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1 er measurements (Fe(NO) and peripheral blood eosinophil count).
2 osinophil-derived neurotoxin levels or blood eosinophil counts).
3 to an increased body mass index or a reduced eosinophil count.
4 revalence, total immunoglobulin E (IgE), and eosinophil count.
5 ations was independent of the baseline blood eosinophil count.
6 ting beta2 agonist, irrespective of baseline eosinophil count.
7 and 1 year after (outcome) their most recent eosinophil count.
8 th vilanterol alone were not associated with eosinophil count.
9 limited to histologic EG based on the tissue eosinophil count.
10 s, as reported by CD41, predicted esophageal eosinophil count.
11 pecified subgroup analysis by baseline blood eosinophil count.
12 f controller asthma medication, and absolute eosinophil count.
13 creased and PCO(2) increased with increasing eosinophil count.
14 cantly predicted the presence of high sputum eosinophil counts.
15 eived placebo, independent of baseline blood eosinophil counts.
16 uid neutrophil and lymphocyte counts but not eosinophil counts.
17 1237 with high (>/=200 cells per muL) blood eosinophil counts.
18 mately 0, including correlations with sputum eosinophil counts.
19 between ETP and vWF with neutrophil but not eosinophil counts.
20 vere, uncontrolled asthma and elevated blood eosinophil counts.
21 -course-persistent asthma had elevated blood eosinophil counts.
22 ced clinicopathologic remission with reduced eosinophil counts.
23 rated the ability to reduce blood and tissue eosinophil counts.
24 re not associated with changes in esophageal eosinophil counts.
25 zation significantly enhanced BAL and tissue eosinophil counts.
26 ma Control Questionnaire 5 scores, and blood eosinophil counts.
27 re is no evidence that it reduces esophageal eosinophil counts.
28 tional polynomials to model continuous blood eosinophil counts.
29 ional exhaled nitric oxide values and sputum eosinophil counts.
30 counts, and so were stratified by mean blood eosinophil count: 1262 patients with low (<200 cells per
31 ively, active vs placebo) and gastric mucosa eosinophils counts (239 eosinophils/mm(2) [59-645] vs 25
32 decrease in FEV(1) and an increase in sputum eosinophil counts 24 hours later (after diluent: median,
33 ents were stratified (2:1) by baseline blood eosinophil counts 300 cells per muL or greater and less
34 f 75.1%, median values of 300/mm(3) of blood eosinophil count, 323 kU/L of serum total IgE, and 24 pp
36 -threatening exacerbations with median blood eosinophil count (5-95th percentiles) of 0.270 x 10(9) /
37 nts or singly increased Feno levels or blood eosinophil counts (85.7% vs 35.8% or 63.3% or 60%, P < .
38 ed nitric oxide values (14.5 ppb), and blood eosinophil counts (96 cells/muL) than all other groups.
39 imary endpoint was the reduction in absolute eosinophil count (AEC) during the first week of DEC trea
41 for the evaluation of eosinophilia (absolute eosinophil count [AEC] > 1500/muL) met the criteria for
42 Seropositive patients had higher absolute eosinophil counts (AECs) than seronegative patients (P =
44 a close relationship between baseline blood eosinophil count and clinical efficacy of mepolizumab in
45 ures of EoE (peak esophageal intraepithelial eosinophil count and EoE histologic scores), endoscopica
46 d persistent asthma irrespective of baseline eosinophil count and had a favourable safety profile, an
47 We investigated the relation between blood eosinophil count and prospective annual asthma outcomes
48 most well established of these are the blood eosinophil count and serum periostin, both of which have
49 IMPACT trial shows that assessment of blood eosinophil count and smoking status has the potential to
51 ifferentials, explaining 71% of variation in eosinophil counts and 64% of variation in neutrophil cou
54 ficantly improved intraepithelial esophageal eosinophil counts and dysregulated esophageal disease-re
55 sess the relationship between baseline blood eosinophil counts and efficacy of mepolizumab we did a s
56 osinophilic inflammation [primary endpoints: eosinophil counts and eosinophil cationic protein (ECP)]
59 roduced a significant decrease in esophageal eosinophil counts and improved dysphagia and endoscopic
60 eactions correlated with reductions in blood eosinophil counts and lung function and increases in nas
61 rleukin-5 monoclonal antibody, reduces blood eosinophil counts and may have value in the treatment of
62 r of controller medications, and total blood eosinophil counts and negatively with the Asthma Control
63 T-cell counts and positively correlated with eosinophil counts and not associated with CD4 T-cell cou
64 nd rs2416257 (A allele associated with lower eosinophil counts and protective against asthma) were co
65 ion of IL33 (A allele associated with higher eosinophil counts and risk for asthma) was correlated wi
67 ts with both increased Feno levels and blood eosinophil counts and subjects with normal Feno levels a
68 ic protein in nasal washes, along with blood eosinophil counts and total and allergen-specific IgE in
69 zed for hemoglobin, white blood cell counts, eosinophil counts and total serum IgE levels, questionna
70 and pre-randomisation measurements of blood eosinophil counts and were of at least 24 weeks in durat
71 score and >75% reduction in gastrointestinal eosinophil count) and the change in total symptom score.
