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Conceived and designed the experiments: AB AMF JB WY LM NP ZY. Performed the experiments: AB. Analyzed the data: AB WY. Contributed reagents/materials/analysis tools: JB LM NP. Wrote the paper: AB. Reviewed and edited manuscript: AB AMF JB WY LM NP ZY.
This study was conducted to generate knowledge useful for developing public health interventions for more effective tuberculosis control in Arkansas.
The study population included 429 culture-confirmed reported cases (January 1, 2004–December 31, 2010). Mycobacterium tuberculosis genotyping data were used to identify cases likely due to recent transmission (clustered) versus reactivation (non-clustered). Poisson regression models estimated average decline rate in incidence over time and assessed the significance of differences between subpopulations. A multinomial logistic model examined differences between clustered and non-clustered incidence.
A significant average annual percent decline was found for the overall incidence of culture-confirmed (9%; 95% CI: 5.5%, 16.9%), clustered (6%; 95% CI: 0.5%, 11.6%), and non-clustered tuberculosis cases (12%; 95% CI: 7.6%, 15.9%). However, declines varied among demographic groups. Significant declines in clustered incidence were only observed in males, non-Hispanic blacks, 65 years and older, and the rural population.
These findings suggest that the Arkansas tuberculosis control program must target both traditional and non-traditional risk groups for successful tuberculosis elimination. The present study also demonstrates that a thorough analysis of TB trends in different population subgroups of a given geographic region or state can lead to the identification of non-traditional risk factors for TB transmission. Similar studies in other low incidence populations would provide beneficial data for how to control and eventually eliminate TB in the U.S.
Following the 1992 peak in tuberculosis (TB) incidence in the United States, the annual TB incidence rate has decreased every year . In 2011, the incidence was 3.4 cases per 100,000 persons, the lowest recorded rate since national TB reporting began in 1953 . However, this rate failed to meet the national goal of TB elimination by 2010, defined as ≤1 case per million persons . TB case rates differ between sexes, among age, racial/ethnic groups, and geographic regions , . Both reactivation of latent TB infection (LTBI) and recent transmission contribute to the overall disease burden in the U.S. Understanding incidence trends and the relative contributions of reactivation and recent transmission to the disease burden in subpopulations can maximize the use of limited resources available for TB elimination programs.
Molecular epidemiological studies can help characterize TB transmission , . Variation in the Mycobacterium tuberculosis (MTB) genome allows genotyping to differentiate among strains and identify cases that are more likely to be related by transmission . Currently, the Centers for Disease Control and Prevention (CDC) supports TB genotyping of at least one MTB isolate from each culture-positive case in the U.S. through the National Tuberculosis Genotyping Service (NTGS) . MTB isolates submitted to NTGS are genotyped using two methods: spacer oligonucleotide typing (spoligotyping) and mycobacterial interspersed repetitive unit-variable number tandem repeat typing (MIRU-VNTR). Cases with indistinguishable isolate genotypes are generally considered part of the same chain of transmission, when having either close geographic proximity or epidemiologic link . Cases with a TB genotype that match that of at least one other case are referred to as clustered. However, as suggested by an earlier molecular epidemiological study conducted in Arkansas, while genotyping clustering provides an estimate of recent transmission, it is not a definitive measure . Thus, a time-restricted cluster definition has been applied in molecular epidemiological studies of TB to improve the accuracy of genotyping clustering in measuring recent TB transmission , . If clustered cases are diagnosed within a short period of time within the same geographic area, then recent transmission is more likely. Cases having unique isolates are more likely due to the reactivation of remotely acquired infection . In the U.S., most molecular epidemiology TB studies have focused on large urban areas with higher TB incidence. However, recent studies have included rural areas and low-incidence populations, which have provided new insights into TB epidemiology –. Different forces may drive TB incidence between rural and urban populations and a better characterization of these forces should lead to better TB control.
TB incidence in Arkansas is relatively low and the case rate declined from 7.9 in 1997 to 2.7 in 2010 , . However, recently the decline began to plateau, only decreasing by 0.2 cases per 100,000 during 2008–2010. Comparatively, during 2004–2006 incidence declined 1.2 cases per 100,000 and during 2006–2008 the decline was 0.7 cases per 100,000 , , . Understanding the trends in TB due to either recent transmission or reactivation of latent infection in different subpopulations in Arkansas is essential to successfully target control efforts. Characterizing these trends will aid in understanding which subpopulations are contributing to the decline.
