Home Elevated levels of renal function tests conferred increased risks of developing various pregnancy complications and adverse perinatal outcomes: insights from a population-based cohort study
Article
Licensed
Unlicensed Requires Authentication

Elevated levels of renal function tests conferred increased risks of developing various pregnancy complications and adverse perinatal outcomes: insights from a population-based cohort study

  • Zhengwen Xu , He S. Yang , Lin Liu , Lanlan Meng , Yifan Lu , Lican Han , Guodong Tang , Jing Wang , Lu Chen , Yue Zhang , Yanhong Zhai EMAIL logo , Shaofei Su EMAIL logo and Zheng Cao ORCID logo EMAIL logo
Published/Copyright: April 6, 2023

Abstract

Objectives

Physiological changes during pregnancy can affect the results of renal function tests (RFTs). In this population-based cohort study, we aimed to establish trimester-specific reference intervals (RIs) of RFTs in singleton and twin pregnancies and systematically investigate the relationship between RFTs and adverse pregnancy outcomes.

Methods

The laboratory results of the first- and third-trimester RFTs, including blood urea nitrogen (BUN), serum uric acid (UA), creatinine (Crea) and cystatin C (Cys C), and the relevant medical records, were retrieved from 29,328 singleton and 840 twin pregnant women who underwent antenatal examinations from November 20, 2017 to January 31, 2021. The trimester-specific RIs of RFTs were estimated with both of the direct observational and the indirect Hoffmann methods. The associations between RTFs and pregnancy complications as well as perinatal outcomes were assessed by logistic regression analysis.

Results

Maternal RFTs showed no significant difference between the direct RIs established with healthy pregnant women and the calculated RIs derived from the Hoffmann method. In addition, elevated levels of RFTs were associated with increased risks of developing various pregnancy complications and adverse perinatal outcomes. Notably, elevated third-trimester RFTs posed strong risks of preterm birth (PTB) and fetal growth restriction (FGR).

Conclusions

We established the trimester-specific RIs of RFTs in both singleton and twin pregnancies. Our risk analysis findings underscored the importance of RFTs in identifying women at high risks of developing adverse complications or outcomes during pregnancy.


Corresponding authors: Zheng Cao, Department of Laboratory Medicine, Beijing Obstetrics and Gynecology Hospital, Capital Medical University, Beijing Maternal and Child Health Care Hospital, Beijing, P.R. China; Center of Clinical Mass Spectrometry, Beijing Obstetrics and Gynecology Hospital, Capital Medical University, Beijing Maternal and Child Health Care Hospital, Beijing, P.R. China, E-mail: ; Shaofei Su, Central Laboratory, Beijing Obstetrics and Gynecology Hospital, Capital Medical University, Beijing Maternal and Child Health Care Hospital, Beijing, P.R. China, E-mail: ; Yanhong Zhai, Department of Laboratory Medicine, Beijing Obstetrics and Gynecology Hospital, Capital Medical University, Beijing Maternal and Child Health Care Hospital, Beijing, P.R. China; and Center of Clinical Mass Spectrometry, Beijing Obstetrics and Gynecology Hospital, Capital Medical University, Beijing Maternal and Child Health Care Hospital, 251 Yaojiayuan Road, 100026 Beijing, P.R. China, Phone: +86 10 52276406, E-mail:
Zhengwen Xu and He S. Yang contributed equally to this work.

Funding source: Beijing Obstetrics and Gynecology Hospital, Capital Medical University

Award Identifier / Grant number: XKGG201802

Award Identifier / Grant number: CCMU2022ZKYXZ006

Funding source: Beijing Municipal Administration of Hospitals Incubating Program

Award Identifier / Grant number: PX2020060

  1. Research funding: This work was supported by the Training Fund for Open Projects at Clinical Institutes and Departments of Capital Medical University (CCMU2022ZKYXZ006), the Beijing Municipal Administration of Hospitals Incubating Program (No. PX2020060) and Beijing Obstetrics and Gynecology Hospital, Capital Medical University, Beijing Maternal and Child Health Care Hospital ‘Discipline Backbone’ Plan Special Funds (No. XKGG201802). The funding bodies did not take part in the design of the study, the collection, analysis and interpretation of the data, or manuscript writing.

