Evaluation of renal function in the Brazilian adult population, according to laboratory criteria from the National Health Survey

Deborah Carvalho Malta Ísis Eloah Machado Cimar Azeredo Pereira André Willian Figueiredo Lilian Kelen de Aguiar Wanessa da Silva de Almeida Maria de Fatima Marinho de Souza Luiz Gastão Rosenfeld Célia Landman Szwarcwald About the authors

ABSTRACT:

Objective:

To evaluate the renal function of the Brazilian adult population, according to laboratory criteria of the National Health Survey (Pesquisa Nacional de Saúde - PNS).

Methodology:

A descriptive study was carried out with laboratory data from the PNS, which was collected between the years 2014 and 2015. Population prevalence of the serum creatinine (CR) and estimated glomerular filtration rate (GFR) according to sociodemographic variables, were analyzed from the PNS laboratory data.

Results:

The sample consisted of 8,535 individuals aged 18 years old or older for the study of CR and 7,457 for the study of GFR. The GFR prevalence < 60 mL/min/1.73 m2 was 6.7% (95%CI 6.0 - 7.4), higher in women (8.2% 95%CI 7.2 - 9.2) than in men (5.0% 95%CI 4.2 - 6.0) p < 0.001, and in elderly > 60 years old it was 21.4%. For the values of CR ≥ 1.3 mg/dL in men were 5.5% (95%CI 4.6 - 6.5), and in women values of CR ≥ 1.1 mg/dL were 4.6% (95%CI 4.0 - 5.4), with no diference between the genders, p = 0.140.

Conclusion:

Results from the PNS laboratory identified a higher prevalence of chronic kidney disease in the Brazilian population than that estimated in self-reported studies, with higher GFR < 60 mL/min/1.73 m2 in women, and reaching one fifth of the elderly. These tests may be useful for the purpose of identifying the disease early on and thus preventing the progression of renal damage and reduce the risk of cardiovascular events and mortality.

Keywords:
Chronic renal insufficiency; Creatinine; Glomerular filtration rate; Risk factors; Health survey; Noncommunicable diseases

INTRODUCTION

Chronic kidney disease (CKD) is the gradual loss of renal structure and function, resulting in progressive loss of physiological function of the kidneys11. Bastos MG. Doença renal crônica no idoso. In: Canziani MEF, Kirsztajn GM, editores. Doença renal crônica: manual prático. São Paulo: Livraria Balieiro, 2013. p.50-65.. The decline in renal function is associated with increased mortality, morbidity, limitations in daily life, physical disability and loss of quality of life22. Chen YC, Weng SC, Liu JS, Chuang HL, Hsu CC, Tarng DC. Severe decline of estimated glomerular filtration rate associates with progressive cognitive deterioration in the elderly: a community-based cohort study. Sci Rep 2017; 7: 42690. http://doi.org/10.1038/srep42690
http://doi.org/10.1038/srep42690...
.

The prevalence of CKD has increased worldwide due to population aging and metabolic risk factors such as hypertension, obesity, diabetes and the use of nephrotoxic agents33. Jha V, Garcia-Garcia G, Iseki K, Li Z, Naicker S, Plattner B, et al. Chronic kidney disease: global dimension and perspectives. Lancet 2013; 382(9888): 260-72. http://doi.org/10.1016/S0140-6736(13)60687-X
http://doi.org/10.1016/S0140-6736(13)606...
.

Early diagnosis of CKD can be performed through routine laboratory tests such as blood creatinine dosage and glomerular filtration rate44. Pena PFA, Silva Júnior AG, Oliveira PTR, Moreira GAR, Libório AB. Cuidado ao paciente com Doença Renal Crônica no nível primário: pensando a integralidade e o matriciamento. Ciênc Saúde Coletiva 2012; 17(11): 3135-44. http://dx.doi.org/10.1590/S1413-81232012001100029
http://dx.doi.org/10.1590/S1413-81232012...
. Creatinine is the most commonly used screening test for renal function assessments and is also used to estimate glomerular filtration rates in CKD screenings55. Vidigal PG. Investigação laboratorial do paciente com disfunção renal. In: Erichsen ES, Iana LG, Faria RMDF, Santos SME, editores. Medicina laboratorial para o clínico. Belo Horizonte: Coopmed; 2009. p.439-68.. It is a residual product of creatine and phosphocreatine metabolism present mainly in skelet al muscles, so people with higher muscle mass tend to have physiologically higher creatinine excretion66. Cirillo M. Evaluation of glomerular filtration rate and of albuminuria/proteinuria. J Nephrol 2010; 23(2): 125-32.. This excretion occurs mainly in renal ducts, 85.0% by glomerular filtration and 15.0% by tubular secretion55. Vidigal PG. Investigação laboratorial do paciente com disfunção renal. In: Erichsen ES, Iana LG, Faria RMDF, Santos SME, editores. Medicina laboratorial para o clínico. Belo Horizonte: Coopmed; 2009. p.439-68.. Due to its availability and low cost, creatinine is the most widespread clinical screening test for renal function assessment.

