{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,16]],"date-time":"2026-10-16T18:31:49Z","timestamp":1792175509156,"version":"4.4.0"},"reference-count":32,"publisher":"Elsevier BV","issue":"4","license":[{"start":{"date-parts":[[2018,7,1]],"date-time":"2018-07-01T00:00:00Z","timestamp":1530403200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2018,7,1]],"date-time":"2018-07-01T00:00:00Z","timestamp":1530403200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2020,7,1]],"date-time":"2020-07-01T00:00:00Z","timestamp":1593561600000},"content-version":"vor","delay-in-days":731,"URL":"http:\/\/www.elsevier.com\/open-access\/userlicense\/1.0\/"}],"funder":[{"DOI":"10.13039\/100000002","name":"NIH","doi-asserted-by":"publisher","award":["R01DK072126"],"award-info":[{"award-number":["R01DK072126"]}],"id":[{"id":"10.13039\/100000002","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100000002","name":"NIH","doi-asserted-by":"publisher","award":["R01DK034108"],"award-info":[{"award-number":["R01DK034108"]}],"id":[{"id":"10.13039\/100000002","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100000897","name":"Cystic Fibrosis Foundation","doi-asserted-by":"publisher","award":["SANDERS11A0"],"award-info":[{"award-number":["SANDERS11A0"]}],"id":[{"id":"10.13039\/100000897","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["clinicalkey.com","clinicalkey.com.au","clinicalkey.es","clinicalkey.fr","clinicalkey.jp","cysticfibrosisjournal.com","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Journal of Cystic Fibrosis"],"published-print":{"date-parts":[[2018,7]]},"DOI":"10.1016\/j.jcf.2018.01.006","type":"journal-article","created":{"date-parts":[[2018,2,1]],"date-time":"2018-02-01T20:41:47Z","timestamp":1517517707000},"page":"528-535","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":49,"title":["Early life growth patterns persist for 12\u202fyears and impact pulmonary outcomes in cystic fibrosis"],"prefix":"10.1016","volume":"17","author":[{"given":"Don B.","family":"Sanders","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Zhumin","family":"Zhang","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Philip M.","family":"Farrell","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"HuiChuan J.","family":"Lai","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"issue":"6","key":"10.1016\/j.jcf.2018.01.006_bb0005","doi-asserted-by":"crossref","first-page":"583","DOI":"10.1016\/0895-4356(88)90063-7","article-title":"A comparison of survival, growth, and pulmonary function in patients with cystic fibrosis in Boston and Toronto","volume":"41","author":"Corey","year":"1988","journal-title":"J Clin Epidemiol"},{"issue":"3","key":"10.1016\/j.jcf.2018.01.006_bb0010","doi-asserted-by":"crossref","first-page":"276","DOI":"10.1002\/ppul.20162","article-title":"Association of body composition and lung function in children with cystic fibrosis","volume":"39","author":"Pedreira","year":"2005","journal-title":"Pediatr Pulmonol"},{"issue":"2","key":"10.1016\/j.jcf.2018.01.006_bb0015","doi-asserted-by":"crossref","first-page":"134","DOI":"10.1016\/j.jpeds.2007.03.006","article-title":"Risk factors for rate of decline in forced expiratory volume in one second in children and adolescents with cystic fibrosis","volume":"151","author":"Konstan","year":"2007","journal-title":"J Pediatr"},{"issue":"3","key":"10.1016\/j.jcf.2018.01.006_bb0020","doi-asserted-by":"crossref","first-page":"374","DOI":"10.1067\/mpd.2000.107891","article-title":"Longitudinal relationship among growth, nutritional status, and pulmonary function in children with cystic fibrosis: analysis of the Cystic Fibrosis Foundation National CF Patient Registry","volume":"137","author":"Zemel","year":"2000","journal-title":"J Pediatr"},{"issue":"3","key":"10.1016\/j.jcf.2018.01.006_bb0025","doi-asserted-by":"crossref","first-page":"588","DOI":"10.1542\/peds.112.3.588","article-title":"Longitudinal changes in growth parameters are correlated with changes in pulmonary function in children with cystic fibrosis","volume":"112","author":"Peterson","year":"2003","journal-title":"Pediatrics"},{"issue":"1","key":"10.1016\/j.jcf.2018.01.006_bb0030","doi-asserted-by":"crossref","first-page":"63","DOI":"10.1513\/AnnalsATS.201309-303OC","article-title":"Risk factors for the progression of cystic fibrosis lung disease throughout childhood","volume":"11","author":"Sanders","year":"2014","journal-title":"Ann Am Thorac Soc"},{"issue":"6","key":"10.1016\/j.jcf.2018.01.006_bb0035","doi-asserted-by":"crossref","first-page":"624","DOI":"10.1067\/mpd.2003.152","article-title":"Growth and nutritional indexes in early life predict pulmonary function in cystic fibrosis","volume":"142","author":"Konstan","year":"2003","journal-title":"J