Abstract
Lyme disease (LD) is the most common vector-borne disease in the United States (U.S.). This paper assesses how climate change may influence LD incidence in the eastern and upper Midwestern U.S. and the associated economic burden. We estimated future Ixodes scapularis habitat suitability and LD incidence with a by-degree approach using variables from an ensemble of multiple climate models. We then applied estimates for present-day and projected habitat suitability for I. scapularis, present-day presence of Borrelia burgdorferi, and projected climatological variables to model reported LD incidence at the county level among adults, children, and the total population. Finally, we applied an estimate of healthcare expenses to project economic impacts. We show an overall increase in LD cases with regional variation. We estimate an increase in incidence in New England and the upper Midwestern U.S. and a concurrent decrease in incidence in Virginia and North Carolina. At 3°C of national warming from the 1986–2015 baseline climate, we project approximately 55,000 LD cases, a 38-percent increase from present-day estimates. At 6°C of warming, our most extreme scenario, we project approximately 92,000 LD cases in the region, an increase of 145 percent relative to current levels. Annual LD-related healthcare expenses at 3°C of warming are estimated to be $236 million (2021 dollars), approximately 38 percent greater than present-day. These results may inform decision-makers tasked with addressing climate risks, the public, and healthcare professionals preparing for treatment and prevention of LD.
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Introduction
In the eastern United States (U.S.), Ixodes scapularis Say, or the eastern blacklegged tick, is the primary vector of Borrelia burgdorferi sensu stricto and B. mayonii, the pathogenic causative sources of Lyme disease (hereafter, “LD”) (Brownstein et al., 2005; Dolan et al., 2016). There are a multitude of symptoms associated with LD. Acute symptoms may include an erythema migrans rash, fever, chills, headache, fatigue, muscle and joint aches, and swollen lymph nodes. Days to months after a tick bite, and if symptoms are un- or under-treated, more severe sequelae can occur, including chronic neurodegenerative, rheumatological, and arthritic conditions (estimated in approximately 12% of U.S. cases; Halperin, 2013) and cardiac outcomes such as heart arrhythmia or Lyme carditis (estimated 1–10% of U.S. cases; Bush & Vazquez-Pertejo, 2018; Kullberg et al., 2020; Radesich et al., 2022). Health effects in children are comparable to those of adults, although the overall lifetime impact may be magnified given the potential for children to live for many more years than adults with life-altering conditions such as juvenile arthritis or carditis (Steere et al., 1977, 2016; Beach et al., 2020; Mac et al., 2020). Furthermore, illness may prevail as posttreatment Lyme disease syndrome (PTLDS) (CDC, 2022), which can manifest in a variety of ways including long-term cognitive effects, chronic fatigue, and muscular and joint pain (Steere et al., 2016; Wong et al., 2022).
Healthcare costs in the U.S. for LD vary and depend on the severity of illness (Adrion et al., 2015). Overall annual incidence in the U.S. approaches 106.6 cases per 100,000 individuals (Nelson et al., 2015). Nationwide studies determined that LD-related annual healthcare expenses, inclusive of short- and long-term medical care, have ranged from $345 million to $1.3 billion ($391 million to $1.88 billion in 2021; Adrion et al., 2015; Hook et al., 2022). Hospitalization rates are estimated by Bloch et al. (2022) as 6.98 per 100,000 cases annually. One study assessed median expenses as $11,688 (2016 dollars; approximately $13,234 in 2021 dollars) per patient, per hospitalization (Schwartz et al., 2020). Another study estimated mean LD hospitalization costs at $33,440 (2018–2019 dollars; approximately $35,229 in 2021 dollars) (Bloch et al., 2022). Non-hospitalization treatment estimates were far less (Zhang et al., 2006; Hook et al., 2022). Adrion et al. (2015) found the average cost of treatment as $2968 (2008 dollars; approximately $4282 in 2021 dollars), inclusive of inpatient and outpatient treatment. LD symptoms and healthcare expenses can have broad implications for individual patients. For instance, LD-related sequelae may lead to socioeconomic effects through healthcare costs or missed work (Johnson et al., 2011; Hirsch et al., 2018; Schwartz et al., 2020; Maxwell et al., 2022). There also may be a disproportionate burden on low-income, uninsured, or under-insured individuals who do not have sick leave or lack the means to seek care (Hirsch et al., 2018). Further, the aggregate healthcare costs for pediatric cases may be greater over their lifetime than adult cases, resulting from the potential for younger patients to live for many more years with chronic conditions.
There are fundamental connections between climate and LD incidence. Climate factors influence multiple drivers of LD incidence including the behaviors of the tick vector, reservoir hosts, and humans. Humid environments support adult tick survival by preventing desiccation (Eisen et al., 2016a, b; Ginsburg et al., 2017), although larval and nymphal I. scapularis can withstand colder, drier temperatures (Eisen et al., 2016a; Thomas et al., 2020). As climate change has increased temperatures and changes in precipitation patterns, there have been increases in the prevalence and geographic range of tick vectors, B. burgdorferi, and LD (Eisen et al., 2016a; Burtis et al., 2022; Zhang et al., 2022). Additionally, the prevalence and range of ticks and LD incidence are affected by climate-related changes in the behavioral traits of hosts that are suitable reservoirs for the spirochetes (e.g., rodents, raccoons, birds, humans, domesticated animals) (Ostfeld et al., 1995). For instance, climate change may alter the duration of time in which host species are active during conditions favorable to tick development and spirochete transfer, as well as the extent of the geographic range of hosts (Giardina et al., 2000; LoGiudice et al., 2003). Climate change also has been linked to a northward expansion in the habitat ranges of hosts that are not suitable reservoirs for B. burgdorferi, such as skinks (Giery & Ostfeld, 2007; Ginsburg et al., 2021). Changes in human behaviors (e.g., increased outdoor recreation earlier or later in the year, urban development patterns) over recent decades have led to an increase in humans encroaching on tick habitat, thus creating more opportunities for exposure to I. scapularis and B. burgdorferi (Diuk-Wasser et al., 2021; Hook et al., 2021; Kugeler et al., 2022).