Glomerular filtration rate (GFR) estimation is commonly used as the standard measure and is an important indicator for the detection, evaluation and prognosis of CKD77. Brito TNS, Oliveira ARS, Silva AKC. Taxa de filtração glomerular estimada em adultos: características e limitações das equações utilizadas. RBAC 2016; 48(1): 7-12.. The progressive decrease in GFR secondary to irreversible loss of functioning nephrons is manifested at first by a persistent increase in plasma levels of the products that are normally excreted by the kidneys such as blood urea and creatinine88. Levey AS, Stevens LA, Schmid CH, Zhang YL,Castro AF 3rd,Feldman HI, et al. A new equation to estimate glomerular filtration rate. Ann Intern Med 2009; 150(9): 604-12. https://doi.org/10.7326/0003-4819-150-9-200905050-00006
https://doi.org/10.7326/0003-4819-150-9-...
. As the damage progresses, other laboratory alterations and clinical manifestations appear. Progressive deterioration over time produces toxic substance accumulation with a variety of biochemical disorders and multiple symptomatology depending on the stage of CKD99. Stevens LA, Coresh J, Greene T, Levey AS. Assessing kidney function - measured and estimated glomerular filtration rate. N Engl J Med 2006; 354(23): 2473-83. http://doi.org/10.1056/NEJMra054415
http://doi.org/10.1056/NEJMra054415...
.

In Brazil, approximately 280 thousand patients registered in dialysis programs in the Unified Health System (Sistema Único de Saúde - SUS) network were identified between 2000 and 2012, which corresponds to 85% of the dialysis performed in the country1010. Moura L de, Prestes IV, Duncan BB, Schmidt MI. Construção de base de dados nacional de pacientes em tratamento dialítico no Sistema Único de Saúde, 2000-2012. Epidemiol Serv Saúde [Internet]. 2014 [acessado em 05 dez. 2018; 23(2): 227-38. Disponível em: Disponível em: http://scielo.iec.gov.br/pdf/ess/v23n2/v23n2a04.pdf http://doi.org/10.5123/S1679-49742014000200004
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.

CKD was initially monitored in Brazil with self-reported research, such as with the National Household Sample Survey (Pesquisa Nacional por Amostra de Domicílio - PNAD) and the National Health Survey (Pesquisa Nacional de Saúde - PNS). However, self-reported surveys may cause underreporting of the disease. Thus, the Brazilian Institute of Geography and Statistics (Instituto Brasileiro de Geografia e Estatística - IBGE) and the Ministry of Health, between 2014 and 2015, added the laboratory component to the PNS, through laboratory creatinine dosage and GFR estimation in the adult population. As such, it is expected to establish population prevalence of CKD, as it is a milestone in the surveillance of the disease in Brazil.

The aim of this study was to analyze the prevalence of chronic kidney disease (CKD) in the Brazilian adult population, according to laboratory criteria from the PNS.

METHODOLOGY

This is a descriptive epidemiological study, using data from PNS laboratory exams from 2014 to 2015. The PNS is a nationwide household-based cross-sectional survey using three-stage probabilistic samples. The primary sampling units (UPAs) were the census tracts or set of sectors, the secondary units, the households, and the tertiary units, the adult residents, aged 18 years or older. Details on the sampling and weighting processes are provided in the publication on the results of PNS1111. Szwarcwald CL, Malta DC, Pereira CA, Vieira MLFP, Conde WL, Souza Júnior PRB, et al. Pesquisa Nacional de Saúde no Brasil: concepção e metodologia de aplicação. Ciênc Saúde Coletiva 2014; 19(2): 333-42. http://dx.doi.org/10.1590/1413-81232014192.14072012
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.

