Non-hispanic whites have higher risk for pulmonary impairment from pulmonary tuberculosis

Health outcome disparities associated with race and ethnicity are well documented for many diseases and patient populations. While there are a variety of explanations for these effects, they are not fully understood [1‐3]. Socio-economic, biological, cultural, demographic, and other factors all contribute to an individual's health before, during and after illness [1, 2, 4]. While some contributors to health disparities are well defined the contribution of biological and gender differences, personal behaviors, value choices, and race/ethnicity on specific diseases and their clinical outcomes are not [1, 3].

It is well established that tuberculosis (TB) is disproportionately prevalent among economically disadvantaged and racial/ethnic minority populations [5‐8]. The health impacts of TB associated with differences in race, ethnicity, and more primary health risks are incompletely known [5‐12]. In a prior study, we measured the frequency and degree of pulmonary impairment in TB patients who were treated with standard regimes delivered by directly observed therapy (DOT) [13]. Spirometry-defined pulmonary impairment after tuberculosis (PIAT) was found in a majority of the cohort, and was more common in US born and older patients [13, 14]. The study's sample size did not allow stratified analysis of PIAT prevalence and severity between race/ethnic and other patient groups. We expanded our sample to allow a comparison of PIAT frequency across self-identified race/ethnicity groups and by socioeconomic status.

Between July 2005 and December 2009, 362 patients with culture confirmed pulmonary tuberculosis were reported to Tarrant County Health and were eligible for study enrolment (Figure 1). Of these, 320 (88%) were enrolled. Sixty-nine (22%) self-identified as non-Hispanic White, 85 (27%) as non-Hispanic Black, 81 (25%) as Asian, 82 (26%) as Hispanic and 3 (0.9%) were combined as "other" racial/ethnic group. The 3 subjects in the "other" racial/ethnic group were all male and included two with mild impairment and one non-impaired and were excluded from further analysis.

TB disease type and site, and patients' access to TB care was similar between race/ethnicity (Table 2). There were significantly different demographic and clinical characteristics between race/ethnicity (Table 2). HIV infection was significantly higher among non-Hispanic Blacks and level of education significantly lower among Hispanics compared to non-Hispanic Whites. Clinical and demographic characteristics, including age and smoking of US-born were significantly different from those who were foreign-born. Both proportion of ever-smokers and level of lifetime cigarette use was significantly higher among Whites (p < 0.001 for both measures) than other groups (Table 2).

The distribution of pulmonary impairment after tuberculosis (PIAT) and its severity among racial/ethnic groups, by smoking status and by socioeconomic status is shown in Figures 2, 3, and 4, respectively. PIAT was more frequent among non-Hispanic Whites compared to other race/ethnic groups (p < 0.001), and was more severe (p = 0.001) (Figure 2). Pulmonary impairment was identified in 71% of non-Hispanic Whites, 58% of non-Hispanic Blacks, 49% of Asians and 32% of Hispanics. PIAT frequency was significantly higher among non-Hispanic Whites compared to other racial/ethnic groups in both ever-smokers and never-smokers, (p < 0.0001) (Figure 3).

The distribution of employment, income, occupation, and education data among subjects was similar to that reported for other US TB patients (9-11). Education and income were significantly correlated (Pearson's correlation coefficient (r) = 0.21, p < 0.001). When occupational status was ranked according to prestige, it also significantly correlated with both education and income (r = 0.33, p < 0.001 and r = 0.15, p = 0.005, respectively). PIAT prevalence was evenly distributed across all levels of socioeconomic status: when the highest level of education attained was used as a proxy for socioeconomic status (Figure 4).

The median "time to beginning TB treatment" for non-impaired persons was 62 days (interquartile range [IQR] was 12-110); 93 days for mildly impaired persons (IQR 61-110), 138 days for moderately impaired subjects (IQR 32-271), and 37 days for severely impaired subjects (IQR 12-60). There was no significant association between race/ethnicity and time to beginning TB treatment, (p = 0.978) (Table 2). Similarly, no association between time to beginning treatment and PIAT was observed (p = 0.058) (data not shown).