Pediatr"},{"issue":"2","key":"10.1016\/j.jcf.2018.01.006_bb0040","doi-asserted-by":"crossref","first-page":"714","DOI":"10.1542\/peds.2007-3089","article-title":"Recovery of birth weight z score within 2\u202fyears of diagnosis is positively associated with pulmonary status at 6\u202fyears of age in children with cystic fibrosis","volume":"123","author":"Lai","year":"2009","journal-title":"Pediatrics"},{"issue":"5","key":"10.1016\/j.jcf.2018.01.006_bb0045","doi-asserted-by":"crossref","first-page":"1081","DOI":"10.1016\/j.jpeds.2015.07.044","article-title":"Early life growth trajectories in cystic fibrosis are associated with pulmonary function at age 6\u202fyears","volume":"167","author":"Sanders","year":"2015","journal-title":"J Pediatr"},{"issue":"5","key":"10.1016\/j.jcf.2018.01.006_bb0050","doi-asserted-by":"crossref","first-page":"832","DOI":"10.1016\/j.jada.2008.02.020","article-title":"Evidence-based practice recommendations for nutrition-related management of children and adults with cystic fibrosis and pancreatic insufficiency: results of a systematic review","volume":"108","author":"Stallings","year":"2008","journal-title":"J Am Diet Assoc"},{"issue":"14","key":"10.1016\/j.jcf.2018.01.006_bb0055","doi-asserted-by":"crossref","first-page":"963","DOI":"10.1056\/NEJM199710023371403","article-title":"Nutritional benefits of neonatal screening for cystic fibrosis","volume":"337","author":"Farrell","year":"1997","journal-title":"N Engl J Med"},{"issue":"1","key":"10.1016\/j.jcf.2018.01.006_bb0060","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1542\/peds.107.1.1","article-title":"Early diagnosis of cystic fibrosis through neonatal screening prevents severe malnutrition and improves long-term growth","volume":"107","author":"Farrell","year":"2001","journal-title":"Pediatrics"},{"key":"10.1016\/j.jcf.2018.01.006_bb0065","first-page":"79","article-title":"Improving the health of patients with cystic fibrosis through newborn screening","volume":"47","author":"Farrell","year":"2000","journal-title":"Adv Pediatr Infect Dis"},{"issue":"6","key":"10.1016\/j.jcf.2018.01.006_bb0070","doi-asserted-by":"crossref","first-page":"723","DOI":"10.1016\/j.jcf.2014.05.009","article-title":"Early attained weight and length predict growth faltering better than velocity measures in infants with CF","volume":"13","author":"Heltshe","year":"2014","journal-title":"J Cyst Fibros"},{"issue":"2","key":"10.1016\/j.jcf.2018.01.006_bb0075","doi-asserted-by":"crossref","first-page":"391","DOI":"10.1542\/peds.2004-2832","article-title":"Temporal associations among energy intake, plasma linoleic acid, and growth improvement in response to treatment initiation after diagnosis of cystic fibrosis","volume":"117","author":"Shoff","year":"2006","journal-title":"Pediatrics"},{"issue":"8","key":"10.1016\/j.jcf.2018.01.006_bb0080","first-page":"415","article-title":"Newborn screening for cystic fibrosis in Wisconsin: first application of population-based molecular genetics testing","volume":"93","author":"Farrell","year":"1994","journal-title":"Wis Med J"},{"key":"10.1016\/j.jcf.2018.01.006_bb0085","first-page":"1","article-title":"2000 CDC growth charts for the United States: methods and development","volume":"246","author":"Kuczmarski","year":"2002","journal-title":"Vital Health Stat"},{"issue":"RR-9","key":"10.1016\/j.jcf.2018.01.006_bb0090","first-page":"1","article-title":"Use of World Health Organization and CDC growth charts for children aged 0\u201359 months in the United States","volume":"59","author":"Grummer-Strawn","year":"2010","journal-title":"MMWR Recomm Rep"},{"issue":"3","key":"10.1016\/j.jcf.2018.01.006_bb0095","doi-asserted-by":"crossref","first-page":"e827","DOI":"10.1542\/peds.2011-3552","article-title":"Breastfeeding and the use of human milk","volume":"129","author":"American Acedemy of Pediatrics","year":"2012","journal-title":"Pediatrics"},{"issue":"5","key":"10.1016\/j.jcf.2018.01.006_bb0100","doi-asserted-by":"crossref","first-page":"1089","DOI":"10.1016\/j.jpeds.2015.07.036","article-title":"Comparing the use of Centers for Disease Control and Prevention and World Health Organization growth charts in children with cystic fibrosis through 2\u202fyears of age","volume":"167","author":"Zhang","year":"2015","journal-title":"J Pediatr"},{"key":"10.1016\/j.jcf.2018.01.006_bb0105","doi-asserted-by":"crossref","first-page":"64","DOI":"10.1002\/ppul.1950110713","article-title":"Growth evaluation at one year of life in infants with cystic fibrosis diagnosed by neonatal screening","volume":"7","author":"Pederzini","year":"1991","journal-title":"Pediatr Pulmonol"},{"issue":"4","key":"10.1016\/j.jcf.2018.01.006_bb0110","doi-asserted-by":"crossref","first-page":"533","DOI":"10.1016\/S0022-3476(05)82478-3","article-title":"Pancreatic