France and coworkers analyzed TB trends in Arkansas during 1997–2003 . Non-Hispanic blacks and individuals aged 65 years or greater had the greatest overall declines in incidence. However, in both subgroups, incidence among non-clustered cases declined the most, suggesting that the primary driver behind the decline was a decrease in the rate of reactivation of past infections . The overall TB incidence trend has changed since 2003, especially as the rate of the decline began to decrease in 2008.
Few studies have focused on understanding TB trends in low-incidence, rural populations –. In 2010, 35 states (70%) had incidence of less than 3.5 cases per 100,000 persons, the rate established in 1989 as the year 2000 interim target for TB elimination , . As the number of low-incidence states increases, understanding incidence trends and factors driving the trends in these populations is vital for achieving TB elimination in the U.S. This study successfully analyzed TB incidence trends in Arkansas during 2004–2010 and the incidence trends in subpopulations based on previously identified TB risk factors, including age , , sex , geographic region , , race/ethnicity , and country of origin  in order to explore recent changes in incidence in these groups and evaluate the impact of recent transmission.
The study sample included culture-confirmed TB cases diagnosed in Arkansas during January 1, 2004–December 31, 2010 for which genotype data (spoligotype and 12-locus MIRU-VNTR results) were available . Only the first isolate collected for each case was included in the analysis. Demographic and clinical information was obtained from a de-identified Arkansas TB surveillance database that is based on information collected by the Arkansas Department of Health using the CDC's “Report of a Verified Case of Tuberculosis” form. Information from the 2010 U.S. Census was used to describe the demographics of the population of Arkansas . Urban and rural areas of Arkansas were defined using methods previously described, based on the Census Bureau Metropolitan Statistical Areas (MSAs) defined by the Office of Management and Budget , . The study was approved by the Institutional Review Board for Health Science and Behavior Science of the University of Michigan.
State TB case rates for culture-confirmed, clustered, and non-clustered TB were calculated from TB surveillance data provided by the Arkansas Department of Health. The annual TB case rates for the total population and each subpopulation were calculated using the July 1st population estimate for each year, obtained from the Bridged-Race Population Estimates provided by the National Center for Health Statistics . The data for the foreign born population were obtained from the American Community Survey .
The study patients were classified as clustered and non-clustered cases, estimating TB due to recent transmission and reactivation of latent TB infection respectively, using a combination of genotype information of M. tuberculosis isolates and diagnostic dates of the study patients. A case was defined as clustered with another case in the state if the isolates of the two cases had an identical spoligotype and 12-locus MIRU-VNTR genotyping pattern and both cases were diagnosed within a one year time period ; a cluster may span more than one year when it involves more than two cases with identical spoligotype and 12-locus MIRU-VNTR genotyping pattern that were diagnosed in different years, but were connected to at least one other case within a one year time frame. When diagnosis date was not available, count date (date the patient was verified as a TB case by the health department) was used as a proxy. This cluster definition has been used previously to estimate recent transmission . Isolates that did not meet this cluster definition were classified as non-clustered.
Chi-squared tests were used to compare the distribution of demographic and clinical factors between the culture-confirmed cases with genotype information and the culture-confirmed cases without genotype information, in order to assess the representativeness of the overall–culture confirmed TB patient population in the study sample. To visually examine the trend in incidence, the culture-confirmed annual incidence rate was plotted over time for each of the population subgroups. Confidence intervals were calculated based on a Poisson distribution, using a method described by Buchanan in Microsoft Excel .
A Poisson model was used to estimate the average percent decline in incidence of culture-confirmed TB over time. To examine whether clustered cases and non-clustered cases had a similar average annual percent decline in incidence during the study period, we used a multinomial logistic model, given that Poisson models do not allow us to directly compare the two types of cases. Since TB incidence is very low in Arkansas, the estimated relative risk ratio of clustered cases compared to non-clustered cases obtained from this model is approximately equal to the incidence ratio. Therefore we used this model to test the difference between the trends of clustered and non-clustered cases.