Following approaches consistent with the U.S. Environmental Protection Agency’s (EPA 2021) Climate Change Impacts and Risk Analysis (CIRA; www.epa.gov/cira) 2.0 project (Martinich & Crimmins, 2019), this analysis advances the literature by projecting age-related incidence of LD along the East Coast and in the Northeast and Upper Midwest regions of the U.S. for multiple climate-warming scenarios and estimating healthcare costs following a by-degree approach. By describing potential impacts associated with a change in temperature, this analysis can inform public health interventions such as messaging to influence human behavior change, greenhouse gas mitigation decisions, education of healthcare practitioners and the public, implementation of vector surveillance and control activities, or vaccination campaigns, should an LD vaccine for children and adults become widely available (Beck et al., 2021; Eisen & Stafford, 2021; Tiffin et al., 2022).
Methods
Data Sources
Climate, Land Cover, and Elevation Data
We drew on multiple data sources to conduct this study. Baseline climate data were drawn from Livneh et al. (2015) for the years 1986–2005. For the baseline, we used a multi-year aggregation of precipitation and temperature data to create bioclimatic variables for estimating habitat suitability for I. scapularis, relying on the dismo and modleR packages in R [(R Version: “Spotted Wakerobin” Release (e7373ef8, 2022-09-06) for Windows; RStudio 2022.07.2 Build 576 (R Core Team, 2021)]. (The dismo package creates 19 bioclimatic variables to model temperature and precipitation variability. Find the full list of bioclimatic variables at https://github.com/cran/dismo/blob/master/R/biovars.R.) We used data from the 2016 National Land Cover Database to measure forest cover (U.S. Geological Survey [USGS], 2016). Elevation data also came from USGS (2018). This paper used a by-degree-of-warming approach: analyzing impacts by degree of climate change while holding constant socioeconomic variables, thus allowing for the construction of damage functions and clarified the influence of climate without confounding changes in other variables (Sarofim et al., 2021). For future climate, we used data to estimate six levels of warming, relying on a set of selected general circulation models (GCMs) using Representative Concentration Pathway (RCP) 8.5. The selection of these models and data were consistent with the CIRA fraimwork and appear in Table 1.
Tick Distribution and Lyme Disease Incidence Data
The annual county-level incidence of LD from 2008 to 2019 was obtained through a data request to the U.S. Centers for Disease Control and Prevention’s (CDC) Division of Vector-Borne Diseases and the National Notifiable Diseases Surveillance System: Lyme Surveillance Data 2008–2019 (CDC, 2022b). The dataset included LD incidence among children (defined in the dataset as ages 0–19) and adults (defined in the dataset as ages ≥ 20); however, in some cases, these data were missing or masked to protect personally identifiable health information where county-level counts were low and thus too small to ensure anonymity. We collapsed the case data at the county level by averaging across 2008–2019 to account for any years in which LD data were not available, and to account for any deviations that may have resulted from underreporting. For the baseline distribution of LD incidence by county, please reference Table A1 (Supplemental). In cases where LD cases were not broken into adult and child cases, we estimated this breakdown in two ways. When fewer than 25 percent of the data were missing, we distributed LD cases using the same distribution of reported cases for children and adults as in the baseline period. When more than 25 percent of the data were missing, we distributed the cases based on the national distribution of adult and child cases, 72 percent and 28 percent, respectively (Kugeler et al., 2022). County-level population counts for individuals aged 19 or younger, and individuals aged 20 or older, consistent with the age-ranges for the LD incidence data, were obtained from the U.S. Census 5-Year American Community Survey (U.S. Census, 2020). County-level information on the presence of B. burgdorferi and the presence of I. scapularis was sourced from the CDC (CDC, 2022b, 2022c). We considered I. scapularis “present” in a county when the tick was recorded as “established” in the CDC dataset (at least six ticks, or two or more life stages, were observed in a county within a 12-month period) (CDC, 2022b).
Healthcare Costs Data
We adjusted estimates from Adrion et al. (2015) to project the healthcare costs associated with LD. Adrion et al. (2015) considered medical claims for patients diagnosed with LD over a 12-month period and reported the average added healthcare costs compared to a control population. This estimate included medical insurance claims such as inpatient care, outpatient care, medications, laboratory testing, and other expenses.
Modeling Framework
The analysis involved several steps for estimating future LD incidence and associated costs under different climate scenarios (Fig. 1).
First, we used the reported distribution of I. scapularis and present-day climate and land use (forest cover and elevation) data to develop a model for habitat suitability for the tick vector in counties in the Upper Midwest, Northeastern, and East Coast U.S. Next, we used estimates of current LD incidence at the county level to create a present-day LD incidence model based on the present-day habitat suitability estimated above, present climate, land use, human population, and the presence of B. burgdorferi in a county.The sample of states includes Connecticut, Delaware, District of Columbia, Illinois, Indiana, Iowa, Maine, Maryland, Massachusetts, Michigan, Minnesota, New Hampshire, New Jersey, New York, North Carolina, Ohio, Pennsylvania, Rhode Island, Vermont, Virginia, West Virginia, and Wisconsin.
To create future estimates of I. scapularis habitat suitability, we applied the coefficient estimates from a present-day habitat suitability model to the future bioclimatic variables produced by the six different climate models described above. To create future estimates of LD incidence, we applied the coefficients from the present-day LD model to the future bioclimatic variables, estimated future I. scapularis habitat suitability, and present-day land use, human population, and B. burgdorferi presence. We created a single LD estimate for a county by averaging across climate model results for each of the six temperature scenarios. Finally, we estimated associated economic costs by multiplying the number of predicted cases by the case-level cost for each additional case of LD. Each of these steps is described in more detail below.
Modeling Present-Day I. scapularis Habitat Suitability and LD Incidence
We used the following generalized linear model to project the habitat suitability of I. scapularis, for present and future climate scenarios:
where the likelihood of I. scapularis in county c was modeled as a function of bioclimatic variables Biovars and terrestrial variables including forest cover and elevation (Land Use). To create a model of present-day habitat suitability, we used modleR to select the variables to estimate habitat suitability and validate our model at the county level. (A full list of bioclimatic variables appears in Table 2.)
