Neutrophil-lymphocyte ratio acts as a novel diagnostic biomarker for kidney stone prevalence and number of stones passed
Introduction
One of the most common urinary diseases is nephrolithiasis, which refers to stones that occur in the renal calyx, renal pelvis and the junction of the renal pelvis and ureter, and its incidence is increasing worldwide (1). Nephrolithiasis occurs when the balance between solubility and precipitation of stone-forming salts in the urinary tract and kidney is disrupted (2). Between 2013 and 2014, the adjusted prevalence of kidney stones in Chinese adults was 5.8% (3). Nephrolithiasis typically involves repeated occurrences, which indicates a higher recurrence rate and worse clinical prognosis (4).
There are few studies on the role of immune responses and inflammatory cells in the formation of kidney stones. Some studies have shown that the retention of crystals is mediated by excessive production of reactive oxygen species and subsequent oxidative stress and inflammation (5-7). The levels of neutrophils, platelets, lymphocytes and acute phase proteins change during this inflammatory response. There are many inflammatory indicators that can be combined to function as biomarkers, including the systemic immune-inflammation index (SII), neutrophil-lymphocyte ratio (NLR), platelet-lymphocyte ratio (PLR) and monocyte-lymphocyte ratio (MLR). Considering the growing evidence of the relationship between kidney stones and inflammatory diseases, we examined whether the levels of key inflammatory biomarkers mentioned above are associated with the prevalence of kidney stones and the number of stones passed
We present the following article in accordance with the STROBE reporting checklist (available at http://dx.doi.org/10.21037/tau-20-890).
Methods
Study population
The National Health and Nutrition Examination Survey (NHANES) uses a complex, probability-based sampling design to collect information from different populations through standardized interviews, physical examinations, and laboratory tests to assess the health and nutritional status of noninstitutionalized civilians in the United States. Since 1999, the data have been released every two years for research use.
In this study, we used public data from four NHANES cycles (2007–2008, 2009–2010, 2011–2011 and 2013–2014). More information about the data are available on the NHANES website (www.cdc.gov/nchs/nhanes/). Between 2007 and 2014, there were 40,617 participants in NHANES. We first excluded 30 participants who reported a history of hematological tumors (n=7) or leukemia (n=23). The subsequent exclusion criteria were as follows: (I) incomplete stone investigation (n=17,201); (II) unknown platelet count (n=1,926); (III) unknown lymphocyte count (n=43); (IV) unknown/abnormal neutrophil count (n=2); (V) unknown body mass index (BMI) (n=269); and (VI) unknown number of kidney stone occurrences (n=40). After excluding these factors, 21,106 participants were included in the final study.
The study was conducted in accordance with the Declaration of Helsinki (as revised in 2013). This study used previously collected deidentified data, which was deemed exempt from review by the Ethics Committee of the Affiliated Zhongda Hospital of Southeast University.
Study variables and outcome
The SII, NLR, PLR and MLR are the main predictors of outcomes measured in this study. The SII is calculated as the platelet count × neutrophil count/lymphocyte count; the NLR is the neutrophil count/lymphocyte count; the PLR is the platelet count/lymphocyte count; and the MLR is the monocyte count/lymphocyte count. The lymphocyte count, platelet count and monocyte count can be obtained directly from laboratory data files. The neutrophil count is calculated from the white blood cell count and neutrophil percentage. Other covariates included sex (male or female), age (20–39 years, 40–59 years and 60+ years), race (non-Hispanic white, non-Hispanic Black, Mexican American, other Hispanic and other), marital status (married, unmarried and other), participation in participation in vigorous recreational activities (yes or no), participation in moderately or vigorous recreational activities (yes or no), education level (less than high school, high school or equivalent, college or above and other), and BMI (<25.0, 25.0–29.9 and ≥30.0 kg/m2). Hypertension and diabetes are defined as self-reported physician-diagnosed hypertension or diabetes.
The end points of the study were the history of kidney stones and the occurrence of kidney stone episodes. The end points were extracted from the questionnaire data file. Participants who answered “No” to the question “Have you ever had kidney stones?” were considered to have no history of kidney stones. For participants who answered “Yes”, we also documented their answer to the “How many times have you passed a kidney stone?” question. For those who answered “0”, we considered them as not having passed stones, and for those who answered “1–80”, we considered them as having passed stones.