  2. Author contributions: Zhengwen Xu: conceptualization, data curation, writing-original draft. He S. Yang: conceptualization, writing-review & editing. Yifan Lu: investigation, methodology. Lanlan Meng, Lin Liu, Lican Han and Guodong Tang: data curation. Jing Wang, Lu Chen and Yue Zhang: data curation, investigation. Yanhong Zhai: conceptualization, data curation, project administration. Shaofei Su: investigation, methodology. Zheng Cao: conceptualization, supervision, funding acquisition, writing – review & editing.

  3. Competing interests: Authors state no conflict of interest.

  4. Informed consent: The need for informed consent from included individuals was waived by the Ethics Committee of Beijing Obstetrics and Gynecology Hospital as all the data used in this study was anonymized before its use.

  5. Ethical approval: The study protocol was approved by the Ethics Committee of Beijing Obstetrics and Gynecology Hospital (2022-KY-007-02).

References

1. Wu, L, Wu, Q, Li, Q, Cao, S, Zhang, Y, Liu, Y, et al.. Consecutive reference intervals for biochemical indices related to serum lipid levels and renal function during normal pregnancy. BMC Pregnancy Childbirth 2022;22:642. https://doi.org/10.1186/s12884-022-04960-0.Search in Google Scholar PubMed PubMed Central

2. Jia, L, Yongmei, J, Leiwen, P, Yi, Y. The reference intervals for renal function indexes in Chinese pregnant women. Pak J Pharm Sci 2017;30:1133–8.Search in Google Scholar

3. Cheung, KL, Lafayette, RA. Renal physiology of pregnancy. Adv Chron Kidney Dis 2013;20:209–14. https://doi.org/10.1053/j.ackd.2013.01.012.Search in Google Scholar PubMed PubMed Central

4. Baylis, C. The determinants of renal hemodynamics in pregnancy. Am J Kidney Dis 1987;9:260–4. https://doi.org/10.1016/s0272-6386(87)80119-1.Search in Google Scholar PubMed

5. Davison, JM, Dunlop, W. Renal hemodynamics and tubular function normal human pregnancy. Kidney Int 1980;18:152–61. https://doi.org/10.1038/ki.1980.124.Search in Google Scholar PubMed

6. Soma-Pillay, P, Nelson-Piercy, C, Tolppanen, H, Mebazaa, A. Physiological changes in pregnancy. Cardiovasc J Afr 2016;27:89–94. https://doi.org/10.5830/cvja-2016-021.Search in Google Scholar

7. de Haas, S, Ghossein-Doha, C, van Kuijk, SMJ, van Drongelen, J, Spaanderman, MEA. Physiological adaptation of maternal plasma volume during pregnancy: a systematic review and meta-analysis. Ultrasound Obstet Gynecol 2017;49:177–87. https://doi.org/10.1002/uog.17360.Search in Google Scholar PubMed

8. Lopes van Balen, VA, van Gansewinkel, TAG, de Haas, S, Spaan, JJ, Ghossein-Doha, C, van Kuijk, SMJ, et al.. Maternal kidney function during pregnancy: systematic review and meta-analysis. Ultrasound Obstet Gynecol 2019;54:297–307. https://doi.org/10.1002/uog.20137.Search in Google Scholar PubMed PubMed Central

9. Girling, JC. Re-evaluation of plasma creatinine concentration in normal pregnancy. J Obstet Gynaecol 2000;20:128–31. https://doi.org/10.1080/01443610062850.Search in Google Scholar PubMed