73 ance, esophageal gene expression, esophageal eosinophil count, and the relationship between clinical
74 ction of exhaled nitric oxide [Feno], sputum eosinophil count, and urinary bromotyrosine [BrTyr] leve
75 t pulmonary function tests, blood and sputum eosinophil counts, and 1.5-T DCE MR imaging within 7 day
77 evere airflow limitation, had elevated blood eosinophil counts, and at least two exacerbations or one
79 ne the predictive value of IgE levels, blood eosinophil counts, and fraction of exhaled nitric oxide
80 d reduced OVA-induced increases in total and eosinophil counts, and IL-4, IL-5, IL-13, IL-1beta, IL-3
81 ling (in 82% of subjects), markedly elevated eosinophil counts, and increased filaria-specific immuno
82 C20, fraction of exhaled nitric oxide, blood eosinophil counts, and inhaled steroid treatment did not
83 s had higher than normal Feno values, sputum eosinophil counts, and urinary BrTyr levels during the s
84 s (phase 2) during which Feno values, sputum eosinophil counts, and urinary BrTyr levels were measure
87 vely with nine ascending categories of blood eosinophil count as compared with a reference category o
89 rushings transcriptional signal versus blood eosinophil counts as well as differential expression usi
91 values of NSBH, and FeNO, as well as sputum eosinophil counts assessed at baseline of the SIC were d
93 FVC ratio, airways responsiveness, and serum eosinophil count at baseline yielded greater than 80% pr
96 n the benralizumab 30 mg Q8W group had blood eosinophil counts at least 300 cells per muL and were in
101 ion of exhaled nitric oxide (Feno) and blood eosinophil count (B-Eos) values, markers of local and sy
104 tment reduces STH prevalence, total IgE, and eosinophil count but has no effect on IR at the communit
105 reduced the peak esophageal intraepithelial eosinophil count by a mean 86.8 eosinophils per high-pow
106 determine the relationship between the blood eosinophil count, clinical characteristics and gene expr
109 ntly increased BAL fluid and biopsy specimen eosinophil counts compared with those found in control s
110 erbations increased in proportion with blood eosinophil count, compared with a non-ICS dual long-acti
111 s, and FEV1 percent predicted, but not blood eosinophil counts, correctly predicted 69% of sputum eos
112 reatening asthma, we found that a spot blood eosinophil count correlates with severity of respiratory
115 etermine whether an algorithm based on blood eosinophil counts could safely reduce systemic corticost
116 ials (conducted between 1998 and 2011), with eosinophil count data available for 10 861 patients with
117 ase from baseline of 61.9% in airway mucosal eosinophil counts (day 28; placebo: +19.6%; P = .28), as
118 200 mg) median reduction of 95.8% in airway eosinophil counts (day 84; placebo, 46.7%; P = .06), as
119 y end point was not met, the mean esophageal eosinophil count decreased by 60% with QAX576 versus an
120 creased in 82% of asthmatic patients, sputum eosinophil counts decreased in 60%, and urinary BrTyr le
122 moderate-to-severe asthma and raised sputum eosinophil counts despite inhaled corticosteroid treatme
123 with recurrent exacerbations and high blood eosinophil counts despite use of inhaled corticosteroids
125 egulatory response, the maintenance of lower eosinophil counts during grass pollen seasons, and sIgE
126 e correlated with improvements in histology, eosinophil counts, endoscopic findings, and symptoms.
