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Incidence of chronic obstructive pulmonary disease based on three spirometric diagnostic criteria in Sao Paulo, Brazil: a nine-year follow-up since the PLATINO prevalence study

Incidência de doença pulmonar obstrutiva crônica com base em três critérios diagnósticos espirométricos em São Paulo, Brasil: seguimento de nove anos após o estudo de prevalência PLATINO

Abstracts

CONTEXT AND OBJECTIVE:

Chronic obstructive pulmonary disease (COPD) is a respiratory disease of high prevalence and socioeconomic impact worldwide. It affects approximately 16% of the population of São Paulo. The incidence of COPD is still unknown in Brazil. The aim of this study was to estimate new cases of COPD in a population-based sample in São Paulo, Brazil, using three different spirometric diagnostic criteria, and to assess the concordance between these criteria.

DESIGN AND SETTING:

Prospective cohort study, in the city of São Paulo, Brazil.

METHODS:

A questionnaire was applied and anthropometry and pre and post-bronchodilator spirometry were performed on the same subjects as in the initial PLATINO study (2003) in São Paulo. Data from this follow-up study were added to the original database of the initial phase. Incident COPD cases refer to subjects who developed the disease in accordance with each spirometric criterion during the nine-year follow-up period. The Statistical Package for the Social Sciences, version 17.0 (SPSS Inc., Chicago, IL, USA) was used in the analysis and the significance level was set at P < 0.05.

RESULTS:

613 subjects participated in the follow-up. New COPD cases ranged in frequency from 1.4% to 4.0%, depending on the diagnostic criterion used. The concordance between the criteria ranged from 35% to 60%.

CONCLUSION:

The incidence of COPD after a nine-year follow-up was high, but varied according to the spirometric criterion used. The agreement between the criteria for identifying new cases of the disease ranged from 35% to 60%.

Pulmonary disease, chronic obstructive; Incidence; Diagnosis; Epidemiology; Spirometry


CONTEXTO E OBJETIVO:

A doença pulmonar obstrutiva crônica (DPOC) é uma enfermidade respiratória de alta prevalência e grande impacto socioeconômico no mundo e afeta aproximadamente 16% da população paulista. A incidência da DPOC ainda é desconhecida no Brasil. O objetivo deste estudo foi avaliar os novos casos de DPOC numa amostra de base populacional em São Paulo, Brasil, considerando três diferentes critérios diagnósticos espirométricos, e avaliar a concordância entre esses critérios.

TIPO DE ESTUDO E LOCAL:

Estudo de coorte prospectivo, na cidade de São Paulo, Brasil.

MÉTODOS:

Foi aplicado um questionário e realizadas a antropometria e espirometria pré e pós-broncodilatador nos mesmos indivíduos do Estudo PLATINO inicial (2003), de São Paulo. Dados deste estudo de seguimento foram adicionados ao banco de dados original da fase inicial. Os casos incidentes da DPOC se referem aos indivíduos que desenvolveram a doença de acordo com cada critério espirométrico durante os nove anos de seguimento. Foi utilizado o programa Statistical Package for the Social Sciences, version 17.0 (SPSS Inc., Chicago, IL, USA) na análise e o nível de significância foi P < 0.05.

RESULTADOS:

Participaram do seguimento 613 indivíduos. Os novos casos de DPOC variaram de 1,4% a 4,0%, dependendo do critério diagnóstico utilizado, e a concordância entre os critérios para identificar os casos incidentes variou de 35% a 60%.

CONCLUSÃO:

A incidência da DPOC após nove anos de seguimento foi alta, porém variável de acordo com o critério espirométrico utilizado. A concordância entre os critérios para identificar os novos casos da doença variou de 35% a 60%.

Doença pulmonar obstrutiva crônica; Incidência; Diagnóstico; Epidemiologia; Espirometria


INTRODUCTION

Chronic obstructive pulmonary disease (COPD) is a respiratory disease that has had great socioeconomic impact due to its high prevalence worldwide.1López Varela MV, Montes de Oca M. Variability in COPD: the PLATINO study viewpoint. Arch Bronconeumol. 2012;48(4):105-6. The prevalence of COPD in a population aged 40 years and older in São Paulo was found to be 15.8%, through the PLATINO study.2Menezes AM, Jardim JR, Pérez-Padilla R, et al. Prevalence of chronic obstructive pulmonary disease and associated factors: the PLATINO Study in Sao Paulo, Brazil. Cad Saude Publica. 2005;21(5):1565-73. Epidemiological studies in European, Asian and North American countries have estimated the prevalence of COPD in their populations to be 5-25%,3Rycroft CE, Heyes A, Lanza L, Becker K. Epidemiology of chronic obstructive pulmonary disease: a literature review. Int J Chron Obstruct Pulmon Dis. 2012;7:457-94. with incidence rates ranging from 1.5-11%.4Johannessen A, Omenaas E, Bakke P, Gulsvik A. Incidence of GOLD-defined chronic obstructive pulmonary disease in a general adult population. Int J Tuberc Lung Dis. 2005;9(8):926-32.

