Genetic and environmental influence on lung function impairment in Swedish twins
© The Author(s) 2010
Received: 13 February 2010
Accepted: 6 July 2010
Published: 6 July 2010
The understanding of the influence of smoking and sex on lung function and symptoms is important for understanding diseases such as COPD. The influence of both genes and environment on lung function, smoking behaviour and the presence of respiratory symptoms has previously been demonstrated for each of these separately. Hence, smoking can influence lung function by co-varying not only as an environmental factor, but also by shared genetic pathways. Therefore, the objective was to evaluate heritability for different aspects of lung function, and to investigate how the estimates are affected by adjustments for smoking and respiratory symptoms.
The current study is based on a selected sample of adult twins from the Swedish Twin Registry. Pairs were selected based on background data on smoking and respiratory symptoms collected by telephone interview. Lung function was measured as FEV1, VC and DLco. Pack years were quantified, and quantitative genetic analysis was performed on lung function data adjusting stepwise for sex, pack years and respiratory symptoms.
Fully adjusted heritability for VC was 59% and did not differ by sex, with smoking and symptoms explaining only a small part of the total variance. Heritabilities for FEV1 and DLco were sex specific. Fully adjusted estimates were10 and 15% in men and 46% and 39% in women, respectively. Adjustment for smoking and respiratory symptoms altered the estimates differently in men and women. For FEV1 and DLco, the variance explained by smoking and symptoms was larger in men. Further, smoking and symptoms explained genetic variance in women, but was primarily associated with shared environmental effects in men.
Differences between men and women were found in how smoking and symptoms influence the variation in lung function. Pulmonary gas transfer variation related to the menstrual cycle has been shown before, and the findings regarding DLco in the present study indicates gender specific environmental susceptibility not shown before. As a consequence the results suggest that patients with lung diseases such as COPD could benefit from interventions that are sex specific.
The adult individuals' lung function is determined both by the maximal level of lung function growth achieved during childhood and adolescence, and by the rate of decline that follows from the early twenties onwards. Both these are likely to be of importance for later development of respiratory disease, such as COPD. Furthermore, factors as FEV1, and VC are powerful predictors of mortality [1, 2].
In healthy populations, level of lung function is strongly genetically determined both early and later in life, for both men and women [3–6]. Lung function will also be affected by, or co-vary, with other factors, such as smoking and chronic respiratory diseases. However, the relationships between these variables are not always obvious as some smokers never develop symptoms and lung function decline, while some never smokers become ill, etc [1, 2]. Interestingly, as smoking behaviour in itself is determined both by genes and environment, it can influence lung function by co-varying not only as an environmental factor, but also by shared genetic pathways [3, 7]. Further, both respiratory symptoms and cigarette smoking have been shown to have a sex related co-variance with pulmonary function measures [8, 9]. This has brought to attention the possibility that an individual's genes affect his or her sensitivity to factors important for respiratory health .
Therefore, the objective of the current cross-sectional study in a Swedish sample of twins was to evaluate heritability for different measures of lung function, and to investigate, by sex, how the estimates are affected by the covariates smoking and respiratory symptoms.
Materials and methods
Available, invited and participating twins from the Swedish Twin Registry.
Symptoms: twin1, twin2
Smoking > 10 PY: twin1, twin2
No of available
No of invited
No of participating
Participation in % of available
Lung function testing
All lung function tests were carried out in a single specialized clinic with highly experienced staff. Lung function in terms of FEV1, VC and DLco was measured according to American Thoracic Society criteria [12, 13], using a Sensormedics 6200 body plethysmograph (SensorMedics; Yorba Linda, CA, USA). Each subject performed several slow and forced vital capacity expirations. FEV1 was compared to the largest obtained VC and individuals with an obstructive pattern (an FEV1/VC ratio 5 units below the predicted value, or FEV1 below 90% of the predicted value) also performed a new test 15 minutes after bronchodilation with a short-acting beta2-agonist (nebulized Salbutamol). The maximum values for VC and FEV1 (measured pre- or post bronchodilation) were then used for analysis. Based on lung function, twins could be classified according to GOLD-criteria .
Self reported cigarette smoking was assessed at the clinical examination and quantified as pack years.
Determination of twin zygosity
Zygosity of the sex-liked pairs was determined by the use of a set of DNA markers from blood drawn at the clinical testing. Blood samples were not available for both members in 14 pairs, and zygosity information for these twins was instead obtained at the time of registry compilation on the basis of questions about childhood resemblance. Four separate validation studies using serology and/or genotyping have shown that with these questions 95-98% of twin pairs are classified correctly .