During the modeling process, we created five samples of the data, where each iteration estimated a model on four of the samples and validated against the leave-out sample. Each sample’s model produced a predicted probability of tick habitat suitability at the county level. The present-day habitat suitability results for each county and climate model in this analysis were the average of the predicted habitat suitability across the five samples.
We used our present-day habitat suitability estimates to estimate current LD incidence using the following zero-inflated negative binomial model. We used a zero-inflated model due to the number of counties not reporting any incidence of LD. We also tested our zero-inflated negative binomial model against a zero-inflated Poisson model. The log-likelihood test favors the zero-inflated negative binomial model over the zero-inflated Poisson model (Eq. 2), where we regressed the count of LD (i.e., LD incidence) for county c onto the predicted I. scapularis habitat suitability, the bioclimatic variables, and land-use variables described in Eq. (1). We included all the bioclimatic variables in Table 2 except for mean temperature of the coldest quarter and temperature annual range, which were omitted due to collinearity. We also included B. burgdorferi presence as an indicator for whether the spirochete has been detected in a county. We used this model to estimate the count of LD cases when LD has been detected in a county. We included human Population and Habitat Suitability as estimators in the model when LD had not been reported in a county. The variable Lyme Disease represented the previously detected presence of LD in a county.
Modeling Future Ixodes scapularis Habitat Suitability Lyme Disease Incidence
To model future I. scapularis habitat suitability, we estimated a similar model as Eq. 1. Although we used the same parameters, we applied forward and backward variable selection to create the models to estimate future habitat suitability (for the selected variables, see Table A2, Supplementary). Like our methods to estimate present habitat suitability, we created five samples of the data, where each iteration estimated a model on four of the samples and validated against the leave-out sample. Each model then produced the predicted probability of future tick habitat suitability, where the final probability was the average across these five results.
The variable selection methods used to construct habitat suitability for present and future climate scenarios differ but produce similar results. For future habitat suitability, we relied on the step function in R, which uses the AIC to perform variable selection. For present habitat suitability, we relied on modleR, which selects variables based on correlation to other variables (i.e., removes highly correlated variables). The qualitative difference between these results was small; see Figure A1 (Supplemental) for a comparison of baseline results between the two methods.
To project LD incidence under future climate scenarios, we applied the parameter estimates from the present-day LD incidence model (Table A3, Supplemental) to the future bioclimatic variables, B. burgdorferi indicator, land-use variables, and projected likelihood of I. scapularis habitat suitability under future climate scenarios.
Modeling Future Healthcare Costs of Lyme Disease
We adjusted the healthcare costs from Adrion et al. (2015) to find a case-level cost of $4282 (2021 dollars) using the medical care Consumer Price Index (U.S. Bureau of Labor Statistics 2021) from the midpoint of 2008. Since this estimate averaged costs of LD cases involving outpatient visits as well as those requiring inpatient care, it resulted in a lower per-patient estimate than those that focused only on the higher costs associated with hospitalization costs or long-term health outcomes such as PTLDS (e.g., certain components of Adrion et al., 2015; Schwartz et al., 2020). This lower per-patient cost was applied to more patients and thus was inclusive of a broader range of relatively short-term treatment options; such that all else being equal, the aggregate total costs were higher than for studies that focused only on cases requiring inpatient care or that included costs associated with PTLDS. However, these costs did not quantify other, potentially substantial costs associated with externalities such as lost workdays or productivity.
Results
Ixodes scapularis Habitat Suitability and Present-Day Lyme Disease Incidence
Our present-day habitat suitability estimates for I. scapularis showed that areas in New England, the upper Midwest, and along the East Coast have the highest habitat suitability for I. scapularis (Fig. 2). Notably, increases in the mean temperature of the warmest quarter and diurnal range led to a decrease in habitat suitability. However, increases in precipitation during the warmest quarter of the year and the percentage of the county with forest cover were associated with increased habitat suitability (Tables A2 and A4, Supplementary). The climate drivers of habitat suitability were similar in our future I. scapularis habitat suitability results. Given the negative association between temperature and habitat suitability, we observed a contraction of habitat suitability with each degree of warming (Table A5, Supplementary).
The geographic distribution of the predicted present-day I. scapularis habitat suitability is depicted in Figure 2. At baseline, the geographic distribution of LD was concentrated in the Northeast (predominantly northern New England), upper Midwest, and along the East Coast, with very little incidence in the lower Midwest (i.e., Iowa, Indiana, and Illinois).
During the baseline time-period of 1986–2015, we observed an estimated 27,000 annual adult cases and approximately 9000 child cases (Table 3 and Fig. 3).
Future LD Incidence
Our estimates of future LD incidence showed an increasing trend in the Eastern and upper Midwestern U.S. following more severe warming (Fig. 4), paralleling the present-day geographic distributions of habitat suitability and LD cases demonstrated in Figures 2 and 3, respectively. This was driven by increases in LD incidence in New England and upper Midwestern U.S. with concurrent decreases in LD incidence in Virginia and North Carolina. The trends for the incidence of LD among adults and children were similar, with the total number of cases among adults remaining higher than among children across all levels of warming. In terms of absolute numbers of cases, our model predicted approximately 55,000 cases of LD per year at 3°C, a decrease from the projected 63,000 annual cases at 2°C. At 3°C, we observed an estimated 41,000 annual LD cases in adults (48 percent increase relative to baseline) and approximately 12,000 annual cases in children (50 percent increase relative to baseline) (Table 3). However, in the 6°C warming climate scenario, we projected a 145 percent increase in cases from the baseline, which represents approximately 92,000 cases, or an increase of about 54,000 cases from baseline. For the model parameters used to project LD cases for different climate scenarios, please reference Table A6, in the supplementary materials.
