RESEARCH ARTICLE
Determinants of Restrictive Spirometric Pattern in a Sub-Saharan Urban Setting: A Cross-sectional Population-based Study
Eric Walter Pefura-Yone1, 2, *, Adamou Dodo Balkissou1, 2, Andre Pascal Kengne3, 4
Article Information
Identifiers and Pagination:
Year: 2016Volume: 10
First Page: 86
Last Page: 95
Publisher ID: TORMJ-10-86
DOI: 10.2174/1874306401610010086
Article History:
Received Date: 08/09/2016Revision Received Date: 21/11/2016
Acceptance Date: 21/11/2016
Electronic publication date: 30/11/2016
Collection year: 2016
open-access license: This is an open access article licensed under the terms of the Creative Commons Attribution-Non-Commercial 4.0 International Public License (CC BY-NC 4.0) (https://creativecommons.org/licenses/by-nc/4.0/legalcode), which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited.
Abstract
Background
Restrictive spirometric pattern is a risk factor for all-cause and cause-specific mortality.
Objective
We assessed the prevalence of restrictive pattern and investigated its determinants in a major sub-Saharan Africa city.
Methods
Participants were adults (≥ 19 years) who took part in a population-based survey in Yaounde (Cameroon) between December 2013 and April 2014. Restrictive pattern was based on a FVC below the lower limit of the normal (LLN) and a ratio forced expiratory volume in one second (FEV1)/FVC ≥ LLN (LLN-based restrictive pattern) or a FVC <80% and FEV1/FVC ≥ LLN (fixed cut-off based restrictive pattern). Determinants were investigated by logistic regressions.
Results
In all, 1003 participants [514 (51.2%) women] with a mean age of 33.7 years were included. The prevalence of restrictive pattern was 18.8% (95%CI: 16.6-21.2) based on LLN and 15.0% (13.0-17.2) based on fixed cut-off. LLN-based restrictive pattern was mild in 148 (78.3%) subjects, moderate in 35 (18.5%) and severe in 6 (3.2%). Determinants of LLN-based restrictive pattern were age ≥ 60 years [adjusted odds ratio 2.90 (95%CI 1.46-5.77), p=0.002), history of pulmonary tuberculosis [3.81(1.42-10.20), p=0.008], prevalent heart diseases [3.81 (1.20-12.12), p=0.024] and underweight [5.15(1.30-20.39), p=0.020]. Determinants were largely similar with slightly different effect sizes for fixed cut-off based restrictive pattern.
Conclusion
Restrictive pattern was very frequent in this city.
Clinical implications
These results enhance the needs to increase the efforts to prevent and control tuberculosis, cardiovascular diseases and underweight in this setting.
INTRODUCTION
Vital capacity (VC) and forced expiratory volume in one second (FEV1) are the commonly used ventilatory parameters in functional evaluation and assessment of severity of respiratory diseases [1]. Studies have reported a relationship between these two parameters and excess all-cause mortality as well as mortality from cardiovascular diseases, respiratory diseases and cancers in the general population [2-5]. Furthermore, in people free of any respiratory symptoms or any known respiratory disease, Burney and Hooper have recently reported a low forced vital capacity (FVC) to be strongly correlated with higher all-cause mortality but not FEV1 and the FEV1/FVC ratio [6]. Moreover, in another recent study by Lee et al. [7], FVC and FEV1 improved mortality risk stratification based upon the Framingham risk equation in intermediate risk individuals. Knowledge of factors associated with low FVC in the general population is therefore important, and can assist risk evaluation and early identification and treatment of high risk individuals.
Few studies originating mostly from developed countries are available on the burden and risk factors for low FVC, also known as restrictive pattern. Across these studies, the prevalence of restrictive pattern in the general population ranged from 5.4% to 10.9% in US [8-10], to 74% in Aboriginal Australians [11]. These studies have also revealed many risk factors for restrictive pattern including high cardio-thoracic index, paralysis, diabetes mellitus and cardiovascular diseases (CVD) in the general population [9, 10]; and abdominal obesity, physical impairment, cognitive impairment and kypho-scoliosis in the elderly population [3].