Lindberg A, Jonsson AC, Rönmark E, et al. Ten-year cumulative incidence of COPD and risk factors for incident disease in a symptomatic cohort. Chest. 2005;127(5):1544-52.

Lindberg A, Eriksson B, Larsson LG, et al. Seven-year cumulative incidence of COPD in an age-stratified general population sample. Chest. 2006;129(4):879-85.

Løkke A, Lange P, Scharling H, Fabricius P, Vestbo J. Developing COPD: a 25 year follow up study of the general population. Thorax. 2006;61(11):935-9.

Pelkonen M, Notkola IL, Nissinen A, Tukiainen H, Koskela H. Thirty-year cumulative incidence of chronic bronchitis and COPD in relation to 30-year pulmonary function and 40-year mortality: a follow-up in middle-aged rural men. Chest. 2006;130(4):1129-37.

de Marco R, Accordini S, Cerveri I, et al. Incidence of chronic obstructive pulmonary disease in a cohort of young adults according to the presence of chronic cough and phlegm. Am J Respir Crit Care Med. 2007;175(1):32-9.

10 Kojima S, Sakakibara H, Motani S, et al. Incidence of chronic obstructive pulmonary disease, and the relationship between age and smoking in a Japanese population. J Epidemiol. 2007;17(2):54-60.
- 1111 de Marco R, Accordini S, Marcon A, et al. Risk factors for chronic obstructive pulmonary disease in a European cohort of young adults. Am J Respir Crit Care Med. 2011;183(7):891-7. This variability can be attributed to the different spirometry criteria used to diagnose the disease.3Rycroft CE, Heyes A, Lanza L, Becker K. Epidemiology of chronic obstructive pulmonary disease: a literature review. Int J Chron Obstruct Pulmon Dis. 2012;7:457-94.

Among the spirometry criteria used in diagnosing airflow obstruction, the ones most commonly used are a fixed ratio of less than 0.7 between forced expiratory volume in one second (FEV1) and forced vital capacity (FVC) (FEV1/FVC < 0.7)1212 Vestbo J, Hurd SS, Agustí AG, et al. Global strategy for the diagnosis, management, and prevention of chronic obstructive pulmonary disease: GOLD executive summary. Am J Respir Crit Care Med. 2013;187(4):347-65. and a FEV1/FVC ratio below the lower limit of normality (LLN),1313 Pellegrino R, Viegi G, Brusasco V, et al. Interpretative strategies for lung function tests. Eur Respir J. 2005;26(5):948-68. which varies according to the subjects' age, height, race and sex, as obtained using reference equations. However, it has been suggested that using forced expiratory volume in six seconds (FEV6) would be an alternative to FVC, since this is approximately 25% less variable than FVC1414 Swanney MP, Jensen RL, Crichton DA, et al. FEV(6) is an acceptable surrogate for FVC in the spirometric diagnosis of airway obstruction and restriction. Am J Respir Crit Care Med. 2000;162(3 Pt 1):917-9. and is a good substitute for detecting airflow obstruction.

Measuring and monitoring a public health problem is the first step in elaborating public health administrative strategies.1515 Soriano JB, Lamprecht B. Chronic obstructive pulmonary disease: a worldwide problem. Med Clin North Am. 2012;96(4):671-80. Spirometry is essential in diagnosing COPD,1616 Joo MJ, Au DH, Lee TA. Use of spirometry in the diagnosis of chronic obstructive pulmonary disease and efforts to improve quality of care. Transl Res. 2009;154(3):103-10. regardless of the spirometric criteria used to identify airflow obstruction. Therefore, this follow-up study, which includes the subjects who took part in the initial phase of the PLATINO study,2Menezes AM, Jardim JR, Pérez-Padilla R, et al. Prevalence of chronic obstructive pulmonary disease and associated factors: the PLATINO Study in Sao Paulo, Brazil. Cad Saude Publica. 2005;21(5):1565-73. in São Paulo, is quite important, given that new cases of COPD can be identified using the same diagnostic procedures and that differences in the estimated incidence can be found in terms of the different spirometric criteria.