We obtained baseline chest x-ray results for 99% of subjects (n = 314), and for 90% (n = 254) of subjects after either 20 weeks or at therapy completion. Pulmonary impairment was significantly (p < 0.001) correlated with the presence and magnitude of abnormal chest x-ray findings for both baseline (Spearman's correlation coefficient (r) = 0.4), and subsequent readings, (r = 0.42). Figure 5 shows the distribution of a standardized severity index among subjects with pulmonary impairment identified by spirometry.

In univariate analysis race/ethnicity, age and US-birth were significantly associated with PIAT (Table 3). The likelihood of PIAT increased by 2% (95% confidence interval [CI] 1, 3) for each 1 year increase in age. PIAT was 2.3 times more common (95% CI 1.46, 3.61) in US-born than foreign-born subjects. Race/ethnic groups and foreign birth were correlated: Spearman's r = 0.69, p < 0.001.

In a multivariate analysis that controlled for potential demographic and clinical confounders; the only significant predictor for PIAT was non-Hispanic White race/ethnicity, among whom PIAT prevalence was 3 times greater (95% C.I. 1.18, 8.40). Since race/ethnic group and foreign birth were significantly correlated, and to avoid confounding, separate multivariate regression models were constructed and are shown in Tables 4 and 5. Risk factors for impairment were variable between race/ethnicity, with age independently predicting impairment in non-Hispanic Whites and non-Hispanic Blacks (Table 4). Smoking was associated with three fold (95% CI 1.15, 7.85) increased risk for impairment among Asians, but was not predictive for impairment among non-Hispanic Whites (Table 4, Figure 3). Table 5 shows the multivariate regression model containing age, smoking and race/ethnicity of 144 US-born persons. In the model, only non-Hispanic White race/ethnicity and age independently predict PIAT. The age-related risk for PIAT increased 5% (95CI 2.0, 8.1) per year of age.

Onset of age-related lung function decline is variable [19, 30, 31]; however, for this study cohort onset of impairment was related to the age at which the different race/ethnic groups acquired tuberculosis. Consequently, the risk for moderate or severe pulmonary impairment is significantly higher among older Whites compared with non-Whites. As an example, the median age was 51 years for non-Hispanic Blacks, 59 for Whites, 56 for Asians and 71 years for Hispanics (Figure 6). Similarly, the probability for developing moderate to severe impairment was higher in non-Hispanic Blacks of younger age groups compared to other race/ethnic groups (Figure 6, panel B). The median age for non-Hispanic Blacks was 63 and that for non-Hispanic Whites was 72, p = 0.0239. The hazard ratio [HR] was 0.45 (0.22, 0.90).

In the U.S., racial/ethnic minorities and foreign-born persons face disparate risks for TB infection and higher levels of poor TB disease outcomes, including mortality [5‐9]. We analyzed the relationship between race/ethnicity and PIAT in a cohort with culture-confirmed pulmonary tuberculosis that had completed a minimum of 20 weeks of therapy. We found that self-identified non-Hispanic White TB patients had disproportionately more frequent and severe pulmonary impairment relative to other race/ethnicities (72% vs. 48%), odds ratio (OR) of 3.15. These differences persist despite control for the effects of age, body mass index, smoking, access to medical treatment, foreign birth and socio-economic status. Among the potential explanatory variables analyzed, only age and race/ethnicity were significant predictors for impairment in US born persons. These data demonstrate a previously unrecognized disparate negative health impact to specific populations of TB patients.

Current U.S. policy does not consider older adults high-priority candidates for testing and treatment of LTBI unless they have specific risks for developing TB disease [17, 32]. These recommendations are based on the potential for adverse drug events associated with LTBI treatment. Predictors for PIAT varied between race/ethnic groups and by country of birth. We found the likelihood for PIAT to increases by an average 5% for each additional increase in age for US-born patients (Table 5; Figure 6). NHANES data showed that poorer lung function is also associated with poor clinical outcomes including premature death [30, 33]. This together with our findings suggests that moderate to severe PIAT may also be associated with earlier mortality. Future versions of LTBI treatment guidelines should consider reduction of tuberculosis burden from preventing PIAT as an additional treatment benefit.