The aim of the present study was to assess the prevalence of restrictive pattern (low FVC in the absence of airway obstruction) and investigate the determinants among adults in the general population from a major sub-Saharan African City.
MATERIALS AND METHODS
Study Design and Participants
This was a cross-sectional population-based survey conducted between December 2013 and April 2014 among adults (19 years of age and above) in Yaounde, the Capital City of Cameroon. Participants were recruited during a population-based survey aiming to quantify the burden of the commonest non-communicable respiratory diseases in Yaounde city. The sampling methods and selection of participants have been described in detail previously [12]. In brief, we used multilevel stratified sampling method to include participants in the current study. We firstly selected 16 enumeration areas (EA) out of the 2000 EAs of Yaounde city. In each enumeration area, we followed the itinerary of the national vaccination campaigns and then we used systematic sampling method to include participants in the study. About every one participant in two was selected for spirometry purpose (and if the spirometry was judged uninterpretable by the field workers, they included the next participant).Were excluded from the survey all participants with any of the following conditions: active tuberculosis, recent pneumonia, physical or mental inability to perform spirometry. Of the 1499 participants selected via multilevel stratified sampling across the seven administrative districts of Yaounde, to undergo spirometry tests during the survey, 212 (14.1%) participants had completely uninterpretable spirometry (lack of reproducibility and incorrect maneuvers); 236 (18.3%) of the remaining 1287 participants had reproducible curves but inadequate end of test plateau. Of the 1051 participants left, 48 (4.7%) had airway obstruction (FEV1/FCV < lower limit of normal [LLN]) and were therefore excluded from the analysis.
Data Collection
Data were collected by purposefully trained final year undergraduate medical students. A pre-tested questionnaire inspired by other questionnaires used in international surveys [13, 14], was used for data collection. The questionnaire was completed during face-to-face interview with consenting participants. Data were collected on the following: 1) socio-demographic details including age, sex and education; 2) exposure to tobacco which was assessed using a series of questions on tobacco use and participants classified as non-smokers (for those who never smoked, or had smoked less than 20 packs in their lifetime), active smokers (for participants who had smoked more than 20 packs in their lifetime, or at least one cigarette per day), and ex-smokers (for participants who had stopped smoking since at least six months) [15]; 3) self-reported history of existing conditions including pulmonary tuberculosis, asthma, pneumonia, cardiovascular diseases, diabetes mellitus, hypertension and cerebrovascular accident ; 4) chronic respiratory signs including chronic cough and expectoration for more than three months per year, dyspnea which was classified into four stages based on the modified Medical Research Council (mMRC) scale [16]; 5) biomass exposure based on exposure to cooking fumes from various solid fuels, and participants who had used solid fuels for cooking purpose for at least six month were classified as having been exposed to biomass [15]; 6) Anthropometric measures including height to the nearest centimeter, which was measured with a stadiometer in a participant without shoes, in the upright position, and weight (in kilograms) which was measured with a CAMRY weight scale (CAMRY, Guangzhou, China).
Spirometric Measurements
Flow-volume curves were acquired following the American Thoracic Society/European Respiratory Society (ATS/ERS) 2005 recommendations [17]. Spirometric examinations used a turbine pneumotachograph (Spiro USB, Care fusion, Yorba Linda-USA) or a Fleisch pneumotachograph (Spirolyser SPL-10 USB, FIM-Medical, Lyon-France), following the international standards, and were performed by a trained technician. All curves were reviewed by an experienced chest physician. Spirometric measurements were performed in a participant at rest for at least 15 minutes, in a sitting position with the back straight, and the nose clipped to allow air flow only per mouth. The ATS/ERS acceptability and reproducibility criteria were applied [17]. All subjects who had an acceptable expiratory plateau were included. At least three tests were done by each participant to establish the FVC curve. Spirometric variables measured included: FEV1, FVC and the FEV1/FVC ratio. FEV1 and FVC values retained were the best out of the three tests which fulfilled the acceptability criteria (maximal difference below 5% or 150 ml). Predicted values were estimated using the reference spirometric values derived from a black African population [18]. Restrictive pattern was defined by a FVC below the age, sex and height specific LLN (LLN-based restrictive pattern). Sensitivity analyses were also conducted using an alternative definition which was based on FVC < 80% of the predicted value (fixed cut-off based restrictive pattern). The severity of restrictive pattern was based on a modification of the classification by Pellegrino et al.: mild restriction for FEV1>70%, moderate restriction for 50% ≤ FEV1≤ 70% and severe for FEV1<50% [1]. The study was approved by the Ethics Committee of the Regional delegation of Health of Center Region of Cameroon.