OBJECTIVE

The aim of the present study was to evaluate new cases of COPD at the end of a nine-year follow-up period, analyzing the same subjects who took part in the initial phase of the population-based PLATINO study in the city of São Paulo and taking into consideration three different diagnostic criteria: FEV1/FVC < 0.70 post-bronchodilator; FEV1/FVC < LLN post-bronchodilator; and FEV1/FEV6< LLN post-bronchodilator; and to identify the concordance of these criteria in the new cases.

METHODS

Sample and study design

The present study population was composed of the same subjects who took part in the initial phase of the population-based PLATINO study in São Paulo in 2003 (n = 1,000), in order to evaluate the prevalence of COPD in this city.

The initial PLATINO study (2003) began with stratification of the metropolitan area into the main municipality and its suburbs. These regions were then divided into socioeconomic segments. Taking into consideration the stratification and a sampling probability proportional to the size and the number of houses, 68 census tracts were selected from each segment (42 in the city of São Paulo and 26 in the other municipalities). The number of individuals within each census tract was updated based on the last census at the location. An average of 15 households (selected from the National Household Sampling Survey, 2002) was visited and systematic sampling was obtained.

A map of each census tract was drawn, and the blocks (or similar units) were numbered. In each sector, one block was randomly selected and one corner of the block was chosen. From the corner selected, every second house was visited until the necessary number of homes had been obtained. Data on the people living in each house were gathered and recorded in order to obtain the distribution according to age and sex. All the adults aged 40 years or older living in the selected households were invited to take part in the study, and they were included in the survey. The sample was self-weighted in each municipality.

The sample size calculations indicated that 800 individuals would be needed in each center if the prevalence was assumed to be up to 30% with a margin of error of less than 4 percentage points. The objective was to interview 20% more subjects per center, with an identical percentage of losses and refusals to participate. The final sample of the initial phase of the PLATINO study in São Paulo included 1,000 subjects.

All of the houses in which the subjects were interviewed in the initial phase of the PLATINO study were visited again in 2012. The initial contact was made by one of four screeners (the addresses were obtained from the evaluation forms of the initial phase of the PLATINO study), who confirmed whether the subjects still lived at those addresses, checked their telephone numbers and informed them about the interviewers' intended visit.

If the subjects no longer lived in the same house, the screeners sought to determine their whereabouts through information from neighbors and inquiries in neighborhood businesses, or by consulting telephone directories. The screeners visited subjects who had moved to another house in the same area. Subjects who had moved to another city within the state of São Paulo were contacted by phone and visited in their new city to determine whether they wished to continue taking part in the study. The names of subjects whose whereabouts were unknown were looked up in the registry of deaths within the state of São Paulo and other Brazilian states. All data obtained by the screeners were sent to the coordinating body responsible for organizing the files for the subsequent scheduling of interviews.

At each respondent's house, the researchers first asked for written informed consent from the subject. If the subject agreed to participate in the study, they proceeded to gather data in accordance with the following sequence: anthropometric assessment for body mass index (BMI) calculation; completion of the questionnaire with exclusion criteria for participation in spirometry; pre-bronchodilator spirometry; administration of a portion of the main questionnaire (during the first 15 minutes after bronchodilator administration); post-bronchodilator spirometry; and administration of the remainder of the main questionnaire.

The main questionnaire (PLATINO questionnaire) was composed of questions relating to demographic and social variables, reports of respiratory symptoms, medication information, diagnoses of respiratory diseases and comorbidities, smoking history, anti-influenza vaccinations, quality of life (SF-12 quality of life questionnaire) and indoor pollution and dust exposure.

Diagnosis

The diagnosis of COPD was confirmed by means of spirometry, using a portable battery-powered spirometer and an ultrasound system (Easy One spirometer; NDD Medical Technologies, Andover, MA, USA, and Zurich, Switzerland) that was identical to those used in the initial phase of the PLATINO study. The subjects performed up to 15 forced expiratory maneuvers (which was the maximum accepted by the team in one session), in order to obtain three acceptable maneuvers yielding the highest FEV1 and FVC values without exceeding a difference of 150 ml. Subsequently, an inhaled bronchodilator (salbutamol, 200 µg) was administered using a 500-ml spacer. The test was then repeated 15 minutes later. All spirometric tests were performed with the subjects seated and using a nose clip and a disposable mouthpiece. Only the expiratory phase was recorded.