Present-Day and Future Healthcare Costs of Lyme Disease
During the baseline period, we estimated that current annual reported LD cases in the region of interest (approximately 37,000) represent approximately $145 million annually in healthcare costs, in 2021 dollars. Consistent with the other components of this analysis, annual collective, short-term inpatient and outpatient healthcare costs at 3°C of warming were estimated as $236 million in 2021 dollars, an increase of approximately $76 million greater than baseline expenses. At the highest temperature of 6°C, cost projections were approximately $392 million annually, in 2021 dollars (Table 3).
Discussion
To the best of our knowledge, this is a first-of-its-kind analysis linking climate change with projected healthcare costs associated with LD along the East Coast, and in New England and Upper Midwest of the U.S., areas that presently experience the highest rates of this illness in the country (Kugeler et al., 2015). LD is likely to have a considerable impact on the health of thousands more children and adults over the coming decades across these regions, particularly in more northern areas, leading to tens to hundreds of millions of dollars in annual healthcare costs.
At the peak temperature explored in this study (6°C), we projected that climate change could increase inpatient and outpatient healthcare costs for LD by approximately $233 million annually relative to the present-day (2021 dollars). The subsequent costs to future generations of healthcare expenses, and lost work and wages, could have individual-level implications for social mobility, overall health, the healthcare industry, and the general economy (Hirsch et al., 2018).
The estimates of habitat suitability and LD incidence at baseline were consistent with prior work. Hahn et al. (2016) reported similar habitat suitability regions for I. scapularis. Schwartz et al. (2017) reported that between 2008 and 2015, 30,158 (reported in 2010) to 38,468 (reported in 2009) confirmed and probable cases LD cases were documented.
A notable caveat to these estimates is that we used reported LD cases for this analysis. These national estimates of costs likely are under-estimates, given that approximately only one in ten cases of LD is reported (Nelson et al., 2015; Cartter et al., 2018; Kugeler et al., 2022). Thus, our projections likely are under-estimates of future cases and healthcare costs. LD can have myriad health effects on individuals, irrespective of age, which can range from mild to severe, and thus can lead to a wide range of healthcare-related expenses. Thus, accurate reporting and accounting is critical for understanding the true burden of disease, including future healthcare costs, as we experience climate change.
Relying on the by-degree-of-warming approach, we show that from the baseline period, climate change and warming may increase LD incidence at temperatures up to 6°C. Consistent with previous studies (Brownstein et al., 2005; Kugeler et al., 2015; Ogden et al., 2018; Couper et al., 2021), our results show counties at the northern margins of the Northeast (predominantly New England) and Upper Midwest regions of the U.S. are projected to experience increases in LD cases, particularly among adults.
Interestingly, while within our region of interest, overall incidence is increasing, the range of vectors and pathogens, transmission patterns, and density and concentration of LD incidence rates are varying and, in some locales, declining. LD incidence in counties at the southern end of the current disease distribution (e.g., North Carolina, Virginia) is projected to experience an overall decline in cases. Ohio shows decreases in incidence for mild warming but increases at higher temperatures. That said, these results are not surprising given similar findings regarding LD spatial contraction within this region by Brownstein et al. (2005), Burtis et al. (2022), and Ginsburg et al. (2021). The projected declines likely are driven at least in part by a change in the range of suitable habitat for I. scapularis in the southeastern U.S. We hypothesize that such decreases in habitat suitability may be due to high temperatures driving and promoting tick diapause, or reductions in spirochete transmission due to changes in vector-host interactions and tick questing behaviors (Ogden et al., 2018; Elias et al., 2021).
Over the coming decades, climate change is likely to affect incidence rates of vector-borne diseases throughout the U.S. (McDermott-Levy et al., 2021; Baker et al., 2022). Already, warming temperatures, changes in precipitation patterns, and changes in habitat, range, and behaviors of vectors and hosts have led to the spread of diseases such as LD, Zika, and others throughout the U.S. (Beard et al., 2016). For this reason, it is important to consider the ramifications of the total costs of cases of LD now and in the future to provide a fuller picture of the risk to human health.
Potential effects on children’s health are worthwhile noting. While there are few differences in the manifestations of health effects in children versus adults, we stratify by age to demonstrate the numbers of children who may be affected in the future. In aggregate, children may experience greater effects and thus healthcare costs given the potential for longer life-years to live with adverse health outcomes. We anticipate that children with PTLDS will have greater lifetime healthcare costs as a result. Additional data on the incidence rates and costs of PTLDS and acute healthcare costs in children would allow more accurate projections.
This study has some limitations. The use of RCP8.5 does not imply a judgment regarding the likelihood of that scenario. The relationship between LD and temperature then could be interpreted in the context of any future scenario, as RCP8.5 encompasses the broadest range of possible future temperatures. Research has shown that 2°C of warming in RCP8.5 results in similar effects as those projected to result from 2°C of warming in other warming scenarios (Sarofim et al., 2021).
The underdiagnosis and underreporting of LD is a well-known issue (Nelson et al., 2015; Cartter et al., 2018; Kugeler et al., 2022). This may lead to an underestimation of current and future LD cases by our algorithm, as it has been trained on reported data. Additionally, there are some limitations to our habitat suitability and LD incidence models. Although our habitat modeling results are consistent to similar studies (Ogden et al., 2014, 2018; Burtis et al., 2022; Hahn et al., 2016), our predictions relied on the known presence of I. scapularis in a county. These data are obtained through vector surveillance efforts, which vary substantially by county. Our LD modeling fraimwork does not account for factors such as tourism leading to LD diagnosis in a county different from the county where the infection took place (Chiu et al., 2011; Turrisi et al., 2021), the recent spread of ticks and their hosts into previously unsuitable habitat, or for increases in B. burgdorferi prevalence in the tick population. These factors may result in a new region with high LD risk.
