{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,1]],"date-time":"2026-09-01T12:05:07Z","timestamp":1788264307302,"version":"build-2803163510"},"reference-count":19,"publisher":"Wiley","issue":"2","license":[{"start":{"date-parts":[[2013,6,28]],"date-time":"2013-06-28T00:00:00Z","timestamp":1372377600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["European J of Haematology"],"published-print":{"date-parts":[[2013,8]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:p>\n                    Systemic mastocytosis (\n                    <jats:styled-content style=\"fixed-case\">SM<\/jats:styled-content>\n                    ) is characterized by the growth of neoplastic mast cells (\n                    <jats:styled-content style=\"fixed-case\">MC<\/jats:styled-content>\n                    s). Most adults with indolent\n                    <jats:styled-content style=\"fixed-case\">SM<\/jats:styled-content>\n                    carry the\n                    <jats:italic>\n                      <jats:styled-content style=\"fixed-case\">KIT<\/jats:styled-content>\n                    <\/jats:italic>\n                    D816V mutation. We recently introduced the D816V+ allele fraction as a disease marker in\n                    <jats:styled-content style=\"fixed-case\">SM<\/jats:styled-content>\n                    using a sensitive and quantitative\n                    <jats:italic>\n                      <jats:styled-content style=\"fixed-case\">KIT<\/jats:styled-content>\n                    <\/jats:italic>\n                    D816V mutation analysis that consistently allows mutation detection in peripheral blood (\n                    <jats:styled-content style=\"fixed-case\">PB<\/jats:styled-content>\n                    ) and bone marrow (\n                    <jats:styled-content style=\"fixed-case\">BM<\/jats:styled-content>\n                    ). The D816V+ allele fraction represents a quantitative measure which allows\n                    <jats:italic>\n                      <jats:styled-content style=\"fixed-case\">KIT<\/jats:styled-content>\n                    <\/jats:italic>\n                    D816V\u2010positivity to be analyzed as a continuous variable instead of a categorical variable (negative\/positive) as previously described. Serum tryptase represents an established disease marker in\n                    <jats:styled-content style=\"fixed-case\">SM<\/jats:styled-content>\n                    , and it remains to be tested whether tryptase and the D816V+ allele fraction are associated or represent independent disease markers. In this study, correlation analysis between serum tryptase, the D816V+ allele fraction in\n                    <jats:styled-content style=\"fixed-case\">PB<\/jats:styled-content>\n                    and\n                    <jats:styled-content style=\"fixed-case\">BM<\/jats:styled-content>\n                    , and the\n                    <jats:styled-content style=\"fixed-case\">MC<\/jats:styled-content>\n                    fraction was performed in 57 indolent systemic mastocytosis (\n                    <jats:styled-content style=\"fixed-case\">ISM<\/jats:styled-content>\n                    ) patients. We detected significant correlations between the D816V+ allele fraction, the mature neoplastic\n                    <jats:styled-content style=\"fixed-case\">MC<\/jats:styled-content>\n                    fraction, and serum tryptase which represent three different biological measures of disease burden. Mutation analysis was performed in two or more\n                    <jats:styled-content style=\"fixed-case\">PB<\/jats:styled-content>\n                    samples in 39 patients, and the results demonstrated high stability with no overall tendency to increasing D816V+ allele fractions over time. Considerable variation was nevertheless observed in the correlation analyses. Serum tryptase reflects the mature\n                    <jats:styled-content style=\"fixed-case\">MC<\/jats:styled-content>\n                    load, whereas the D816V+ allele fraction includes cells other than mature\n                    <jats:styled-content style=\"fixed-case\">MC<\/jats:styled-content>\n                    s to a variable extent. We conclude that tryptase and the D816V+ allele fraction represent different, although correlated, measures of disease status in\n                    <jats:styled-content style=\"fixed-case\">SM<\/jats:styled-content>\n                    .\n                  <\/jats:p>","DOI":"10.1111\/ejh.12128","type":"journal-article","created":{"date-parts":[[2013,4,27]],"date-time":"2013-04-27T10:00:48Z","timestamp":1367056848000},"page":"106-111","source":"Crossref","is-referenced-by-count":26,"title":["Serum tryptase correlates with the\n                    <i>\n                      <scp>KIT<\/scp>\n                    <\/i>\n                    D816V mutation burden in adults with indolent systemic mastocytosis"],"prefix":"10.1111","volume":"91","author":[{"given":"Thomas","family":"Kristensen","sequence":"first","affiliation":[{"name":"Department of Pathology Odense University Hospital Odense Denmark"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sigurd","family":"Broesby\u2010Olsen","sequence":"additional","affiliation":[{"name":"Department of Dermatology and Allergy Centre Odense University Hospital Odense Denmark"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Hanne","family":"Vestergaard","sequence":"additional","affiliation":[{"name":"Department of Haematology Odense University Hospital Odense Denmark"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Carsten","family":"Bindslev\u2010Jensen","sequence":"additional","affiliation":[{"name":"Department of Dermatology and Allergy Centre Odense University Hospital Odense Denmark"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Michael Boe","family":"M\u00f8ller","sequence":"additional","affiliation":[{"name":"Department of Pathology Odense University Hospital Odense Denmark"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"name":"the Mastocytosis Centre Odense University Hospital (MastOUH)","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2013,6,28]]},"reference":[{"key":"e_1_2_5_2_1","first-page":"54","volume-title":"WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues","author":"Horny 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