The PNS sample was calculated in 81,254 households, the survey was conducted in 64,348households, and 60,202 adults were interviewed. The laboratory subsample was defined in 25% of the census tracts, assuming a non-response rate of 20%. The expected number of individuals with laboratory data was 12,000. However, there were several losses in the collection process. Among them, the difficulty of locating the research participants’ address and the selected residents’ refusal to perform the biological material collection. Thelaboratory sample consisted of 8,952 people, however due to the loss of biological material and the lack of information such as age, the plasma creatinine values of 8,535 participants and the GFR of 7,457 were obtained.

We considered the sampling process weights, and the post-stratification weights were performed according to gender, age, education and region, in order to correct for possible biases. Thus, the laboratory sample represents the Brazilian adult population. More details of the sampling process can be found in other publications1111. Szwarcwald CL, Malta DC, Pereira CA, Vieira MLFP, Conde WL, Souza Júnior PRB, et al. Pesquisa Nacional de Saúde no Brasil: concepção e metodologia de aplicação. Ciênc Saúde Coletiva 2014; 19(2): 333-42. http://dx.doi.org/10.1590/1413-81232014192.14072012
http://dx.doi.org/10.1590/1413-812320141...
,1212. Instituto Brasileiro de Geografia e Estatística. Nota Técnica - Resultados dos Exames Laboratoriais da Pesquisa Nacional de Saúde. Rio de Janeiro: Instituto Brasileiro de Geografia e Estatística; 2018..

The collection and analysis of the biological material were carried out through a consortium with private laboratories. The laboratories were chosen based on those that met the quality control criteria of the Ministry of Health and those that ensured the compliance with current rules for collection, transport and processing of biological material1212. Instituto Brasileiro de Geografia e Estatística. Nota Técnica - Resultados dos Exames Laboratoriais da Pesquisa Nacional de Saúde. Rio de Janeiro: Instituto Brasileiro de Geografia e Estatística; 2018..

Having the data of the household location and the selected individual, the laboratory technician informed the participant about the procedure to be performed. The participant was asked to fill out the Free and Informed Consent Form. After that they were presented with the collection kit and were given guidance on how to receive the report containing the results.

Full details of the laboratory sample collection procedure for testing are available in other publications1212. Instituto Brasileiro de Geografia e Estatística. Nota Técnica - Resultados dos Exames Laboratoriais da Pesquisa Nacional de Saúde. Rio de Janeiro: Instituto Brasileiro de Geografia e Estatística; 2018..