Cigarette smoking, an established cause of pulmonary impairment, was significantly more prevalent among non-Hispanic Whites compared to other racial/ethnic groups. The proportion of non-Hispanic Whites impaired among never-smokers was 70% compared to 78% among ever-smokers. PIAT was more frequently encountered among non-Hispanic Whites compared to other racial/ethnic groups (p < 0.001), and when encountered was more likely to be severe (p = 0.001) (Figure 2) even after controlling for age and smoking (Figure 3, Tables 4). While there were more non-Hispanic Whites who smoked our data shows this difference is not sufficient to explain the more severe impairment found in non-Hispanic Whites.

Previous studies have investigated pulmonary sequelae of TB from a number of perspectives, but these are not readily generalized to US populations [31, 34‐37]. Poh et al evaluated patients hospitalized for treatment with non-rifampin chemotherapy regimens and identified older age, disease severity at presentation and heavy smoking as predictors for pulmonary impairment [36]. A population-based study from Latin America demonstrated that older age and repeated TB disease were associated with pulmonary impairment [31]. Two South African studies of patients receiving inpatient treatment [34, 37] similarly demonstrated that repeated TB disease significantly increased risks for pulmonary impairment. Race/ethnicity was not explored in these studies [31,34,37. Despite management with best currently available therapy for tuberculosis we identified some PIAT in over half (52%) of patients and severe PIAT, in which less than 50% of personal lung function remains, in almost 1 in 10 patients (9%). Prevalence and severity of PIAT were not associated with diagnostic or treatment delay, suggesting that it occurs early among those with TB. Therefore, strategies to mitigate PIAT must primarily rely on prevention of active TB.

Our study failed to detect association between socioeconomic status and pulmonary impairment. This was an unexpected and novel finding. Poorer health outcomes are consistently associated with low socioeconomic status [1, 5, 23]. Despite Hispanics' lower socioeconomic status in our study cohort, and their higher TB incidence rates relative to other racial/ethnic groups in the US [5]; they enjoyed apparent protection against pulmonary impairment compared to other racial/ethnic groups. This finding supports what has been called the "healthy Hispanic Paradox," in which Hispanics experience disproportionately greater life expectancy relative to other racial/ethnic groups [38, 39]. Equity in health care access within the study area allowed by the public treatment of TB may explain health outcomes' independence from socioeconomic status.

There are several areas within our study vulnerable to ascertainment bias: such as the fact that race/ethnicity was self-reported, identification and grading of pulmonary impairment was biased towards an obstructive pattern and that the chest x-ray grading of impairment lacks consensus of standardization. Both race and ethnicity are contextual, mutually contradictory and usually assume socially defined constructs with no biologic basis such that even the definitions used by U.S. federal agencies change with every 10-year census [2, 40]. Even though mixed race/ethnicity is rare among self-identified non-Hispanic Whites, the US Hispanic population has a heterogeneous ethnic ancestry comprising of American Indian, European and African origins [41]. In addition, 30% of self-identified US-born Blacks consider themselves of mixed race [41, 42]. As a result, the true effects of race/ethnicity on health outcomes may be difficult to clearly distinguish and are subject to confounding. Indeed, AMA grading is biased towards impairment that is obstructive in nature; hence patients with restrictive patterns might be under-represented in these estimates [18‐20]. Given these limitations, it cannot be excluded that the findings reflect different phenotypic disease entities among different groups, of which some might be influenced by smoking and some not.

In conclusion, we found that pulmonary TB patients, who self-identified as non-Hispanic White, had more prevalent and more severe pulmonary impairment. The risk for pulmonary impairment remained after several factors such as smoking and socioeconomic status were controlled. Since race/ethnicity was self reported and race is not a biological construct, these findings must be interpreted with caution. However, because since race/ethnicity is a proxy for several other unmeasured host, pathogen or environment factors that may contribute to disparate health outcomes, these results are meant to suggest hypotheses for further research. Nevertheless, if these findings are confirmed among other populations in other locations, they suggest that the decision-making thresholds of risk of TB prevention strategies should be reconsidered to include the benefits of preventing PIAT.