127 haled breath (FENO ), spirometry (FEV1 ) and eosinophil count (EOS) in 36 patients with allergic, ste
128 ere evaluated with respect to baseline blood eosinophil counts (eosinophils <300/muL [low] vs >/=300/
129 Intraepithelial peak eosinophil and blood eosinophil counts, esophageal-related symptoms, serum to
130 inophil counts, rather than sputum or tissue eosinophil counts, evolved as a pharmacodynamic and pred
132 on with sputum eosinophil percentages, blood eosinophil counts, Feno levels, and total IgE levels did
133 tionship between observed efficacy and blood eosinophil count for moderate or severe exacerbations, T
135 eas ethnicity, sex, atopy, IgE level, sputum eosinophil count, fraction of exhaled nitric oxide, asth
137 end point was the change in gastrointestinal eosinophil count from baseline to 2 weeks after the fina
138 revious 12 months, and had a screening blood eosinophil count greater than or equal to 1000 cells/muL
141 Using either a PC20 </=16 mg/mL or a sputum eosinophil count >/=1% increased the sensitivity to 94%.
143 NSBH despite a positive SIC showed a sputum eosinophil count >/=2%, a FeNO level >/=25 ppb, or both
144 2.832, 95%-CI 1.508-5.321, P = 0.001), peak eosinophil count >10 eosinophils/HPF (OR 0.724, 95%-CI 0
146 phenotype were stratified according to blood eosinophil count (>/=150 per cubic millimeter at screeni
148 ) ratio versus placebo, analysed by baseline eosinophil counts (>/=0, >/=150, >/=300, or >/=450 cells
149 creased Feno levels (>/=20-25 ppb) and blood eosinophil counts (>/=0.3 x 10(9)/L) had a higher preval
150 erbations in patients stratified by baseline eosinophil counts (>/=150 cells per muL, >/=300 cells pe
151 itric oxide values in relationship to sputum eosinophil counts (>2%), as well as to determine whether
153 , 40 (3.8%) patients with less than 2% blood eosinophil counts had a pneumonia event versus 48 (2.4%)
154 reshold, patients with COPD with lower blood eosinophil counts had more pneumonia events than did tho
156 ificance of the "treatable trait" high blood eosinophil count in COPD is the same as for asthma remai
157 led corticosteroids (ICS) and baseline blood eosinophil count in patients with chronic obstructive pu
158 rimary outcome was change in mean esophageal eosinophil count in the 5 high-power fields (hpfs) with
160 tiple-dose subcutaneous benralizumab reduced eosinophil counts in airway mucosa/submucosa and sputum
161 with eosinophilic asthma and its effects on eosinophil counts in airway mucosal/submucosal biopsy sp
163 lter symptoms of eosinophilic esophagitis or eosinophil counts in biopsy samples compared with placeb
164 y mucosa/submucosa and sputum and suppressed eosinophil counts in bone marrow and peripheral blood.
165 Here we report an increase of blood or heart eosinophil counts in humans and mice after myocardial in
166 inary eicosanoid metabolite levels and blood eosinophil counts in patients with AERD who tolerate and
168 investigate increased Feno levels and blood eosinophil counts in relation to lung function, bronchia
169 ) and is correlated with high IgE levels and eosinophil counts in subjects bearing the risk genotype.
175 treatment for COPD have shown that the blood eosinophil count is associated with the risk of COPD exa
176 ng with aeroallergen sensitization and blood eosinophil counts is useful for guiding treatment select
177 with mepolizumab versus placebo in the blood eosinophil count less than 150 cells/muL subgroup (72% v
178 erol was 0.88 (95% CI 0.74 to 1.04) at blood eosinophil count less than 90 cells per muL and 0.56 (0.
