SciELO - Scientific Electronic Library Online

 
vol.51 issue12Insights on the epigenetic mechanisms underlying pulmonary arterial hypertensionMicroRNA-221 promotes cell proliferation, migration, and differentiation by regulation of ZFPM2 in osteoblasts author indexsubject indexarticles search
Home Pagealphabetic serial listing  

Services on Demand

Journal

Article

Indicators

Related links

Share


Brazilian Journal of Medical and Biological Research

Print version ISSN 0100-879XOn-line version ISSN 1414-431X

Braz J Med Biol Res vol.51 no.12 Ribeirão Preto  2018  Epub Oct 18, 2018

https://doi.org/10.1590/1414-431x20187558 

Research Article

Cat ownership is associated with increased asthma prevalence and dog ownership with decreased spirometry values

C.S. Simoneti1 

E. Ferraz2 

M.B. Menezes1 

T.R. Icuma3 

E.O. Vianna1 

1Departamento de Clínica Médica, Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, Ribeirão Preto, SP, Brasil

2Departamento de Fisioterapia, Centro Regional Universitário de Espírito Santo do Pinhal, Espírito Santo do Pinhal, SP, Brasil

3Departamento de Medicina Social, Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, Ribeirão Preto, SP, Brasil


ABSTRACT

The association between pet ownership and the development of allergic and respiratory diseases has been the aim of several studies, however, the effects of exposure in adults remain uncertain. The aims of the present study were to investigate the prevalence of asthma and lung function status among dog and cat owners. This cross-sectional study was performed at two universities with students and workers who were allocated into 3 groups according to pet ownership in the previous year: cat owners, dog owners, and no pets (control group). Subjects underwent spirometry, bronchial challenge test with mannitol, skin prick tests, and questionnaires about animal exposures and respiratory symptoms. Control group comprised 125 subjects; cat owner group, 51 subjects; and dog owner group, 140 subjects. Cat owners had increased asthma prevalence (defined by symptoms and positive bronchial challenge test), but no changes in lung function compared to the control group. The dog owner group had lower spirometry values (forced expiratory volume in one second and lower forced vital capacity), but similar asthma prevalence, compared to the control group. In the cat owner group, excess of asthma may have an immunological basis, since we found an association with atopy. Although we did not have endotoxin data from volunteers' households, we postulated that low values of lung function were associated to exposure to endotoxins present in environments exposed to dogs.

Key words: Respiratory tract diseases; Animals; Bronchial hyperreactivity; Lung function; Pets

Introduction

The effect of exposure to pets on the respiratory system has long been studied and is still controversial. In the 1990's, it was shown that sensitization to cats was a risk factor for asthma (1). In turn, exposure to cat allergen was associated with increased bronchial responsiveness (2). Subsequently, it was demonstrated that in atopic people, total IgE above 100 kU/L and specific IgE against cats above 0.35 kU/L were associated with new-onset asthma (3). In another study, daytime attacks of breathlessness were associated with cat ownership (4).

However, the same authors found a negative association with having a dog and infections of the airways, thus suggesting a possible protective effect (4). A systematic review involving studies with children and adults concludes that there is not enough evidence to indicate a relationship between keeping a pet and subsequent development of asthma (5). This lack of consensus and the discrepancy of the effects of pets reinforce the need for further studies. Thus, the aim of the present study was to investigate the prevalence of asthma and lung function status among dog and cat owners.

Material and Methods

The present cross-sectional study was conducted among adults working or studying at two Brazilian universities, the University of São Paulo at Ribeirão Preto campus and the State University of Campinas. For the present analysis, we selected individuals who had owned a cat or a dog as a pet in the year prior to the study; individuals who had not owned pets were selected as the control group. Consequently, the present study comprised three groups: cat owner, dog owner, and control groups. Subjects had no work exposure to laboratory animals or other animals.

Subjects answered a questionnaire and underwent a skin prick test (SPT), pulmonary function test, and bronchial challenge test with mannitol. Lung function was measured using a Koko spirometer and software (PDS Instrumentation, Inc., USA). Measurements were performed in the sitting position with the volunteer wearing a nose clip. At least 3 technically satisfactory maneuvers were attempted for each volunteer. If at least 3 technically satisfactory maneuvers were not obtained after 8 attempts, lung function testing was discontinued.

In order to perform the bronchial challenge test, an inhalation device and capsules (Pharmaxis Ltd., Australia) containing dry powdered mannitol were used. The challenge began with an empty capsule (used for training), followed by inhalation of 5, 10, 20, 40, 80, 160, 160, and 160 mg of dry powdered mannitol. Forced expiratory volume in one second (FEV1) was measured 60 s after every inhalation. This procedure was repeated for each dose until inhalation of 635 mg of mannitol or 15% fall in FEV1. The bronchial challenge test was considered positive when a 15% decrease in FEV1 was observed, indicating bronchial hyperresponsiveness (BHR). An individual was considered to be an asthmatic subject if he or she had BHR and had experienced symptoms of wheezing, chest tightness during the night, or dyspnea during the day or at night in the previous 12 months.