To collect creatinine (CR), a sample was collected in a gel tube. Thirty minutes passed until clot retraction, and centrifugation was performed at 3,200 revolutions per minute (RPM) for 12 minutes. The analysis was performed using the Jaffé method without deproteinization. For serum creatinine, the following ranges were adopted: for men (CR): <0.6 mg/dL; 0.6 to <1.3 mg/dL, normal values; ≥ 1.3 to <3 mg/dL, slight change; ≥3to <7mg/dL, moderate change, and ≥ 7mg/dL, high change, and for women: <0.6mgdL; 0.6 to <1.1 mg/dL, normal values; ≥ 1.1 to <3 mg/dL, slight change; ≥ 3 to <7­mg/­dL, moderate change, and ≥ 7 mg/dL, high change. For the dichotomous analysis, the values ≥ 1.3 mg/dL were considered increased for males and ≥ 1.1 mg/dL were considered increased for females. It is worth noting that there are differences between the cutoffs adopted in several studies1313. Kidney Disease Improving Global Outcomes. KDIGO 2012 Clinical Practice Guideline for the Evaluation and Management of Chronic Kidney Disease. Kidney Int Suppl. [Internet]. 2013 [acessado em 11 jan. 2018]; 3(1): 1-150. Disponível em: Disponível em: https://kdigo.org/wp-content/uploads/2017/02/KDIGO_2012_CKD_GL.pdf
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,1414. Barreto SM, Ladeira RM, Duncan BB, Schmidt MI, Lopes AA, Benseñor IM, et al. Chronic kidney disease among adult participants of the ELSA-Brazil cohort: association with race and socioeconomic position. J Epidemiol Community Health 2016; 70(4): 380-9. http://doi.org/10.1136/jech-2015-205834
http://doi.org/10.1136/jech-2015-205834...
, although there is consensus that CR values are higher among men1313. Kidney Disease Improving Global Outcomes. KDIGO 2012 Clinical Practice Guideline for the Evaluation and Management of Chronic Kidney Disease. Kidney Int Suppl. [Internet]. 2013 [acessado em 11 jan. 2018]; 3(1): 1-150. Disponível em: Disponível em: https://kdigo.org/wp-content/uploads/2017/02/KDIGO_2012_CKD_GL.pdf
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,1414. Barreto SM, Ladeira RM, Duncan BB, Schmidt MI, Lopes AA, Benseñor IM, et al. Chronic kidney disease among adult participants of the ELSA-Brazil cohort: association with race and socioeconomic position. J Epidemiol Community Health 2016; 70(4): 380-9. http://doi.org/10.1136/jech-2015-205834
http://doi.org/10.1136/jech-2015-205834...
,1515. Szwarcwald CL, Malta DC, Pereira CA, Figueiredo AW, Almeida WS, Machado ÍE, et al. Valores de referência para exames laboratoriais de colesterol, hemoglobina glicosilada e creatinina da população adulta brasileira segundo a Pesquisa Nacional de Saúde. Rev Bras Epidemiol 2019. (no prelo.). Higher creatinine reference values among men were also confirmed in another PNS laboratory study1515. Szwarcwald CL, Malta DC, Pereira CA, Figueiredo AW, Almeida WS, Machado ÍE, et al. Valores de referência para exames laboratoriais de colesterol, hemoglobina glicosilada e creatinina da população adulta brasileira segundo a Pesquisa Nacional de Saúde. Rev Bras Epidemiol 2019. (no prelo.).

The GFR was calculated based on creatinine, by predictive equations using correction factors (age and gender)1313. Kidney Disease Improving Global Outcomes. KDIGO 2012 Clinical Practice Guideline for the Evaluation and Management of Chronic Kidney Disease. Kidney Int Suppl. [Internet]. 2013 [acessado em 11 jan. 2018]; 3(1): 1-150. Disponível em: Disponível em: https://kdigo.org/wp-content/uploads/2017/02/KDIGO_2012_CKD_GL.pdf
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and by employing regression techniques to model it in a given population99. Stevens LA, Coresh J, Greene T, Levey AS. Assessing kidney function - measured and estimated glomerular filtration rate. N Engl J Med 2006; 354(23): 2473-83. http://doi.org/10.1056/NEJMra054415
http://doi.org/10.1056/NEJMra054415...
. The GFR (in mL/min/1.73 m2)1616. da Silva MMH, Brune MFSS. Importância do cálculo da taxa de filtração glomerular na avaliação da função renal de adultos. Rev Bras Farm 2011; 92(3): 160-5. was calculated by separate equations for men and women and, according to the following formulas, according to gender:

  • If female: (175 * ((1 / serum creatinine result) 1,154) * ((1 / patient’s age in years) 0.203) * 0.742);

  • If male: 175 * ((1/serum creatinine result) 1,154) * ((1/ patient’s age in years) 0.203).

For GFR, cutoff points were adopted according to the guidelines of the Chronic Kidney Disease1313. Kidney Disease Improving Global Outcomes. KDIGO 2012 Clinical Practice Guideline for the Evaluation and Management of Chronic Kidney Disease. Kidney Int Suppl. [Internet]. 2013 [acessado em 11 jan. 2018]; 3(1): 1-150. Disponível em: Disponível em: https://kdigo.org/wp-content/uploads/2017/02/KDIGO_2012_CKD_GL.pdf
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group. A diagnosis of renal insufficiency is considered when GFR is less than 60­mL/­min /1.73 m2, and severe renal insufficiency or renal failure is considered when GFR is less than 15 mL/min/1.73 m213,14.

  • Normal (≥ 90 and <120 mL/min/1.73 m2);

  • Slight decrease in GFR (≥ 60 and <90 mL/min/1.73 m2);

  • Moderate decrease in GFR (≥ 30 and <60 mL/min/1.73 m2);

  • Severe decrease in GFR (≥ 15 and <30 mL/min/1.73 m2).