Statistical Analysis
Data analysis used the IBM-SPSS v.20 for Windows (IBM, Chicago, USA). Qualitative variables are presented as count and frequencies, and quantitative variables as mean and standard deviation (SD) or median and 25th-75th percentiles. Graphical plots and Shapiro-Wilk test were used to assess the normality of the quantitative variables. There was indication of departure from normal distribution for all the quantitative variables included in the analysis. Group comparisons used chi square test for qualitative variables, and Mann-Whitney U test for quantitative variables. Age-standardized prevalence was calculated using the Cameroon National population’s age structure in 2010 as the standard population [19], and direct standardization methods. Logistic regression models were employed to investigate the determinants of restrictive pattern. Significant predictors in univariable analysis (based on a threshold p<0.10) were entered altogether in the same multivariable model and the significant ones retained as the final determinants. A p-value < 0.05 was used to characterize statistically significant results.
RESULTS
General Characteristics of the Study Population
The general characteristics of the included participants are described in Table 1. Of the 1003 participants included, 514 (51.2%) were women. The mean age (SD) was 33.7 (12.1) years and 44 (4.4%) participants were aged 60 years and above. Women were less educated than men with 66.2% vs. 58.3% having achieved at most secondary school level education (p<0.001). Compared with women, men were more likely to be current smokers (16% vs. 2.3%, p<0.001), and as expected women were more likely to have been exposed to biomass than men (8.4% vs. 7%, p<0.001). With the exception of dyspnea which was more frequent in women than men (31.7% vs. 18.4%, p<0.001), chronic respiratory symptoms were equally distributed between men and women. The mean predicted FVC (SD) was 96.98% (18.51%) overall and the predicted value did not differ between men and women. Predicted FEV1 was also similar between men and women (98.52% vs. 96.77%, p=0.336).
| Characteristics | Overall, n=1003 (%) | Men, n=489 (%) | Women, n=514 (%) | p-value |
|---|---|---|---|---|
| Age, years | ||||
| Mean (SD) | 33.7 (12.1) | 33.5 (12.3) | 34.0 (11.8) | 0.237 |
| Median (25th -75th percentiles) | 30 (24-41) | 29 (24-40) | 30 (25-41) | |
| Age group, years | ||||
| 19-39 | 730 (72.8) | 364 (74.4) | 366 (71.2) | 0.231 |
| 40-59 | 229 (22.8) | 101 (20.7) | 128 (24.9) | |
| ≥ 60 | 44 (4.4) | 24 (4.9) | 20 (3.9) | |
| Education | ||||
| ≤ secondary | 664 (66.2) | 285 (58.3) | 379 (73.7) | < 0.001 |
| Higher | 339 (33.8) | 204 (41.7) | 135 (26.3) | |
| Subject/bedrooms | ||||
| ≤ 2 | 561 (56) | 307 (62.8) | 254 (49.5) | <0.001 |
| > 2 | 441 (44) | 182 (37.2) | 259 (50.5) | |
| Tobacco smoking | ||||