In both the initial and the follow-up (2012) phase, the subjects were diagnosed using three criteria: FEV1/FVC < 0.70 post-bronchodilator;1212 Vestbo J, Hurd SS, Agustí AG, et al. Global strategy for the diagnosis, management, and prevention of chronic obstructive pulmonary disease: GOLD executive summary. Am J Respir Crit Care Med. 2013;187(4):347-65. FEV1/FVC < LLN post-bronchodilator;1313 Pellegrino R, Viegi G, Brusasco V, et al. Interpretative strategies for lung function tests. Eur Respir J. 2005;26(5):948-68. and FEV1/FEV6 < LLN post-bronchodilator.1717 Perez-Padilla R, Wehrmeister FC, Celli BR, et al. Reliability of FEV1/FEV6 to diagnose airflow obstruction compared with FEV1/FVC: the PLATINO longitudinal study. PLoS One. 2013;8(8):e67960.

The reference equation derived from the PLATINO study was used to calculate the predicted values and the LLN for FEV1, FEV6, FVC, FEV1/FVC, and FEV1/FEV6.1818 Perez-Padilla R, Torre Bouscoulet L, Vazquez-Garcia JC, et al. Valores de referencia para la espirometría después de la inhalación de 200 microg de salbutamol [Spirometry reference values after inhalation of 200 microg of salbutamol]. Arch Bronconeumol. 2007;43(10):530-4.

The present study was approved by the university's Research Ethics Committee (no. 04234/10). After being informed about the study and its procedures, all the subjects who agreed to participate provided written informed consent.

Statistical analysis

The data gathered during the follow-up phase of the PLATINO study were added to the original database of the initial phase of the study, which had been conducted in the city of São Paulo, Brazil, in 2003. The data analysis was performed using the Statistical Package for the Social Sciences, version 17.0 (SPSS Inc., Chicago, IL, USA), and the statistical significance level was set at P < 0.05.

Cumulative incidence refers to the number of onsets in a population at risk during a certain period. In this study, the new cases of COPD were obtained from among the subjects who developed the disease, in accordance with each spirometric diagnostic criterion, over the nine-year follow-up period. Preexisting cases, individuals who did not take part in the follow-up phase and individuals who did not undergo spirometry in either the initial or the follow-up phase of the PLATINO study were not included in the incidence calculation. Subjects who reported having a medical diagnosis of asthma and cases of FEV1 reversibility, as seen in the post-bronchodilator spirometry were considered eligible for analysis.

RESULTS

Out of the 1,000 subjects who took part in the initial phase of the PLATINO study, 944 were found again or information on their whereabouts after nine years was obtained. The reasons for the loss of follow-up were as follows: subject not found (n = 56), death (n = 135), refusal to participate (n = 141) and subject moved to another state/city and considered to be a "loss" (n = 55). Out of these 944 subjects, 613 took part in the follow-up phase of the study and 594 provided consent and underwent pre-bronchodilator and post-bronchodilator spirometry. The participants and non-participants (i.e. refusals, subject not found and subject who had moved to another state/city) of the follow-up PLATINO study had the same characteristics as the participants who took part in the initial phase of the study, in terms of sex, age, education level and pulmonary function. The only significant difference was in the proportion of former smokers, which was higher in the group of subjects who took part in the follow-up phase of the study, in relation to non-participants (37.6% versus 23.8%; P < 0.001). The data regarding the subjects who took part in the follow-up PLATINO study in São Paulo are presented in Figure 1.

Figure 1.
Flowchart for final sample in follow-up PLATINO study, São Paulo, Brazil.

The demographic and clinical data on the subjects who took part in the initial phase (n = 1,000) and follow-up phase (n = 613) of the PLATINO study are presented in Table 1. At the end of the nine-year follow-up period, the subjects showed deterioration in the physical domain of quality of life. The proportion of smokers was different, and thus, the proportion of former smokers was higher.

