{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,3]],"date-time":"2026-10-03T23:49:53Z","timestamp":1791071393697,"version":"4.1.0"},"reference-count":41,"publisher":"Wiley","issue":"4","license":[{"start":{"date-parts":[[2009,1,12]],"date-time":"2009-01-12T00:00:00Z","timestamp":1231718400000},"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":[[2009,4]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:p>\n                    Mutations in GBA1 gene that encodes lysosomal glucocerebrosidase result in Type 1 Gaucher Disease (GD), the commonest lysosomal storage disorder; the most prevalent disease mutation is N370S. We investigated the heterogeneity and natural course of N370S GD in 403 patients. Demographic, clinical, and genetic characteristics of GD at presentation were examined in a cross\u2010sectional study. In addition, the relative risk (RR) of cancer in patients compared with age\u2010, sex\u2010, and ethnic\u2010group adjusted national rates of cancer was determined. Of the 403 patients, 54% of patients were homozygous (N370S\/N370S) and 46% were compound heterozygous for the N370S mutation (N370S\/other). The majority of N370S\/N370S patients displayed a phenotype characterized by late onset, predominantly skeletal disease, whereas the majority of N370S\/other patients displayed early onset, predominantly visceral\/hematologic disease,\n                    <jats:italic>P<\/jats:italic>\n                    &lt; 0.0001. There was a striking increase in lifetime risk of multiple myeloma in the entire cohort (RR 25, 95% CI 9.17\u201354.40), mostly confined to N370S homozygous patients. The risk of other hematologic malignancies (RR 3.45, 95% CI 1.49\u20136.79), and overall cancer risk (RR 1.80, 95% CI 1.32\u20132.40) was increased. Homozygous N370S GD leads to adult\u2010onset progressive skeletal disease with relative sparing of the viscera, a strikingly high risk of multiple myeloma, and an increased risk of other cancers. High incidence of gammopathy suggests an important role of the adaptive immune system in the development of GD. Adult patients with GD should be monitored for skeletal disease and cancers including multiple myeloma. Am. J. Hematol., 2009. \u00a9 2009 Wiley\u2010Liss, Inc.\n                  <\/jats:p>","DOI":"10.1002\/ajh.21362","type":"journal-article","created":{"date-parts":[[2009,1,12]],"date-time":"2009-01-12T19:26:27Z","timestamp":1231788387000},"page":"208-214","source":"Crossref","is-referenced-by-count":144,"title":["The underrecognized progressive nature of N370S Gaucher disease and assessment of cancer risk in 403 patients"],"prefix":"10.1002","volume":"84","author":[{"given":"Tamar H.","family":"Taddei","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Katherine 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