In addition, univariate Poisson regression was used to assess whether there was any difference in the trends of percentage decline in culture-confirmed, clustered, and non-clustered TB incidence over the study period between age groups (20 to 64 years vs. 65 and older), race/ethnic groups (non-Hispanic whites vs. non-Hispanic blacks), geographic regions (urban vs. rural counties), country of origin (foreign born vs. US born), and sexes, respectively. Analysis of these demographic factors was done one at a time. The age groups were chosen to allow for comparison to the previous Arkansas study. Cases less than 20 years of age were excluded from the analysis because the sample size is too small to allow for meaningful statistical analysis. For each analysis, the model included one demographic variable, the time variable, and the interaction between time and the demographic variable. If a regression coefficient of the interaction term is significantly different from zero, it indicates that the particular demographic variable is significantly associated with a percent decline in the rate of TB. Similar analyses were also done separately on clustered TB cases and non-clustered cases to estimate the association of the above demographic factors on the decline rate of recent transmission and reactivation, respectively. For each of the above regression analyses, we compared a linear time function and a quadratic time function of log of TB incidence rate. For all analyses, a model with the linear time function yielded a better fit for our data and therefore was used in all analyses. These statistical analyses were performed in SAS version 9.2 . All analyses were completed using de-identified data. In all analyses, P-value<0.05 was considered to be statistically significant.
A total of 699 cases of TB were reported in Arkansas during the study period (January 1, 2004–December 31, 2010). Of the total reported cases, 494 (70.7%) were confirmed by mycobacterial culture of sputum, tissue, or body fluids. Genotyping information was available for 429 (86.8%) of the 494 culture-confirmed TB cases. Most of the reported cases were either non-Hispanic white or non-Hispanic black (Table 1). A majority of the cases were male and in the 20 to 64 year age range. Almost 70% of the cases were born in the United States.
We included all 429 culture-confirmed cases with available genotyping information in our study sample. To assess the sample representativeness, we compared the distribution of patient characteristics among genotyped cases with that among all the non-genotyped culture-confirmed cases. The distributions of age group and site of disease (pulmonary vs. extrapulmonary) were significantly different (P<0.05) between genotyped and the non-genotyped culture-confirmed cases (Table 2). The distributions of sex, race/ethnicity, place of birth, and type of residential area were not significantly different between the genotyped and non-genotyped cases.
Of the 429 genotyped cases, 178 (41.5%) were clustered and 251 (58.5%) were non-clustered. The clustered cases consisted of a total of 60 clusters, of which 47 (78.3%) had between two and four related cases and 7 (11.7%) clusters had between five and nine related cases. The remaining 6 (10%) clusters had 10 or more cases, with the largest cluster containing 20 cases. The time spans of clusters with 10 or more cases ranged from four years to the entire study period of seven years.
During January 1, 2004–December 31, 2010, the annual incidence of culture-confirmed cases in Arkansas declined by 1.4 cases per 100,000 persons (Figure 1). However, during January 1, 2008–December 31, 2010 the annual incidence of such cases declined only by 0.2 per 100,000. During the study period, the annual incidence of clustered TB and non-clustered TB declined by 0.4 and 0.8 cases per 100,000, respectively (Figure 1). The average annual percent decline in incidence for culture-confirmed cases was approximately 9% (95% CI: 5.5%, 16.9%). Based on the results from the multinomial logistic model, the annual percent decline in incidence for the clustered cases and non-clustered cases was 6% (95% CI: 0.5%, 11.6%) and 12% (95% CI: 7.6%, 15.9%), respectively. Although the non-clustered TB experienced a higher average annual percent decline than clustered TB, the observed difference was not statistically significant (P=0.11).
