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. 2016 Jun 16;150(4):869–876. doi: 10.1016/j.chest.2016.06.011

Differences in Health-Related Quality of Life Between New Mexican Hispanic and Non-Hispanic White Smokers

Alejandro A Diaz a,, Hans Petersen b, Paula Meek c, Akshay Sood d, Bartolome Celli a, Yohannes Tesfaigzi b
PMCID: PMC5812751  PMID: 27321735

Abstract

Background

Smoking is associated with impaired health-related quality of life (HRQL) across all populations. Because decline in lung function and risk for COPD are lower in New Mexican Hispanic smokers compared with their non-Hispanic white (NHW) counterparts, the goal of this study was to ascertain whether HRQL differs between these two racial/ethnic groups and determine the factors that contribute to this difference.

Methods

We compared the score results of the Medical Outcomes Short-Form 36 Health Survey (SF-36) and St. George’s Respiratory Questionnaire (SGRQ) in 378 Hispanic subjects and 1,597 NHW subjects enrolled in the Lovelace Smokers’ Cohort (LSC) from New Mexico. The associations of race/ethnicity with SGRQ and SF-36 were assessed by using multivariable regression.

Results

Physical functioning (difference, –4.5; P = .0008) but not mental health or role emotional domains of the SF-36 was worse in Hispanic smokers than in their NWH counterparts in multivariable analysis. SGRQ total score and its activity and impact subscores were worse in Hispanic (vs NHW) smokers after adjustment for education level, current smoking, pack-years smoked, BMI, number of comorbidities, and FEV1 % predicted (difference range, 2.9-5.0; all comparisons, P ≤ .001). Although the difference in the SGRQ activity domain was above the clinically important difference of four units, the total score was not.

Conclusions

New Mexican Hispanic smokers have clinically relevant, lower HRQL than their NHW counterparts. A perception of diminished physical functioning and impairment in daily life activities contribute to the poorer HRQL among Hispanic subjects.

Key Words: health-related quality of life, Hispanic, quality of life, racial disparities, smokers, smoking, SQRQ

Abbreviations: HRQL, health-related quality of life; NHW, non-Hispanic white; SF-36, Medical Outcomes 36-item Short Form Health Survey; SGRQ, St. George’s Respiratory Questionnaire


Despite a major reduction in smoking rates over the past decade, an estimated 40 million adults were current smokers in the United States in 2014.1 The effects of smoking on mortality, risk for chronic diseases, and impairment in health-related quality of life (HRQL) are well known.2, 3, 4, 5 However, health status perceptions of smokers from different races and ethnic groups are not well known.6 Minority subjects with smoking-related lung diseases seem to experience a worse HRQL. For example, African-American subjects who smoke and have COPD report worse HRQL than their non-Hispanic white (NHW) counterparts. Although Hispanic ethnicity is the largest and fastest growing minority in the United States,7 ethnic differences in health status among Hispanic and NHW smokers have not been studied. The lack of literature on HRQL in this minority group may be due to their infrequent inclusion in large studies.8 Understanding health status perception in this population is of importance to better inform the burden of smoking on Hispanic subjects.

In a New Mexico-based cohort, Hispanic female smokers had higher expiratory airflow and lower risk of airflow obstruction than NHW subjects.9 Furthermore, Hispanic smokers had a reduced risk of rapid decline in lung function.10 Despite this advantage, previous investigations in smoking-related diseases (eg, obstructive lung disease, coronary artery disease, stroke) have shown that Hispanic subjects seem to experience greater impairment in HRQL than NHW subjects.11, 12, 13 A limitation of those studies is that they used a generic questionnaire or a single question from a generic instrument as a measure of HRQL. Using both a generic (eg, Medical Outcomes 36-item Short Form Health Survey [SF-36])14 and a respiratory disease-specific instrument (eg, the St. George’s Respiratory Questionnaire [SGRQ])15 would improve the objective assessment of the health status in Hispanic subjects who smoke. Although the SGRQ has been used in smokers,16 we are unaware of reports of SGRQ results restricted to US Hispanic subjects. Therefore, the goal of the present study was to compare SF-36 and SGRQ responses between Hispanic and NHW smokers. Although Hispanic smokers have better lung function, based on results of previous studies,11, 12 we hypothesized that Hispanic subjects would have a lower HRQL than NHW subjects. We also investigated the risk factors associated with HRQL in Hispanic smokers.

