Serum pancreatic enzymes define the pancreatic phenotype in patients with Shwachman-Diamond syndrome
- PMID: 12183724
- DOI: 10.1067/mpd.2002.125849
Serum pancreatic enzymes define the pancreatic phenotype in patients with Shwachman-Diamond syndrome
Abstract
Objective: To evaluate the role of serum enzymes for defining the pancreatic phenotype in Shwachman-Diamond syndrome (SDS), an inherited multisystem condition.
Study design: Serum pancreatic trypsinogen and isoamylase were measured in 164 patients known or presumed to have SDS. The diagnosis was confirmed in 90 patients. Among 74 unconfirmed cases, 35 ("probable SDS") had hematologic dysfunction but lacked documented pancreatic dysfunction, whereas 39 patients ("improbable SDS") lacked both documented pancreatic and hematologic dysfunction. Classification and regression tree (CART) analysis was performed in 90 patients with SDS and 134 control patients to establish a rule for defining the pancreatic phenotype of SDS; the rule was then applied to the patients with unconfirmed diagnosis.
Results: In the control patients, serum trypsinogen showed little variation with age, whereas serum isoamylase values rose from birth on, attaining adult values by 3 years. For patients with SDS, serum trypsinogen values were low in young patients and tended to increase with age, whereas serum isoamylase values remained low at all ages. The CART rule combined results from both enzymes and classified the pancreatic phenotype in all but one SDS patient, who was <3 years of age. Excluding patients <3 years of age, CART identified the pancreatic phenotype in 82% and 7% of the "probable SDS" and "improbable SDS" cases, respectively.
Conclusions: Serum pancreatic enzymes are useful for determining the pancreatic phenotype and confirming the diagnosis of SDS.
Similar articles
-
Evidence of a generalized defect of acinar cell function in Shwachman-Diamond syndrome.J Pediatr Gastroenterol Nutr. 2010 Jul;51(1):8-13. doi: 10.1097/MPG.0b013e3181d67e78. J Pediatr Gastroenterol Nutr. 2010. PMID: 20512054
-
[Serum pancreatic enzymes in the diagnosis of carcinoma of the pancreas].G Ital Oncol. 1989 Jan-Mar;9(1):7-13. G Ital Oncol. 1989. PMID: 2468605 Italian.
-
Mutation analysis of SBDS in pediatric acute myeloblastic leukemia.Pediatr Blood Cancer. 2005 Dec;45(7):920-4. doi: 10.1002/pbc.20416. Pediatr Blood Cancer. 2005. PMID: 16007594
-
Shwachman-Diamond syndrome: clinical phenotypes.Pancreatology. 2001;1(5):543-8. doi: 10.1159/000055858. Pancreatology. 2001. PMID: 12120235 Review.
-
Shwachman-Diamond syndrome.Pediatr Blood Cancer. 2005 Dec;45(7):892-901. doi: 10.1002/pbc.20478. Pediatr Blood Cancer. 2005. PMID: 16047374 Review.
Cited by
-
Predisposition to myeloid malignancies in Shwachman-Diamond syndrome: biological insights and clinical advances.Blood. 2023 Mar 30;141(13):1513-1523. doi: 10.1182/blood.2022017739. Blood. 2023. PMID: 36542827 Free PMC article. Review.
-
Sixth International Congress on Shwachman-Diamond syndrome: from patients to genes and back.Ann N Y Acad Sci. 2011 Dec;1242:26-39. doi: 10.1111/j.1749-6632.2011.06348.x. Ann N Y Acad Sci. 2011. PMID: 22191554 Free PMC article.
-
Erythrocyte adenosine deaminase: diagnostic value for Diamond-Blackfan anaemia.Br J Haematol. 2013 Feb;160(4):547-54. doi: 10.1111/bjh.12167. Epub 2012 Dec 17. Br J Haematol. 2013. PMID: 23252420 Free PMC article.
-
Clinical approach to marrow failure.Hematology Am Soc Hematol Educ Program. 2009:329-37. doi: 10.1182/asheducation-2009.1.329. Hematology Am Soc Hematol Educ Program. 2009. PMID: 20008218 Free PMC article. Review.
-
A Case of Shwachman-Diamond Syndrome who Presented with Hypotonia.J Pediatr Genet. 2018 Sep;7(3):117-121. doi: 10.1055/s-0038-1636997. Epub 2018 Mar 7. J Pediatr Genet. 2018. PMID: 30105119 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources