dc.contributor.author |
Boss, Marti |
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dc.contributor.author |
Rottenburger, Christof |
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dc.contributor.author |
Brenner, Winfried |
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dc.contributor.author |
Blankenstein, Oliver |
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dc.contributor.author |
Prasad, Vikas |
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dc.contributor.author |
Prasad, Sonal |
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dc.contributor.author |
de Coppi, Paolo |
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dc.contributor.author |
Kuhnen, Peter |
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dc.contributor.author |
Buitinga, Mijke |
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dc.contributor.author |
Nuutila, Pirjo |
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dc.contributor.author |
Otonkoski, Timo |
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dc.contributor.author |
Hussain, Khalid |
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dc.contributor.author |
Brom, Maarten |
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dc.contributor.author |
Eek, Annemarie |
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dc.contributor.author |
Bomanji, Jamshed |
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dc.contributor.author |
Shah, Pratik |
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dc.contributor.author |
Gotthardt, Martin |
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dc.date.accessioned |
2022-03-25T08:17:01Z |
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dc.date.available |
2022-03-25T08:17:01Z |
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dc.date.issued |
2022-02-01 |
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dc.identifier.citation |
Boss , M , Rottenburger , C , Brenner , W , Blankenstein , O , Prasad , V , Prasad , S , de Coppi , P , Kuhnen , P , Buitinga , M , Nuutila , P , Otonkoski , T , Hussain , K , Brom , M , Eek , A , Bomanji , J , Shah , P & Gotthardt , M 2022 , ' Ga-68-NODAGA-Exendin-4 PET/CT Improves the Detection of Focal Congenital Hyperinsulinism ' , The Journal of Nuclear Medicine , vol. 63 , no. 2 , pp. 310-315 . https://doi.org/10.2967/jnumed.121.262327 |
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dc.identifier.other |
PURE: 175720155 |
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dc.identifier.other |
PURE UUID: 3695c5b5-15aa-4d91-b429-1a40639e9ecc |
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dc.identifier.other |
WOS: 000749772400024 |
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dc.identifier.uri |
http://hdl.handle.net/10138/342040 |
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dc.description.abstract |
Surgery with curative intent can be offered to congenital hyperinsulinism (CHI) patients, provided that the lesion is focal. Radiolabeled exendin-4 specifically binds the glucagonlike peptide 1 receptor on pancreatic beta-cells. In this study, we compared the performance of F-18-DOPA PET/CT, the current standard imaging method for CHI, and PET/CT with the new tracer Ga-68-NODAGA-exendin-4 in the preoperative detection of focal CHI. Methods: Nineteen CHI patients underwent both F-18-DOPA PET/CT and Ga-68-NODAGA-exendin-4 PET/CT before surgery. The images were evaluated in 3 settings: a standard clinical reading, a masked expert reading, and a joint reading. The target (lesion)-to-nontarget (normal pancreas) ratio was determined using SUVmax. Image quality was rated by pediatric surgeons in a questionnaire. Results: Fourteen of 19 patients having focal lesions underwent surgery. On the basis of clinical readings, the sensitivity of Ga-68-NODAGA-exendin-4 PET/CT (100%; 95% CI, 77%-100%) was higher than that of F-18-DOPA PET/CT (71%; 95% CI, 42%-92%). Interobserver agreement between readings was higher for Ga-68-NODAGA-exendin-4 than for F-18-DOPA PET/CT (Fleiss kappa = 0.91 vs. 0.56). Ga-68-NODAGA-exendin-4 PET/CT provided significantly (P = 0.021) higher target-to-nontarget ratios (2.02 +/- 0.65) than did F-18-DOPA PET/CT (1.40 +/- 0.40). On a 5-point scale, pediatric surgeons rated Ga-68-NODAGA-exendin-4 PET/CT as superior to F-18-DOPA PET/CT. Conclusion: For the detection of focal CHI, Ga-68-NODAGA-exendin-4 PET/CT has higher clinical sensitivity and better interobserver correlation than F-18-DOPA PET/CT. Better contrast and image quality make Ga-68-NODAGA-exendin-4 PET/CT superior to F-18-DOPA PET/CT in surgeons' intraoperative quest for lesion localization. |
en |
dc.format.extent |
6 |
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dc.language.iso |
eng |
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dc.relation.ispartof |
The Journal of Nuclear Medicine |
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dc.rights |
cc_by |
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dc.rights.uri |
info:eu-repo/semantics/openAccess |
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dc.subject |
congenital hyperinsulinism |
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dc.subject |
focal CHI |
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dc.subject |
diagnostic imaging |
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dc.subject |
Ga-68-NODAGA-exendin-4 PET/CT |
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dc.subject |
F-18-DOPA PET/CT |
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dc.subject |
11P15 IMPRINTED GENES |
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dc.subject |
DIAGNOSIS |
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dc.subject |
LOCALIZATION |
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dc.subject |
MANAGEMENT |
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dc.subject |
MUTATION |
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dc.subject |
CHILDREN |
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dc.subject |
INFANCY |
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dc.subject |
DIFFUSE |
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dc.subject |
FORMS |
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dc.subject |
3126 Surgery, anesthesiology, intensive care, radiology |
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dc.title |
Ga-68-NODAGA-Exendin-4 PET/CT Improves the Detection of Focal Congenital Hyperinsulinism |
en |
dc.type |
Article |
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dc.contributor.organization |
Helsinki One Health (HOH) |
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dc.contributor.organization |
STEMM - Stem Cells and Metabolism Research Program |
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dc.contributor.organization |
Centre of Excellence in Stem Cell Metabolism |
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dc.contributor.organization |
HUS Children and Adolescents |
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dc.contributor.organization |
Clinicum |
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dc.contributor.organization |
Research Programs Unit |
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dc.contributor.organization |
Timo Pyry Juhani Otonkoski / Principal Investigator |
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dc.contributor.organization |
Children's Hospital |
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dc.description.reviewstatus |
Peer reviewed |
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dc.relation.doi |
https://doi.org/10.2967/jnumed.121.262327 |
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dc.relation.issn |
0161-5505 |
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dc.rights.accesslevel |
openAccess |
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dc.type.version |
publishedVersion |
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