10. Chen, Q, Izumi, A, Minakami, H, Sato, I. Comparative changes in uterine artery blood flow waveforms in singleton and twin pregnancies. Gynecol Obstet Invest 1998;45:165–9. https://doi.org/10.1159/000009948.Search in Google Scholar PubMed

11. MacGillivray, I, Campbell, D, Duffus, GM. Maternal metabolic response to twin pregnancy in primigravidae. J Obstet Gynaecol Br Commonw 1971;78:530–4. https://doi.org/10.1111/j.1471-0528.1971.tb00311.x.Search in Google Scholar PubMed

12. Campbell, DM, MacGillivray, I. The importance of plasma volume expansion and nutrition in twin pregnancy. Acta Genet Med Gemellol 1984;33:19–24. https://doi.org/10.1017/s0001566000007431.Search in Google Scholar PubMed

13. Thomsen, JK, Fogh-Andersen, N, Jaszczak, P. Atrial natriuretic peptide, blood volume, aldosterone, and sodium excretion during twin pregnancy. Acta Obstet Gynecol Scand 1994;73:14–20. https://doi.org/10.3109/00016349409013386.Search in Google Scholar PubMed

14. Sima, RM, Findeklee, S, Bădărău, IA, Poenaru, MO, Scheau, C, Pleș, L. Comparison of maternal third trimester hemodynamics between singleton pregnancy and twin pregnancy. J Perinat Med 2021;49:566–71. https://doi.org/10.1515/jpm-2020-0169.Search in Google Scholar PubMed

15. Igarashi, M, Miyake, H, Suzuki, S. Hemodynamic changes in maternal renal arteries in twin pregnancy. Gynecol Obstet Invest 2010;69:88–92. https://doi.org/10.1159/000260331.Search in Google Scholar PubMed

16. Gao, Y, Jia, J, Liu, X, Guo, S, Ming, L. Trimester-specific reference intervals of serum urea, creatinine, and uric acid among healthy pregnant women in Zhengzhou, China. Lab Med 2021;52:267–72. https://doi.org/10.1093/labmed/lmaa088.Search in Google Scholar PubMed

17. Roberts, JM, Bodnar, LM, Lain, KY, Hubel, CA, Markovic, N, Ness, RB, et al.. Uric acid is as important as proteinuria in identifying fetal risk in women with gestational hypertension. Hypertension 2005;46:1263–9. https://doi.org/10.1161/01.hyp.0000188703.27002.14.Search in Google Scholar

18. Hawkins, TLA, Roberts, JM, Mangos, GJ, Davis, GK, Roberts, LM, Brown, MA. Plasma uric acid remains a marker of poor outcome in hypertensive pregnancy: a retrospective cohort study. BJOG 2012;119:484–92. https://doi.org/10.1111/j.1471-0528.2011.03232.x.Search in Google Scholar PubMed

19. Laughon, SK, Catov, J, Roberts, JM. Uric acid concentrations are associated with insulin resistance and birthweight in normotensive pregnant women. Am J Obstet Gynecol 2009;201:582.e1–e6. https://doi.org/10.1016/j.ajog.2009.06.043.Search in Google Scholar PubMed PubMed Central

20. Dockree, S, Brook, J, James, T, Shine, B, Impey, L, Vatish, M. Pregnancy-specific reference intervals for C-reactive protein improve diagnostic accuracy for infection: a longitudinal study. Clin Chim Acta 2021;517:81–5. https://doi.org/10.1016/j.cca.2021.02.015.Search in Google Scholar PubMed

21. Lu, Y, Jia, Z, Su, S, Han, L, Meng, L, Tang, G, et al.. Establishment of trimester-specific reference intervals of serum lipids and the associations with pregnancy complications and adverse perinatal outcomes: a population-based prospective study. Ann Med 2021;53:1632–41. https://doi.org/10.1080/07853890.2021.1974082.Search in Google Scholar PubMed PubMed Central

