline habit would be a “type-V solvatomorph of Chadha” ([3] see Figure 5f) in our patient. It has not been previously described.

Figure-1: 
Microscopic imaging.
Light-microscopy images of urinary methotrexate crystals, where the four structures (I–IV quoted in the text) can be observed (A). Polarized light-microscopy image: (B) polarizer and analyzer placed at right angle and (C) nearly parallel (“DM-LSP” [Leica Microsystems, Wetzlar, Germany]).
Figure-1:

Microscopic imaging.

Light-microscopy images of urinary methotrexate crystals, where the four structures (I–IV quoted in the text) can be observed (A). Polarized light-microscopy image: (B) polarizer and analyzer placed at right angle and (C) nearly parallel (“DM-LSP” [Leica Microsystems, Wetzlar, Germany]).

The rarity of this precipitate made it necessary the positive identification to authenticate the nature of these crystals. A mass spectrometry (MS) procedure was used for this purpose [4]. The spectra confirm that this drug is the major component of the floccular, whitish and bulky precipitate appeared in the case urine of the patient (Figure 2A), as well as its “in vivo” metabolites (Figure 2B). To our knowledge, this is the first case positively confirmed of a urinary methotrexate precipitate in patients without intravenous administration [5], [6], [7], [8], [9], [10].

Figure-2: 
Spectral data of the precipitate after washing and concentration steps.
(A) MS and MS/MS spectra (“4800 MALDI ToF/ToF MS” [AB-SCIEX, Framingham, MA, USA]) with the methotrexate ion-molecular peak (m/z=456; up, red arrow) and its defining fragments (m/z=455.67, 339.88, 251.07, 180.09; down, red asterisks). (B) MS peaks of “in vivo” metabolites (m/z=325: 2,4-diamino-N10-methylpteroic acid (DAMPA) and m/z=471: 7-hydroxymethotrexate [7-OH-MTX]) resulting from additional spectral data, an unambiguous demonstration of the nature of this well formed crystalline habit.
Figure-2:

Spectral data of the precipitate after washing and concentration steps.

(A) MS and MS/MS spectra (“4800 MALDI ToF/ToF MS” [AB-SCIEX, Framingham, MA, USA]) with the methotrexate ion-molecular peak (m/z=456; up, red arrow) and its defining fragments (m/z=455.67, 339.88, 251.07, 180.09; down, red asterisks). (B) MS peaks of “in vivo” metabolites (m/z=325: 2,4-diamino-N10-methylpteroic acid (DAMPA) and m/z=471: 7-hydroxymethotrexate [7-OH-MTX]) resulting from additional spectral data, an unambiguous demonstration of the nature of this well formed crystalline habit.

Following seven weeks (continuing oral treatment), a new control analysis showed normal results again: Creatinine 70 µmol/L, eGFR >90 mL/min/1.73 m2, albumin 44 g/L, urea 4.66 mmol/L, GGT 17 IU/L, sodium 144 mmol/L, potassium 4.3 mmol/L and erythrocyte count 4.39 × 1012/L. Normal urine (negative results for elemental analysis), specific gravity 1015 and pH 7.0 and absence of crystals. Furthermore, the lack of symptoms of acute renal impairment did not support a renal biopsy. This fact demonstrates the need for a skillfull and more closely urine sediments even in low-dose treatment.


Corresponding author: Santiago A. Lojo-Rocamonde, Clinical Analysis Service, Montecelo Hospital, r/Mourente s/n, 36701, Pontevedra, Spain. E-mail: .

  1. Research funding: None declared.

  2. Author contributions: Both authors have accepted responsibility for the entire content of this manuscript and approved its submission.

  3. Competing interests: None of the authors states no conflict of interest.

  4. Informed consent: Informed consent was obtained from the individual included in this study.

  5. Ethical approval: Not applicable.

References

1. Sand, TE, Jacobsen, S. Effect of urine pH and flow on renal clearance of methotrexate. Eur J Clin Pharmacol 1981;19:453–6. https://doi.org/10.1007/bf00548590.Search in Google Scholar PubMed

2. Santucci, R, Levêque, D, Herbrecht, R. Cola beverage and delayed elimination of methotrexate. Br J Clin Pharmacol 2010;70:762–4. https://doi.org/10.1111/j.1365-2125.2010.03744.x.Search in Google Scholar PubMed PubMed Central

3. Chadha, R, Arora, P, Kaur, R, Saini, A, Singla, ML, Jain, DS. Characterization of solvatomorphs of methotrexate using thermoanalytical and other techniques. Acta Pharm 2009;59:245–7. https://doi.org/10.2478/v10007-009-0024-9.Search in Google Scholar PubMed

4. Bouquié, R, Deslandes, G, Nieto-Bernáldez, B, Renaud, C, Dailly, E, Jolliet, P. A fast LC-MS/MS assay for methotrexate monitoring in plasma: validation, comparison to FPIA and application in the setting of carboxypeptidase therapy. Anal Meth 2014;6:178–86. https://doi.org/10.1039/c3ay40815a.Search in Google Scholar

5. Mallipattu, SK, Ross, MJ. Methotrexate in the urine. Kidney Int 2011;80:226. https://doi.org/10.1038/ki.2011.97.Search in Google Scholar PubMed

6. Luciano, RL, Perazella, MA. Crystalline-induced kidney disease: a case for urine microscopy. Clin Kidney J 2015;8:131–6. https://doi.org/10.1093/ckj/sfu105.Search in Google Scholar PubMed PubMed Central