The incidence of culture-confirmed TB was consistently higher in the older age group (≥65) than in the younger age group (20–64) during each year of the study period. However, a larger absolute decline in the annual incidence of culture-confirmed TB was observed in the ≥65 years age group (6.1 per 100,000) than in the 20–64 year age group (0.5 per 100,000) (Figure 2). In the older age group, clustered incidence declined by 0.8 per 100,000 and non-clustered declined by 4.1 per 100,000. No change in clustered TB was observed in the younger age group, while non-clustered declined by 0.5 per 100,000. The older age group (11.9%, 95% CI: 8.2%, 15.5%) experienced a significantly higher average annual percent decline in incidence than the younger age group (1.8%, 95% CI: −5.3%, 8.3%) in culture-confirmed TB (P=0.0082). A similar trend was also observed in the clustered TB cases, the older age group (12.5%, 95% CI: 5.6%, 18.9%) experienced a significantly higher average annual percent decline (P=0.0062) than the younger age group (−3.9%, 95% CI: −14.5%, 5.7%). In contrast, the average annual percent decline in incidence in the non-clustered cases was not significantly different between the two age groups (Table 3).
The incidence of culture-confirmed TB was consistently higher in males than females over the study period (Figure 3). Males experienced a larger absolute overall decline in the culture-confirmed TB incidence than females (3.5 vs. 0.4 per 100,000). A larger decline was observed in non-clustered TB (1.3 per 100,000) than in clustered TB (0.4 per 100,000) among males. However, among females the decline was similar, with non-clustered declining by 0.1 per 100,000 and clustered declining by 0.2 per 100.000. Despite these differences, the average annual percent decline in incidence in culture-confirmed, clustered, or non-clustered TB was similar between females and males (Table 3).
Across the entire study period, the annual incidence of culture-confirmed TB was lower for non-Hispanic whites than for non-Hispanic blacks (Figure 4). The absolute decline in the incidence of culture-confirmed TB was 0.5 and 2.6 per 100,000 for non-Hispanic whites and non-Hispanic blacks, respectively. Among non-Hispanic whites, non-clustered TB declined by 0.5 per 100,000 while clustered TB increased by 0.2 cases per 100,000. Among non-Hispanic blacks, the declines in non-clustered TB (1.2 per 100,000) and clustered TB (1.0 per 100,000) were similar. The average annual percent decline in incidence for culture-confirmed TB was significantly higher (P=0.0067) in non-Hispanic blacks (14.5%, 95% CI: 9.4%, 19.4%) than in non-Hispanic whites (5.3%, 95% CI: 0.9%, 10.4%). A statistically significant (P=0.034) difference in the incidence trend of clustered TB was also found between the groups (Table 3). The annual incidence of clustered TB in non-Hispanic whites showed little change, with an average annual percent decline in incidence of 0.8% (95% CI: −7.5%, 8.4%) while it declined significantly in non-Hispanic blacks, with an average annual percent decline in incidence of 12.9% (95% CI: 4.7%, 20.3%). In contrast, the incidence of non-clustered TB declined significantly in both races/ethnicities with no significant different between them (Table 3).
The incidence rates of culture-confirmed TB in individuals from counties classified as rural and individuals from urban counties were similar over the study time period. The absolute decline in overall culture-confirmed TB incidence was 2.0 and 1.0 per 100,000 persons in the rural population and the urban population, respectively. Clustered TB declined by 0.1 per 100,000 and non-clustered TB declined by 0.8 per 100,000 in the urban population. Among rural residents, the declines were similar with clustered declining by 0.9 per 100,000 and non-clustered by 0.8 per 100,000. The average annual percent decline in incidence of all the culture-confirmed cases, whether clustered or non-clustered TB, was not significantly different between rural and urban residents (Table 3).
Over the study period, the incidence of culture-confirmed TB in the foreign born was greater than in U.S. born individuals. However, in the foreign born population, culture-confirmed TB declined by 30.2 per 100,000 persons while in the U.S. born population, the decline was 1.1 per 100,000 persons. In the foreign born population, clustered TB declined by 8.4 per 100,000 persons and non-clustered by 5.7 per 100,000. In the U.S. born population, the decline in clustered incidence was 0.8 per 100,000 persons and 0.7 per 100,000 in non-clustered cases. The average annual percent decline in incidence of culture-confirmed TB was significantly higher (P=0.022) in the foreign born individuals (15.6%, 95% CI: 9.6%, 28.8%) than in the U.S. born individuals (7.2%, 95% CI: 3.0%, 11.2%). The average annual percent decline in the incidence of clustered TB was higher among foreign born individuals compared to U.S. born individuals; however, the observed difference was not statistically significant (Table 3). The average annual percent decline in the incidence of non-clustered TB was also similar between the two groups.