Patients and Methods

Data were used from the Lovelace Smokers’ Cohort (LSC), which has been described elsewhere.10 In brief, this is a cohort recruited based on smoking status (former and current smokers) including mainly NHW subjects and Hispanic subjects from the Albuquerque metropolitan area of New Mexico. Recruitment to this cohort was initiated in 2001 and is ongoing with follow-up visits of recruited subjects. Participants were aged 40 to 75 years, had smoked ≥ 20 pack-years, and were able to understand English. Approximately 96% of Hispanic participants were born in the United States, and they were therefore long-term residents in the country.17 Subjects from other racial/ethnic groups were excluded from this analysis. From the 2,273 initial participants enrolled, exclusion of participants from other racial/ethnic groups and those with missing data on self-reported race/ethnicity (N = 298) resulted in 1,975 subjects eligible for analysis (New Mexican Hispanic subjects, n = 378; NHW subjects, n = 1,597).

All subjects gave their consent to participate in the study. The study protocol was approved by the Western Institutional Review Board (No. 20031684).

Lung Function Assessment

Spirometry was performed by adhering to the 1994 American Thoracic Society guidelines18 as described previously.19 Spirometric measures of lung function were obtained prior to and following the administration of albuterol. FEV1 % predicted and FVC % predicted were calculated by using equations based on race/ethnicity. Mexican-American reference standards were used for the New Mexican Hispanic subjects.20

Outcome

The outcome was health status as measured by using the generic questionnaire SF-36 and the disease-specific, self-administered SGRQ. The SF-36 encompasses eight domains, and the following five domains were used: physical functioning, bodily pain, role emotional, mental health, and general health. The SF-36 scores range from 0 to 100, with higher scores indicating better HRQL.14 The SGRQ total score and its activity, symptom, and impact domain subscores were used for analyses. The SGRQ total score and its domain subscores range from 0 to 100, with higher score indicating a worse HRQL.21 A minimal clinically important difference in SGRQ total score and domain subscores is 4.22

Covariates

Clinical information was collected in a standardized manner, including demographic characteristics, education level (dichotomized as high school or beyond level or lower), smoking intensity (pack-years), current smoking status, and comorbidities. COPD was defined as a postbronchodilator ratio of FEV1 to FVC < 0.7, according to criteria of the Global Initiative for Chronic Obstructive Lung Disease.23 Asthma was defined as participants’ self-report of physician diagnosis for this condition. Chronic bronchitis was based on self-reported cough productive of phlegm for ≥ 3 months per year for at least 2 consecutive years.24 Information on other comorbidities (diabetes, hypertension, congestive heart failure, rheumatic disease, TB, cancer, peripheral vascular disease, renal disease, liver disease, and transient ischemic attack) was also collected based on self-reported data as described elsewhere.19 The number of comorbidities was dichotomized as 0 to 2 and ≥ 3.25

Statistical Analyses

Main analyses for SGRQ total score and subscores, as well as SF-36 and its domains, were conducted by using multivariable regression models in which New Mexican Hispanic ethnicity was the main predictor, and NHW was the reference group. The models were adjusted for education level, BMI, pack-years smoked, current smoking status, FEV1 % predicted, and the number of comorbidities. The main analysis was conducted in all smokers, but ethnic differences in subgroups with asthma, chronic bronchitis, or COPD were also explored. For the subgroup analyses, subjects with multiple diseases were excluded. To assess potential factors associated with SGRQ scores within the minority population, multivariable models in Hispanic subjects only were also assessed.

A P value < .05 was considered significant. All analyses were conducted by using SAS version 9.3 (SAS Institute, Inc).

Results

Participants’ Characteristics

Hispanic subjects compared with NHW smokers were younger and more likely to be current smokers but had smoked fewer pack-years, had lower education levels, and higher BMI. In addition, Hispanic subjects who smoked had a higher incidence of diabetes and rheumatic disease but less hypertension, TB, and cancer than their NHW counterparts. As was previously reported,9, 10 Hispanic smokers had a higher FEV1 % predicted and lower prevalence of COPD confirmed with spirometry, as well as a higher prevalence of chronic bronchitis, with no significant differences in asthma prevalence (Table 1).