| Current smoker | 90 (9) | 78 (16) | 12 (2.3) | <0.001 |
| Ex-smokers | 64 (6.4) | 57 (11.7) | 7 (1.4) | |
| Non smokers | 845 (84.6) | 353 (72.3) | 492 (96.3) | |
| Cooking fuel | ||||
| Biomass | 76/982 (7.7) | 33/473 (7) | 43/509 (8.4) | <0.001 |
| Mixed | 454/982 (46.2) | 183/473 (38.7) | 271/509 (53.2) | |
| Clean | 452/982 (46) | 257/473 (54.3) | 195/509 (38.3) | |
| Past history of tuberculosis | ||||
| Yes | 18 (1.8) | 9 (1.8) | 9 (1.8) | 0.915 |
| No | 985 (98.2) | 480 (98.2) | 505 (98.2) | |
| Past history of pneumonia | ||||
| Yes | 28 (2.8) | 17 (3.5) | 11 (2.1) | 0.199 |
| No | 975 (97.2) | 472 (96.5) | 503 (97.9) | |
| Self-reported asthma | ||||
| Yes | 23 (2.3) | 7 (1.4) | 16 (3.1) | 0.075 |
| No | 980 (97.7) | 482 (98.6) | 498 (96.9) | |
| History of stroke | ||||
| Yes | 4 (0.4) | 3 (0.6) | 1 (0.2) | 0.362 |
| No | 999 (99.6) | 486 (99.4) | 513 (99.8) | |
| Self-reported diabetes mellitus | ||||
| Yes | 12 (1.2) | 6 (1.2) | 6 (1.2) | 0.931 |
| No | 991 (98.8) | 483 (98.8) | 508 (98.8) | |
| Self-reported hypertension | ||||
| Yes | 40 (4) | 15 (3.1) | 25 (4.9) | 0.146 |
| No | 963 (96) | 474 (96.9) | 489 (95.1) | |
| History of cardiac disease | ||||
| Yes | 14 (1.4) | 9 (1.8) | 5 (1) | 0.242 |
| No | 989 (98.6) | 480 (98.2) | 509 (99) | |
| Self-reported HIV infection | ||||
| Yes | 7 (0.7) | 3 (0.6) | 4 (0.8) | < 0.001 |
| No | 787 (78.5) | 358 (73.2) | 429 (83.5) | |
| Don’t know | 209 (20.8) | 128 (26.2) | 81 (38.8) | |
| Respiratory symptoms | ||||
| Chronic cough | 22 (2.2) | 10 (2) | 12 (2.3) | 0.754 |
| Chronic expectoration | 8 (0.8) | 4 (0.8) | 4 (0.8) | >0.999 |
| Recent wheezing | 24 (2.4) | 11 (2.2) | 13 (2.5) | 0.772 |
| Dyspnea | 253 (25.2) | 90 (18.4) | 163 (31.7) | <0.001 |
| Any symptoms | 271 (27) | 98 (20) | 173 (33.7) | <0.001 |
| BMI, Kg/m2, Mean (SD) | 26.1 (5.3) | 25.4 (4.3) | 27.4 (5.9) | <0.001 |
| FEV1 | ||||
| Mean (SD), L | 3.08 (0.85) | 3.59 (0.82) | 2.60 (0.54) | <0.001 |
| % predicted (SD) | 97.63 (18.56) | 98.52 (19.23) | 96.77 (17.87) | 0.144 |
| FVC | ||||
| Mean (SD), L | 3.56 (0.97) | 4.14 (0.92) | 3.0 (0.63) | <0.001 |
| % predicted (SD) | 96.98 (18.51) | 96.57 (18.86) | 97.36 (18.19) | 0.336 |
| FEV1/FVC | 0.87 (0.05) | 0.87 (0.05) | 0.87 (0.05) | 0.813 |
Prevalence and Severity of Restrictive Pattern
A total of 189 participants had a FVC < LLN; therefore, the crude prevalence of LLN-based restrictive pattern was 18.8% (95% confidence interval [CI] 16.6-21.2). The age-standardized prevalence was 20.3% (17.8-22.2%). LLN-based restrictive pattern was mild in 148 (78.3%) participants, moderate in 35 (18.5%) and severe in 6 (3.2%) participants. Furthermore, 127 (67.2%) of participants with LLN-based restrictive pattern had a FEV1 <80% of the predicted value. Based on a FVC <80%, 180 participants had a low FVC; therefore the prevalence of fixed cut-off based restrictive pattern was 15% (95%CI: 13.0-17.2%).