Respiratory symptoms and pack years were assessed as covariates in the linear multivariate regression models stratified by sex. Analyses were performed with the Stata 9.2 software package (StataCorp LP, College Station, TX, USA)
Quantitative genetic analysis
Quantitative genetic analysis aims to provide estimates of the importance of genes and environment for the variation of a trait or disease (phenotype). The phenotypic variance is assumed to be due to three latent, or unmeasured, factors: additive genetic factors (a2), shared environmental factors (c2) or dominant genetic factors (d2), and non-shared environmental factors (e2), which also include measurement error. Heritability is a term that describes the proportion of total phenotypic variation directly attributable to genetic effects . Twins are ideal for these types of studies as we know how they are genetically related: identical (monozygotic (MZ)) twins share the same genes, whereas fraternal (dizygotic (DZ)) twins share, on average, half of their segregating genes. We also assume that shared environment (for example the presence of a childhood cat, or parental socioeconomic status) contributes to within-pair likeness to the same extent in MZ and DZ twin pairs. By calculating similarity within and between MZ and DZ twin pairs, we can obtain information about the importance of genetic and environmental factors to the variance of the trait in question. One such measure of twin similarity is the intra-class correlation (ICC) .
In order to test for sex differences, i.e. whether the same genes and environment contribute to the phenotypic variance in both men and women, different versions of the models can be compared . In the first variance model, we allow the genetic and environmental variance components to be different for men and women, and the genetic correlation (ra) is free to be estimated for opposite-sexed DZ twins. For instance, if the genetic correlation is estimated at 0, it indicates that completely different genes influence the trait in men and women. Variance model 2 tests whether the genetic and environmental variance components are allowed to be different for women and men (e.g. if genetic variance is more important in men than in women), constraining the genetic correlation for members of the opposite-sex twin pairs to 0.5. Variance model 3 has equal genetic and environmental variance components for men and women. If the fit of this models is not significantly different compared to the previous, we can assume that there are no sex differences in the magnitude of genetic and environmental influences. In summary, the difference in chi-squares between nested models is calculated in order to test which of the models fits better. A significant chi square difference indicates that the model with fewer parameters to be estimated fits the data worse. Model fitting was performed with the Mx program .
All models were tested using lung function in percent of predicted value, the same adjusted for pack years, and finally also adjusted for presence of respiratory symptoms.
A summary of the available and participating twins is presented in table 1.
Mean value (± Standard Deviation) for lung function measures and covariates, by sex and zygosity.
Opposite sexed pairs (n = 42)
MZ (n = 28)
DZ(n = 14)
MZ(n = 65)
DZ(n = 27)
60.5 ± 9.0
59.8 ± 7.3
59.1 ± 8.3
60.1 ± 9.6
58.5 ± 8.7
58.5 ± 8.8
178.7 ± 5.7
180.1 ± 5.3
164.4 ± 6.2
163.9 ± 5.5
178.3 ± 5.5
165.0 ± 4.8
11.6 ± 17.6
22.4 ± 20.2
9.5 ± 14.0
13.6 ± 16.9
15.5 ± 16.2
11.9 ± 16.5
VC in % pred.
100.64 ± 13.00
97.86 ± 15.83
111.99 ± 15.42
108.89 ± 13.94
101.97 ± 13.04
113.81 ± 14.90
FEV1 in % pred.
92.97 ± 14.91
89.70 ± 18.37
98.96 ± 16.60
98.21 ± 15.77
96.27 ± 15.53
102.68 ± 14.99
DLco2 in % pred.
95.06 ± 18.44
92.45 ± 19.58
87.11 ± 16.08
79.97 ± 14.54
91.83 ± 18.99
89.33 ± 15.97
Intraclass correlations (with 95% confidence intervals) for unadjusted and adjusted FEV1, VC and DLco in a Swedish twin sample by sex and zygosity status.
MZ (n = 28)
DZ (n = 14)
MZ (n = 65)
DZ (n = 27)
(n = 42)
Adj. PY, symptoms
Adj. PY, symptoms
Adj. PY, symptoms
Sex differences in the genetic influence on measures of lung function
Fit statistics from structural equation modelling for VC.
Model 2 vs. 1
Model 3 vs.2
Model 2 vs.1
Model 3 vs.2
Adj. PY, sympt.
Model 2 vs.1
Model 3 vs.2
Fit statistics from structural equation modelling for FEV1.
Model 2 vs. 1
Model 3 vs. 2
Model 2 vs. 1
Model 3 vs. 2
Adj. PY, sympt.
Model 2 vs. 1
Model 3 vs. 2
Fit statistics from structural equation modelling for DLco.
DLco: adj. PY
DLco: adj. PY, symptoms
DLco: adj. PY
DLco: adj. PY, symptoms
Contribution of genes and environment to the total variance
Unadjusted data show that mainly genetic, but also non-shared environmental influences were of importance for the variance of VC. For FEV1 and DLco, analyses had to be separated by sex, as indicated above. For both measures, the variance was attributable to both genetic and environmental factors for women, but only to environmental factors in men (figure 2).
Influence of smoking and symptoms on the total variance
Adjustment for pack-years and respiratory symptoms resulted in a decrease of the total variance of all lung function measures (VC, FEV1, and DLco) between 7 and 37%.
