Skip to main content
Log in

Discrimination model applied to urinalysis of patients with diabetes and hypertension aiming at diagnosis of chronic kidney disease by Raman spectroscopy

  • Original Article
  • Published:
Lasers in Medical Science Aims and scope Submit manuscript

Abstract

Higher blood pressure level and poor glycemic control in diabetic patients are considered progression factors that cause faster decline in kidney functions leading to kidney damage. The present study aimed to develop a quantification model of biomarkers creatinine, urea, and glucose by means of selected peaks of these compounds, measured by Raman spectroscopy, and to estimate the concentration of these analytes in the urine of normal subjects (G_N), diabetic patients with hypertension (G_WOL) patients with chronic renal failure doing dialysis (G_D). Raman peak intensities at 680 cm−1 (creatinine), 1004 cm−1 (urea), and 1128 cm−1 (glucose) from normal, diabetic, and hypertensive and doing dialysis patients, obtained with a dispersive 830 nm Raman spectrometer, were estimated through Origin software. Spectra of creatinine, urea, and glucose diluted in water were also obtained, and the same peaks were evaluated. A discrimination model based on Mahalanobis distance was developed. It was possible to determine the concentration of creatinine, urea, and glucose by means of the Raman peaks of the selected biomarkers in the urine of the groups G_N, G_WOL, and G_D (r = 0.9). It was shown that the groups G_WOL and G_D had lower creatinine and urea concentrations than the group G_N (p < 0.05). The classification model based on Mahalanobis distance applied to the concentrations of creatinine, urea, and glucose presented a correct classification of 89% for G_N, 86% for G_WOL, and 79% for G_D. It was possible to obtain quantitative information regarding important biomarkers in urine for the assessment of renal impairment in patients with diabetes and hypertension, and this information can be correlated with clinical criteria for the diagnosis of chronic kidney disease.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5

Similar content being viewed by others

References

  1. Eknoyan G, Lameire N, Barsoum R, Eckardt KU, Levin A, Locatelli F et al (2004) The burden of kidney disease: improving global outcomes. Kidney Int 66:1310–1314

    Article  PubMed  Google Scholar 

  2. Sesso RCC, Lopes AA, Thomé FS, Lugon JR, Santos DR (2011) Chronic dialysis in Brazil—report of the Brazilian dialysis census. J Bras Nefrol 34:272–277

    Article  Google Scholar 

  3. Hall JE (2011) Guyton and hall textbook of medical physiology, 12th edn. Elsevier Saunders, Philadelphia

    Google Scholar 

  4. Kumar V, Abbas AK, Aster JC (2014) Robbins & Cotran pathologic basis of disease, 9th edn. Elsevier Saunders, Philadelphia

    Google Scholar 

  5. National Kidney Foundation (2003) K/DOQI clinical practice guidelines for chronic kidney disease: evaluation, classification and stratification. Am J Kidney Dis 39:1–266

    Google Scholar 

  6. Bishop ML, Fody EP, Shoeff LE (2013) Clinical chemistry: principles, techniques, and correlations, 7th edn. Lippincott Williams & Wilkins, Philadelphia

    Google Scholar 

  7. Nelson DL, Cox MM (2008) Lehninger principles of biochemistry, 5th edn. W.H. Freeman, New York

    Google Scholar 

  8. Apps DK, Cohen BB, Steel CM (1992) Biochemistry: a concise text for medical students, 5th edn. Bailliere Tindall, London

    Google Scholar 

  9. Assessment of kidney function serum creatinine, BUN, and GFR, Retrieved Spring, 2008. Available at http://www.uptodate.com. Accessed 04 Dec 2014

  10. Jaffe M (1986) Uber den niederschlag welchen pikrinsaure in normalen harn erzeugt und uber eine neue reaktion des kreatinins. Hoppe Seyler's Z Physiol Chem 10:391–400

    Google Scholar 

  11. Oh MS (2011) Evaluation of renal function, water, electrolytes and acid-base balance. In: McPerson RA, Pincus MR (eds) Henry's clinical diagnosis and management by laboratory methods, 22nd edn. Saunders Elsevier, Philadelphia

    Google Scholar 

  12. Bastos MG, Kirsztajn GM (2011) Chronic kidney disease: importance of early diagnosis, immediate referral and structured interdisciplinary approach to improve outcomes in patients not yet on dialysis. J Bras Nefrol 22:93–108

    Article  Google Scholar 

  13. Hanlon EB, Manoharan R, Koo TW, Shafer KE, Motz JT, Fitzmaurice M et al (2000) Prospects for in vivo Raman spectroscopy. Phys Med Biol 45:R1–R59

    Article  CAS  PubMed  Google Scholar 

  14. De Almeida ML, Saatkamp CJ, Fernandes AB, Pinheiro AL, Silveira L (2016) Estimating the concentration of urea and creatinine in the human serum of normal and dialysis patients through Raman spectroscopy. Lasers Med Sci 31:1415–1423