Determinants of Restrictive Pattern
Univariable associations of baseline characteristics with LLN-based restrictive pattern are shown in Table 2. Participants with restrictive pattern were older (37.2 vs. 32.1 years, p<0.001) and less educated (secondary school education or less: 72.5% vs. 64.7%, p=0.043). Other univariable correlates of restrictive pattern included a history of pulmonary tuberculosis [odds ratio (95% CI): 4.47 (1.75-11.43), p=0,002], history of heart disease [5.95 (2.04-17.38), p=0.001], exposure to biomass [1.98 (1.14-3.45), p=0.015)], chronic cough [2.53 (1.04-6.11), p=0.040], dyspnea stage 3 and 4 [2.02 (1.05-3.88), p=0.031], and body mass index (BMI) < 18.5 kg/m2 [5.32 (1.40-20.21), p=0.014]. Univariable determinants were similar for the outcome of fixed cut-off based restrictive pattern, with the exception of exposure to biomass for which the association was borderline (Supplementary Table 1).
| Determinants | Restrictive pattern N=189 (%) |
Normal FVC N=814 (%) |
Crude odds ratio (95%CI) | p-value |
|---|---|---|---|---|
| Gender | ||||
| Male | 92 (48.7) | 397 (48.8) | 1.00 (0.73-1.37) | 0.981 |
| Female | 97 (51.3) | 417 (51.2) | 1 | |
| Age, mean (SD), years | 37.2 (14.5) | 32.1 (11.3) | 1.03 (1.02-1.04) | <0.001 |
| Age group, years | ||||
| 19-39 | 123 (65.1) | 607 (74.6) | 1 | |
| 40-59 | 47 (24.9) | 182 (22.4) | 1.27 (0.88-1.85) | 0.205 |
| ≥ 60 | 19 (10,1) | 25 (3.1) | 3.75 (2.00-7.02) | <0.001 |
| Ethnic group | ||||
| Bantou | 174(92.1) | 771(94.7) | 0.63(0.23-1.78) | 0.384 |
| Fulani | 10(5.3) | 29(3.6) | 0.97(0.28-3.37) | 0.956 |
| Sudanese | 5(2.6) | 14(1.7) | 1 | |
| Education | ||||
| ≤ secondary | 137 (72.5) | 527 (64.7) | 1.44 (1.01-2.04) | 0.043 |
| Higher | 52 (27.5) | 287 (35.3) | 1 | |
| Subject/bedrooms | ||||
| ≤ 2 | 108 (57.1) | 453/813 (55.7) | 1.06 (0.77-1.46) | 0.723 |
| > 2 | 81 (42.9) | 360/813 (44.3) | 1 | |
| Tobacco smoking | ||||
| Current smoker | 19 (10.1) | 71/810 (8.8) | 1.16 (0.68-1.99) | 0.579 |
| Ex-smokers | 12 (6.3) | 52/810 (6.4) | 1.00 (0.52-1.92) | 0.992 |
| Non smokers | 158 (83.6) | 687/810 (84.8) | 1 | |
| Cooking fuel | ||||
| Biomass | 22/186 (46.8) | 54/796 (6.8) | 1.98 (1.14-3.45) | 0.015 |
| Mixed | 87/186 (46.8) | 367/796 (46.1) | 1.15 (0.82-1.62) | 0.406 |
| Clean | 77/186 (41.1) | 796/796 (47.1) | 1 | |
| Past history of TB | ||||
| Yes | 9 (4.8) | 9 (1.1) | 4.47 (1.75-11.43) | 0.002 |