For VC, the decrease in total variance was due to a small reduction of genetic variance, whilst the non-shared environmental variance was stable after adjustments. For FEV1 and DLco, the effect of smoking and symptoms was found to be larger in men than in women. The total variance decrease was due to a reduction attributed to genetic variance in women, and shared environmental variance in men.
In the current study all lung function measures (VC, FEV1 and DLco) were shown to be influenced by genetic factors. FEV1 and DLco showed sex differences in the relative importance of genes and environment, as well as in how smoking and respiratory symptoms influence the genetic and environmental estimates of the trait. Heritability of FEV1 has been studied before, but for the gas transfer measure DLco, related to clinical findings such as emphysema, the information is new. VC heritability was higher, and without sex differences.
The relationship between smoking and the presence of respiratory symptoms as well as impaired lung function has been long known. More recently, studies of general twin populations have suggested that genetic factors are of importance in individual differences in lung function [4, 6, 20], and family studies have shown that relatives of subjects with COPD had a higher risk of airflow obstruction than controls [21–23]. In another study of unselected elderly twins in the Swedish twin registry , heritability estimates adjusted for smoking were lower for FEV1 (24-41% vs. 67%) but more similar for VC (61% vs. 48%) than the current results. In that study no sex differences were found in heritability estimates, but opposite sexed pairs were not included, reducing power to find such differences. Heritability is population specific and will differ between samples that differ in the distribution of environmental risk factors. Even though both populations were of the same nationality and age range, the prevalence of smoking habits and symptoms would have been lower in the unselected second material, which could explain why differences between studies were seen particularly for FEV1, which, as stated above, is known to be susceptible to these factors.
Genes and environments contributed differently to the lung function parameters for men and women. Since it is known that genes influence smoking habits, we chose to present results both with and without the adjustment of pack years. Symptoms on the other hand can be a part of COPD. Adjusting for symptoms give estimates of heritability for lung function not associated with symptoms. The differing results for how much these covariates influenced the three measures used in the current study are not unreasonable as the measures represent different aspects of lung function. Smoking induced pathology is likely to be primarily seen in FEV1 and DLco, while VC can remain, at least initially, essentially normal. The approach of adjusting for covariates can however underestimate heritability for the disease itself particularly if they share genetic and environmental effects in common. In women, smoking accounted for some part of the genetic variance, while in men, it accounted for parts of the shared environmental variance. It has been suggested that due to differences in how smoking has been socially accepted in men and women, it is possible that men are more influenced by cultural reasons for smoking than women . Another explanation to the apparent greater proportion in genetic variance in women could be that there is a reduction in absolute range of environmental variance for smoking in women during the mid 1900's, resulting in a proportionate greater observed genetic variance. Thus, genetic variance per se may not have changed, but when seen in relation to environmental variance, it appears to have increased .
Hence, smoking and respiratory symptoms could have differential effects on the variance components of men and women. The literature also provides examples of sex-specific effects on different aspect of lung function by genetic determination of physiological and hormonal patterns, such as the connection between aerobic capacity and risk for development of COPD , the impact of oestrogen on smoke toxins in the lung , and variations in gas transfer over the menstrual cycle .
On the phenotypic level, sex differences in the relationship between smoking and lung function impairment have been described in the literature, where women smoke less but have more severe lung function decline and more symptoms [3, 8, 9]. Two recent studies [28, 29] have suggested the presence gene-environment interaction, i.e. that the effect of smoking on lung function (here FEV1) is dependent on the genotype of the individual. Given our results, we suggest that there are sex differences of importance to the genetic and environmental influence on lung disease. However, the number of twin pairs in the current study was insufficient to evaluate possible interactions. Age is an important covariate in lung disease, but in the current study the number of participants prevented further modelling.
We have in a sample of twins with and without smoking and respiratory symptoms, shown that not only environment but also genes determine the variability in VC, FEV1 and DLco. Differences between men and women were found in the size of the relative importance of genes, but also in the type of genetic pattern (additive vs. dominant). Adjustments of smoking and respiratory symptoms had also differential effect on men and women for FEV1 and DLco. Further studies on gene-environment interaction are needed to fully understand the sex differences in respiratory disease. The present study highlights the importance of evaluating genetic and environmental influence on lung function by sex, and suggests that patients with lung diseases such as COPD could benefit from interventions that are sex specific both on the genetic and environmental level.
Specification of questions from the SALT questionnaire
Do you have recurrent periods of coughing?
Do you regularly cough up phlegm?
Do you have or have you had:
Chronic bronchitis (bronchitis)
Chronic bronchitis was defined as:
Recurrent cough with phlegm production, and/or self reported chronic bronchitis and/or self reported emphysema (positive answers to questions 1+2 or 3 or 4).
The authors thank the hospital team Kristina Daniels, Kerstin Magnusson, Isabella Norgren, and Astrid Fernstedt at Södersjukhuset for excellent technical assistance. The study was supported with substantial grants from AstraZeneca, but without any reservations in terms of control of the results. The data collection in SALT was supported by grants from the Swedish Research Council and NIH grant AG 08724. The study was also supported by grants from the Swedish Heart and Lung Foundation.
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