21 research outputs found
Population characteristics (n = 2906).
<p>All data posted as mean (SE) unless otherwise indicated. Geometric means are presented for all variables log-transformed in presented analyses.</p><p>*ferritin < 20ng/ml</p><p>SE = linearized standard error</p><p><sup>§</sup>n = 2678;</p><p><sup>†</sup>n = 2415;</p><p><sup>$</sup>n = 2378;</p><p><sup>‡</sup>n = 2444;</p><p><sup>ᶿ</sup>n = 2374;</p><p><sup>ᶲ</sup>n = 2470;</p><p><sup>λ</sup>n = 2901</p><p>Population characteristics (n = 2906).</p
Iron Status is Associated with Asthma and Lung Function in US Women
<div><p>Background</p><p>Asthma and iron deficiency are common conditions. Whether iron status affects the risk of asthma is unclear.</p><p>Objective</p><p>To determine the relationship between iron status and asthma, lung function, and pulmonary inflammation.</p><p>Methods</p><p>Relationships between measures of iron status (serum ferritin, serum soluble transferrin receptor (sTfR), and sTfR/log10ferritin (sTfR-F Index)) and asthma, lung function, and pulmonary inflammation were examined in women 20-49 years in the National Health and Nutrition Examination Survey. Logistic, linear, and quadratic regression models accounting for the survey design of NHANES were used to evaluate associations between iron status and asthma-related outcomes and were adjusted for race/ethnicity, age, smoking status, income, and BMI.</p><p>Results</p><p>Approximately 16% reported a lifetime history of asthma, 9% reported current asthma, and 5% reported a recent asthma episode/attack (n = 2906). Increased ferritin (iron stores) was associated with decreased odds of lifetime asthma, current asthma, and asthma attacks/episodes in the range of ferritin linearly correlated with iron stores (20-300ng/ml). The highest quintile of ferritin (>76 ng/ml) was also associated with a decreased odds of asthma. Ferritin levels were not associated with FEV1. Increased values of the sTfR-F Index and sTfR, indicating <i>lower</i> body iron and <i>higher</i> tissue iron need, respectively, were associated with decreased FEV1, but neither was associated with asthma. None of the iron indices were associated with FeNO.</p><p>Conclusion</p><p>In US women, higher <i>iron stores</i> were inversely associated with asthma and lower <i>body iron</i> and higher <i>tissue iron need</i> were associated with lower lung function. Together, these findings suggest that iron status may play a role in asthma and lung function in US women.</p></div
Predicted relationships between the full range of ferritin concentrations and asthma- related outcomes, generated from regression models: (a) lifetime asthma and (b) current asthma.
<p>95% confidence intervals are depicted by the shaded areas. Vertical line represents approximately 20ng/ml ferritin.</p
Relationships between iron status and asthma outcomes.