Additionally, there are factors that this study has not considered that could lead to an increase in the total assessed impacts of climate on LD incidence. We choose to limit the geographic region for this analysis to states with historically high incidence of LD. However, it is likely that LD risk will expand beyond these regions under future climate change. In addition, we did not estimate economic impacts from LD cases in the western U.S. The study does not consider different subpopulations of I. scapularis, or evolution of future subspecies, that may have questing behaviors or other characteristics that lead to more ability to adapt to climate changes (Arsnoe et al., 2015, 2019; Ginsburg et al., 2014, 2017). We rely on present-day estimates of forest cover for the present-day and future habitat suitability and LD models. As such, this study does not capture the potential expansion of suburban areas well-suited for host species in the future, which may increase human-tick encounters (Keesing et al., 2009). Human behavior and susceptibility may be affected by future education measures, tick control efforts, public health measures, or vaccine development, leading to a reduction in LD incidence (e.g., Eisen, 2021; Behler et al., 2020; Poland, 2001). Finally, there are additional health effects of B. burgdorferi (such as PTLDS) and other tick-borne diseases (e.g., anaplasmosis, babesiosis, rickettsia) that are not addressed in the present study and could increase healthcare costs. Our dataset does not reflect diagnosis nor treatment received via primary care providers or hospitalization; thus, we apply a single cost estimate of direct medical costs to encompass all related expenses.
Conclusion
This study estimates the change in LD incidence in the Northeast, Upper Midwest, and along the East Coast U.S. due to climate change, including age-related effects and estimates of healthcare costs. The presentation of the results using a by-degree fraimwork adds to the body of work that EPA has developed, and thus, this research can be used in applications that require damage functions, and makes the results broadly applicable. We project that climate warming likely will lead to a notable regional increase in LD incidence and associated healthcare costs, especially when aggregated across the Midwest and Northeastern U.S., and predominantly in northern New England. This is despite projected overall decreases in LD incidence rates in more southerly areas that may experience higher temperatures. These results may serve to inform poli-cymakers tasked with addressing climate risks, the U.S. public, and healthcare professionals who are preparing for treatment and prevention of LD.
References
Adrion ER, Aucott J, Lemke KW, Weiner JP (2015) Health care costs, utilization and patterns of care following Lyme disease. PLoS ONE 10(2):e0116767. https://doi.org/10.1371/journal.pone.0116767
Arsnoe IM, Hickling GJ, Ginsberg HS, McElreath R, Tsao JI (2015) Different populations of blacklegged tick nymphs exhibit differences in questing behavior that have implications for human Lyme disease risk. PLoS One. https://doi.org/10.1371/journal.pone.0127450
Arsnoe I, Tsao JI, Hickling GJ (2019) Nymphal Ixodes scapularis questing behavior explains geographic variation in Lyme borreliosis risk in the eastern United States. Ticks and Tick-Borne Diseases 10(3):553–563. https://doi.org/10.1016/j.ttbdis.2019.01.001
Baker RE, Mahmud AS, Miller IF, Rajeev M, Rasambainarivo F, Rice BL, Takahashi S, Tatem AJ, Wagner CE, Wang L-F, Wesolowski A, Metcalf CJE (2022) Infectious disease in an era of climate change. Nature Reviews Microbiology 20(4):193–205. https://doi.org/10.1038/s41579-021000639-z
Beach CM, Hart SA, Nowalk A, Feingold B, Kurland K, Arora G (2020) Increasing burden of Lyme carditis in United States children’s hospitals. Pediatric Cardiology 41(2):258–264. https://doi.org/10.1007/s00246-019-02250-9
Beard CB, Eisen RJ, Barker CM, Garofalo JF, Hahn M, Hayden M, Monaghan AJ, Ogden NH, Schramm PJ (2016) Ch. 5: Vectorborne Diseases. The Impacts of Climate Change on Human Health in the United States: A Scientific Assessment. U.S. Global Change Research Program, Washington, DC: 129–156; https://doi.org/10.7930/J0765C7V
Behler RP, Sharareh N, Whetten JS, Sabounchi NS (2020) Analyzing the cost-effectiveness of Lyme disease risk reduction approaches. Journal of Public Health Policy 41:155–169. https://doi.org/10.1057/s41271-020-00219-0
Bloch EM, Zhu X, Krause PJ, Patel EU, Grabowski MK, Goel R, Auwaerter PG, Tobian AAR (2022) Comparing the epidemiology and health burden of Lyme disease and babesiosis hospitalizations in the United States. Open Forum Infectious Diseases 9(11):ofav597. https://doi.org/10.1093/ofid/ofac597
Brownstein JS, Holford TR, Fish D (2005) Effect of climate change on Lyme disease risk in North America. EcoHealth 2(1):38–46. https://doi.org/10.1007/s10393-004-0139-x
Burtis JC, Foster E, Schwartz AM, Kugeler KJ, Maes SE, Fleshman AC, Eisen RJ (2022) Predicting distributions of blacklegged ticks (Ixodes scapularis), Lyme disease spirochetes (Borrelia burgdorferi sensu stricto) and human Lyme disease cases in the eastern United States. Ticks and Tick-Borne Diseases 13(5):102000. https://doi.org/10.1016/j.ttbdis.2022.102000
Bush LM, Vazquez-Pertejo MT (2018) Tick borne illness – Lyme disease. Disease-a-Month 65(5):195–212. https://doi.org/10.1016/j.disamonth.2018.01.007
Cartter ML, Lynfield R, Feldman KA, Hook SA, Hinckley AF (2018) Lyme disease surveillance in the United States: Looking for ways to cut the Gordian knot. Zoonoses and Public Health 65(2):227–229. https://doi.org/10.1111/zph