| No | 180 (95.2) | 805 (98.9) | 1 | |
| Past history of pneumonia | ||||
| Yes | 7 (3.7) | 21 (2.6) | 1.45 (0.61-3.47) | 0.398 |
| No | 182 (96.3) | 793 (97.4) | ||
| Self-reported asthma | ||||
| Yes | 3 (1.6) | 20 (2.5) | 0.64 (0.19-2.18) | 0.475 |
| No | 186 (98.4) | 794 (97.5) | 1 | |
| History of stroke | ||||
| Yes | 2 (1.1) | 2 (0.2) | 4.34 (0.61-31.03) | 0.143 |
| No | 187 (98.9) | 812 (00.8) | 1 | |
| Self-reported diabetes mellitus | ||||
| Yes | 4 (2.1) | 8 (1.0) | 2.19 (0.65-7.31) | 0.208 |
| No | 185 (97.9) | 806 (99.0) | 1 | |
| Self-reported hypertension | ||||
| Yes | 10 (5.3) | 30 (3.7) | 1.46 (0.71-3.04) | 0.312 |
| No | 179 (94.7) | 784 (96.3) | 1 | |
| History of heart disease | ||||
| Yes | 8 (4.2) | 6 (0.7) | 5.95 (2.04-17.37) | 0.001 |
| No | 181 (95.8) | 808 (99.3) | 1 | |
| Self-reported HIV infection | ||||
| Yes | 1 (0.5) | 6 (0.7) | 0.71 (0.09-5.97) | 0.756 |
| No | 149 (78.8) | 638 (78.4) | 1 | |
| Don’t know | 39 (20.6) | 170 (20.9) | 0.98 (0.66-1.45) | 0.929 |
| Respiratory symptoms | ||||
| Chronic cough | 8 (4.2) | 14 (1.7) | 2.53 (1.04-6.11) | 0.040 |
| Chronic expectoration | 2 (1.1) | 6 (0.7) | 1.44 (0.29-7.19) | 0.657 |
| Recent wheezing | 5 (2.6) | 19 (2.3) | 1.14 (0.42-3.09) | 0.801 |
| Dyspnea | 59 (31.2) | 194 (23.8) | 1.45 (1.03-2.05) | 0.035 |
| mMRC dyspnea > 2 | 14 (7.4) | 31 (3.8) | 2.02 (1.05-3.88) | 0.031 |
| Any respiratory symptoms | 62 (32.8) | 209 (25.7) | 1.41 (1.00-1.99) | 0.047 |
| BMI, Kg/m2, Mean (SD) | 26.6 (6.7) | 26.4 (4.9) | 1.01 (0.98-1.04) | 0.618 |
| BMI classes | ||||
| Underweight | 5/188 (2.7) | 4/812 (0.5) | 5.32 (1.40-20.21) | 0.014 |
| Overweight | 46 (24.5) | 264 (32.5) | 0.74 (0.50-1.09) | 0.131 |
| Obese | 47 (25) | 161 (19.8) | 1.24 (0.84-1.85) | 0.285 |
| Normal | 90 (47.9) | 383 (47.2) | 1 |
In multivariable regression models, independent determinants of LLN-based restrictive pattern were age ≥ 60 years [adjusted odds ratio (95%CI): 2.90 (1.46-5.77), p = 0.002], history of pulmonary tuberculosis [3.81 (1.42-10.20), p = 0.008], past history of heart disease [3.81 (1.20-12.12), p = 0.024] and underweight [5.15 (1.30-20.39), p = 0.020] (Table 3). The pattern of the associations was similar for fixed cut-off based restrictive pattern, although the association with prevalent heart disease was no longer significant [1.64 (0.45-5.94, p=0.450] (Supplementary Table 2).
