{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,6]],"date-time":"2026-10-06T13:57:48Z","timestamp":1791295068421,"version":"4.1.0"},"reference-count":31,"publisher":"Wiley","issue":"7","license":[{"start":{"date-parts":[[2010,3,24]],"date-time":"2010-03-24T00:00:00Z","timestamp":1269388800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["American J Hematol"],"published-print":{"date-parts":[[2010,7]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Hyperferritinemia occurs in Gaucher disease but its clinical spectrum or its association with systemic iron overload and <jats:italic>HFE<\/jats:italic> mutations are not known. In 114 patients with Type 1 Gaucher disease, we determined serum ferritin, transferrin saturation and <jats:italic>HFE<\/jats:italic> genotype. The results were correlated with the extent of hepatosplenomegaly, overall Gaucher disease severity score index, and response to enzyme replacement therapy. In a subset of patients with radiological and\/or laboratory evidence of systemic iron overload, liver biopsy was performed. There was a mean 3.7\u2010fold elevation of serum ferritin over the upper limit of normal (ULN). Prior splenectomy was associated with most severe hyperferritinemia compared to patients with intact spleen (6.53 \u00d7 ULN vs. 2.69 \u00d7 ULN, <jats:italic>P<\/jats:italic> = 0.003). <jats:italic>HFE<\/jats:italic> genotyping revealed two patients homozygous for H63D mutation and 30% of patients heterozygote carriers of <jats:italic>H63D<\/jats:italic> mutation; no patients harbored <jats:italic>C282Y<\/jats:italic> mutation; there was no correlation of ferritin with <jats:italic>HFE<\/jats:italic> genotype. Ferritin level correlated with liver volume (Pearson correlation coefficient = 0.254, <jats:italic>P<\/jats:italic> = 0.035) and it was negatively correlated with hemoglobin (<jats:italic>r<\/jats:italic> = \u22120.315, <jats:italic>P<\/jats:italic> = 0.004); there was no relationship with other indicators of Gaucher disease activity. Enzyme replacement therapy (ERT) resulted in amelioration of hyperferritinemia: 707 \u00b1 898 ng\/ml vs. 301 \u00b1 310 ng\/ml (<jats:italic>P<\/jats:italic> = 0.001), transferrin saturation remained normal. Three patients were suspected of clinical iron overload, confirmed on liver biopsy. Iron accumulation was variably noted in hepatocytes and Kupffer cells. There is a high prevalence of hyperferritinemia in Type 1 Gaucher disease that is associated with indicators of disease severity, reversed by ERT and is not related to <jats:italic>HFE<\/jats:italic> mutations. Am. J. Hematol. 2010. \u00a9 2010 Wiley\u2010Liss, Inc.<\/jats:p>","DOI":"10.1002\/ajh.21721","type":"journal-article","created":{"date-parts":[[2010,3,25]],"date-time":"2010-03-25T04:31:57Z","timestamp":1269491517000},"page":"472-476","source":"Crossref","is-referenced-by-count":68,"title":["Hyperferritinemia and iron overload in type 1 Gaucher disease"],"prefix":"10.1002","volume":"85","author":[{"given":"Philip","family":"Stein","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Hannah","family":"Yu","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Dhanpat","family":"Jain","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Pramod K.","family":"Mistry","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2010,6,23]]},"reference":[{"key":"e_1_2_1_2_2","doi-asserted-by":"publisher","DOI":"10.1016\/S0140-6736(08)61522-6"},{"key":"e_1_2_1_3_2","first-page":"659","article-title":"Gaucher's disease: Clinical features and natural history","volume":"10","author":"Cox TM","year":"1997","journal-title":"Bailliere's