Table 1.

Baseline Characteristics of the Participants According to Disease and Racial/Ethnic Group

Characteristic All Participants (N = 1,975) Hispanic (n = 378) Non-Hispanic White (n = 1,597) P Value
Female sex 1,518 (77) 281 (74) 1,237 (78) .20
Age, y 56 ± 10 53 ± 9 56 ± 10 < .0001
High school or higher education level 1,373 (70) 172 (46) 1,201 (75) < .0001
Pack-years smoked 39.9 ± 20.7 33.7 ± 15.5 41.3 ± 21.5 < .0001
Current smoking status 1149 (58) 288 (76) 861 (54) < .0001
BMI, kg/m2 28.1 ± 6.2 28.7 ± 6.0 28.0 ± 6.2 .04
FEV1, L 2.5 ± 0.8 2.6 ± 0.7 2.5 ± 0.8 .19
FEV1/FVC, % 73.1 ± 10.4 76.6 ± 9.0 72.3 ± 10.6 < .0001
FVC, L 3.5 ± 0.9 3.4 ± 0.9 3.5 ± 0.9 .03
FEV1 % predicted 88 ± 18 92 ± 17 87 ± 18 < .0001
FVC % predicted 94 ± 15 95 ± 15 93 ± 15 .01
Chronic pulmonary diseases
 Asthma only 172 (9) 34 (9) 138 (9) .83
 Chronic bronchitis only 294 (15) 78 (21) 216 (14) < .0001
 COPD only 194 (10) 19 (5) 175 (11) .001
Comorbidities
 ≥ 3 Comorbidities 165 (8) 22 (6) 143 (9) < .0001
 Hypertension 654 (33) 100 (27) 554 (35) .002
 Chronic heart failure 15 (1) 2 (1) 13 (1) .56
 Peripheral vascular disease 164 (8) 24 (6) 140 (9) .13
 Liver disease 164 (8) 38 (10) 126 (8) .17
 Transient ischemic attack 82 (4) 15 (4) 67 (4) .84
 Renal disease 107 (5) 21 (6) 86 (5) .90
 Rheumatic disease 106 (5) 31 (8) 75 (5) .007
 Diabetes 145 (7) 45 (12) 100 (6) .0002
 TB 197 (10) 16 (4) 181 (11) < .0001
 Cancer 330 (17) 33 (9) 297 (19) < .0001
Health status: SF-36
 Physical functioning 76.4 ± 24.9 72.9 ± 26.5 77.2 ± 24.5 .002
 Bodily pain 67.1 ± 25.0 64.6 ± 27.5 67.7 ± 24.4 .03
 Role emotional 75.2 ± 39.6 71.7 ± 41.6 76.0 ± 39.1 .06
 Mental health 73.4 ± 19.7 69.8 ± 21.5 74.3 ± 19.1 < .0001
 General health 66.6 ± 21.6 64.0 ± 22.6 67.3 ± 21.3 .009
Health status: SGRQ
 Total score 21.9 ± 17.9 25.3 ± 19.2 21.1 ± 17.5 < .0001
 Activity domain 31.7 ± 24.9 36.2 ± 26.3 30.6 ± 24.4 < .0001
 Symptom domain 31.2 ± 23.5 34.8 ± 24.7 30.4 ± 23.1 .001
 Impact domain 11.9 ± 14.3 14.7 ± 16.2 11.2 ± 13.7 < .0001

Data are presented as no. (%) or mean ± SD. SF-36 = Medical Outcomes 36-item Short Form Health Survey; SGRQ = St. George’s Respiratory Questionnaire.

Hispanic Smokers Have Worse HRQL

In univariate analysis, physical functioning, bodily pain, mental health, and general health domains of the SF-36 questionnaire were worse (lower) in Hispanic smokers than in NHW smokers (P ≤ .03 for all comparisons) (Table 1). However, in adjusted models, physical functioning was the only domain in the SF-36 questionnaire that remained significantly lower (Table 2). Hispanic smokers also had worse (ie, higher) SGRQ total score (3.4 more points) and subscores (range, 3.4-5.6) than their NHW counterparts in univariate analysis. In adjusted analyses, the racial/ethnic differences in the SGRQ domain subscores (range, 2.9-5.0) were attenuated but remained significant (P ≤ .0003), with the exception of the symptom subscale (P = .09). Although the difference in the activity subscore was above the minimal clinically important difference, the total score and impact subscores were not. We tested for an interaction between sex and ethnicity for SGRQ total score, which was not significant (P = .48).