7. Perazella, MA, Luciano, RL. Review of select causes of drug-induced acute renal impairment. Expert Rev Clin Pharmacol 2015;8:367–71. https://doi.org/10.1586/17512433.2015.1045489.Search in Google Scholar PubMed

8. Garneau, AP, Riopel, J, Isenring, P. N Eng J Med 2015;373:2691–3. https://doi.org/10.1056/nejmc1507547.Search in Google Scholar PubMed

9. Pazhayattil, GS, Brewster, UC, Perazella, MA. A case of crystalline nephropathy. Kidney Int 2015;87:1265–6. https://doi.org/10.1038/ki.2014.317.Search in Google Scholar PubMed

10. Mamlouk, O, Hninn, WY, Mandayam, S, Workeneh, B. Acute kidney injury associated with high dose methotrexate. J Onco-Nephrol 2020;4:64–5. https://doi.org/10.1177/2399369319886865.Search in Google Scholar

Received: 2020-08-19
Accepted: 2020-10-08
Published Online: 2020-10-22
Published in Print: 2021-03-26

© 2020 Santiago A. Lojo-Rocamonde and Susana B. Bravo-López, published by De Gruyter, Berlin/Boston

This work is licensed under the Creative Commons Attribution 4.0 International License.

Articles in the same Issue

  1. Frontmatter
  2. Editorials
  3. Perspectives in developments of mass spectrometry for improving diagnosis and monitoring of multiple myeloma and other plasma cell disorders
  4. Cytokine “storm”, cytokine “breeze”, or both in COVID-19?
  5. Review
  6. Clinical relevance of biological variation of cardiac troponins
  7. General Clinical Chemistry and Laboratory Medicine
  8. Development of novel methods for non-canonical myeloma protein analysis with an innovative adaptation of immunofixation electrophoresis, native top-down mass spectrometry, and middle-down de novo sequencing
  9. Falsely markedly elevated 25-hydroxyvitamin D in patients with monoclonal gammopathies
  10. Development of a pregnancy-specific reference material for thyroid biomarkers, vitamin D, and nutritional trace elements in serum
  11. Applying the concept of uncertainty to the sFlt-1/PlGF cut-offs for diagnosis and prognosis of preeclampsia
  12. Reducing sample rejection in Durban, South Africa
  13. Quality benchmarking of smartphone laboratory medicine applications: comparison of laboratory medicine specialists’ and non-laboratory medicine professionals’ evaluation
  14. Urine soluble CD163 (sCD163) as biomarker in glomerulonephritis: stability, reference interval and diagnostic performance
  15. Measurement of urine albumin by liquid chromatography-isotope dilution tandem mass spectrometry and its application to value assignment of external quality assessment samples and certification of reference materials
  16. Choice of faecal immunochemical test matters: comparison of OC-Sensor and HM-JACKarc, in the assessment of patients at high risk of colorectal cancer
  17. Reference Values and Biological Variations
  18. Reference values of trace elements in blood and/or plasma in adults living in Belgium
  19. Cancer Diagnostics
  20. Clinical performance of calcitonin and procalcitonin Elecsys® immunoassays in patients with medullary thyroid carcinoma
  21. Cardiovascular Diseases
  22. Analytical assessment of ortho clinical diagnostics high-sensitivity cardiac troponin I assay
  23. Evaluation of the 0 h/1 h high-sensitivity cardiac troponin T algorithm in diagnosis of non-ST-segment elevation myocardial infarction (NSTEMI) in Han population
  24. Diabetes
  25. Are hemoglobin A1c point-of-care analyzers fit for purpose? The story continues
  26. Infectious Diseases
  27. Diagnostic and prognostic role of presepsin in patients with cirrhosis and bacterial infection
  28. Hemocytometric characteristics of COVID-19 patients with and without cytokine storm syndrome on the sysmex XN-10 hematology analyzer
  29. Letters to the Editor
  30. Letter in reply to the letter to the editor of Geerts N and Schanhorst V with the title “Roche Troponin T hs-STAT meets all expert opinion analytical laboratory practice recommendations for the use of the differential diagnosis of acute coronary syndrome”
  31. Improving measurement uncertainty of plasma electrolytes: a complex but not impossible task
  32. Truncation limits of patient-based real-time quality control: a new model derived from between-subject biological variations
  33. Plasma xanthine oxidoreductase activity change over 12 months independently associated with change in serum uric acid level: MedCity21 health examination registry
  34. Exogenous triglycerides interfere with a point of care CRP assay: a pre-analytical caveat
  35. Monoclonal components in alpha-2 region should not be neglected in capillary electrophoresis
  36. Do not measure an extra high value monoclonal IgM by immunoturbidity: a case report
  37. Reference values for plasma neurofilament light chain (NfL) in healthy Chinese
  38. Diagnosis of vitamin B12 deficiency: combined indicator of B12-status should be interpreted with caution in the case of renal impairment
  39. Could the UKNEQAS program “Manual Differential Blood Count” be performed by the use of an automated digital morphology analyzer (Sysmex DI-60)? A feasibility study
  40. Low-dose oral methotrexate-induced crystalluria
Downloaded on 12.9.2025 from https://www.degruyterbrill.com/document/doi/10.1515/cclm-2020-1268/html
Scroll to top button