Statistical analysis
The participants were divided into four groups: the no stone group, the no-stones-passed group, the stones-passed 1–5 times group and the stones-passed >5 times group. We used MedCalc software (version 15.2.0) to determine the cutoff values for the SII, NLR, PLR, and MLR. The mean ± standard deviation is used to describe the distribution of continuous variables, and the proportion is used to describe the distribution of categorical variables. Chi-square analysis was used to evaluate the clinical characteristics of all participants. A multivariate logistic regression model was used to evaluate the adjusted odds ratio (OR) and 95% confidence interval (CI) of factors related to kidney stones and the number of kidney stones passed. All statistical analyses were performed using SPSS (version 24.0), and graphs were generated by GraphPad (version 8.0.2). P<0.05 (two-tailed) was considered to indicate statistical significance.
Results
Based on the screening criteria in Figure 1, we included 21,106 qualified participants from the NHANES database from 2007 to 2014. Table 1 shows the clinical characteristics of all participants. Among them, 19,242 were in the no stone group, 292 in the no-stones-passed group, 1,462 in the stones passed 1-5 times group and 110 in the stones passed >5 times group. The chi-square test showed significant differences among several variables, including sex (P<0.001), age (P<0.001), race (P<0.001), marital status (P<0.001), participation in moderately or vigorous recreational activities (P<0.001), hypertension (P<0.001), diabetes (P<0.001), BMI (P=0.004), the SII (P=0.001), the NLR (P<0.001) and the MLR (P<0.001). We found that the proportion of males, non-Hispanic whites, no participation in activities, married, college or above, hypertension, diabetes/borderline, obese, SII >44.37, NLR >1.72 and MLR >0.29 in the group with stones passed >5 times was significantly higher than that in the other three groups.
Full table
We focused on investigating the expression of four inflammatory biomarkers (the SII, NLR, PLR and MLR) in the four groups. We found that the levels of the SII (534.26±336.33, 545.91±370.32, 557.27±330.87, and 613.39±405.50) and NLR (2.18±1.94, 2.30±1.19, 2.35±1.30, and 2.52±1.31) increased progressively (Figure 2) in the no stone group, no stones passed group, stones passed 1-5 times group and stones passed >5 times group, and the proportion of participants with the SII >44.37, NLR >1.72 and MLR >0.29 showed an increase in each subsequent group (Figure 3).
To further determine the risk factors related to the prevalence of kidney stones and the number of stones passed, we subsequently conducted a multivariate logistic regression analysis (Table 2). The results showed that the prevalence of kidney stones and the number of stones passed were related to sex, age, race, participation in moderately or vigorous recreational activities, BMI and the NLR. We found that female participants had a lower risk of kidney stones (vs. male participants OR =0.73, 95% CI: 0.66–0.81, P<0.001). Patients aged 40–59 years (vs. 20–39 years OR =1.21, 95% CI: 1.08–1.36, P=0.001), 60+ years (vs. 20–39 years OR =1.83, 95% CI: 1.58–2.13, P<0.001), who did not participate in activities (vs. participation in activities OR =1.20, 95% CI: 1.03–1.40, P=0.017), who did not participate in moderately vigorous recreational activities (vs. participation in moderately vigorous recreational activities OR =1.13, 95% CI: 1.02–1.26, P=0.022), who were overweight (vs. normal OR =1.15, 95% CI: 1.03–1.29, P=0.015) and who had obesity (vs. normal OR =1.50, 95% CI: 1.31–1.71, P<0.001) had a higher risk of kidney stones. In addition, of the four inflammatory biomarkers, only the NLR was associated with the prevalence of kidney stones and the number of stones passed (NLR >1.72 vs. NLR ≤1.72 OR =1.18, 95% CI: 1.03–1.36, P=0.019).