| Determinants | Adjusted odds ratio | 95% confidence interval | p-value |
|---|---|---|---|
| Male gender | 1.06 | 0.75-1.50 | 0.754 |
| Age group, years | |||
| 19-39 | 1.00 (reference) | ||
| 40-59 | 1.16 | 0.76-1.76 | 0.489 |
| ≥ 60 | 2.90 | 1.46-5.77 | 0.002 |
| Education ≤ secondary | 1.33 | 0.91-1.94 | 0.118 |
| Cooking fuel | |||
| Biomass | 1.70 | 0.94-3.09 | 0.080 |
| Mixed | 1.13 | 0.79-1.62 | 0.497 |
| Clean | 1.00 (reference) | ||
| Past history of TB | 3.81 | 1.42-10.20 | 0.008 |
| History of cardiac disease | 3.81 | 1.20-12.12 | 0.024 |
| Chronic cough | 1.92 | 0.71-5.14 | 0.197 |
| mMRC dyspnea > 2 | 1.50 | 0.72-3.14 | 0.279 |
| BMI classes | |||
| Underweight | 5.15 | 1.30-20.39 | 0.020 |
| Overweight | 0.70 | 0.47-1.06 | 0.093 |
| Obese | 0.95 | 0.61-1.51 | 0.843 |
| Normal | 1.00 (reference) |
TB, tuberculosis; mMRC, modified Medical Research Council scale; BMI, body mass index.
DISCUSSION
In this population of urban dwellers from a major sub-Saharan African city, we found that about one in five adults had a low FVC, which was essentially driven by advanced age, history of pulmonary tuberculosis, prevalent heart diseases and underweight. These findings were largely robust to changes in criteria for defining low FVC. Since loss of respiratory functions, and particularly low FVC is important determinant of mortality risk in the general population [2-6, 8, 20], our findings indicate the importance of using the identified determinants to select from the general population, those who are more likely to be diagnosed with restrictive pattern, and to benefit from targeted risk factors control to mitigate the risk of adverse outcomes.
“Although to establish the diagnosis of lung restriction, a lung volume measurement is needed, we used the term restrictive spirometric pattern to design the population with a low FVC with a FEV1/FVC > lower limit of normal [LLN])” The prevalence of restrictive spirometric pattern in our study was higher than the 6.6% (fixed cut-off based) and 5.4% (LLN-based) reported respectively by Mannino et al., and Kurth et al. in the general population in the USA, using data from the third National Nutrition and Health Examination Survey [8, 10]. Similarly, Scarlata et al. found a prevalence of 10.9% for restrictive pattern among elderly people in the general population in Italy [3], which was by far lower than the 43.2% found among the 60 years old and above in our sample. However, prevalence of restrictive pattern as higher as 74% has been reported among Aboriginal population, while it is around 9.7% in non-Aboriginal Australians [11]. In the study by Mannino et al. comprising people age 40 years and above from 14 sites across different continents who took part in the Burden of Obstructive Lung Disease (BOLD) study, the prevalence of restrictive pattern defined by a ratio FEV1/FVC ≥70% and a FVC<80% varied from 6.1% in Sydney (Australia) to 29.3% in Cape Town (South Africa) and 45.9% in Manilla (Philippines) [21]. Soriano et al. also found a point prevalence of 12.7% in subjects aged 40 years and above in Spain [22]. In the ≥40 years of age particpants in our study, the prevalence of restrictive pattern was 24.2% (LLN-based) and 20.1% (fixed cut-off based), which is closer to the South African figures in BOLD [21]. Global variations in the prevalence of restrictive pattern can be explained by regional differences in the distribution of a number of factors including socio-economic conditions, prevalence of obesity and underweight, birth weight, and prevalence of restrictive lung diseases. However, that restrictive diseases are rather rare in the general population [23] suggests that they contribute less to the burden of restrictive pattern across published studies.
The prevalence of restrictive pattern was four times higher in the ≥ 60 years age group in our sample compared with those in the lower age stratum, and after adjustment for potential extraneous factors. The increasing prevalence of restrictive pattern with increasing age was very well characterized in the study by Mannino et al. where restrictive pattern was 2 to 2.5 times more frequent among the 50 years old and above compared with less older participants [9]. This is likely explained by the combined effect of several phenomena occurring with ageing which include deformation of the axial skeleton, restrictive lung diseases and lung ageing.