22. Cheung, KL, Lafayette, RA. Renal physiology of pregnancy. Adv Chron Kidney Dis 2013;20:209–14. https://doi.org/10.1053/j.ackd.2013.01.012.Search in Google Scholar PubMed PubMed Central

23. Defining, establishing, and verifying reference intervals in the clinical laboratory, approved guideline—3rd ed. CLSI document C28-A3c; 2008. [Online]. Available from: https://webstore.ansi.org/preview-pages/CLSI/preview_CLSI+C28-A3.pdf.Search in Google Scholar

24. Lahti, A, Hyltoft Petersen, P, Boyd, JC, Fraser, CG, Jørgensen, N. Objective criteria for partitioning Gaussian-distributed reference values into subgroups. Clin Chem 2002;48:338–52. https://doi.org/10.1093/clinchem/48.2.338.Search in Google Scholar

25. Igarashi, M, Miyake, H, Suzuki, S. Effect of changes in renal circulation on serum uric acid levels in women with twin pregnancy. Clin Exp Nephrol 2010;14:436–9. https://doi.org/10.1007/s10157-010-0306-z.Search in Google Scholar PubMed

26. Han, L, Zheng, W, Zhai, Y, Xie, X, Zhang, J, Zhang, S, et al.. Reference intervals of trimester-specific thyroid stimulating hormone and free thyroxine in Chinese women established by experimental and statistical methods. J Clin Lab Anal 2018;32:e22344. https://doi.org/10.1002/jcla.22344.Search in Google Scholar PubMed PubMed Central

27. Davison, JM. Kidney function in pregnant women. Am J Kidney Dis 1987;9:248–52. https://doi.org/10.1016/s0272-6386(87)80117-8.Search in Google Scholar PubMed

28. Zemek, R, Barrowman, N, Freedman, SB, Gravel, J, Gagnon, I, McGahern, C, et al.. Clinical risk score for persistent postconcussion symptoms among children with acute concussion in the ED. JAMA 2016;315:1014–25. https://doi.org/10.1001/jama.2016.1203.Search in Google Scholar PubMed

29. Dai, Y, Liu, J, Yuan, E, Li, Y, Wang, Q, Jia, L, et al.. Gestational age-specific reference intervals for 15 biochemical measurands during normal pregnancy in China. Ann Clin Biochem 2018;55:446–52. https://doi.org/10.1177/0004563217738801.Search in Google Scholar PubMed

30. Larsson, A, Palm, M, Hansson, LO, Axelsson, O. Reference values for clinical chemistry tests during normal pregnancy. BJOG 2008;115:874–81. https://doi.org/10.1111/j.1471-0528.2008.01709.x.Search in Google Scholar PubMed

31. Greenberg, N, Roberts, WL, Bachmann, LM, Wright, EC, Dalton, RN, Zakowski, JJ, et al.. Specificity characteristics of 7 commercial creatinine measurement procedures by enzymatic and Jaffe method principles. Clin Chem 2012;58:391–401. https://doi.org/10.1373/clinchem.2011.172288.Search in Google Scholar PubMed

32. Bellos, I, Pergialiotis, V, Loutradis, D, Daskalakis, G. The prognostic role of serum uric acid levels in preeclampsia: a meta-analysis. J Clin Hypertens 2020;22:826–34. https://doi.org/10.1111/jch.13865.Search in Google Scholar PubMed PubMed Central

33. Franceschini, N, Qiu, C, Barrow, DA, Williams, MA. Cystatin C and preeclampsia: a case control study. Ren Fail 2008;30:89–95. https://doi.org/10.1080/08860220701742229.Search in Google Scholar PubMed

34. Cunningham, FG, Cox, SM, Harstad, TW, Mason, RA, Pritchard, JA. Chronic renal disease and pregnancy outcome. Am J Obstet Gynecol 1990;163:453–9. https://doi.org/10.1016/0002-9378(90)91175-c.Search in Google Scholar PubMed