Full table
Discussion
In this retrospective study, we used the NHANES database, which can be assumed to represent the population of the United States. Our results showed for the first time that the SII, NLR and MLR increased, and the proportion of the SII >444.37 and MLR >0.29 increased as the incidence of kidney stones increased from the no-stone group, no-stones-passed group, stones passed 1–5 times group and stones passed >5 times group. There was a significant correlation between higher SII, NLR and MLR values and the self-reported prevalence of kidney stones and the number of stones passed. After adjusting for other confounding factors, only the NLR was associated with the prevalence of kidney stones and the number of stones passed. This indicates that the upregulated NLR can be regarded as a powerful indicator for the diagnosis of kidney stone prevalence and number of stones passed.
Kidney stones are a common and frequently occurring condition that seriously affects human health, and as the prevalence of stones increases, the cost of medical care related to stones significantly increases as well (8). Among kidney stones, calcium oxalate stones are the most common, accounting for approximately 80% (9). The recurrence rate of kidney stones is very high, 50% in 5–10 years, and patients with recurrent stones are more likely to have more recurrences (10). The specific pathogenesis of kidney stones is still unclear. In recent years, the role of oxidative stress and the inflammatory response in the occurrence and development of kidney stones has provoked widespread concern among scholars. An increasing number of studies have confirmed that oxidative stress and inflammatory responses are closely related to the formation of kidney stones (6,11,12).
Oxidative stress and inflammatory responses play an important role in a variety of crystal-related diseases, such as gout (uric acid crystals), silicosis (silica crystals), and atherosclerosis (cholesterol crystals) (13-15). Kidney stones are also a crystal-related disease, and oxalate crystals and other components in urine can lead to oxidative stress and inflammatory responses in tissue and cells, resulting in the release of inflammatory cells and inflammatory factors (16).
During inflammation, the levels of neutrophils, lymphocytes and C-reactive protein (CRP) change. Neutrophils can release inflammatory factors (such as IL-8, IL-6, and neutrophil elastase), and lymphocytes can secrete cytokines (e.g., interferon-γ and tumor necrosis factor-α) (17). As a simple peripheral blood indicator that can better reflect the level of systemic inflammation compared with lymphocytes, an increase in the NLR indicates an increase in neutrophils, which promote inflammation (18). As a biomarker of acute and chronic phase inflammation (19,20), CRP has been proven to be associated with kidney stones. Shoag et al. (21) found a significant correlation between serum CRP levels and self-reported kidney stones in younger individuals.
Because routine blood examination is economical, easy to perform and encompasses a large number of useful parameters, it should be fully applied in the diagnosis and management of kidney stones, which is worthy of further discussion.
Our research also has certain limitations. First, our study is based on the NHANES database, which is a cross-sectional study; further research requires a prospective study. Second, there is no information in the NHANES database about the type of kidney stones. Moreover, NHANES survey results are based on participants’ self-reported data and require the use of a diagnostic test; further, the complete kidney stone history is not available.
Conclusions
Overall, this study found that a higher NLR was closely associated with self-reported kidney stones and the number of stones passed. Because the NLR is a convenient and economical biomarker derived from a routine blood examination, it may play an important role in the screening and prevention of kidney stones in future clinical practice.
Acknowledgments
The authors are grateful for the invaluable support and useful discussions with other members of the urological department.
Funding: This work was supported by the National Natural Science Foundation of China (No. 81572517 and 81872089), Natural Science Foundation of Jiangsu Province (BK20161434), Jiangsu Provincial Medical Innovation Team (CXTDA2017025), and Jiangsu Provincial Medical Talent (ZDRCA2016080).
Footnote
Reporting Checklist: The authors have completed the STROBE reporting checklist. Available at http://dx.doi.org/10.21037/tau-20-890
Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at http://dx.doi.org/10.21037/tau-20-890). The authors have no conflicts of interest to declare.
Ethical Statement: The authors are accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved. The study was conducted in accordance with the Declaration of Helsinki (as revised in 2013). This study used previously collected deidentified data, which was deemed exempt from review by the Ethics Committee of the Affiliated Zhongda Hospital of Southeast University.
Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.