The same equation was used for the black population, as has been proposed by most methods1313. Kidney Disease Improving Global Outcomes. KDIGO 2012 Clinical Practice Guideline for the Evaluation and Management of Chronic Kidney Disease. Kidney Int Suppl. [Internet]. 2013 [acessado em 11 jan. 2018]; 3(1): 1-150. Disponível em: Disponível em: https://kdigo.org/wp-content/uploads/2017/02/KDIGO_2012_CKD_GL.pdf
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. Albuminuria parameters were not considered for the diagnosis of CKD, as it was not collected in the PNS.

In the current study, creatinine and GFR prevalence were stratified by gender, age group (18-29, 30-49, 40-59, 60 years or older), skin color, education, and region.

The data analysis were obtained with the aid of the statistical software Stata, version 14.0. A set of commands for the data analysis of surveys with a complex sample (survey) were used.

The PNS was approved by the National Research Ethics Commission (Comissão Nacional de Ética em Pesquisa - CONEP) of the National Health Council (Conselho Nacional de Saúde - CNS), of the Ministry of Health. Adult participation in the research was voluntary and confidentiality of their information was guaranteed.

RESULTS

The results were calculated by the stratified formulas according to gender. Table 1 shows the distribution of the different ranges of GFR estimates. GFR ≥120 mL/min/1.73 m2 and GFR ≥ 90 and <120 mL/min/1.73 m2 showed no difference according to gender, and was higher in the groups aged 18 to 29 years old.

Table 1.
Glomerular filtration rate according to different cutoff points. Brazil, National Health Survey (PNS), 2014-2015.

The prevalence found for GFR > 30 to <60 mL/min/1.73 m2 was 6.4%, ≥ 15 to <30­mL/­min/1.73 m2 of 0.1% and <15 mL/min/1.73 m2 was 0.2%. GFR values ≥ 30 and <60 mL/min/1.73 m2 were higher in women (7.8% 95%CI 6.9 - 8.8) than in men (4.8% 95%CI 4.0 - 5.8), with an increase in the age group 60 years or older (20.8%95%CI 17.9 - 24.1) and among less educated individuals (9.1% CI95 % 7.9 - 10.4) (Table 1).

Table 2 shows the prevalences of GFR below <60 mL/min/1.73 m2. Reduced GFR was higher in women (8.2% 95%CI 7.2 - 9.2) p <0.001, increased with age, was higher in the age group of 60 years or older (21.4% 95%CI 18.4 - 24.7) p <0.001, and had no change according to skin color. The population with a higher level if education had a lower prevalence (4.8% 95%CI 4.0 - 5.7) p <0.001, and was higher among residents of the Northern Region (9.295%CI7.7-10.9) p <0.001 (Table 2).

Table 2.
Glomerular filtration rate < 60 mL/min/1.73 m2, according to gender. Brazil, National Health Survey (PNS), 2014-2015.

The different creatinine strata are described in Table 3. Creatinine values between 0.6 and <1.3 mg/dL were found in 93.9% of men and between 0.6 and <1.1 mg/dL in 83.9% of women. Altered creatinine in men, CR ≥ 1.3 to <3 mg/dL was 5.3% and in women, CR≥1.1 to <3 mg/dL was 4.4%. Values between CR ≥ 3 to <7 mg/dL and CR ≥ 7 mg/dL were 0.1% in both sexes and strata (Table 3).

Table 3.
Plasma creatinine values, according to sociodemographic variables. Brazil, National Health Survey (PNS), 2014-2015.

Increased creatinine in men (CR ≥ 1.3 mg/dL) was found to be 5.5% 95%CI 4.6 - 6.5, and in women (CR ≥ 1.1 mg/dL), it was found to be 4.6% (95%CI 4 - 5.4). It was higher in the population aged 60 years or older (12.2% 95% CI 10.4 - 14.2), had lower prevalence in the population with an education of 12 years or more (3.8% 95% CI 3.1 - 4.7) and was higher in the Northern Region (8.1% 95%CI 6.8 - 9.7) (Table 4).

Table 4.
Frequency of creatinine values ≥ 1.3 mg/dl for males and ≥ 1.1 mg/dl for females, Brazil, National Health Survey (PNS), 2014-2015.