Table 1.
Clinical, anthropometric and functional characteristics of initial PLATINO participants (n = 1,000) and follow-up PLATINO participants (n = 613)

The new cases of COPD at the end of the nine-year follow-up period varied in terms of the spirometric criterion used to diagnose the disease: FEV1/FVC < 0.7 showed the highest proportion of onsets (Table 2). The three diagnostic criteria were concordant with regard to classifying six subjects who had COPD (Figure 2). The criterion FEV1/FEV6 < LLN with FEV1/FVC < LLN presented the highest level of concordance (60.0%) in classifying new COPD cases, followed by FEV1/FVC < 0.7 with FEV1/FEV6 < LLN (40.0%), and lastly, FEV1/FVC < 0.7 with FEV1/FVC < LLN (35.0%). The results regarding smoking status among the incident cases for the three criteria were as follows: GOLD criterion1212 Vestbo J, Hurd SS, Agustí AG, et al. Global strategy for the diagnosis, management, and prevention of chronic obstructive pulmonary disease: GOLD executive summary. Am J Respir Crit Care Med. 2013;187(4):347-65. (40% nonsmokers, 35% smokers and 25% former smokers); FEV1/FVC < LLN (43% nonsmokers, 43% smokers and 14% former smokers); and FEV1/FEV6 < LLN (23% nonsmokers, 44% smokers and 33% former smokers).

Table 2.
Incident cases of chronic obstructive pulmonary disease (COPD) in São Paulo, Brazil, based on three different spirometric diagnostic criteria

Figure 2.
Incident cases of chronic obstructive pulmonary disease (COPD) and agreement among three spirometric diagnostic criteria: FEV1/FVC < 0.7 post-bronchodilator; FEV1/FVC < LLN post-bronchodilator; and FEV1/FEV6 < LLN post-bronchodilator.

DISCUSSION

The results from this study showed that, at the end of a nine-year follow-up period, the rate of diagnosing new cases of COPD in a population-based sample in the city of São Paulo ranged from 1.4% to 4.0%, depending on the spirometric diagnostic criterion used. The guidelines available regarding COPD diagnosis and treatment1212 Vestbo J, Hurd SS, Agustí AG, et al. Global strategy for the diagnosis, management, and prevention of chronic obstructive pulmonary disease: GOLD executive summary. Am J Respir Crit Care Med. 2013;187(4):347-65. , 1919 Standards for the diagnosis, and care of patients with chronic obstructive pulmonary disease. American Thoracic Society. Am J Respir Crit Care Med. 1995;152(5 Pt 2):S77-121.

20 Siafakas NM, Vermeire P, Pride NB, et al. Optimal assessment and management of chronic obstructive pulmonary disease (COPD). The European Respiratory Society Task Force. Eur Respir J. 1995;8(8):1398-420.
- 2121 BTS guidelines for the management of chronic obstructive pulmonary disease. The COPD Guidelines Group of the Standards of Care Committee of the BTS. Thorax. 1997;52 Suppl 5:S1-28. differ in relation to the spirometric criteria used for identifying airflow obstruction, and there is controversy regarding which criterion is the most appropriate for diagnosing the disease.

The spirometric diagnostic criterion that takes a fixed FEV1/FVC ratio or a FEV1/FVC of 0.7 is simple and practical. However, it can increase the rates of false-positive results among older subjects and might not detect the disease in younger subjects (false-negative results).2222 Celli BR, Halbert RJ, Isonaka S, Schau B. Population impact of different definitions of airway obstruction. Eur Respir J. 2003;22(2):268-73. , 2323 Borrego LM, Couto M, Almeida I, et al. Avaliação da função respiratória: comparação entre valores de referência percentuais fixos e o 5o percentil para diagnóstico de obstrução das vias aéreas [Lung function evaluation: comparing fixed percentage reference values vs. the 5th percentile in the diagnosis of airway obstruction]. Braz J Allergy Immunol. 2013;1(4):229-35. The increase in the number of false-positive results is minimized when this criterion is based on the fifth percentile or taken as below the LLN. On the other hand, it has already been demonstrated that false-negative results are more common when such a criterion is used. Because of the resulting misdiagnoses, COPD patients are undertreated or even not treated in the initial stages of the disease, when they could benefit from treatment.2424 Güder G, Brenner S, Angermann CE, et al. "GOLD or lower limit of normal definition? A comparison with expert-based diagnosis of chronic obstructive pulmonary disease in a prospective cohort-study". Respir Res. 2012;13(1):13. The criterion FEV1/FEV6 < 0.75 or FEV1/FEV6 < LLN has the advantages of being easy to apply, both for the evaluator and for the patient. This criterion can eliminate the limitation on low-flow accuracy at the end of the FVC maneuver and can reduce the time needed to perform the spirometry, as well as the chances of possible complications during the examination, such as syncope.2525 Ferguson GT, Enright PL, Buist AS, Higgins MW. Office spirometry for lung health assessment in adults: A consensus statement from the National Lung Health Education Program. Chest. 2000;117(4):1146-61.