<p>*Adjusted for race/ethnicity, age, smoking, income, and BMI</p><p><b>Bolded</b> results are statistically significant, with p<0.05</p><p><sup>‡</sup>n = 2906 for unadjusted, n = 2663 for adjusted; ferritin Q1–4: 1.8–76.0ng/ml, Q5: >76.0ng/ml</p><p><sup>§</sup>Ferritin restricted to values from 20 to 300 ng/ml, inclusive; n = 2134 for unadjusted, n = 1963 for adjusted</p><p><sup>†</sup>n = 2901 for unadjusted, n = 2658 for adjusted</p><p>Relationships between iron status and asthma outcomes.</p
Salivary Inflammatory Mediator Profiling and Correlation to Clinical Disease Markers in Asthma
<div><p>Rationale</p><p>There is a need for a readily available, non-invasive source of biomarkers that predict poor asthma control.</p><p>Objectives</p><p>We sought to determine if there is an association between the salivary inflammatory profile and disease control in children and adults with asthma.</p><p>Methods</p><p>In this cross-sectional study, we collected demographic and clinical information from two independent populations at different sites, resulting in convenience samples of 58 pediatric and 122 adult urban asthmatics. Control was assessed by symptom questionnaire (children) and by Asthma Control Questionnaire and current exacerbation (adults). Saliva was collected in all subjects. We applied principal component analysis to a 10-plex panel of relevant inflammatory markers to characterize marker profiles and determined if profiles were associated with asthma control.</p><p>Results</p><p>There were similar, strong correlations amongst biologically related markers in both populations: eosinophil-related: eotaxin-1/CCL11, RANTES/CCL5, and IL-5 (p<.001); myeloid/innate: IL-1β, IL-6, MCP-1/CCL2, and IL-8/CXCL8 (p<.001). The first three principal components captured ≥74% of variability across all ten analytes in both populations. In adults, the Principal Component 1 score, broadly reflective of all markers, but with greater weight given to myeloid/innate markers, was associated with Asthma Control Questionnaire score and exacerbation. The Principal Component 3 score, reflective of IP-10/CXCL10, was associated with current exacerbation. In children, the Principal Component 1, 2, and 3 scores were associated with recent asthma symptoms. The Principal Component 2 score, reflective of higher eosinophil markers, was inversely correlated with symptoms. The Principal Component 3 score was positively associated with all symptom outcomes.</p><p>Conclusion</p><p>The salivary inflammatory profile is associated with disease control in children and adults with asthma.</p></div
Asthma and Allergic Disease Characteristics, Pediatric Population.
<p>*n = 57,</p><p>n = 55,</p><p>n = 56.</p><p>F<sub>E</sub>NO: Fractional Exhaled Nitric Oxide, SPT: Skin Prick Test, FEV1: Forced Expiratory Volume in the 1<sup>st</sup> second, FVC: Forced Vital Capacity.</p
Three-dimensional display of subject principal component scores with respect to clinician-determined exacerbation in adults, n = 120.
<p>Three-dimensional display of subject principal component scores with respect to clinician-determined exacerbation in adults, n = 120.</p
Asthma and Allergic Disease Characteristics, Adult Population.
<p>*n = 120.</p><p>ACQ: Asthma Control Questionnaire, ACT: Asthma Control Test.</p
A pilot feeding study for adults with asthma: The healthy eating better breathing trial
<div><p>Rationale</p><p>Evidence from observational studies and to a lesser extent clinical trials suggest that a healthy diet may improve symptoms and lung function in patients with asthma. We conducted a pilot study to determine the feasibility of conducting a larger scale dietary trial and to provide preliminary evidence on the impact of a healthy diet on asthma outcomes.</p><p>Methods</p><p>In a randomized, two period cross-over trial, participants with asthma received a 4-week dietary intervention followed by a usual diet (or vice versa), separated by a 4-week washout. The dietary intervention was a healthy diet rich in unsaturated fat. During the dietary intervention, participants ate three meals per week on site at the Johns Hopkins ProHealth Research Center. All remaining meals and snacks were provided for participants to consume off-site. During the control diet, participants were instructed to continue their usual dietary intake. Relevant biomarkers and asthma clinical outcomes were assessed at 0, 2, and 4 weeks after starting each arm of the study.</p><p>Results</p><p>Eleven participants were randomized, and seven completed the full study protocol. Among these seven participants, average age was 42 years, six were female, and six were African American. Participant self-report of dietary intake revealed significant increases in fruit, vegetable, and omega-3 fatty acid intake with the dietary intervention compared to usual diet. Serum carotenoids (eg. lutein and beta-cryptoxanthin) increased in the intervention versus control. Total cholesterol decreased in the intervention versus control diet. There was no consistent effect on asthma outcomes.</p><p>Conclusions</p><p>The findings suggest that a feeding trial in participants with asthma is feasible. Larger trials are needed to definitively assess the potential benefits of dietary interventions on pulmonary symptoms and function in patients with asthma.</p></div