DISCUSSION

This is the first national study to present a renal function assessment using laboratory criteria for the Brazilian adult population. The estimates given here were up to four times higher compared to the self-reported studies, suggesting the under-diagnosis of CKD in the country. The prevalence of GFR <60 was 6.7%, and was higher in women, the elderly and individuals with lower levels of education. Increased creatinine values were found in 5.0% of the population and were higher in the elderly, in people with low levels of education, and people living in the Northern Region. The study is innovative in that it uses equations that do not increase GFR among black people, so there was no difference in the prevalence of CKD between white and black people.

Age is an important factor in increased CKD. US survey data from the National Health and Nutrition Examination Surveys (NHANES)1717. Centers for Disease Control and Prevention. National Health and Nutrition Examination Survey [Internet]. Atlanta: Centers for Disease Control and Prevention; 2018 [acessado em 7 dez. 2018]. Disponível em: Disponível em: https://www.cdc.gov/visionhealth/vehss/data/national-surveys/national-health-and-nutrition-examination-survey.html
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show a gradual increase, rising from 6.6% in the 20 to 39 age group, to 10.6% in individuals aged 40 to 59, and increasing of 32.6% in those 60 and older, increasing Medicare health spending1818. Saran R, Robinson B, Abbott KC, Agodoa LY, Albertus P, Ayanian J, et al. US Renal Data System 2016 Annual Data Report: Epidemiology of Kidney Disease in the United States. Am J Kidney Dis 2017; 69(3 Supl. 1): A7-A8. http://doi.org/10.1053/j.ajkd.2016.12.004
http://doi.org/10.1053/j.ajkd.2016.12.00...
. Reduction in GFR is expected with increasing age as a function of physiological aging, in which renal blood flow decreases and glomerular membrane permeability increases1919. Bolignano D, Mattace-Raso F, Sijbrands EJ, Zoccali C. The aging kidney revisited: a systematic review. Ageing Res Rev 2014; 14: 65-80. http://doi.org/10.1016/j.arr.2014.02.003
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,2020. Karam Z, Tuazon J. Anatomic and physiologic changes of the aging kidney. Clin Geriatr Med 2013; 29(3): 555-64. http://doi.org/10.1016/j.cger.2013.05.006
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. Among the main causes for reduced renal function in the elderly are systemic arterial hypertension, smoking exposure, dyslipidemia, obesity, and polypharmacy2121. El Essawy AB, Mousa D, Al-Sulaiman M. Dilemma of renal disease in elderly. Saudi J Kidney Dis Transpl 2008; 19(4): 669-77.. Possible overestimation of the prevalence of CKD in the elderly has been discussed in the literature, and some studies suggest that a lower cutoff point should be adopted for the classification of CKD in this population.

The literature also indicates that male sex are more associated with loss of renal function, with lower GFR 2121. El Essawy AB, Mousa D, Al-Sulaiman M. Dilemma of renal disease in elderly. Saudi J Kidney Dis Transpl 2008; 19(4): 669-77.,2424. Moura L, Andrade SSCA, Malta DC, Pereira CA, Passos JEF. Prevalência de autorrelato de diagnóstico médico de doença renal crônica no Brasil: Pesquisa Nacional de Saúde, 2013. Rev Bras Epidemiol 2015; 18(Supl. 2): 181-91. http://dx.doi.org/10.1590/1980-5497201500060016
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,2525. Cherchiglia ML, Machado EL, Szuster DAC, Andrade EIG, Acúrcio FA, Caiaffa WT, et al. Perfil epidemiológico dos pacientes em terapia renal substitutiva no Brasil, 2000-2004. Rev Saúde Pública 2010; 44(4): 639-49. http://dx.doi.org/10.1590/S0034-89102010000400007
http://dx.doi.org/10.1590/S0034-89102010...
, differing from the current study, which identified a higher prevalence in women.

Creatine metabolism, creatinine metabolite, originates mainly from skelet al muscle, and because men have higher muscle mass, they tend to have higher physiological CR values66. Cirillo M. Evaluation of glomerular filtration rate and of albuminuria/proteinuria. J Nephrol 2010; 23(2): 125-32.. This origin explains why creatinine reference values within the normal range are higher in men (0.8 - 1.3 mg/dL) than in women (0.6 - 1.0 mg/dL)66. Cirillo M. Evaluation of glomerular filtration rate and of albuminuria/proteinuria. J Nephrol 2010; 23(2): 125-32.. Thus, cutoff points and GFR estimation equations were different considering gender and age differences1313. Kidney Disease Improving Global Outcomes. KDIGO 2012 Clinical Practice Guideline for the Evaluation and Management of Chronic Kidney Disease. Kidney Int Suppl. [Internet]. 2013 [acessado em 11 jan. 2018]; 3(1): 1-150. Disponível em: Disponível em: https://kdigo.org/wp-content/uploads/2017/02/KDIGO_2012_CKD_GL.pdf
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.