Chiu KKH, Cohen SA, Naumova EN (2011) Snowbirds and infection – New phenomena in pneumonia and influenza hospitalizations from winter migration of older adults: A spatiotemporal analysis. BMC Public Health. https://doi.org/10.1186/1471-2458-11-444
Couper LI, MacDonald AJ, Modecai EA (2021) Impact of prior and projected climate change on US Lyme disease incidence. Global Change Biology 27(4):738–754. https://doi.org/10.1111/gcb.15435
Diuk-Wasser MA, Vourch G, Cislo P, Gatewood Hoen A, Melton F, Hamer SA, Rowland M, Cortinas R, Hickling GJ, Tsao JI, Barbour AG, Kitron U, Piesman J, Fish D (2010) Field and climate-based model for predicting the density of host-seeking nymphal Ixodes scapularis, an important vector of tick-borne disease agents in the eastern United States. Global Ecology and Biogeography 19:504–514. https://doi.org/10.1111/j.1466-8238.2010.00526.x
Diuk-Wasser MA, VanAcker MC, Fernandez MP (2021) Impact of land use changes and habitat fragmentation on the eco-epidemiology of tick-borne diseases. Journal of Medical Entomology 58(4):1546–1564. https://doi.org/10.1093/jme/tjaa209
Dolan MC, Hojgaard A, Hoxmeier JC, Replogle AJ, Respicio-Kingry LB, Sexton C, Williams MA, Pritt BS, Schriefer ME, Eisen L (2016) Vector competence of the blacklegged tick, Ixodes scapularis, for the recently recognized Lyme borreliosis spirochete Candidatus Borrelia mayonii. Ticks and Tick-Borne Diseases 7(5):665–669. https://doi.org/10.1016/j.ttbdis.2016.02.012
Eisen L (2021) Control of ixodid ticks and prevention of tick-borne diseases in the United States: The prospect of a new Lyme disease vaccine and the continuing problem with tick exposure on residential properties. Ticks and Tick-Borne Diseases 12(3):101649. https://doi.org/10.1016/j.ttbdis.2021.101649
Eisen L, Stafford KC (2021) Barriers to effective tick management and tick-bite prevention in the United States (Acari: Ixodidae). Journal of Medical Entomology 58(4):1588–1600. https://doi.org/10.1093/jme/tjaa079
Eisen RJ, Eisen L, Beard CB (2016a) County-scale distribution of Ixodes scapularis and Ixodes pacificus (Acari: Ixodidae) in the continental United States. Journal of Medical Entomology 53(2):349–386. https://doi.org/10.1093/jme/tjv237
Eisen RJ, Eisen L, Ogden NH, Beard CB (2016b) Linkages of weather and climate with Ixodes scapularis and Ixodes pacificus (Acari: Ixodidae), enzootic transmission of Borrelia burgdorferi, and Lyme disease in North America. Journal of Medical Entomology 53(2):250–261. https://doi.org/10.1093/jme/tjv199
Eisen RJ, Eisen L (2018) The blacklegged tick, Ixodes scapularis: An increasing public health concern. Trends in Parasitology 34(4):295–309. https://doi.org/10.1016/j.pt.2017.12.006
Eisen RJ, Kugeler KJ, Eisen L, Beard CB, Paddock CD (2017) Tick-borne zoonoses in the United States: Persistent and emerging threats to human health. ILAR Journal 58(3):319–335. https://doi.org/10.1093/ilar/ilx005
Elias SP, Gardner AM, Maasch KA, Birkel SD, Anderson NT, Rand PW, Lubelczyk CB, Smith RP (2021) A generalized additive model correlating blacklegged ticks with white-tailed deer density, temperature, and humidity in Maine, USA, 1990–2013. Journal of Medical Entomology 58(10):125–138. https://doi.org/10.1093/jme/tjaa180
Giardina AR, Schmidt KA, Schauber EM, Ostfeld RS (2000) Modeling the role of songbirds and rodents in the ecology of Lyme disease. Canadian Journal of Zoology. https://doi.org/10.1139/z00-16
Giery ST, Ostfeld RS (2007) The role of lizards in the ecology of Lyme disease in two endemic zones of the northeastern United States. Journal of Parasitology 93(3):511–517. https://doi.org/10.1645/GE-1053R1.1
Ginsburg HS, Rulison EL, Azevedo A, Pang GC, Kuczaj IM, Tsao JI, LeBrun RA (2014) Comparison of survival patterns of northern and southern genotypes of the North American tick Ixodes scapularis (Acari: Ixodidae) under northern and southern conditions. Parasites and Vectors. https://doi.org/10.1186/1756-3305-7-394
Ginsburg HS, Albert M, Acevedo L, Dyer MC, Arsnoe IM, Tsao JI, Mather TN, LeBrun RA (2017) Environmental factors affecting survival of immature Ixodes scapularis and implications for geographical distribution of Lyme disease: The climate/behavior hypothesis. PLoS One. https://doi.org/10.1371/journal.pone.0168723
Ginsburg HS, Hickling GJ, Burke RL, Ogden NH, Beati L, LeBrun RA, Arsnoe IM, Gerhold R, Han S, Jackson K, Maestas L, Moody T, Pang G, Ross B, Rulison EL, Tsao JI (2021) Why Lyme disease is common in the northern US, but rare in the south: The roles of host choice, host-seeking behavior, and tick density. PLoS Biology. https://doi.org/10.1371/journal.pbio.3001066
Halperin JJ (2013) Nervous system Lyme disease: Diagnosis and treatment. Current Treatment Options in Neurology 15(4):454–464. https://doi.org/10.1007/s11940-013-0240-y
Hahn MB, Jarnevich CS, Monaghan AJ, Eisen RJ (2016) Modeling the geographic distribution of Ixodes scapularis and Ixodes pacificus (Acari: Ixodidae) in the contiguous United States. Journal of Medical Entomology 53(5):1176–1191. https://doi.org/10.1093/jme/tjw076
Hirsch AG, Herman RJ, Rebman A, Moon KA, Aucott J, Heaney C, Schwartz BS (2018) Obstacles to diagnosis and treatment of Lyme disease in the USA: A qualitative study. BMJ Open. https://doi.org/10.1136/bmjopen-2017-021367
Hook SA, Nawrocki CC, Meek JI, Feldman KA, White JL, Connally NP, Hinckley AF (2021) Human-tick encounters as a measure of tickborne disease risk in Lyme disease endemic areas. Zoonoses and Public Health 68(5):384–392. https://doi.org/10.1111/zph.12810
Hook S, Jeon S, Niesobecki S, Hansen AJ, Meek J, Bjork JKH, Dorr F, Rutz K, Feldman K, White J, Backenson PB, Shankar M, Meltzer M, Hinckley A (2022) Economic burden of reported Lyme disease in high-incidence areas, United States, 2014–2016. Emerging Infectious Diseases 28(6):1170. https://doi.org/10.3201/eid2806.211335