Clin Haematol"},{"key":"e_1_2_1_4_2","doi-asserted-by":"publisher","DOI":"10.1016\/j.ymgme.2004.08.015"},{"key":"e_1_2_1_5_2","doi-asserted-by":"publisher","DOI":"10.1111\/j.1651-2227.2005.tb02110.x"},{"key":"e_1_2_1_6_2","doi-asserted-by":"publisher","DOI":"10.1093\/qjmed\/90.1.19"},{"key":"e_1_2_1_7_2","doi-asserted-by":"publisher","DOI":"10.1136\/bmj.286.6381.1864"},{"key":"e_1_2_1_8_2","doi-asserted-by":"publisher","DOI":"10.1006\/bcmd.1995.0012"},{"key":"e_1_2_1_9_2","doi-asserted-by":"publisher","DOI":"10.1002\/ajh.20908"},{"key":"e_1_2_1_10_2","doi-asserted-by":"publisher","DOI":"10.1002\/ajh.21362"},{"key":"e_1_2_1_11_2","doi-asserted-by":"publisher","DOI":"10.1074\/jbc.M301804200"},{"key":"e_1_2_1_12_2","doi-asserted-by":"publisher","DOI":"10.1016\/j.cca.2007.02.042"},{"key":"e_1_2_1_13_2","doi-asserted-by":"publisher","DOI":"10.1016\/S0074-7696(06)52001-7"},{"key":"e_1_2_1_14_2","doi-asserted-by":"publisher","DOI":"10.1182\/blood-2003-05-1612"},{"key":"e_1_2_1_15_2","doi-asserted-by":"publisher","DOI":"10.1001\/archinte.158.16.1754"},{"key":"e_1_2_1_16_2","doi-asserted-by":"publisher","DOI":"10.1097\/00005792-199211000-00002"},{"key":"e_1_2_1_17_2","doi-asserted-by":"publisher","DOI":"10.1056\/NEJM199909023411002"},{"key":"e_1_2_1_18_2","doi-asserted-by":"publisher","DOI":"10.1002\/path.1700840107"},{"key":"e_1_2_1_19_2","doi-asserted-by":"publisher","DOI":"10.1002\/hep.1840170107"},{"key":"e_1_2_1_20_2","doi-asserted-by":"publisher","DOI":"10.1006\/bcmd.2002.0511"},{"key":"e_1_2_1_21_2","doi-asserted-by":"publisher","DOI":"10.1007\/s10545-005-4416-9"},{"key":"e_1_2_1_22_2","doi-asserted-by":"publisher","DOI":"10.1016\/0002-9343(67)90070-8"},{"key":"e_1_2_1_23_2","first-page":"404","article-title":"Adult\u2010type Gaucher's disease: A secondary disorder of iron metabolism","volume":"37","author":"Lorber M","year":"1970","journal-title":"Mt Sinai J Med"},{"key":"e_1_2_1_24_2","doi-asserted-by":"publisher","DOI":"10.1056\/NEJM197408012910521"},{"key":"e_1_2_1_25_2","doi-asserted-by":"publisher","DOI":"10.1146\/annurev.pathol.4.110807.092205"},{"key":"e_1_2_1_26_2","doi-asserted-by":"publisher","DOI":"10.1172\/JCI0214530"},{"key":"e_1_2_1_27_2","doi-asserted-by":"publisher","DOI":"10.1016\/j.bcmd.2005.07.006"},{"key":"e_1_2_1_28_2","doi-asserted-by":"publisher","DOI":"10.1007\/BF00441877"},{"key":"e_1_2_1_29_2","doi-asserted-by":"publisher","DOI":"10.1182\/blood.V96.1.76"},{"key":"e_1_2_1_30_2","unstructured":"ICGG Annual Report 2009. Available athttp:\/\/www.lsdregistry.net\/gaucherregistry."},{"key":"e_1_2_1_31_2","doi-asserted-by":"publisher","DOI":"10.1016\/S0002-9343(02)01150-6"},{"key":"e_1_2_1_32_2","doi-asserted-by":"publisher","DOI":"10.1182\/blood-2004-01-0177"}],"container-title":["American Journal of Hematology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1002%2Fajh.21721","content-type":"unspecified","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1002\/ajh.21721","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,11,22]],"date-time":"2023-11-22T03:23:05Z","timestamp":1700623385000},"score":1,"resource":{"primary":{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/ajh.21721"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2010,6,23]]},"references-count":31,"journal-issue":{"issue":"7","published-print":{"date-parts":[[2010,7]]}},"alternative-id":["10.1002\/ajh.21721"],"URL":"https:\/\/doi.org\/10.1002\/ajh.21721","archive":["Portico"],"relation":{},"ISSN":["0361-8609","1096-8652"],"issn-type":[{"value":"0361-8609","type":"print"},{"value":"1096-8652","type":"electronic"}],"subject":[],"published":{"date-parts":[[2010,6,23]]}}}