    Article  PubMed  Google Scholar 

  15. Silveira L, Borges RC, Navarro RS, Giana HE, Zângaro RA, Pacheco MT, Fernandes AB (2017) Quantifying glucose and lipid components in human serum by Raman spectroscopy and multivariate statistics. Lasers Med Sci (in press)

  16. McMurdy JW, Berger AJ (2003) Raman spectroscopy-based creatinine measurement in urine samples from a multipatient population. Appl Spectrosc 57:522–525

    Article  CAS  PubMed  Google Scholar 

  17. Saatkamp CJ, de Almeida ML, Bispo JA, Pinheiro AL, Fernandes AB, Silveira L (2016) Quantifying creatinine and urea in human urine through Raman spectroscopy aiming at diagnosis of kidney disease. J Biomed Opt 21:37001

    Article  PubMed  Google Scholar 

  18. Premasiri WR, Clarke RH, Womble ME (2001) Urine analysis by laser Raman spectroscopy. Lasers Surg Med 28:330–334

    Article  CAS  PubMed  Google Scholar 

  19. Teo BW, Loh PT, Wong WK, Ho PJ, Choi KP, Toh QC, Xu H, Saw S, Lau T, Sethi S, Lee EJ (2015) Spot urine estimations are equivalent to 24-hour urine assessments of urine protein excretion for predicting clinical outcomes. Int J Nephrol 2015:156484

    Article  PubMed  PubMed Central  Google Scholar 

  20. Xin G, Wang M, Jiao LL, Xu GB, Wang HY (2004) Protein-to-creatinine ratio in spot urine samples as a predictor of quantitation of proteinuria. Clin Chim Acta 350:35–39

    Article  CAS  PubMed  Google Scholar 

  21. Park C, Kim K, Choi J, Park K (2007) Classification of glucose concentration in diluted urine using the low-resolution Raman spectroscopy and kernel optimization methods. Physiol Meas 28:583–593

    Article  PubMed  Google Scholar 

  22. Wang H, Malvadkar N, Koytek S, Bylander J, Reeves WB, Demirel MC (2010) Quantitative analysis of creatinine in urine by metalized nanostructured parylene. J Biomed Opt 15:027004

    Article  PubMed  Google Scholar 

  23. Li M, Du Y, Zhao F, Zeng J, Mohan C, Shih WC (2015) Reagent- and separation-free measurements of urine creatinine concentration using stamping surface enhanced Raman scattering (S-SERS). Biomed Opt Express 6:849–858

    Article  PubMed  PubMed Central  Google Scholar 

  24. Bispo JA, Vieira EES, Silveira L, Fernandes AB (2013) Correlating the amount of urea, creatinine, and glucose in urine from patients with diabetes mellitus and hypertension with the risk of developing renal lesions by means of Raman spectroscopy and principal component analysis. J Biomed Opt 18:1–8

    Article  Google Scholar 

  25. Ciaccio EJ, Dunn SM, Akay M (1994) Biosignal pattern-recognition and interpretation systems. IEEE Eng Med Biol 13:129–135

    Article  Google Scholar 

  26. The MathWorks Inc (2016) Documentation. Classify. The Mathworks Inc. https://www.mathworks.com/help/stats/classify.html. Accessed 20 Oct 2016

  27. Filho AC, Silveira L, Yanai AL, Fernandes AB (2015) Raman spectroscopy for a rapid diagnosis of sickle cell disease in human blood samples: a preliminary study. Lasers Med Sci 30:247–253

    Article  PubMed  Google Scholar 

Download references

Acknowledgments

L. Silveira Jr. thanks the FAPESP (São Paulo Research Foundation) for the partial financial support (process no. 2009/01788-5) and CNPq (National Council for Scientific and Technological Development) for the Productivity Fellowship (process no. 305680/2014-5). E. E. S. Vieira and J. A. M. Bispo thank the Regional Public Hospital of Western Pará and Santarém Municipal Hospital for authorizing this research in the Nephrology Clinic.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Adriana Barrinha Fernandes.

Ethics declarations

Conflict of interest

The authors declare that they have no conflict of interest.

Role of funding sources

The project has been supported in part by a public funding agency (São Paulo Research Foundation—FAPESP), Process FAPESP no. 2009/01788-5, that allowed to purchase the Raman spectrometer.

Ethical approval

This study was approved by Research Ethics Committee from UNICASTELO (protocols nos. 64116 and 8926).

Informed consent

All volunteers agreed and signed an informed consent form to participate this study.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

de Souza Vieira, E.E., Bispo, J.A.M., Silveira, L. et al. Discrimination model applied to urinalysis of patients with diabetes and hypertension aiming at diagnosis of chronic kidney disease by Raman spectroscopy. Lasers Med Sci 32, 1605–1613 (2017). https://doi.org/10.1007/s10103-017-2288-5

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10103-017-2288-5

Keywords

Navigation