References
- Sorokin I, Mamoulakis C, Miyazawa K, et al. Epidemiology of stone disease across the world. World J Urol 2017;35:1301-20. [Crossref] [PubMed]
- Han H, Segal AM, Seifter JL, et al. Nutritional Management of Kidney Stones (Nephrolithiasis). Clin Nutr Res 2015;4:137-52. [Crossref] [PubMed]
- Zeng G, Mai Z, Xia S, et al. Prevalence of kidney stones in China: an ultrasonography based cross-sectional study. BJU Int 2017;120:109-16. [Crossref] [PubMed]
- Parks JH, Coe FL. An increasing number of calcium oxalate stone events worsens treatment outcome. Kidney Int 1994;45:1722-30. [Crossref] [PubMed]
- Fujii Y, Okada A, Yasui T, et al. Effect of adiponectin on kidney crystal formation in metabolic syndrome model mice via inhibition of inflammation and apoptosis. PLoS One 2013;8:e61343. [Crossref] [PubMed]
- Khan SR. Reactive Oxygen Species as the Molecular Modulators of Calcium Oxalate Kidney Stone Formation: Evidence from Clinical and Experimental Investigations. J Urol 2013;189:803-11. [Crossref] [PubMed]
- Lee HJ, Jeong SJ, Park MN, et al. Gallotannin Suppresses Calcium Oxalate Crystal Binding and Oxalate-Induced Oxidative Stress in Renal Epithelial Cells. Biol Pharm Bull 2012;35:539-44. [Crossref] [PubMed]
- Antonelli JA, Maalouf NM, Pearle MS, et al. Use of the National Health and Nutrition Examination Survey to calculate the impact of obesity and diabetes on cost and prevalence of urolithiasis in 2030. Eur Urol 2014;66:724-9. [Crossref] [PubMed]
- Evan AP. Physiopathology and etiology of stone formation in the kidney and the urinary tract. Pediatr Nephrol 2010;25:831-41. [Crossref] [PubMed]
- Khan SR, Pearle MS, Robertson WG, et al. Kidney stones. Nat Rev Dis Primers 2016;2:16008. [Crossref] [PubMed]
- de Water R, Leenen PJ, Noordermeer C, et al. Cytokine production induced by binding and processing of calcium oxalate crystals in cultured macrophages. Am J Kidney Dis 2001;38:331-8. [Crossref] [PubMed]
- Evan AP, Lingeman JE, Worcester EM, et al. Renal histopathology and crystal deposits in patients with small bowel resection and calcium oxalate stone disease. Kidney Int 2010;78:310-7. [Crossref] [PubMed]
- Moutzouri E, Tsimihodimos V, Tselepis AD. Inflammatory biomarkers and cardiovascular risk assessment. Current knowledge and future perspectives. Curr Pharm Des 2013;19:3827-40. [Crossref] [PubMed]
- Pineda C, Fuentes-Gomez AJ, Hernandez-Diaz C, et al. Animal model of acute gout reproduces the inflammatory and ultrasonographic joint changes of human gout. Arthritis Res Ther 2015;17:37. [Crossref] [PubMed]
- Nardi J, Nascimento S, Goethel G, et al. Inflammatory and oxidative stress parameters as potential early biomarkers for silicosis. Clin Chim Acta 2018;484:305-13. [Crossref] [PubMed]
- Canales BK, Anderson L, Higgins L, et al. Second prize: Comprehensive proteomic analysis of human calcium oxalate monohydrate kidney stone matrix. J Endourol 2008;22:1161-7. [Crossref] [PubMed]
- Ohtani H. Focus on TILs: prognostic significance of tumor infiltrating lymphocytes in human colorectal cancer. Cancer Immun 2007;7:4. [PubMed]
- Capone M, Giannarelli D, Mallardo D, et al. Baseline neutrophil-to-lymphocyte ratio (NLR) and derived NLR could predict overall survival in patients with advanced melanoma treated with nivolumab. J Immunother Cancer 2018;6:74. [Crossref] [PubMed]
- Lech M, Rommele C, Anders HJNDT. Pentraxins in nephrology: C-reactive protein, serum amyloid P and pentraxin-3. 2013;28:803-11.
- Ansar W, Ghosh SJIR. C-reactive protein and the biology of disease. Immunol Res 2013;56:131-42. [Crossref] [PubMed]
- Shoag J, Eisner BH. Relationship between C-reactive protein and kidney stone prevalence. J Urol 2014;191:372-5. [Crossref] [PubMed]