179 l due to clinical relevance]), rectal biopsy eosinophil count less than or equal to 32 cells per high
180 e that patients with COPD and baseline blood eosinophil counts less than 2% have a poorer response to
183 and allergic mediators, lower mast cells and eosinophil counts, lower protein expressions of Th2 cyto
185 the end of the double-blind phase and a peak eosinophil count <5 eosinophils/high power field.
186 >/=3%, and <5% and >/=5%) and absolute blood eosinophil count (<150 cells/mul, 150 to <300 cells/mul,
187 eumonia events, stratified by baseline blood eosinophil count (<2% vs >/=2% of blood leucocytes) and
189 mly allocated them (1:1; stratified by blood eosinophil count [<300 cells per muL vs >/=300 cells per
190 gnificant decrease in bronchoalveolar lavage eosinophil counts, lung interleukin-13 and interleukin-5
191 cidate the relationship between a spot blood eosinophil count-measured at the onset of a life-threate
192 al serum IgE level (median, 733 kU/L), blood eosinophil count (median, 400 cells/mm(3)), and allergen
194 % and it was therefore postulated that blood eosinophil count might also have an effect on the risk o
196 h T(H)2 axis decreases, serum IgE levels and eosinophil counts negatively correlated with age in pati
197 s ratio, 32.6; P = 6.9 x 10(-7)), high blood eosinophil counts (odds ratio, 9.1; P = 2.6 x 10(-6)), a
199 one acute exacerbation of COPD, and a sputum eosinophil count of 3.0% or more within the previous yea
201 e hypereosinophilic syndrome and an absolute eosinophil count of at least 1000 cells per cubic millim
202 ic rhinitis aOR = 1.96 [95% CI = 1.58-2.42]; eosinophil count of at least 150 cells per microliter aO
204 actors, including asthma, allergic rhinitis, eosinophil count of at least 150 cells per microliter, a
205 her prevalence of asthma, allergic rhinitis, eosinophil count of at least 150 cells per microliter, a
206 0.39-0.58) in patients with a baseline blood eosinophil count of at least 150 cells per muL to 70%; 0
208 stent, moderate-to-severe asthma and a blood eosinophil count of at least 300 cells per microliter or
210 ts and among subgroups with a baseline blood eosinophil count of less than 150 cells/muL, baseline OG
211 ol alone, were 24% in patients with baseline eosinophil counts of >/=2-<4%, 32% for those with counts
213 received benralizumab every 4 weeks who had eosinophil counts of 0 or more cells per muL, AER was 0.
214 patient per year; p<0.0001) in patients with eosinophil counts of 2% or higher, and by 10% (0.79 vs 0
219 ds of asthma control for patients with blood eosinophil counts of 400 cells per muL or less versus gr
220 had eosinophilia, with median peak absolute eosinophil counts of 726/mL (interquartile range, 594-99
221 eat analysis, the subjects had baseline peak eosinophil counts of 73 and 77 eos/hpf in the OVB and MD
223 ients were stratified 2:1 according to blood eosinophil counts of at least 300 cells per muL and less
225 (FEV1 in L) in patients with baseline blood eosinophil counts of at least 300 eosinophils per muL as
227 exhaled nitric oxide (Feno) levels and blood eosinophil counts offer additive information in relation
228 ed the trends and correlations between blood eosinophil count on admission with arterial blood gas va
230 icant attenuation of allergen-induced sputum eosinophil count on Day 4 following GSK2190915: mean tre
235 BHR than having normal Feno levels and blood eosinophil counts or singly increased Feno levels or blo
237 the ICS-continuation group in patients with eosinophil counts (out of total white blood cell count)
238 levels significantly correlated with sputum eosinophil counts (P < .0001), suggesting that CCL26 par
239 d subjects with normal Feno levels and blood eosinophil counts (P = .02) after adjusting for confound
240 .001) and the highest quartile of peripheral eosinophil counts (P = .03) but not wheezing symptoms, b
241 scores correlated with increased airway wall eosinophil counts (P = 0.003), blood eosinophil percenta
243 ncreased and plasma tryptase correlated with eosinophil counts (Pearson r = 0.514; P < 0.01) on aspir
244 027) positively correlated with peak gastric eosinophil counts (Pearson r(2) = .8102, P < .0001).