35. Wang, J, Hu, H, Liu, X, Zhao, S, Zheng, Y, Jia, Z, et al.. Predictive values of various serum biomarkers in women with suspected preeclampsia: a prospective study. J Clin Lab Anal 2021;35:e23740. https://doi.org/10.1002/jcla.23740.Search in Google Scholar PubMed PubMed Central

36. Furukawa, S, Fujita, T, Shimabukuro, M, Iwaki, M, Yamada, Y, Nakajima, Y, et al.. Increased oxidative stress in obesity and its impact on metabolic syndrome. J Clin Invest 2004;114:1752–61. https://doi.org/10.1172/jci21625.Search in Google Scholar

37. Cook, S, Hugli, O, Egli, M, Vollenweider, P, Burcelin, R, Nicod, P, et al.. Clustering of cardiovascular risk factors mimicking the human metabolic syndrome X in eNOS null mice. Swiss Med Wkly 2003;133:360–3. https://doi.org/10.4414/smw.2003.10239.Search in Google Scholar PubMed

38. Sautin, YY, Nakagawa, T, Zharikov, S, Johnson, RJ. Adverse effects of the classic antioxidant uric acid in adipocytes: NADPH oxidase-mediated oxidative/nitrosative stress. Am J Physiol Cell Physiol 2007;293:C584–96. https://doi.org/10.1152/ajpcell.00600.2006.Search in Google Scholar PubMed

39. Nakagawa, T, Tuttle, KR, Short, RA, Johnson, RJ. Hypothesis: fructose-induced hyperuricemia as a causal mechanism for the epidemic of the metabolic syndrome. Nat Clin Pract Nephrol 2005;1:80–6. https://doi.org/10.1038/ncpneph0019.Search in Google Scholar PubMed

40. Roy, D, Perreault, M, Marette, A. Insulin stimulation of glucose uptake in skeletal muscles and adipose tissues in vivo is NO dependent. Am J Physiol 1998;274:E692–9. https://doi.org/10.1152/ajpendo.1998.274.4.e692.Search in Google Scholar PubMed

41. Laughon, SK, Catov, J, Provins, T, Roberts, JM, Gandley, RE. Elevated first-trimester uric acid concentrations are associated with the development of gestational diabetes. Am J Obstet Gynecol 2009;201:402.e1–e5. https://doi.org/10.1016/j.ajog.2009.06.065.Search in Google Scholar PubMed PubMed Central

42. Wolak, T, Sergienko, R, Wiznitzer, A, Paran, E, Sheiner, E. High uric acid level during the first 20 weeks of pregnancy is associated with higher risk for gestational diabetes mellitus and mild preeclampsia. Hypertens Pregnancy 2012;31:307–15. https://doi.org/10.3109/10641955.2010.507848.Search in Google Scholar PubMed

43. Gursoy, AY, Tasci, Y, Celik, H, Caglar, GS, Kiseli, M, Candar, T, et al.. The prognostic value of first-trimester cystatin C levels for gestational complications. J Perinat Med 2016;44:295–9. https://doi.org/10.1515/jpm-2015-0061.Search in Google Scholar

44. Amini, E, Sheikh, M, Hantoushzadeh, S, Shariat, M, Abdollahi, A, Kashanian, M. Maternal hyperuricemia in normotensive singleton pregnancy, a prenatal finding with continuous perinatal and postnatal effects, a prospective cohort study. BMC Pregnancy Childbirth 2014;14:104. https://doi.org/10.1186/1471-2393-14-104.Search in Google Scholar

45. Yalamati, P, Bhongir, AV, Betha, K, Verma, R, Dandge, S. Relationship of serum uric acid, serum creatinine and serum cystatin C with maternal and fetal outcomes in rural Indian pregnant women. Int J Reprod Contracept Obstet Gynecol 2015;4:1505–10. https://doi.org/10.18203/2320-1770.ijrcog20150737.Search in Google Scholar

