{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,10]],"date-time":"2026-09-10T17:41:48Z","timestamp":1789062108434,"version":"build-2803163510"},"reference-count":30,"publisher":"Wiley","issue":"5","license":[{"start":{"date-parts":[[2012,3,22]],"date-time":"2012-03-22T00:00:00Z","timestamp":1332374400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Allergy"],"published-print":{"date-parts":[[2012,5]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:sec>\n                    <jats:title>Background<\/jats:title>\n                    <jats:p>\n                      Risk indicators of indolent systemic mastocytosis (\n                      <jats:styled-content style=\"fixed-case\">ISM<\/jats:styled-content>\n                      ) in adults with clinical suspicion of\n                      <jats:styled-content style=\"fixed-case\">ISM<\/jats:styled-content>\n                      without accompanying skin lesions [urticaria pigmentosa (\n                      <jats:styled-content style=\"fixed-case\">UP<\/jats:styled-content>\n                      )] are lacking. This study aimed at creating a decision tree using clinical characteristics, serum tryptase, and the urinary histamine metabolites methylimidazole acetic acid (\n                      <jats:styled-content style=\"fixed-case\">MIMA<\/jats:styled-content>\n                      ) and methylhistamine (\n                      <jats:styled-content style=\"fixed-case\">MH<\/jats:styled-content>\n                      ) to select patients for bone marrow investigations to diagnose\n                      <jats:styled-content style=\"fixed-case\">ISM<\/jats:styled-content>\n                      .\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>\n                      Retrospective data analysis of all adults, in whom bone marrow investigations were performed to diagnose\n                      <jats:styled-content style=\"fixed-case\">ISM<\/jats:styled-content>\n                      , was carried out.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      In total, 142 patients were included.\n                      <jats:styled-content style=\"fixed-case\">SM<\/jats:styled-content>\n                      was absent in all 44 patients with tryptase &lt;10\u00a0\u03bcg\/l, in 45 of 98 (46%) patients with tryptase \u226510\u00a0\u03bcg\/l and in 18 of 52 patients (35%) with tryptase &gt;20\u00a0\u03bcg\/l. Above 43\u00a0\u03bcg\/l, all patients had\n                      <jats:styled-content style=\"fixed-case\">ISM<\/jats:styled-content>\n                      (\n                      <jats:italic>n<\/jats:italic>\n                      \u00a0=\u00a011). Male gender, insect venom anaphylaxis as presenting symptom, tryptase,\n                      <jats:styled-content style=\"fixed-case\">MIMA<\/jats:styled-content>\n                      , and\n                      <jats:styled-content style=\"fixed-case\">MH<\/jats:styled-content>\n                      were independent\n                      <jats:styled-content style=\"fixed-case\">ISM<\/jats:styled-content>\n                      predictors. If tryptase was \u226510\u00a0\u03bcg\/l, the diagnostic accuracy of\n                      <jats:styled-content style=\"fixed-case\">MIMA<\/jats:styled-content>\n                      and\n                      <jats:styled-content style=\"fixed-case\">MH<\/jats:styled-content>\n                      was high (areas under the\n                      <jats:styled-content style=\"fixed-case\">ROC<\/jats:styled-content>\n                      curve 0.92).\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>\n                      In suspected patients without\n                      <jats:styled-content style=\"fixed-case\">UP<\/jats:styled-content>\n                      , the\n                      <jats:styled-content style=\"fixed-case\">ISM<\/jats:styled-content>\n                      risk is very low (if present at all) if tryptase is &lt;10\u00a0\u03bcg\/l. If tryptase is \u226510\u00a0\u03bcg\/l, this risk depends on\n                      <jats:styled-content style=\"fixed-case\">MIMA<\/jats:styled-content>\n                      and\n                      <jats:styled-content style=\"fixed-case\">MH<\/jats:styled-content>\n                      , being low if these are normal, but high if these are elevated. Male gender and insect venom anaphylaxis are additional risk indicators. We recommend refraining from bone marrow examinations in suspected patients without\n                      <jats:styled-content style=\"fixed-case\">UP<\/jats:styled-content>\n                      if tryptase is &lt;10\u00a0\u03bcg\/l. Our results question the reliability of the minor diagnostic\n                      <jats:styled-content style=\"fixed-case\">W<\/jats:styled-content>\n                      orld\n                      <jats:styled-content style=\"fixed-case\">H<\/jats:styled-content>\n                      ealth\n                      <jats:styled-content style=\"fixed-case\">O<\/jats:styled-content>\n                      rganization criterion of tryptase &gt;20\u00a0\u03bcg\/l.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1111\/j.1398-9995.2012.02809.x","type":"journal-article","created":{"date-parts":[[2012,3,23]],"date-time":"2012-03-23T02:38:44Z","timestamp":1332470324000},"page":"683-690","source":"Crossref","is-referenced-by-count":57,"title":["Tryptase and histamine metabolites as diagnostic indicators of indolent systemic mastocytosis without skin lesions"],"prefix":"10.1111","volume":"67","author":[{"given":"J. J.","family":"van Doormaal","sequence":"first","affiliation":[{"name":"Departments of Allergology University Medical Center Groningen University of Groningen Groningen The Netherlands"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"E.","family":"van der Veer","sequence":"additional","affiliation":[{"name":"Department of Laboratory Medicine University Medical Center Groningen University of Groningen Groningen The Netherlands"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"P. C.","family":"van Voorst Vader","sequence":"additional","affiliation":[{"name":"Department of Dermatology University Medical Center Groningen University of Groningen Groningen The Netherlands"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"P. M.","family":"Kluin","sequence":"additional","affiliation":[{"name":"Department of Pathology University Medical Center Groningen University of Groningen Groningen The Netherlands"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"A. B.","family":"Mulder","sequence":"additional","affiliation":[{"name":"Department of Laboratory Medicine University Medical Center Groningen University of Groningen Groningen The Netherlands"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"S.","family":"van der Heide","sequence":"additional","affiliation":[{"name":"Department of Laboratory Medicine University Medical Center Groningen University of Groningen Groningen The Netherlands"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"S.","family":"Arends","sequence":"additional","affiliation":[{"name":"Department of Reumatology and Clinical Immunology University Medical Center Groningen University of Groningen Groningen The Netherlands"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"J. C.","family":"Kluin\u2010Nelemans","sequence":"additional","affiliation":[{"name":"Department of Hematology University Medical Center Groningen University of Groningen Groningen the Netherlands"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"J. N. G.","family":"Oude Elberink","sequence":"additional","affiliation":[{"name":"Departments of Allergology University Medical Center Groningen University of Groningen Groningen The Netherlands"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"J. G. 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