246 Primary outcomes were post-treatment maximum eosinophil counts per high-power field (eos/hpf) and a v
249 sk allele at the IL6 lead variant and higher eosinophil count, pulse pressure, systolic blood pressur
251 sion was negatively correlated with absolute eosinophil counts (r = -0.46, P < .001), and soluble pla
252 ation found was between IgE levels and blood eosinophil counts (r = 0.33, P < .001); furthermore, all
253 a levels correlated positively with absolute eosinophil counts (r = 0.69, P < .001), suggesting modul
254 inical development program showed that blood eosinophil counts, rather than sputum or tissue eosinoph
255 weak but significant association with sputum eosinophil counts (receiver operating characteristic are
256 d reduced bronchoalveolar lavage (BAL) fluid eosinophil counts, reduced airway resistance in response
258 (worsening of HES-related symptoms or blood eosinophil count requiring therapeutic escalation) in th
259 risons of symptoms, lung function, and blood eosinophil counts revealed differences that were more pr
260 ho = 0.48), C-reactive-protein (rho = 0.43), eosinophil counts (rho = -0.45), and serum albumin (rho
261 EC) in the first 24 hours posttreatment, the eosinophil count rose significantly in both groups, peak
264 antly greater than AUCs for peripheral blood eosinophil counts, sputum neutrophil counts, and combine
265 ry end points included changes in esophageal eosinophil counts, symptoms assessed by questionnaire sc
268 tly higher total IgE levels and higher blood eosinophil counts than those with the lower-risk genotyp
269 neutrophilia, and despite the wide range in eosinophil counts, the T(H)2 mediators that are thought
271 gies may be effective in reducing esophageal eosinophil counts to <15 per high-power field over a sho
272 orticosteroids effectively reduce esophageal eosinophil counts to <15 per high-power field over a sho
275 lesions, treatment of rash, peripheral blood eosinophil count, tumor response, and skin histologic ch
276 f IL-6 (non-Type 2 asthma) and FeNO or blood eosinophil count (Type 2 asthma) identified asthma endot
277 e mean percentage change in gastrointestinal eosinophil count was -86% in the combined AK002 group, a
280 um of up to 4 days) on days when their blood eosinophil count was at least 0.3 x 10(9) cells per L.
282 riod, a treatment based on the last measured eosinophil count was prescribed for the remaining days w
284 DSQ scores were 29.3 and 29.0, and mean peak eosinophil counts were 156 and 130 per hpf in the BOS an
285 DSQ scores were 15.0 and 21.5, and mean peak eosinophil counts were 39 and 113 per high-power field,
286 ine to the end of therapy in peak esophageal eosinophil counts were 59%, 67%, 64%, and 24% in the 1,
288 ionships with pulmonary function testing and eosinophil counts were assessed by using Pearson correla
291 score was reduced by 0.47 points, and blood eosinophil counts were reduced by 78%, with similar impr
292 f gastric biopsy specimens, as well as blood eosinophil counts, were analyzed in patients with EG and
294 t positive association with the linear blood eosinophil count, whereas in U-BIOPRED, 1197 genes showe
295 hilic inflammation, some have an increase in eosinophil counts, which might be orchestrated by TH2 ce
296 b in patients with asthma and elevated blood eosinophil counts who are inadequately controlled on inh
297 he T2 phenotype was defined by using a blood eosinophil count with a threshold of 300 cells/muL.
298 protocol presented a significant increase in eosinophil counts with increased extracellular DNA in br
299 mined, patients with elevated baseline blood eosinophil counts, with three or more exacerbations in t
300 whether patients with COPD with higher blood eosinophil counts would be more likely to have exacerbat