Table 2.

Racial/Ethnic Differences in Health-Related Quality of Life in All Smokers

SF-36 Domains
Physical Functioning
P Value Bodily Pain
P Value Role emotional
P Value Mental Health
P Value General Health
P Value
Hispanic-NHW Diff (95% CI) Hispanic-NHW Diff (95% CI) Hispanic-NHW Diff (95% CI) Hispanic-NHW Diff (95% CI) Hispanic-NHW Diff (95% CI)
–4.5 (–5.8 to –3.2) .0008 –1.4 (–2.9 to 0.1) .35 –1.1 (–3.5 to 1.3) .63 –1.8 (–3.0 to –0.6) .11 –1.2 (–2.4 to 0.0) .31
SGRQ Domains
SGRQ Total Score
P Value Activity
P Value Symptom
P Value Impact
P Value
Hispanic-NHW Diff (95% CI) Hispanic-NHW Diff (95% CI) Hispanic-NHW Diff (95% CI) Hispanic-NHW Diff (95% CI)
3.4 (4.3 to 2.5) .0003 5.0 (3.7 to 6.3) .0002 2.1 (0.8 to 3.4) .09 2.9 (2.1 to 3.7) .0002

The values for the differences in scores between Hispanic subjects and non-Hispanic white (NHW) subjects represent the parameter estimates (95% CI) from multivariable regression models, with NHW as the reference group and adjusted for education level (high school or beyond vs less than high school), pack-years smoked, current smoking status, BMI, the number of comorbidities (≥ 3 vs < 3), and FEV1 % predicted.

Diff = difference. See Table 1 legend for expansion of other abbreviation.

Risk Factors for SGRQ Total Score in Hispanic Smokers

In analyses of Hispanic smokers only, current smoking status, greater pack-years smoked, greater BMI, and lower FEV1 % predicted were independently associated with worse (ie, higher) SGRQ total score. Similar relationships with predictive factors were found for the domains of activity, impact, and symptoms (Table 3).

Table 3.

Multivariable Models for SGRQ Total Score and Subscores in All New Mexican Hispanic Smokers Only

Variable Total Score
Activity Subscore
Symptom Subscore
Impact Subscore
β (95% CI) P Value β (95% CI) P Value β (95% CI) P Value β (95% CI) P Value
High school or higher education level –3.2 (–3.3 to –3.1) .09 –3.9 (–6.5 to –1.3) .13 –0.9 (–3.3 to 1.5) .70 –3.4 (–5.0 to –1.8) .04
BMI 0.5 (0.3 to 0.7) .004 0.8 (0.6 to 1.0) .0002 0.3 (0.1 to 0.5) .19 0.3 (0.2 to 0.4) .04
Pack-years smoked 0.1 (0.04 to 0.16) .02 0.1 (0.0 to 0.2) .12 0.1 (0.0 to 0.2) .15 0.2 (0.1 to 0.3) .003
Smoking status 8.5 (6.3 to 10.7) .0001 9.9 (6.8 to 13) .001 17.5 (14.6 to 20.4) <.0001 4.2 (2.3 to 6.1) .02
≥3 Comorbidities 4.7 (0.3 to 9.1) .24 7.1 (1.4 to 12.8) 0.21 0.9 (–4.3 to 6.1) <.0001 4.6 (1.2 to 8.0) .18
FEV1 % predicted –0.2 (–0.3 to –0.1) <.0001 –0.2 (–0.3 to –0.1) <.0001 –0.3 (–0.4 to –0.2) <.0001 –0.2 (–0.24 to –0.16) <.0001

β = beta value. See Table 1 legend for expansion of abbreviation.

