Decreased Pulmonary Function Measured in Children Exposed to High Environmental Relative Moldiness Index Homes

1.. INTRODUCTION

Exposure to water-damaged, moldy homes/buildings has been linked to respiratory disease [1, 2], including asthma [3, 4]. Many methods have been used to estimate the water-damage and/or mold contamination in homes/buildings but probably a visual and/or olfactory inspection is the most common. This is not highly quantitative. Similarly, many diverse methods have been used to estimate the respiratory health impact from exposures to water-damaged environments including, caregiver diaries, healthcare utilization records, phone surveys, etc. [5]. These are not clinically precise. In this study, a standard metric for quantifying water-damage/mold contamination in homes, the Environmental Relative Moldiness Index (ERMI), and a clinically-based spirometry test called FEV1% or “forced expiratory volume in 1 second, percent predicted” were utilized to quantitatively relate exposures to lung function.

The US Environmental Protection Agency (US EPA) in conjunction with the Department of Housing and Urban Development (HUD) created a standardized assessment to quantify water-damage and mold contamination in US homes called the ERMI [6]. For the ERMI analysis, a DNA-based technology, mold specific quantitative polymerase chain reaction, was used to measure the concentration of 36 indicator molds in settled-dust samples. The concentration of each of the 36 molds is mathematically treated to produce a single number, the ERMI value for that home [6, 7]. The ERMI scale ranges from -10 to 20 for most homes but a few homes have ERMI values up to about 40. For convenience of use, the ERMI scale is divided into quartiles. About 50% of homes in the US have low ERMI values of -10 to 0. Those in the third quartile range from 0 to 5 and the highest quartile is above 5 [6].

Clinical testing with spirometry of a child’s lung function provides a standardized evaluation of a child’s respiratory health. Measurement of lung function by spirometry is reportedly both objective and reproducible [8]. The goal of this analysis was to determine the correlation between the water-damage, i.e. ERMI value, in an asthmatic child’s home and the child’s pulmonary function, as measured by FEV1%. This analysis utilized data obtained from the “Heads-off Environmental Asthma in Louisiana” (HEAL) study [9-12] but was not part of the original HEAL study design. The HEAL study concerned the impact of the 29 August 2005 hurricane Katrina on the children in the affected homes in New Orleans, LA.

2.. MATERIALS AND METHODOLOGY

The HEAL study was approved by the National Institute of Environmental Health Sciences and the Tulane and Louisiana State Universities’ Institutional Review Boards. Many previous publications have describe the HEAL study, the methods used, the population demographics, the exposures measured, and the outcomes [9-12]. No attempt will be made to repeat this background but it is briefly summarized below.

Hurricane Katrina impacted the city of New Orleans in August of 2005 and recruitment for the HEAL study began in February 2007 and was completed by March 2008 [9]. Children (n=182) were recruited from New Orleans schools and pre-screened by telephone. They were eligible if they were 4-12 years old and a parent or guardian reported they had asthma; lived in Orleans Parish or neighboring parishes that were affected by the hurricane Katrina and subsequent flooding; and met criteria for moderate-to-severe asthma at the time of the baseline clinical evaluation, as described earlier [9]. At the time of the study, about 60% of homes had completed some level of renovation/remediation, in 26% of homes efforts were on-going and in 13% work had not started [11].

Many of the participants were not necessarily receiving appropriate care for their asthma. As a result of their enrollment, each participant received excellent standard of care and therapy for their asthma [12]. At the time of the baseline clinical visit spirometry testing was completed using a EasyOne Spirometer (ndd Medical, Inc., Andover, MA) and the calculation of FEV1% was completed following American Thoracic Society protocol (https://www. thoracic.org/statements/resources/pfet/PFT2.pdf). Shortly after the clinical evaluation, a home visit was made for dust collection and other environmental evaluations [9].

Of the children enrolled in HEAL, 67% were African American, and 25% came from households with annual incomes < $15K and 51% making < 30K [12]. Therefore the participants were generally of low socioeconomic status. HEAL children were symptomatic, averaging 6.6 symptom days in the 2 weeks before the baseline sampling, and had frequent unscheduled visits to clinics or emergency departments (76% had at least one unscheduled visit in the preceding 3 months) [9].

This current analysis only included the 109 children who were at least 6 years of age and therefore eligible to perform spirometry testing. They had to have completed at least one spirometry evaluation and a dust sample had to have been obtained from the home at approximately the same time as the spirometry testing. For 50 of the children, the spirometry testing and dust collecting and ERMI analysis were performed twice during this 12 month study (repeats at least 6 months apart).

Methods and MSQPCR assays have been reported previously for performing the ERMI analysis [13]. Briefly, the standard reaction assays contained 12.5 µl of “Universal Master Mix” (Applied Biosystems Inc., Foster City, CA), 1 µl of a mixture of forward and reverse primers at 25 µM each, 2.5 µl of a 400 nM TaqMan probe (Applied Biosystems Inc.), 2.5 µl of 2 mg/ml fraction V bovine serum albumin (Sigma Chemical, St. Louis, MO) and 2.5 µl of DNA free water (Cepheid, Sunnyvale, CA). To this mix was added 5 µl of the DNA extract from the sample. All primer and probe sequences used in the assays have been published [14]. Primers and probes were synthesized commercially (Applied Biosystems, Inc.).