26 Swanney MP, Beckert LE, Frampton CM, et al. Validity of the American Thoracic Society and other spirometric algorithms using FVC and forced expiratory volume at 6 s for predicting a reduced total lung capacity. Chest. 2004;126(6):1861-6.
- 2727 Hansen JE, Sun XG, Wasserman K. Should forced expiratory volume in six seconds replace forced vital capacity to detect airway obstruction?. Eur Respir J. 2006;27(6):1244-50. These diagnostic criteria present different sensitivities, specificities and positive and negative predictive values.2323 Borrego LM, Couto M, Almeida I, et al. Avaliação da função respiratória: comparação entre valores de referência percentuais fixos e o 5o percentil para diagnóstico de obstrução das vias aéreas [Lung function evaluation: comparing fixed percentage reference values vs. the 5th percentile in the diagnosis of airway obstruction]. Braz J Allergy Immunol. 2013;1(4):229-35. , 2424 Güder G, Brenner S, Angermann CE, et al. "GOLD or lower limit of normal definition? A comparison with expert-based diagnosis of chronic obstructive pulmonary disease in a prospective cohort-study". Respir Res. 2012;13(1):13. , 2828 Aggarwal AN, Gupta D, Agarwal R, Jindal SK. Comparison of the lower confidence limit to the fixed-percentage method for assessing airway obstruction in routine clinical practice. Respir Care. 2011;56(11):1778-84. , 2929 Vandevoorde J, Verbanck S, Schuermans D, Kartounian J, Vincken W. FEV1/FEV6 and FEV6 as an alternative for FEV1/FVC and FVC in the spirometric detection of airway obstruction and restriction. Chest. 2005;127(5):1560-4.

Although the positive and negative points of each COPD diagnostic criterion have been identified, the historical divergences regarding the use of fixed ratios, LLN, and other criteria still remain in the literature.3030 Celli BR, Halbert RJ. Point: should we abandon FEV1/FVC < 070 to detect airway obstruction? . No. Chest. 2010;138(5):1037-40. , 3131 Enright P, Brusasco V. Counterpoint: should we abandon FEV1/FVC < 070 to detect airway obstruction? . Yes. Chest. 2010;138(5):1040-2; discussion 1042-4. Therefore, further studies that aim to identify the diagnostic and prognostic markers of this disease are needed.

Hence, the present study evaluated the findings from new COPD cases in the city of São Paulo based on three different spirometric criteria. The incidence rate of COPD was lower (n = 7) when FEV1/FVC < LLN was used, followed by FEV1/FEV6 < LLN (n = 10) and the fixed-ratio criterion FEV1/FVC < 0.7 (n = 20). Thus, according to the diagnostic criterion used, the number of new COPD cases may triple. This difference in the results was also reported previously in an incidence study1111 de Marco R, Accordini S, Marcon A, et al. Risk factors for chronic obstructive pulmonary disease in a European cohort of young adults. Am J Respir Crit Care Med. 2011;183(7):891-7. in which the results indicated that the number of cases could double. This large disparity probably reflects differences in sensitivity and specificity.3232 de Marco R. What evidence could validate the definition of COPD?. Thorax. 2008;63(9):756-7. In divergent cases of airflow obstruction (e.g. FEV1/FVC < 0.7 and FEV1/FVC ≥ LLN), the subjects would not have clinically significant obstruction but would have a clinical profile characterized by significant comorbidities, thereby indicating that they could be at risk of developing COPD and should be followed up carefully.3333 Lamprecht B, Schirnhofer L, Kaiser B, et al. Subjects with Discordant Airways Obstruction: Lost between Spirometric Definitions of COPD. Pulm Med. 2011;2011:780215.

Despite the disparities among the criteria, six subjects showed concordance regarding the incidence of airflow obstruction. The concordance between the criteria FEV1/FVC < 0.7 and FEV1/FVC < LLN was 35.0%, while de Marco et al. 1111 de Marco R, Accordini S, Marcon A, et al. Risk factors for chronic obstructive pulmonary disease in a European cohort of young adults. Am J Respir Crit Care Med. 2011;183(7):891-7. reported concordance of 48% for these same criteria. The most discordant cases were associated with the criterion FEV1/FVC < 0.7, which was the only one to classify 11 subjects as new cases.