In order to identify the challenges and opportunities for a continued decline in TB incidence in Arkansas, we analyzed the incidence trends of culture-confirmed, clustered, and non-clustered TB in different subpopulations, using a combination of TB surveillance data and genotyping results of MTB isolates from culture-confirmed cases reported during January 1, 2004–December 31, 2010. The relative contributions of declines in ongoing TB transmission and declines in reactivation of latent infection were assessed.
The most important finding was that although the incidence of culture-confirmed, clustered, and non-clustered TB declined significantly in Arkansas during 2004–2010, the decline in recent transmission was uneven across different subpopulations. The lack of significant decline in estimated recent transmission among females, non-Hispanic whites, the younger age group (20–64 years), the urban population, and the U.S. born population has an important implication for TB control. Both non-Hispanic whites and females have not been a previously identified risk group for clustering , but our data show that TB transmission in these two groups has remained stable. Young age (less than 65 years of age) has previously been identified as a risk factor for being part of large clusters . These data indicate the need for strengthening targeted TB control in subpopulations previously identified as risk groups, but also in subpopulations not previously identified as risk groups.
A second important finding was that the incidence of TB due to reactivation declined similarly among different age, gender, race/ethnicity groups and residence types, as measured by average annual percent decline of incidence. The lower incidence in the younger age group is likely due to the previously described cohort effect where each successive birth cohort has a lower risk of exposure to TB due to the decreasing incidence. As the older members, who have the highest prevalence of latent infection, are removed from the population, the incidence of reactivation of latent infection continues to decrease , . The foreign born population had the highest incidence of non-clustered TB throughout the time period and the lack of significant decline represents another target for better control. However, it is important to note that the confidence intervals for the estimated rate of decline among foreign born individualsare wide as the number of foreign born individuals in Arkansas is relatively small (range of foreign born population: 101,169 to 131,667; range of US born population: 2,701,431 to 2,771,280). This relatively small sample size somewhat limits the power to examine the effect of country of origin.
One possible limitation of this study is the use of 12-locus MIRU instead of 24-locus MIRU-VNTR in the cluster definition. This approach might have overestimated the amount of clustering as the 24-locus typing method shows greater discriminatory power than 12-locus method –. The concern about overestimation of clustering may have been offset by the time restriction used in identifying clustered cases in this study. Time-restricted clusters are considered more specific for indicating recent transmission compared to just clustering alone . Furthermore, this study looked at trends over time and any overestimate is expected to be consistent over time. Another potential limitation of this study is the significantly different distributions of age and disease sites between genotyped cases (the study sample) and culture-confirmed cases that were not genotyped. However, given that the study sample included as high as 87% of all culture-confirmed cases, the findings are informative for the development of an improved strategy for TB transmission control in Arkansas. Another possible limitation of the study is some cases classified as non-clustered may theoretically be index cases from other states, which may have overestimated the number of non-clustered cases.
Despite these possible limitations, the lessons learned from this study have important implications for the future of TB control in Arkansas. The significant declines are encouraging signs for control of this disease in Arkansas. However, for greater success in the future, more resources should be direct towards controlling recent transmission. The findings of the study suggest that the Arkansas tuberculosis control program must target both traditional and non-traditional risk groups for successful tuberculosis elimination. Although the implication of the current study findings for TB control seems to be limited to Arkansas, the present study demonstrates that a thorough analysis of TB trends in different population subgroups of a given geographic region or state can lead to a better understanding of the dynamics of TB in this geographic region or state and the identification of non-traditional risk factors for TB transmission. Similar studies in other low incidence populations would provide beneficial data for how to control and eventually eliminate TB in the U.S.
The authors acknowledge the contribution of Nancy Brannon, Michelle Herndon, Ndeye Diatta, and Elizabeth Karpoff for the collection of the Arkansas TB Surveillance data and thank Jane Voyles for her assistance to isolate and collect the study isolates for genotyping. CDC Disclaimer: The findings and conclusions in this paper are those of the authors and do not necessarily represent the views of the Centers for Disease Control and Prevention.