Studies from the NHANES found a higher prevalence of CKD in African Americans (16.9%) thanin white Americans (15.2%)1717. Centers for Disease Control and Prevention. National Health and Nutrition Examination Survey [Internet]. Atlanta: Centers for Disease Control and Prevention; 2018 [acessado em 7 dez. 2018]. Disponível em: Disponível em: https://www.cdc.gov/visionhealth/vehss/data/national-surveys/national-health-and-nutrition-examination-survey.html
https://www.cdc.gov/visionhealth/vehss/d...
,1818. Saran R, Robinson B, Abbott KC, Agodoa LY, Albertus P, Ayanian J, et al. US Renal Data System 2016 Annual Data Report: Epidemiology of Kidney Disease in the United States. Am J Kidney Dis 2017; 69(3 Supl. 1): A7-A8. http://doi.org/10.1053/j.ajkd.2016.12.004
http://doi.org/10.1053/j.ajkd.2016.12.00...
. However, these results differ from the current study, which did not identify differences according to skin color. The Brazilian Longitudinal Study of Adult Health (Elsa Brazil) used similar equations for whites and blacks, which is more adequate for the reality of the country and, after these adjustments, found no differences due to skin color1414. Barreto SM, Ladeira RM, Duncan BB, Schmidt MI, Lopes AA, Benseñor IM, et al. Chronic kidney disease among adult participants of the ELSA-Brazil cohort: association with race and socioeconomic position. J Epidemiol Community Health 2016; 70(4): 380-9. http://doi.org/10.1136/jech-2015-205834
http://doi.org/10.1136/jech-2015-205834...
. A cross-sectional study in Rio de Janeiro also did not apply the 20% correction in GFR, and similarly there were no differences between blacks and whites in CKD prevalence88. Levey AS, Stevens LA, Schmid CH, Zhang YL,Castro AF 3rd,Feldman HI, et al. A new equation to estimate glomerular filtration rate. Ann Intern Med 2009; 150(9): 604-12. https://doi.org/10.7326/0003-4819-150-9-200905050-00006
https://doi.org/10.7326/0003-4819-150-9-...
. In light of these results, we strongly suggest revising these equations to estimate GFR, regarding the correction factor according to skin color.

The GFR increased in individuals with lower levels of education, proxy of socioeconomic status, due to greater difficulty in accessing health systems and diagnoses and due to inadequate control of the disease2626. Zambonato TK, Thomé FS, Gonçalves LFS. Perfil socioeconômico dos pacientes com doença renal crônica em diálise na região noroeste do Rio Grande do Sul. J Bras Nefrol 2008; 30(3): 192-9.. A study that analyzed the socioeconomic profile of patients with CKD found that patients on hemodialysis had significantly lower levels of education2626. Zambonato TK, Thomé FS, Gonçalves LFS. Perfil socioeconômico dos pacientes com doença renal crônica em diálise na região noroeste do Rio Grande do Sul. J Bras Nefrol 2008; 30(3): 192-9.. Another study found that 3.2% of CKD patients were not literate and 34.9% had not completed elementary school2727. Oliveira CS, Cardoso da Silva E, Ferreira LW, Skalinski LM. Perfil dos pacientes renais crônicos em tratamento hemodialítico. Rev Baiana Enferm 2015; 29(1): 1-8. http://dx.doi.org/10.18471/rbe.v29i1.12633
http://dx.doi.org/10.18471/rbe.v29i1.126...
. In addition, low levels of education can interfere in the adherence and access to proper treatment, as well as quality of life, since it compromises access to health information and represents difficulties in understanding guidelines provided by health professionals2828. Marinho CLA, de Oliveira JF, Borges JES, da Silva RS, Fernandes FECV. Qualidade de vida de pessoas com doença renal crônica em hemodiálise. Rev Rene 2017; 18(3): 396-403.. In the Elsa Brazil study, the prevalence of CKD also increased in those with primary and secondary education when compared with those with higher levels of education1414. Barreto SM, Ladeira RM, Duncan BB, Schmidt MI, Lopes AA, Benseñor IM, et al. Chronic kidney disease among adult participants of the ELSA-Brazil cohort: association with race and socioeconomic position. J Epidemiol Community Health 2016; 70(4): 380-9. http://doi.org/10.1136/jech-2015-205834
http://doi.org/10.1136/jech-2015-205834...
.