From investigating the characteristics of these 11 subjects in relation to the COPD cases with concordance in three criteria (n = 6), we found that 64% were 68 years of age or older (P = 0.04). Considering that aging contributes to airflow limitation, mainly due to increased thoracic wall rigidity and decreased pulmonary elastic recoil,3434 Meyer KC. Aging. Proc Am Thorac Soc. 2005;2(5):433-9. , 3535 Stanojevic S, Wade A, Stocks J, et al. Reference ranges for spirometry across all ages: a new approach. Am J Respir Crit Care Med. 2008;177(3):253-60. these findings corroborate the assumption that the criterion FEV1/FVC < 0.7 may lead to misdiagnosing of COPD among the elderly through precluding the clinical distinction between disease and airflow limitation that is caused by the aging process.1313 Pellegrino R, Viegi G, Brusasco V, et al. Interpretative strategies for lung function tests. Eur Respir J. 2005;26(5):948-68. , 3636 Hansen JE, Sun XG, Wasserman K. Spirometric criteria for airway obstruction: Use percentage of FEV1/FVC ratio below the fifth percentile, not < 70%. Chest. 2007;131(2):349-55. Mannino et al. 3737 Mannino DM, Sonia Buist A, Vollmer WM. Chronic obstructive pulmonary disease in the older adult: what defines abnormal lung function?. Thorax. 2007;62(3):237-41. confirmed that there is uncertainty regarding whether discordant cases obtained through using different criteria represent misdiagnosis, COPD phenotypes or overlapping between COPD and any other associated disease.

The use of different criteria can lead to variability in diagnosing new COPD cases, which can affect public health decisions regarding strategic planning, allocation of resources and establishment of priorities.2222 Celli BR, Halbert RJ, Isonaka S, Schau B. Population impact of different definitions of airway obstruction. Eur Respir J. 2003;22(2):268-73. A study published in 20131717 Perez-Padilla R, Wehrmeister FC, Celli BR, et al. Reliability of FEV1/FEV6 to diagnose airflow obstruction compared with FEV1/FVC: the PLATINO longitudinal study. PLoS One. 2013;8(8):e67960. demonstrated that using the FEV1/FEV6 criterion was more reliable than using FEV1/FVC, given that FVC varies with expiratory time during the forced maneuvers required for spirometry. The present study also suggests that FEV1/FEV6 is the most appropriate criterion, considering its greater concordance with the other two spirometric diagnostic criteria (FEV1/FVC < 0.7 and FEV1/FVC < LLN), which produced extreme numbers of new COPD cases, i.e. a higher and a lower proportion of cases, respectively. Thus, further studies are needed, especially longitudinal population-based studies, in order to identify the best diagnostic criterion to use.

When considering the use of different criteria to evaluate the diagnoses of new cases of COPD, care should be taken in comparing the rate found in the present study with the rates obtained in other studies. This is because, in addition to the criterion used for diagnosing the disease,3838 Gershon AS, Wang C, Wilton AS, Raut R, To T. Trends in chronic obstructive pulmonary disease prevalence, incidence, and mortality in Ontario, Canada, 1996 to 2007: a population-based study. Arch Intern Med. 2010;170(6):560-5. there were differences in incidence rate,9de Marco R, Accordini S, Cerveri I, et al. Incidence of chronic obstructive pulmonary disease in a cohort of young adults according to the presence of chronic cough and phlegm. Am J Respir Crit Care Med. 2007;175(1):32-9.