Analysis According to Disease Group

Compared with smokers who had no chronic pulmonary diseases (asthma, chronic bronchitis, COPD), participants with asthma (SGRQ difference range, –4.3 [impact] to –9.0 [symptom], chronic bronchitis (–8.1 [impact] to –23.5 [symptom]), or COPD (–3.6 [impact] to –7.7 [activity]) had a worse (ie, higher) SGRQ total score and subscores (P < .0001 for all comparisons). However, the multivariable analysis within disease showed no differences in most of the SF-36 and SGRQ scores and subscores (all comparisons, P > .05) between New Mexican Hispanic and NHW smokers: asthma (SF-36 difference range, –3.8 [bodily pain] to 3.7 [role emotional]; SGRQ difference range, –0.5 [impact] to 4.6 [activity]); chronic bronchitis (SF-36, –3.6 [role emotional] to 3.9 [general health]; SGRQ, 0.8 [symptom] to 3.4 [activity]); and COPD (SF-36, –0.4 [role emotional] to 4.4 [general health]; SGRQ, 0.1 [symptom] to –1.2 [impact]). One exception was observed in patients with asthma: New Mexican Hispanic subjects reported significantly worse SF-36 physical functioning (difference, –7.9; P = .04). None of the interactions between disease statuses and ethnicity for SGRQ total score and subscores were significant (P range, .10-.82).

Discussion

In the present study, we evaluated > 1,500 LSC participants and found that New Mexican Hispanic subjects compared with NHW subjects reported worse generic and disease-specific HRQL. In New Mexican Hispanic smokers, diminished physical functioning and impairment in daily life activities were the primary contributors to HRQL impairment. Current smoking status, greater pack-years smoked, higher BMI, and lower FEV1 % predicted were identified as risk factors for a worse SGRQ score in this population.

The so-called “Hispanic paradox” states that despite socioeconomic disadvantages, Hispanic subjects vs NHW subjects have comparable or more favorable health outcomes (eg, lower general mortality rates, better birth outcomes).26, 27 However, whether this paradox includes HRQL in smokers is unknown. Our results found that the Hispanic paradox is not applicable to health status because smokers of this ethnicity experienced worse HRQL than their NHW counterparts. The racial/ethnic differences in SGRQ activity subscore are particularly relevant because they exceed the minimum clinically important difference for this instrument and are higher than those reported between women and men with COPD.28 Although our cohort is female predominant, and women tend to report worse HRQL and more respiratory symptoms (eg, dyspnea) than men,29 the proportion of women was similar in both populations, and an interaction term between sex and ethnicity was not significant, suggesting that the observed differences were independent of sex. In addition, because Hispanic subjects from the LSC were long-term residents in New Mexico and are fluent in English, the “healthy migrant effect” and language barrier are likely not to be relevant explanations for the observed ethnic differences in HRQL.17, 30 Together, our novel findings suggest that although New Mexican Hispanic smokers have less airway obstruction and fewer pack-years of smoking exposure than their NHW counterparts, they perceive their health status to be on average poorer based on their reports of diminished ability to perform activities of daily living and of experiencing more severe disease impact. The results of both SF-36 and SGRQ are consistent in revealing that the discrepancy between desired and real well-being among New Mexican Hispanic smokers seems to be related to a reduced ability to perform activities of daily living or being less physically functional. The absence of ethnic differences in the SF-36 mental, role emotional, and general health domain scores emphasizes that physical limitations seem more relevant to health status in New Mexican Hispanic smokers. These findings suggest that culturally sensitive interventions targeted to improve physical functioning may be most appropriate for the well-being of Hispanic subjects.

The factors contributing to the racial/ethnic differences in HRQL are multifactorial and include disparities in access to health care and adequate health literacy, and health behavior. A recent report indicated that compared with NHW subjects, US Hispanic subjects are three times less likely to have health insurance,31 a key factor to health care access. Martinez et al11 demonstrated that access to health care was one of the main contributors to differences in health status between Mexican-American subjects and NHW subjects. Prior investigation has documented that education level is directly related to health literacy.32 The 2003 National Assessment of Adult Literacy showed that Hispanic subjects have the lowest health literacy level of all ethnic groups in the United States.33 Because the majority of the Hispanic smokers in the present study had only a high school education, it is also likely that they have inadequate health literacy. Low health literacy is reportedly associated with worse HRQL in Hispanic subjects with asthma.34, 35 Furthermore, leisure-time physical activity is a behavior associated with improved HRQL likely because it involves improvement in mobility, reduced pain, and higher emotional well-being.36, 37 Hispanic subjects report less leisure-time physical activity compared with NHW subjects,38 which might explain the differences in observed HRQL.