Subjects underwent SPT with 11 allergens. A wheal diameter of at least 3 mm was considered positive. The volunteers also responded to a questionnaire adapted from the European Community Respiratory Health Survey (ECRHS), translated and tested in Brazil. Further information on all the procedures performed can be found elsewhere (6).

Statistical analysis

Univariate analysis (chi-squared test) was performed to compare prevalence of asthma among control, and cat and dog owner groups. ANOVA was used to compare age and spirometric data (continuous variables) among groups. Relative risk (RR) was estimated using a modified Poisson regression approach, i.e., Poisson regression with a robust error variance. The model was adjusted using the Package Geepack in the R Software (R Foundation for Statistical Computing, Austria), version 3.2.2 and confidence intervals for the RR were obtained with the Package doBy in the R Software (R Foundation for Statistical Computing). Linear regression was used to make predictions about forced vital capacity (FVC) and FEV1.

Results

A total of 316 volunteers were included. Of these, 125 had not been pet owners in the previous year (control group), 51 individuals reported having had a cat, and 140 subjects reported having had a dog. Table 1 presents the general characteristics and the outcomes studied. The group of individuals exposed to dogs had lower FEV1 (reported in percentage of predicted values) and lower forced vital capacity (in percentage of predicted values) than the control group.

Table 1 Characteristics and outcomes of the study sample. 

Control group (n=125) Cat owner group (n=51) Dog owner group (n=140) P value
Age 32.5±9.8 32.8±11.4 32.0±10.3 0.844
Sex
Female 83 (66.4%) 34 (66.7%) 97 (69.3%) 0.868
Male 42 (33.6%) 17 (33.3%) 43 (30.7%) 0.868
Smoking 13 (10.4%) 10 (19.6%) 25 (16.7%) 0.151
SPT positive 50 (40.0%) 23 (45.1%) 71 (50.7%) 0.216
Confirmed asthma 6 (4.8%) 8 (15.7%) 15 (10.7%) 0.053
FEV1 (%) 99.4±13.1 99.6±13.4 96.0±10.1 0.035*
FVC (%) 100.4±13.2 101.5±13.5 97.2±10.8 0.038*

Data for age, FEV1, and FVC are reported as means±SD. SPT: skin prick test; FEV1: forced expiratory volume in 1 s (% of predicted value); FVC: forced vital capacity (% of predicted value). Statistical analysis was done with chi-squared test. *Pairwise comparisons are shown in Table 3.

Multivariate analysis showed that individuals exposed to cats had increased risk of confirmed asthma compared to individuals in the control group (RR: 3.24; 95% confidence interval (CI): 1.31 to 7.99) (Table 2). Linear regression showed that dog exposure was associated with lower FVC in percentage of predicted values (adjusted coefficient: –3.61, 95%CI: –6.62 to –0.60) and lower FEV1 in percentage of predicted (adjusted coefficient: –3.50, 95%CI: –6.45 to –0.55) compared to the control group. Cat ownership was not associated with changes in lung function (Table 3).

Table 2 Assessment of risk factors for confirmed asthma. 

Risk factors Crude model Adjusted model
RR 95%CI P value RR 95%CI P value
Group (cat vs control) 3.28 1.20 8.97 0.02 3.24 1.31 7.99 0.01
Group (dog vs control) 2.21 0.89 5.52 0.08 1.74 0.73 4.16 0.21
Age (continuous) 0.94 0.89 0.99 0.01 0.96 0.91 1.01 0.09
Sex (female vs male) 0.66 0.29 1.48 0.31 0.54 0.25 1.15 0.10
SPT (positive vs negative) 15.75 3.81 65.09 <0.001 14.12 3.58 55.69 <0.001
Smoking (yes vs no) 0.42 0.10 1.70 0.22 0.58 0.15 2.26 0.43

RR: relative risk; CI: confidence interval; SPT: skin prick test.

Table 3 Assessment of risk factors for reduction in FVC and FEV1

Risk factors FVC FEV1
Adjusted coefficient 95%CI P value Adjusted coefficient 95%CI P value
Group (cat vs control) 0.28 –3.77 4.34 0.89 –0.15 –4.13 3.82 0.94
Group (dog vs control) –3.61 –6.62 –0.60 0.01 –3.50 –6.45 –0.55 0.02
Age (continuous) 0.09 –0.05 0.24 0.20 0.02 –0.12 0.17 0.73
Sex (female vs male) –1.65 –4.67 1.37 0.28 –1.45 –4.41 1.51 0.33
SPT (positive vs negative) 0.44 –2.39 3.26 0.76 –1.85 –4.62 0.92 0.19
Smoking (yes vs no) 4.28 0.14 8.42 0.04 2.27 –1.78 6.33 0.27

FVC: forced vital capacity (% of predicted value); FEV1: forced expiratory volume in 1 s (% of predicted value); CI: confidence interval; SPT: skin prick test.

