<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Abou Alaiwa MH</submitter><funding>Howard Hughes Medical Institute</funding><funding>NIEHS NIH HHS</funding><funding>Program Project Grant</funding><funding>NHLBI NIH HHS</funding><funding>Cystic Fibrosis Foundation Research Development Program</funding><pagination>373-7</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4060428</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>13(4)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Disrupted HCO3(-) transport and reduced airway surface liquid (ASL) pH in cystic fibrosis (CF) may initiate airway disease. We hypothesized that ASL pH is reduced in neonates with CF.&lt;h4>Methods&lt;/h4>In neonates with and without CF, we measured pH of nasal ASL. We also measured nasal pH in older children and adults.&lt;h4>Results&lt;/h4>In neonates with CF, nasal ASL (pH5.2 ± 0.3) was more acidic than in non-CF neonates (pH6.4 ± 0.2). In contrast, nasal pH of CF children and adults was similar to values measured in people without CF.&lt;h4>Conclusions&lt;/h4>At an age when infection, inflammation and airway wall remodeling are minimal, neonates with CF had an acidic nasal ASL compared to babies without CF. The CF:non-CF pH difference disappeared in older individuals, perhaps because </pubmed_abstract><journal>Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society</journal><pubmed_title>Neonates with cystic fibrosis have a reduced nasal liquid pH; a small pilot study.</pubmed_title><pmcid>PMC4060428</pmcid><funding_grant_id>R458</funding_grant_id><funding_grant_id>P01 HL091842</funding_grant_id><funding_grant_id>P30 ES005605</funding_grant_id><funding_grant_id>P01 HL051670</funding_grant_id><funding_grant_id>HL51670</funding_grant_id><pubmed_authors>Abou Alaiwa MH</pubmed_authors><pubmed_authors>Launspach JL</pubmed_authors><pubmed_authors>Welsh MJ</pubmed_authors><pubmed_authors>Beer AM</pubmed_authors><pubmed_authors>Starner TD</pubmed_authors><pubmed_authors>Zabner J</pubmed_authors><pubmed_authors>Pezzulo AA</pubmed_authors><pubmed_authors>Stoltz DA</pubmed_authors><pubmed_authors>Horan RA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Neonates with cystic fibrosis have a reduced nasal liquid pH; a small pilot study.</name><description>&lt;h4>Background&lt;/h4>Disrupted HCO3(-) transport and reduced airway surface liquid (ASL) pH in cystic fibrosis (CF) may initiate airway disease. We hypothesized that ASL pH is reduced in neonates with CF.&lt;h4>Methods&lt;/h4>In neonates with and without CF, we measured pH of nasal ASL. We also measured nasal pH in older children and adults.&lt;h4>Results&lt;/h4>In neonates with CF, nasal ASL (pH5.2 ± 0.3) was more acidic than in non-CF neonates (pH6.4 ± 0.2). In contrast, nasal pH of CF children and adults was similar to values measured in people without CF.&lt;h4>Conclusions&lt;/h4>At an age when infection, inflammation and airway wall remodeling are minimal, neonates with CF had an acidic nasal ASL compared to babies without CF. The CF:non-CF pH difference disappeared in older individuals, perhaps because </description><dates><release>2014-01-01T00:00:00Z</release><publication>2014 Jul</publication><modification>2025-04-21T16:57:18.623Z</modification><creation>2019-03-27T01:30:21Z</creation></dates><accession>S-EPMC4060428</accession><cross_references><pubmed>24418186</pubmed><doi>10.1016/j.jcf.2013.12.006</doi></cross_references></HashMap>