46. Harel, Z, Park, AL, McArthur, E, Hladunewich, M, Dirk, JS, Wald, R, et al.. Prepregnancy renal function and risk of preterm birth and related outcomes. CMAJ 2020;192:E851–7. https://doi.org/10.1503/cmaj.200089.Search in Google Scholar

47. Ananth, CV, Vintzileos, AM. Ischemic placental disease: epidemiology and risk factors. Eur J Obstet Gynecol Reprod Biol 2011;159:77–82. https://doi.org/10.1016/j.ejogrb.2011.07.025.Search in Google Scholar

48. Piccoli, GB, Conijn, A, Attini, R, Biolcati, M, Bossotti, C, Consiglio, V, et al.. Pregnancy in chronic kidney disease: need for a common language. J Nephrol 2011;24:282–99. https://doi.org/10.5301/jn.2011.7978.Search in Google Scholar

49. Leguizamon, G, Reece, EA. Effect of medical therapy on progressive nephropathy: influence of pregnancy, diabetes and hypertension. J Matern Fetal Med 2000;9:70–8. https://doi.org/10.1002/(sici)1520-6661(200001/02)9:1<70::aid-mfm15>3.0.co;2-#.10.1002/(SICI)1520-6661(200001/02)9:1<70::AID-MFM15>3.0.CO;2-#Search in Google Scholar

50. Senra, JC, Yoshizaki, CT, Doro, GF, Ruano, R, Gibelli, MABC, Rodrigues, AS, et al.. Kidney impairment in fetal growth restriction: three-dimensional evaluation of volume and vascularization. Prenat Diagn 2020;40:1408–17. https://doi.org/10.1002/pd.5778.Search in Google Scholar

51. Malamitsi-Puchner, A, Briana, DD, Kontara, L, Boutsikou, M, Baka, S, Hassiakos, D, et al.. Serum cystatin C in pregnancies with normal and restricted fetal growth. Reprod Sci 2007;14:37–42. https://doi.org/10.1177/1933719106298196.Search in Google Scholar

52. Brien, M-E, Duval, C, Palacios, J, Boufaied, I, Hudon-Thibeault, A-A, Nadeau-Vallée, M, et al.. Uric acid crystals induce placental inflammation and alter trophoblast function via an IL-1-dependent pathway: implications for fetal growth restriction. J Immunol 2017;198:443–51. https://doi.org/10.4049/jimmunol.1601179.Search in Google Scholar

53. Kang, J, Hwang, S, Lee, TS, Cho, J, Seo, DM, Choi, SJ, et al.. Gestational age-specific serum creatinine can predict adverse pregnancy outcomes. Sci Rep 2022;12:11224. https://doi.org/10.1038/s41598-022-15450-w.Search in Google Scholar PubMed PubMed Central

54. Naylor, CD, Sermer, M, Chen, E, Farine, D. Selective screening for gestational diabetes mellitus. Toronto trihospital gestational diabetes project investigators. N Engl J Med 1997;337:1591–6. https://doi.org/10.1056/nejm199711273372204.Search in Google Scholar

55. Artzi, NS, Shilo, S, Hadar, E, Rossman, H, Barbash-Hazan, S, Ben-Haroush, A, et al.. Prediction of gestational diabetes based on nationwide electronic health records. Nat Med 2020;26:71–6. https://doi.org/10.1038/s41591-019-0724-8.Search in Google Scholar PubMed

56. Wu, Y-T, Zhang, C-J, Mol, BW, Kawai, A, Li, C, Chen, L, et al.. Early prediction of gestational diabetes mellitus in the Chinese population via advanced machine learning. J Clin Endocrinol Metab 2021;106:e1191–205. https://doi.org/10.1210/clinem/dgaa899.Search in Google Scholar PubMed PubMed Central


Supplementary Material

This article contains supplementary material (https://doi.org/10.1515/cclm-2023-0104).