Discussion

The risks and/or benefits of keeping a pet have been the subject of several studies. This knowledge becomes even more important for regions or countries with relevant prevalence of pet ownership, such as the United Kingdom (7) and Italy (8). Pets (dogs or cats) are found in 9% of households of asthmatics in Spain (9).

Data from the present study showed that cat ownership was associated with increased risk of asthma but not with reduced lung function, while dog ownership was associated with reduced pulmonary function (FEV1 and FVC), without an increased risk of asthma. Previous studies have shown that exposure to cats is associated with increased risk of asthma among adults (10,11), however, to our knowledge, this is the first study to show concomitantly that dog ownership is associated with changes in lung function in adults. It is noteworthy that although we found a statistically significant reduction of lung function in dog owners, such reduction was not clinically worrisome. Reductions in spirometric values should be taken with caution. Values were still in the normal range and changes were small, approximately, 3.5% of predicted value. This fall is not a reason for concern among the general population; however, the change is important due to its mechanisms, its implications in patients with severe respiratory disease, and its relevance for disease understanding.

We believe that the increased risk of asthma among individuals exposed to cats is associated with immunological mechanisms because, as expected, atopy was a risk factor for asthma. In turn, changes in lung function of individuals exposed to dogs were not associated with atopy. It has been shown that households in which there are dogs have greater levels of airborne endotoxins (12) and exposure to endotoxins may worsen lung function (13,14).

Among sewage treatment plant workers, low levels of endotoxin had a significant impact on the observed across-shift (during 6 h shift) decline in FEV1 (13). In another study, workers of a factory that produced bioproteins derived from a bacterial species (Methylococcus capsulatum), exposed to low concentrations of endotoxin, presented lower FVC during the period of occupational exposure, compared to the period without occupational exposure. In addition, the authors detected increased leukocyte count during the exposure period (14). These findings reveal the association between exposure to endotoxin and inflammatory activity in the workers' lungs.

In urban areas, pets frequently live in apartments with no sufficient ventilation and upholstered furniture and carpets, where the level of exposure to pet allergens is very high (15). In residences not exposed to dogs and cats in the previous 6 months, the geometric mean concentrations of dog and cat allergens were 1.33 μg/g and 1.47 μg/g, respectively. In households exposed to dogs and cats, the geometric mean concentrations were 69.23 μg/g and 199.70 μg/g, respectively (16). Threshold values generally recognized as sufficient to induce sensitization and trigger respiratory symptoms are, respectively, 1 μg and 8–10 μg of allergen/g of dust (17). Thus, concentrations of dog and cat allergens in households not exposed to such animals would be insufficient to induce symptoms. In addition, exposure to animals is associated with the presence of other agents, such as the endotoxins, previously mentioned (12). In a recent study to evaluate home fungal and bacterial microbiomes, bacterial evenness and diversity, but not richness, were significantly increased by the presence of a dog, but not by the presence of a cat. Homes with dogs contained four times more putative bacterial species compared to homes without a dog (18).

Our data demonstrated that exposure to cats was associated with increased risk of asthma, while exposure to dogs is associated with reduced lung function. We speculate that the outcomes have different pathways for their development. Asthma would have an immunological basis (marked by atopy as a risk factor), and there may be a latency period between the onset of cat exposure and the development of asthma. On the other hand, reduction of pulmonary function can be associated with endotoxin exposure, which causes inflammation and may rapidly lead to changes in lung function.

References

1. Litonjua AA, Sparrow D, Weiss ST, O'Connor GT, Long AA, Ohman JLJr. Sensitization to cat allergen is associated with asthma in older men and predicts new-onset airway hyperresponsiveness. Am J Respir Crit Care Med 1997; 156: 23–27, doi: 10.1164/ajrccm.156.1.9608072. [ Links ]

2. Chinn S, Heinrich J, Antó JM, Janson C, Norbäck D, Olivieri M, et al. Bronchial responsiveness in atopic adults increases with exposure to cat allergen. Am J Respir Crit Care Med 2007; 176: 20–26, doi: 10.1164/rccm.200612-1840OC. [ Links ]

3. Antó JM, Sunyer J, Basagaãa X, Garcia-Esteban R, Cerveri I, De Marco R, et al. Risk factors of new-onset asthma in adults: a population-based international cohort study. Allergy 2010; 65: 1021–1030, doi: 10.1111/j.1398-9995.2009.02301.x. [ Links ]