History of tuberculosis was a significant determinant of restrictive pattern in our study. This has not been reported previously in studies conducted in western countries, likely due to the low incidence of tuberculosis in those settings. Restrictive functional sequels of tuberculosis are very common [24, 25], mostly reflecting the exent of the parenchymatous involvement duing pulmonary tuberculosis [26]. Prevalent heart disease was also an independent determinant of restriction in our study. This result has not been reported in other studies [9], but Kurth et al. found a significant association between pulmonary restriction and cardiovascular diseases including congestive heart failure, stroke and heart attacks [10]. Cardiovascular diseases, when complicated with left heart failure can lead to pulmonary oedema, which in turn can reduce the vital capacity. Furthermore, heart diseases are often associated with cardiomegaly and muscle deconditioning, which are both associated with decreasing vital capacity [2, 9].
Obesity has been classically associated with functional restrictive lung involvments [27]. Considering that FVC is not in perfect agreement with the total lung capacity (TLC) which is used as gold standard to diagnose pulmonary restriction, it is possible that the non-association of obesity with restrictive pattern in our sample was a chance finding. Furthermore, the majority of obese participants in our sample had moderate obesity. However, underweight was associated with restrictive pattern, in line with the findings of the GOLD study [21]. These association could reflect some underlying conditions which are actually correlated with restrictive pattern. Furthermore, there are suggestions of an inverse relationship between birth weight (not assessed in our study) and lung funtions [28].
The non-association of respiratory symptoms with restrictive pattern in our multivariable analyses reflects the correlation of those symptoms with other significant predictors of restrictive pattern, such as pulmonary tuberculosis and heart diseases. Diabetes and hypertension which have been reported to be associated with restrictive pattern [21] were not confirmed in our sample. It is of note however that statuses for diabetes and hypertension were based on self-report in a setting where under-diagnosis of those conditions is very common. The presence of a high number of undiagnosed diabetes and/or hypertension among those with negative history, which is very likely, can erase any true association.
The present study has some limitations. FVC alone is not sufficient to clinically diagnose pulmonary restriction, for which measurement of the TLC via plethysmography or gas dilution is required. While FVC has very good specificity and negative predictive value to diagnose pulmonary restriction, the sensitivity hardly crosses 75% [29-31]. However, measurement of TLC in community-based study is a very challenging undertaking, while FVC-diagnosed restrictive pattern has been reported to be correlated all-cause and cause-specific mortality [4, 6, 7, 9, 20]. Furthermore, it is possible that the high prevalence of restrictive pattern found in this study is related to a high proportion of false positive related to the definition of the restriction used. Also, the relatively frequent exposure to the biomass of the population studied can lead to the obstruction of the distal airways causing the decline in FVC. The study was cross-sectional; hence it is not possible to reliably establish the sequence of happening between outcome of interest and exposure to potential determinants. Otherwise, the exclusion of patients with incorrect spirometric maneuvers may have influenced the prevalence of restrictive pattern. Our study also has major strengths and in particular the large representative community based sample, which will improve the generalizability of our findings.
CONCLUSION
Restrictive pattern was very frequent in this city.
CLINICAL IMPLICATIONS
These results enhance the needs to increase the efforts to prevent and control tuberculosis, cardiovascular diseases and underweight in this setting.
SUPPLEMENTARY MATERIAL
Supplementary material is available on the publishers Website along with the published article.
LIST OF ABBREVIATIONS
| ATS/ERS | = American Thoracic Society/European Respiratory |
| BMI | = Body Mass Index |
| CI | = Society |
| BOLD | = Burden of Obstructive Lung Disease |
| CVD | = Cardiovascular Disease |
| FEV1 | = Forced Expiratory Volume in First Second |
| FVC | = Low Forced Vital Capacity |
| mMRC | = Modified Medical Research Council Scale |
| SD | = Standard Deviation |
| VC | = Vital Capacity |
CONFLICT OF INTEREST
The authors confirm that this article content has no conflict of interest.
ACKNOWLEDGEMENTS
Declared none.
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