insufficiency, growth, and nutrition in infants identified by newborn screening as having cystic fibrosis","volume":"120","author":"Bronstein","year":"1992","journal-title":"J Pediatr"},{"issue":"3","key":"10.1016\/j.jcf.2018.01.006_bb0115","doi-asserted-by":"crossref","first-page":"578","DOI":"10.1093\/ajcn\/54.3.578","article-title":"Nutritional status of infants with cystic fibrosis associated with early diagnosis and intervention","volume":"54","author":"Marcus","year":"1991","journal-title":"Am J Clin Nutr"},{"issue":"3","key":"10.1016\/j.jcf.2018.01.006_bb0120","doi-asserted-by":"crossref","first-page":"478","DOI":"10.1016\/S0022-3476(98)70024-1","article-title":"Growth status in children with cystic fibrosis based on the National Cystic Fibrosis Patient Registry data: evaluation of various criteria used to identify malnutrition","volume":"132","author":"Lai","year":"1998","journal-title":"J Pediatr"},{"issue":"3","key":"10.1016\/j.jcf.2018.01.006_bb0125","doi-asserted-by":"crossref","first-page":"230","DOI":"10.1002\/ppul.10336","article-title":"Longitudinal evaluation of bronchopulmonary disease in children with cystic fibrosis","volume":"36","author":"Farrell","year":"2003","journal-title":"Pediatr Pulmonol"},{"issue":"2","key":"10.1016\/j.jcf.2018.01.006_bb0130","doi-asserted-by":"crossref","first-page":"75","DOI":"10.1002\/ppul.1950150204","article-title":"Pulmonary function between 6 and 18\u202fyears of age","volume":"15","author":"Wang","year":"1993","journal-title":"Pediatr Pulmonol"},{"issue":"1","key":"10.1016\/j.jcf.2018.01.006_bb0135","doi-asserted-by":"crossref","first-page":"24","DOI":"10.1542\/peds.63.1.24","article-title":"The chest roentgenogram in cystic fibrosis: a new scoring system","volume":"63","author":"Brasfield","year":"1979","journal-title":"Pediatrics"},{"issue":"2","key":"10.1016\/j.jcf.2018.01.006_bb0140","doi-asserted-by":"crossref","first-page":"488","DOI":"10.1542\/peds.91.2.488","article-title":"Wisconsin cystic fibrosis chest radiograph scoring system","volume":"91","author":"Weatherly","year":"1993","journal-title":"Pediatrics"},{"issue":"6","key":"10.1016\/j.jcf.2018.01.006_bb0145","doi-asserted-by":"crossref","first-page":"457","DOI":"10.1002\/(SICI)1099-0496(200006)29:6<457::AID-PPUL8>3.0.CO;2-9","article-title":"Wisconsin cystic fibrosis chest radiograph scoring system: validation and standardization for application to longitudinal studies","volume":"29","author":"Koscik","year":"2000","journal-title":"Pediatr Pulmonol"},{"issue":"1 Pt 1","key":"10.1016\/j.jcf.2018.01.006_bb0150","doi-asserted-by":"crossref","first-page":"53","DOI":"10.1542\/peds.105.1.53","article-title":"Nutritional status of patients with cystic fibrosis with meconium ileus: a comparison with patients without meconium ileus and diagnosed early through neonatal screening","volume":"105","author":"Lai","year":"2000","journal-title":"Pediatrics"},{"issue":"3","key":"10.1016\/j.jcf.2018.01.006_bb0155","first-page":"246","article-title":"Consensus report on nutrition for pediatric patients with cystic fibrosis","volume":"35","author":"Borowitz","year":"2002","journal-title":"J Pediatr Gastroenterol Nutr"},{"issue":"6 Suppl","key":"10.1016\/j.jcf.2018.01.006_bb0160","doi-asserted-by":"crossref","first-page":"S73","DOI":"10.1016\/j.jpeds.2009.09.001","article-title":"Cystic Fibrosis Foundation evidence-based guidelines for management of infants with cystic fibrosis","volume":"155","author":"Borowitz","year":"2009","journal-title":"J Pediatr"}],"container-title":["Journal of Cystic Fibrosis"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1569199318300092?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1569199318300092?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,10,27]],"date-time":"2025-10-27T21:39:09Z","timestamp":1761601149000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1569199318300092"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2018,7]]},"references-count":32,"journal-issue":{"issue":"4","published-print":{"date-parts":[[2018,7]]}},"alternative-id":["S1569199318300092"],"URL":"https:\/\/doi.org\/10.1016\/j.jcf.2018.01.006","relation":{},"ISSN":["1569-1993"],"issn-type":[{"value":"1569-1993","type":"print"}],"subject":[],"published":{"date-parts":[[2018,7]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Early life growth patterns persist for 12\u202fyears and impact pulmonary outcomes in cystic fibrosis","name":"articletitle","label":"Article Title"},{"value":"Journal of Cystic Fibrosis","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.jcf.2018.01.006","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2018 European Cystic Fibrosis Society. Published by Elsevier B.V.","name":"copyright","label":"Copyright"}]}}