Received: 2023-01-29
Accepted: 2023-03-27
Published Online: 2023-04-06
Published in Print: 2023-09-26

© 2023 Walter de Gruyter GmbH, Berlin/Boston

Articles in the same Issue

  1. Frontmatter
  2. Editorial
  3. Laboratory Medicine: from just testing to saving lives
  4. Reviews
  5. Serum biomarkers of remodeling in severe asthma with fixed airway obstruction and the potential role of KL-6
  6. Safety monitoring of drug-induced muscle injury and rhabdomyolysis: a biomarker-guided approach for clinical practice and drug trials
  7. Mini Review
  8. Concise review on the combined use of immunocapture, mass spectrometry and liquid chromatography for clinical applications
  9. Opinion Paper
  10. Recommendation for the design of stability studies on clinical specimens
  11. General Clinical Chemistry and Laboratory Medicine
  12. Assessment of WHO 07/202 reference material and human serum pools for commutability and for the potential to reduce variability among soluble transferrin receptor assays
  13. veRification: an R Shiny application for laboratory method verification and validation
  14. Impact of storage temperature and time before analysis on electrolytes (Na+, K+, Ca2+), lactate, glucose, blood gases (pH, pO2, pCO2), tHb, O2Hb, COHb and MetHb results
  15. The stability of blood gases and CO-oximetry under slushed ice and room temperature conditions
  16. Elevated levels of renal function tests conferred increased risks of developing various pregnancy complications and adverse perinatal outcomes: insights from a population-based cohort study
  17. Poor comparability of plasma renin activity measurement in determining patient samples: the status quo and recommendations for harmonization
  18. Salivary cortisol and cortisone in diagnosis of Cushing’s syndrome – a comparison of six different analytical methods
  19. Improved diagnostics of purine and pyrimidine metabolism disorders using LC-MS/MS and its clinical application
  20. Analytical evaluation of a GAD65 antibodies chemiluminescence immunoassay for CSF in neurological syndromes
  21. Reference Values and Biological Variations
  22. Evaluation of low-density lipoprotein cholesterol equations by cross-platform assessment of accuracy-based EQA data against SI-traceable reference value
  23. Highly sensitive tandem mass spectrometric measurement of serum estradiol without derivatization and pediatric reference intervals in children and adolescents
  24. Cancer Diagnostics
  25. Practical delta check limits for tumour markers in different clinical settings
  26. Comparison between free β subunit of human chorionic gonadotropin (hCG) and total hCG assays in adults with testicular cancer
  27. Hematology and Coagulation
  28. Value of monocyte distribution width for predicting severe cholecystitis: a retrospective cohort study
  29. Performance of digital morphology analyzer Medica EasyCell assistant
  30. Validation of non-invasive point of care blood content analysis using the TensorTip™ MTX device: a method comparison study
  31. Infectious Diseases
  32. Kinetics and ability of binding antibody and surrogate virus neutralization tests to predict neutralizing antibodies against the SARS-CoV-2 Omicron variant following BNT162b2 booster administration
  33. Letters to the Editor
  34. The first case of VEXAS syndrome in Austria
  35. Acetylcholine receptor and muscle-specific tyrosine kinase antibodies detection: is it time for a change?
  36. Performance of the 2009 CKDEPI, 2021 CKDEPI, and EKFC equations among high-risk patients in Denmark
  37. Biotin interference in immunoassays: water under the bridge?
  38. The new synthetic benzimidazole opioid etonitazepipne: an emerging fatal harm and a challenge for laboratory medicine
  39. Unexplained increase of serum carcinoembryonic antigen: don’t forget the thyroid!
  40. Falsely elevated cortisol serum levels in preterm infants due to use of immunoassay
  41. Misdiagnosis of Hb Bart’s disease: prenatal screening and diagnosis of thalassemia in special population
Downloaded on 1.11.2025 from https://www.degruyterbrill.com/document/doi/10.1515/cclm-2023-0104/html
Scroll to top button