4. Takaoka M, Suzuki K, Norbäck D. Current asthma, respiratory symptoms and airway infections among students in relation to the school and home environment in Japan. J Asthma 2017; 54: 652–661, doi: 10.1080/02770903.2016.1255957. [ Links ]

5. Chen CM, Tischer C, Schnappinger M, Heinrich J. The role of cats and dogs in asthma and allergy - a systematic review. Int J Hyg Environ Health 2010; 213: 1–31, doi: 10.1016/j.ijheh.2009.12.003. [ Links ]

6. Ferraz E, Arruda LK, Bagatin E, Martinez EZ, Cetlin AA, Simoneti CS, et al. Laboratory animals and respiratory allergies: The prevalence of allergies among laboratory animal workers and the need for prophylaxis. Clinics (Sao Paulo) 2013; 68: 750–759, doi: 10.6061/clinics/2013(06)05. [ Links ]

7. Murray JK, Gruffydd-Jones TJ, Roberts MA, Browne WJ. Assessing changes in the UK pet cat and dog populations: numbers and household ownership. Vet Rec 2015; 177: 259, doi: 10.1136/vr.103223. [ Links ]

8. Capello K, Bortolotti L, Lanari M, Baioni E, Mutinelli F, Vascellari M. Estimate of the size and demographic structure of the owned dog and cat population living in Veneto region (north-eastern Italy). Prev Vet Med 2015; 118: 142–147, doi: 10.1016/j.prevetmed.2014.10.017. [ Links ]

9. Fernandez R, Ariza M, Iscar M, Martinez C, Rubinos G, Gagatek S, et al. Impact of environmental air pollutants on disease control in asthmatic patients. Lung 2015; 193: 195–198, doi: 10.1007/s00408-015-9695-9. [ Links ]

10. Linneberg A, Nielsen NH, Madsen F, Frølund L, Dirksen A, Jørgensen T. Pets in the home and the development of pet allergy in adulthood. The Copenhagen Allergy Study. Allergy 2003; 58: 21–26, doi: 10.1034/j.1398-9995.2003.23639.x. [ Links ]

11. Noertjojo K, Dimich-Ward H, Obata H, Manfreda J, Chan-Yeung M. Exposure and sensitization to cat dander: asthma and asthma-like symptoms among adults. J Allergy Clin Immunol 1999; 103: 60–65, doi: 10.1016/S0091-6749(99)70526-9. [ Links ]

12. Park JH, Spiegelman DL, Gold DR, Burge HA, Milton DK. Predictors of airborne endotoxin in the home. Environ Health Perspect 2001; 109: 859–864, doi: 10.1289/ehp.01109859. [ Links ]

13. Cyprowski M, Sobala W, Buczyńska A, Szadkowska-Stańczyk I. Endotoxin exposure and changes in short-term pulmonary function among sewage workers. Int J Occup Med Environ Health 2015; 28: 803–811, doi: 10.13075/ijomeh.1896.00460. [ Links ]

14. Skogstad M, Sikkeland LIB, Øvstebø R, Haug KBF, Heldal KK, Skare Ø, et al. Long-term occupational outcomes of endotoxin exposure and the effect of exposure cessation. Occup Environ Med 2012; 69: 107–112, doi: 10.1136/oem.2010.062414. [ Links ]

15. Liccardi G, D'Amato G, Russo M, Canonica GW, D'Amato L, De Martino M, et al. Focus on cat allergen (Fel d 1): immunological and aerodynamic characteristics, modality of airway sensitization and avoidance strategies. Int Arch Allergy Immunol 2003; 132: 1–12, doi: 10.1159/000073259. [ Links ]

16. Arbes SJJr, Cohn RD, Yin M, Muilenberg ML, Friedman W, Zeldin DC. Dog allergen (Can f 1) and cat allergen (Fel d 1) in US homes: results from the national survey of lead and allergens in housing. J Allergy Clin Immunol 2014; 114: 111–117, doi: 10.1016/j.jaci.2004.04.036. [ Links ]

17. Chapman MD, Wood RA. The role and remediation of animal allergens in allergic diseases. J Allergy Clin Immunol 2001; 107(3 Suppl): S414–S421, doi: 10.1067/mai.2001.113672. [ Links ]

18. Kettleson EM, Adhikari A, Vesper S, Coombs K, Indugula R, Reponen T. Key determinants of the fungal and bacterial microbiomes in homes. Environ Res 2015; 138: 130–135, doi: 10.1016/j.envres.2015.02.003. [ Links ]

Received: March 19, 2018; Accepted: August 15, 2018

Correspondence: E.O. Vianna: <evianna@fmrp.usp.br>

Creative Commons License This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.