When we examined the factors associated with HRQL in New Mexican Hispanic smokers only, we consistently identified modifiable risk factors such as current smoking status, pack-years smoked, and BMI. The current smoking status in this study was higher in New Mexican Hispanic subjects than in NHW subjects, and current smoking remains higher in national surveys.31 Our findings thus support the need of culturally sensitive smoking cessation interventions in this population. Consistent with national data,39 a higher BMI was also observed in New Mexican Hispanic subjects than in NHW subjects, and BMI was associated with worse health status. A previous study reported a modest decrease in HRQL in obese (vs nonobese) Hispanic subjects.40 A high BMI may affect HRQL by further limiting daily activities or causing sleep disturbances.24

In the analysis according to disease group, we found no racial/ethnic differences in most of the SF-36 scales and for all SGRQ domains. The exception was in participants with asthma only, in whom SF-36 physical functioning was, again, worse in New Mexican Hispanic subjects. This finding suggests that the burden of asthma is worse for this minority group. As for COPD, initial New Mexican Hispanic/NHW differences in SGRQ scores and subscores disappeared after adjustment for lung function. FEV1 % predicted was inversely associated with SGRQ in this population, suggesting that this factor partly explains the lack of HRQL difference based on race/ethnicity in COPD.

The present study has several limitations. First, all LSC participants are heavy smokers, the majority are female, and the enrolled Hispanic subjects are predominantly long-term residents of New Mexico. Thus, the cohort is not representative of the diverse Hispanic subgroups in the United States, limiting the generalizability of our results. The term Hispanic in this study applies solely to Hispanic subjects living in the New Mexico area. Ancestry studies by our group have shown that this population has an average 33% Native American ancestry,10 which may not be present in other ancestry groups that are also identified as Hispanic subjects in the United States. A further limitation is that some potential confounders such as access to health care, physical activity, depression, and dyspnea in the health status/ethnicity relationships were not accounted for.6 When we examined dyspnea frequency by using the SGRQ individual item, no ethnic differences were evident (33% vs 30% for New Mexican Hispanic subjects and NHW subjects, respectively; P = .20); this finding is consistent with a previous study.41 Finally, we used the SGRQ with the assumption that it is an appropriate instrument to capture the true health status of a minority population. However, although the instrument was originally validated in a nonminority population from six countries,42, 43 several subsequent studies44, 45 have used the SGRQ in Hispanic subjects outside of the United States, supporting its use in this population.

Conclusions

The present study found that, compared with NHW smokers, New Mexican Hispanic smokers had clinically relevant decreases in HRQL, which seemed to be driven by less physical functioning and limitations in performing daily life activities.

Acknowledgments

Author contributions: H. P. had full access to all of the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis. A. A. D., H. P., P. M., A. S., B. C., and Y. T. contributed to conception and design of this study and creation, revision, and final approval of this manuscript A. A. D., H. P., P. M., A. S., B. C., and Y. T. contributed to analysis and interpretation; H. P., A. S., and Y. T. contributed to data acquisition; and A. A. D., H. P., P. M., B. C., A. S., and Y. T. drafted the manuscript for important intellectual content.

Financial/nonfinancial disclosures: The authors have reported to CHEST the following: A. A. D. has received speaker fees from Novartis, Inc. None declared (H. P., P. M., A. S., B. C., Y. T.).

Role of sponsors: The sponsors had no role in the design of the study, the collection and analysis of the data, or the preparation of the manuscript.

Footnotes

FUNDING/SUPPORT: This work was supported by the State of New Mexico (appropriation from the Tobacco Settlement Fund) and grants from the National Institutes of Health (A. A. D., K01HL118714; A. S., K23 HL 094531-01 and 5M01 RR00997; Y. T., R01 HL068111 and R01 ES015482). A. A. D. is also supported by the Brigham and Women’s Hospital Minority Faculty Career Development Award.

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