Statistical evaluation of the correlation between ERMI values and FEV1% was performed using the Spearman’s Rank Correlation analysis. Outliers in the data were evaluated using the Grubbs test. Among subjects with ERMI and FEV1% measurements at both time points (N=50), differences between base line and follow-up were evaluated via the Wilcoxon signed rank test. Neither ERMI nor FEV1% were found to differ significantly from baseline to follow-up (p=0.96 and p=0.89, respectively). The average values for the ERMI and FEV1% test results were utilized in the Spearman’s Rank Correlation analysis. The relationship between ERMI values and FEV1% was performed using B-spline regression [15] showing the 95% confidence interval. The analyses were performed in SAS version 9.3 (SAS Institute, Cary NC) and R version 2.14 (R Foundation for Statistical Computing, Vienna, Austria).

3.. RESULTS

The average ERMI value for the homes in the HEAL study was 7.3 (standard deviation ± 4.6) and the average FEV1% value was 95% (standard deviation ± 15). The Grubbs’ test identified one ERMI value of 30.61 in a single home as an outlier, compared to the average ERMI of 7.3. Similarly, the FEV1% levels for two of the children were measured at 38% and 43% in their initial clinic visit, compared to 95% for the average. Therefore these two sets of results were also removed from further analysis, leaving 106 ERMI and FEV1% data pairs. The paired ERMI and FEV1% data is shown in Fig. (1) with the regression line for FEV1% showing a downward slope as the homes’ ERMI values increased.

The possible relationship between the ERMI value of the home and the FEV1% value for the child’s lung function was visualized by plotting a B-spline regression using two interior quantile knots and 95% confidence intervals (Fig. 2). (We also examined spline curves with one and three knots, but the two knot spline curve provided the best fit to the data.) The first knot or change in curve direction fell in the third quartile of the ERMI scale, which is bounded on the low side by an ERMI value of 0 and on the high side with an ERMI value of 5 [6]. Therefore, the value of 2.5 was selected, precisely in the middle of the third quartile, to divide the homes into two groups; those with ERMI values below 2.5 and those with ERMI values above 2.5.

For the set of homes with ERMI values below 2.5, there was no significant correlation between ERMI values and FEV1% results (Spearman’s rho -0.1; p=0.7). For the set of

homes with ERMI values between 2.5 and 15, there was a significant inverse correlation with the child’s lung function or FEV1% measurement (Spearman’s rho -0.23; p= 0.03), i.e. as the ERMI value increased, the FEV1% value decreased. (There were only six homes with ERMI values above 15; too few to evaluate the relationship between ERMI and FEV1%, as noted by the flattening of the B-spline at about that point). The peak FEV1% of about 100% was at an ERMI value of approximately 2.5. The FEV1% values declined to a low of about 70% at an ERMI value of 15 (Fig. 2).

4.. DISCUSSION

Exposure of a child to a New Orleans home with water damage above 2.5 on the ERMI scale was likely to result in a deficit in the child’s normal lung function. Norbäck et al. [16] similarly demonstrated that the lung function of adults declined over time when exposed to damp homes. Of course, there are many chemical and biological exposures in water-damaged homes. Therefore, no specific cause(s) for the respiratory deficit can be assigned. Rather this analysis adds to the growing scientific literature that indicates that exposure to water-damaged homes should be reduced [2].

Reponen et al. [3, 4] conducted a prospective study of asthma development from infancy to age seven and the physician-based diagnosis of asthma. They found that infants exposed to homes with ERMI values above 5 were much more likely to develop asthma. In a study of three widely dispersed cities in the US (Boston, Kansas City, and San Diego), the homes of the children with asthma had average ERMI values of 8.7 [17]. This is very similar to the average ERMI value of 7.3 found in the water-damaged homes of the asthmatic children in New Orleans.

We acknowledge that this analysis has many limitations. Since this analysis was not specifically a part of the original study plan, we were limited to a relative small sample size in which the environmental sampling and clinical testing coincided. In addition, we did not have large enough data set for a multivariate analysis. However, previous results from the HEAL study showed exposures to allergens of mice (Mus m 1), dust mites (Der p 1) and cockroach (Bla g 1) in only 60%, 35% and 20% of homes respectively and at low mean concentrations [11]. These exposures do not appear to be significant confounding exposures but of course we have not measured all possible exposures including indoor air pollution, pesticides, etc. In spite of these limitations, our results do suggest, but do not prove, that there is a quantitative relationship between exposures to water-damaged homes and the exposed child’s respiratory function.

It does not take a hurricane to create water-damaged homes. In fact, each year millions of homes suffer water-damage from obvious sources like flooding and “hidden” problems like the dripping pipe in the wall. These water-damaged homes may be contributing to the asthma epidemic [18] which costs the US billions of dollars each year [19]. Since the costs continue to escalate, methods to prevent asthma development or exacerbation are needed. One important step might be remediating water-damaged homes. Combining more quantitative measures of water-damage like the ERMI and clinical assessments of the child’s health through spirometry might provide the motivation to prevent children from being exposed to water-damaged homes.

REFERENCES