The literature indicates that creatinine has been the most widespread screening test in clinical practice, due to its availability and low cost 55. Vidigal PG. Investigação laboratorial do paciente com disfunção renal. In: Erichsen ES, Iana LG, Faria RMDF, Santos SME, editores. Medicina laboratorial para o clínico. Belo Horizonte: Coopmed; 2009. p.439-68.,2929. Bastos MG, Carmo WB, Abrita RR, Almeida EC, Mafra D, Costa DMN, et al. Doença renal crônica: problemas e soluções. J Bras Nefrol 2004; 26(4): 202-15.. The authors suggest that serum creatinine dosage enables the calculation of endogenous glomerular filtration and/or renal clearance. However, its use may be a late parameter in detecting impaired renal function, since the change occurs after the patient loses about 50 to 60% of GFR. Therefore, CKD may be under-diagnosed when using only creatinine as a parameter for the disease. Thereare other markers such as cystatin, inulin among others, which would be more specific, though more expensive and not used in clinical practice3030. Masson I, Maillard N, Tack I, Thibaudin L, Dubourg L, Delanaye P, et al. GFR estimation using standardized cystatin C in kidney transplant recipients. Am J Kidney Dis 2013; 61(2): 279-84. http://doi.org/10.1053/j.ajkd.2012.09.010
http://doi.org/10.1053/j.ajkd.2012.09.01...
.

Limitations of the study include the use of serum creatinine to estimate GFR and the fact that other tests, such as albuminuria, which is included in the laboratory classification criteria for CKD, were not considered, which may have underestimated the prevalence found in this study. There are different equations for GFR, and there may be large variations in estimates depending on the method employed, which may change the sensitivity and specificity of the test.

CONCLUSION

The present study evaluated renal function in the Brazilian population through serum creatinine and GFR, analyzing laboratory data from the PNS. The biochemical data analyzed here indicate higher population prevalence when compared to surveys using self-reported questions from previous medical diagnoses. The GFR <60 was higher in the elderly, in women, and in less educated populations. The study points out that there was no difference according to skin color and suggests a review of the equations that estimate GFR according to this parameter, confirming that the 20% increase in GFR calculation among black people should not be included to the formula. The equation in the form as it has been used may underestimate the diagnosis of CKD among black people, delaying the diagnosis of declining renal function among them.

The PNS was a landmark in surveillance by including laboratory tests and estimating underreporting of CKD in the Brazilian population. CKD is considered a public health problem, with an important impact on morbidity and mortality and loss of quality of life. CKD surveillance, including monitoring of population and patient epidemiological data, can improve care planning as well as treatment effectiveness, and thus, can support coping with this problem. The higher prevalence of CKD in the elderly demonstrates the need for an early diagnosis, especially in at-risk groups. The use of measures of creatinine and GFR may be useful in the early identification of the disease, which can thus prevent the progression of renal damage and reduce the risk of cardiovascular events and mortality.

ACKNOWLEDGMENTS

To Dr. Jarbas Barbosa and Dr. Gonzalo Vecina, for their support in conducting the National Health Survey (PNS). To Dr. Lenildo de Moura, for introducing the idea of working with the PNS. To the National Council for Scientific and Technological Development/CNPq, the Junior Postdoctoral fellowship received by author IEM and the Research Productivity grant received by author DCM.

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  • Financial support: Health Surveillance Secretariat, Ministry of Health (TED 147/2018).

Publication Dates

  • Publication in this collection
    07 Oct 2019
  • Date of issue
    2019

History

  • Received
    19 Dec 2018
  • Reviewed
    24 Jan 2019
  • Accepted
    12 Feb 2019
Associação Brasileira de Pós -Graduação em Saúde Coletiva São Paulo - SP - Brazil
E-mail: revbrepi@usp.br