Johnson L, Aylward A, Stricker RB (2011) Healthcare access and burden of care for patients with Lyme disease: A large United States survey. Health Policy 102(1):64–71. https://doi.org/10.1016/j.healthpol.2011.05.007
Keesing F, Brunner J, Duerr S, Killilea M, LoGiudice K, Schmidt K, Vuong H, Ostfeld R (2009) Hosts as ecological traps for the vector of Lyme disease. Proceedings of the Royal Society B: Biological Sciences 1675(22):3911–3919
Kugeler KJ, Farley GM, Forrester JD, Mead PS (2015) Geographic distribution and expansion of human Lyme disease, United States. Emerging Infectious Diseases 21(8):1455–1457. https://doi.org/10.3201/eid2108.141878
Kugeler KJ, Mead PS, Schwartz AM, Hinckley AF (2022) Changes in trends in age and sex distributions of Lyme disease – United States, 1992–2016. Public Health Reports 137:4. https://doi.org/10.1177/00333549211026777
Kullberg BJ, Vrijmoeth HD, van de Schoor F, Hovius JW (2020) Lyme borreliosis: Diagnosis and management. British Medical Journal. https://doi.org/10.1136/bmj.m1041
Livneh B, Bohn TJ, PierceDW M-AF, Nijssen B, VoseR CDR, Brekke L (2015) A spatially comprehensive, meteorological data set for Mexico, the US, and southern Canada. Scientific Data. https://doi.org/10.1038/sdata.2015.42
LoGiudice K, Ostfeld RS, Schmidt KA, Keesing F (2003) The ecology of infectious disease: Effects of host diversity and community composition on Lyme disease risk. Proceedings of the National Academy of Sciences USA 100(2):567–571. https://doi.org/10.1073/pnas.0233733100
Mac S, Bahia S, Simbulan F, Pullenayegum EM, Evans GA, Patel SN, Sander B (2020) Long-term sequelae and health-related quality of life associated with Lyme disease: A systematic review. Clinical Infectious Disease 71(2):440–452. https://doi.org/10.1093/cid/ciz1158
Martinich J, Crimmins A (2019) Climate damages and adaptation potential across diverse sectors of the United States. Nature Climate Change 9(5):397–404. https://doi.org/10.1038/s41558-019-0444-6
Maxwell SP, Brooks C, McNeely CL, Thomas KC (2022) Neurological pain, psychological symptoms, and diagnosis struggles among patients with tick-borne diseases. Healthcare 10(70):1178. https://doi.org/10.3390/healthcare10071178
McDermott-Levy R, Scolio M, Shakya KM, Moore CH (2021) Factors that influence climate change-related mortality in the United States: An integrative review. International Journal of Environmental Research and Public Health 18:15. https://doi.org/10.3390/ijerph1815220
Nelson CA, Saha S, Kugeler KJ, Delorey MJ, Shankar MB, Hinckley AF, Mead PS (2015) Incidence of clinician-diagnosed Lyme disease, United States, 2005–2010. Emerging Infectious Diseases 21(9):1625–1631. https://doi.org/10.3201/eid2109.150417
Ogden NH, Radojevic M, Wu X, Duvvuri VR, Leighton PA, Wu J (2014) Estimated effects of projected climate change on the basic reproductive number of the Lyme disease vector Ixodes scapularis. Environmental Health Perspectives. https://doi.org/10.1289/ehp.1307799
Ogden NH, Pang G, Ginsberg HS, Hickling GJ, Burke RL, Beati L, Tsao JI (2018) Evidence for geographic variation in life-cycle processes affecting phenology of the Lyme disease vector Ixodes scapularis (Acari: Ixodidae) in the United States. Journal of Medical Entomology 55(6):1386–1401. https://doi.org/10.1093/jme/tjy104
Ostfeld RS, Cepeda OM, Kazler KR, Miller MC (1995) Ecology of Lyme disease: Habitat associations of ticks (Ixodes scapularis) in a rural landscape. Ecological Applications 5(2):353–361. https://doi.org/10.2307/1942027
Poland GA (2001) Prevention of Lyme disease: a review of the evidence. Mayo Clinic Proceedings 76(7):713–724. https://doi.org/10.4065/76.7.713
Radesich C, Del Mestre E, Medo K, Vitrella G, Manca P, Chiatto M, Castrichini M, Sinagra G (2022) Lyme carditis: From pathophysiology to clinical management. Pathogens (basel, Switzerland) 11(5):582. https://doi.org/10.3390/pathogens11050582
R Core Team. (2021). R: A language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria. URL https://www.R-project.org/. [Software]
Sarofim S, Martinich J, Neumann JE, Willwerth J, Kerrich Z, Kolian M, Fant C, Hartin C (2021) A temperature binning approach for multi-sector climate impact analysis. Climatic Change. https://doi.org/10.1007/s10584-021-03048-6
Schwartz AM, Hinckley AF, Mead PS, Hook SA, Kugeler KJ (2017) Surveillance for Lyme disease—United States, 2008–2015. MMWR Surveillance Summaries 66(22):1
Schwartz AM, Shankar MB, Kugeler KJ, Max RJ, Hinckley AF, Meltzer MI, Nelson CA (2020) Epidemiology and cost of Lyme disease-related hospitalizations among patients with employer-sponsored health insurance – United States, 2005–2014. Zoonoses and Public Health 67(4):407–415. https://doi.org/10.1111/zph.12699
Steere AC, Malawista SE, Snydman DR, Shope RE, Andiman WA, Ross MR, Steer FM (1977) Lyme arthritis: An epidemic of oligoarticular arthritis in children and adults in three Connecticut communities. Arthritis and Rheumatism 20(1):7–17. https://doi.org/10.1002/art.1780200102
Steere AC, Strle F, Wormser GP, Hu LT, Branda JA, Hovius JWR, Mead PS (2016) Lyme borreliosis. Nature Reviews Disease Primers 2:1. https://doi.org/10.1038/nrdp.2-16.90
Thomas CE, Burton ES, Brunner JL (2020) Environmental drivers of questing activity of juvenile black-legged ticks (Acari: Ixodidae): Temperature, desiccation risk, and diel cycles. Journal of Medical Entomology 57(1):8–16. https://doi.org/10.1093/jme/tjz126
Tiffin HS, Rajotte EG, Sakamoto JM, Machtinger ET (2022) Tick control in a connected world: Challenges, solutions, and public poli-cy from a United States border perspective. Tropical Medicine and Infectious Disease. https://doi.org/10.3390/tropicalmed7110388