10 Kojima S, Sakakibara H, Motani S, et al. Incidence of chronic obstructive pulmonary disease, and the relationship between age and smoking in a Japanese population. J Epidemiol. 2007;17(2):54-60.
- 1111 de Marco R, Accordini S, Marcon A, et al. Risk factors for chronic obstructive pulmonary disease in a European cohort of young adults. Am J Respir Crit Care Med. 2011;183(7):891-7. , 3838 Gershon AS, Wang C, Wilton AS, Raut R, To T. Trends in chronic obstructive pulmonary disease prevalence, incidence, and mortality in Ontario, Canada, 1996 to 2007: a population-based study. Arch Intern Med. 2010;170(6):560-5. follow-up duration,5Lindberg A, Jonsson AC, Rönmark E, et al. Ten-year cumulative incidence of COPD and risk factors for incident disease in a symptomatic cohort. Chest. 2005;127(5):1544-52. , 7Løkke A, Lange P, Scharling H, Fabricius P, Vestbo J. Developing COPD: a 25 year follow up study of the general population. Thorax. 2006;61(11):935-9. , 8Pelkonen M, Notkola IL, Nissinen A, Tukiainen H, Koskela H. Thirty-year cumulative incidence of chronic bronchitis and COPD in relation to 30-year pulmonary function and 40-year mortality: a follow-up in middle-aged rural men. Chest. 2006;130(4):1129-37. , 3838 Gershon AS, Wang C, Wilton AS, Raut R, To T. Trends in chronic obstructive pulmonary disease prevalence, incidence, and mortality in Ontario, Canada, 1996 to 2007: a population-based study. Arch Intern Med. 2010;170(6):560-5. population studied,5Lindberg A, Jonsson AC, Rönmark E, et al. Ten-year cumulative incidence of COPD and risk factors for incident disease in a symptomatic cohort. Chest. 2005;127(5):1544-52. , 8Pelkonen M, Notkola IL, Nissinen A, Tukiainen H, Koskela H. Thirty-year cumulative incidence of chronic bronchitis and COPD in relation to 30-year pulmonary function and 40-year mortality: a follow-up in middle-aged rural men. Chest. 2006;130(4):1129-37. , 1010 Kojima S, Sakakibara H, Motani S, et al. Incidence of chronic obstructive pulmonary disease, and the relationship between age and smoking in a Japanese population. J Epidemiol. 2007;17(2):54-60. age distribution9de Marco R, Accordini S, Cerveri I, et al. Incidence of chronic obstructive pulmonary disease in a cohort of young adults according to the presence of chronic cough and phlegm. Am J Respir Crit Care Med. 2007;175(1):32-9. , 1111 de Marco R, Accordini S, Marcon A, et al. Risk factors for chronic obstructive pulmonary disease in a European cohort of young adults. Am J Respir Crit Care Med. 2011;183(7):891-7. and exclusion criteria.7Løkke A, Lange P, Scharling H, Fabricius P, Vestbo J. Developing COPD: a 25 year follow up study of the general population. Thorax. 2006;61(11):935-9. , 9de Marco R, Accordini S, Cerveri I, et al. Incidence of chronic obstructive pulmonary disease in a cohort of young adults according to the presence of chronic cough and phlegm. Am J Respir Crit Care Med. 2007;175(1):32-9.

10 Kojima S, Sakakibara H, Motani S, et al. Incidence of chronic obstructive pulmonary disease, and the relationship between age and smoking in a Japanese population. J Epidemiol. 2007;17(2):54-60.
- 1111 de Marco R, Accordini S, Marcon A, et al. Risk factors for chronic obstructive pulmonary disease in a European cohort of young adults. Am J Respir Crit Care Med. 2011;183(7):891-7. This high variability in identifying new cases of COPD among different studies may be associated with the fact that the samples of some of the studies did not include subjects who reported asthma,9de Marco R, Accordini S, Cerveri I, et al. Incidence of chronic obstructive pulmonary disease in a cohort of young adults according to the presence of chronic cough and phlegm. Am J Respir Crit Care Med. 2007;175(1):32-9. , 1111 de Marco R, Accordini S, Marcon A, et al. Risk factors for chronic obstructive pulmonary disease in a European cohort of young adults. Am J Respir Crit Care Med. 2011;183(7):891-7. as well as differences in follow-up periods, which ranged from 7 to 25 years.

One of the limitations of the present study is the rate of losses from the follow-up, which exceeded 20%. However, a European multicenter longitudinal study over a similar follow-up period reported a participation rate of 63.3%.1111 de Marco R, Accordini S, Marcon A, et al. Risk factors for chronic obstructive pulmonary disease in a European cohort of young adults. Am J Respir Crit Care Med. 2011;183(7):891-7. In addition, the group formed by the cases of loss from the follow-up and refusal to participate had the same clinical and pulmonary function characteristics as shown by the participants in the follow-up phase of the PLATINO study. Another limitation is the fact that there was only one re-evaluation after a period of nine years, which does not allow the incidence rates to be expressed as numbers of cases/year, although the perceptual value could be presented and used in comparisons with other studies.

CONCLUSION

We conclude that the rate of diagnosing new cases of COPD in the city of São Paulo at the end of a nine-year follow-up period was similar to the percentages found in European, Asian and North American countries, with a range from 1.4% to 4.0%, depending on the spirometric criterion used for diagnosing the disease, with concordance levels of 35-60%. Therefore, researchers should concentrate their efforts on determining which spirometric criterion is the most accurate one for diagnosing COPD, so that epidemiological studies can better report the impact of this disease and the real responses of subjects to the treatment prescribed.

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  • This study was presented to Universidade Federal de São Paulo (Unifesp) as part of a doctoral degree thesis in 2013 (Sep 25)
  • Sources of funding: Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (Capes)

Publication Dates

  • Publication in this collection
    June 2015

History

  • Received
    10 Sept 2014
  • Reviewed
    26 Jan 2015
  • Accepted
    09 Feb 2015
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