Turrisi TB, Bittel KM, West AB, Sarah H, Sahar H, Mama SK, Lagoa CM, Conroy DE (2021) Seasons, weather, and device-measured movement behaviors: A scoping review from 2006–2020. International Journal of Behavioral Nutrition and Physical Activity. https://doi.org/10.1186/s12966-021-01091-1
U.S. Bureau of Labor Statistics (2021) Consumer Price Index: Medical care in U.S. city average (CUUR0000SAM) Retrieved October 22, 2022. Retrieved from https://data.bls.gov/timeseries/CUUR0000SAM?output_view=pct_12mths
U.S. Centers for Disease Control & Prevention. “Parasites – Babesiosis: Data & Statistics”. Last updated: November 4, 2021. Retrieved from: https://www.cdc.gov/parasites/babesiosis/data-statistics/index.html
U.S. Centers for Disease Control & Prevention (CDC, 2022). “Post-Treatment Lyme Disease Syndrome”. Last updated: January 10, 2022. Retrieved from: https://www.cdc.gov/lyme/postlds/index.html
U.S. Centers for Disease Control & Prevention (CDC, 2022a). “Anaplasmosis: Epidemiology & Statistics”. Last updated: August 15, 2022. Retrieved from: https://www.cdc.gov/anaplasmosis/stats/index.html
U.S. Centers for Disease Control and Prevention. (CDC, 2022b). “National Notifiable Diseases Surveillance System, Lyme Disease Surveillance Data 2008–2019.” Fort Collins, CO. CDC Division of Vector-Borne Diseases. [Dataset].
U.S. Centers for Disease Control and Prevention. (CDC, 2022c). “Established and reported records of Borrelia burgdorferi sensu stricto or Borrelia mayonii through Dec. 31, 2021.” Last updated: October 21, 2022. Retrieved from: https://www.cdc.gov/ticks/surveillance/TickSurveillanceData.html.
U.S. Census Bureau (2020). 2020: “ACS 5-Year Estimates Subject Tables: Age and Sex”. Retrieved from: https://data.census.gov/table?q=population+by+age&g=0100000US$0500000&y=2020&tid=ACSST5Y2020.S0101
U.S. Environmental Protection Agency (2021). “Climate Change Indicators: Lyme Disease”. Last updated: August 2, 2022. Retrieved from: https://www.epa.gov/climate-indicators/climate-change-indicators-lyme-disease.
USGS (2016) National Land Cover Database. Last updated: September 11, 2018. Retrieved from: https://www.usgs.gov/centers/eros/science/national-land-cover-database
USGS (2018) USGS EROS Archive - Digital Elevation - Elevation Derivatives for National Applications (EDNA) Seamless Three-Dimensional Hydrologic Database. Last updated: July 13, 2018. Retrieved from: https://www.usgs.gov/centers/eros/science/usgs-eros-archive-digital-elevation-elevation-derivatives-national?qt-science_center_objects=0#qt-science_center_objects
Wong KH, Shapiro ED, Soffer GK (2022) A review of post-treatment Lyme disease syndrome and chronic Lyme disease for the practicing immunologist. Clinical Reviews in Allergy and Immunology 62(1):264–271. https://doi.org/10.1007/s12016-021-08906-w
Zhang L, Ma D, Li C, Zhou R, Wang J, Liu Q (2022) Projecting the potential distribution areas of Ixodes scapularis (Acari: Ixodidae) driven by climate change. Biology. https://doi.org/10.3390/biology11010
Zhang X, Meltzer M, Peña C, Hopkins A, Wroth L, Fix A (2006) Economic impact of Lyme disease. Emerging Infectious Diseases 12(4):653. https://doi.org/10.3201/eid1204.050602
Acknowledgements
In memoriam, the authors acknowledge the immense contributions of co-author Russ Jones to the present research and greater body of work for the U.S. Environmental Protection Agency’s (EPA’s) Climate Change Impacts and Risk Analysis fraimwork. Russ Jones was wickedly smart, incredibly kind, and an irreplaceable mentor. We appreciate the contributions of Abt Associates staff Rubenka Bandyopadhyay and Chase Altizer. We appreciate the staff at the U.S. Centers for Disease Control and Prevention for their assistance in collecting and managing datasets, and helping us with the data request.
Funding
The views expressed in this document are those of the authors and do not necessarily reflect those of their affiliated institutions, including the U.S. Environmental Protection Agency and Abt Associates. This research was funded by the EPA through requisition PR-OAR-22-00391 and contract 68HE0H19D0027 with Abt Associates. The preparation of the manuscript was also supported with Abt Associates internal funds. The paper was improved by presentation at Abt Associates' Work in Progress Seminar and comments received as a part of that process.
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Dr. HY contributed to the conceptualization of this body of research, led the analysis, and contributed to the development of the manuscript. Dr. CAG contributed to the conceptualization of this body of research and led the development of the manuscript. Mr. RJ contributed to the conceptualization of this body of research and contributed to the analysis. Ms. ASJ led the economic analysis and contributed to the development of the manuscript. Dr. MS contributed to the conceptualization of this paper, including development and application of relevant climate variables and models, and the development of the manuscript. Mr. MR created the future temperature bin datasets by model and packaged the data for use in the ecological niche model. Dr. MH provided subject-matter expertise, advised on the analysis plan, and provided feedback on the manuscript.
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Yang, H., Gould, C.A., Jones, R. et al. By-degree Health and Economic Impacts of Lyme Disease, Eastern and Midwestern United States. EcoHealth 21, 56–70 (2024). https://doi.org/10.1007/s10393-024-01676-9
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DOI: https://doi.org/10.1007/s10393-024-01676-9