Publication:
Risk factors for mortality caused by hypothalamic obesity in children with hypothalamic tumours

dc.contributor.authorBEREKET, ABDULLAH
dc.contributor.authorHALİLOĞLU, BELMA
dc.contributor.authorDEMİRCİOĞLU, SERAP
dc.contributor.authorGÜRAN, TÜLAY
dc.contributor.authorsHaliloglu, B.; Atay, Z.; Guran, T.; Abali, S.; Bas, S.; Turan, S.; Bereket, A.
dc.date.accessioned2022-03-14T08:13:47Z
dc.date.accessioned2026-01-11T10:27:13Z
dc.date.available2022-03-14T08:13:47Z
dc.date.issued2016-10
dc.description.abstractBackgroundHypothalamic obesity (HyOb) is a common complication of childhood hypothalamic tumours. Patients with HyOb probably have a higher mortality rate than those with other types of obesity due in many cases to obstructive sleep apnoea/hypoventilation. ObjectivesTo identify predictive factors for mortality caused by HyOb in children. MethodsTwenty children with HyOb secondary to hypothalamic tumours that were followed-up for 3 years and aged <15 years at diagnosis, and received supraphysiological glucocorticoid treatment for 1 month. ResultsMean age at diagnosis was 6.363.60 years. Mean body mass index (BMI) Standard deviation of the samples (SDS) increased from 0.77 +/- 1.26 to 2.66 +/- 1.45 during the first 6 months, but slowed from month 6-12 (2.73 +/- 1.35). BMI SDS at 0-6 months was significantly higher in patients aged <6 years at diagnosis than in those aged >6 years at diagnosis (3.71 +/- 1.96 vs. 0.83 +/- 0.73, P<0.001). Maximum BMI SDS was also significantly higher in the younger group (3.88 +/- 1.39 vs. 2.79 +/- 0.64, P<0.05). In all, four patients died and the mortality rate was significantly higher in the patients with a further increase in BMI SDS>1 SDS after 6 months of therapy (RR: 8.4, P<0.05). Both overall mortality and obesity-related mortality rates were higher in the patients aged <6 years at diagnosis (4.5-fold, 7.2-fold higher, respectively, P>0.05). The mortality rate was also 3.7-fold higher in the patients with a maximum BMI SDS3 at any time during the first 3 years after therapy(P>0.05). ConclusionsAn increase in BMI SDS after 6 months of therapy was observed to be a risk factor for mortality caused by HyOb. In addition, age <6 years at diagnosis and a maximum BMI SDS3 were associated with a higher mortality rate, indicating that earlier and more aggressive treatment of obesity is required.
dc.identifier.doi10.1111/ijpo.12076
dc.identifier.eissn2047-6302
dc.identifier.issn2047-6310
dc.identifier.pubmed26463004
dc.identifier.urihttps://hdl.handle.net/11424/241145
dc.identifier.wosWOS:000385378800013
dc.language.isoeng
dc.publisherWILEY-BLACKWELL
dc.relation.ispartofPEDIATRIC OBESITY
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectBrain tumour
dc.subjectcraniopharyngioma
dc.subjectmortality
dc.subjectBODY-MASS INDEX
dc.subjectCHILDHOOD CRANIOPHARYNGIOMA
dc.subjectMORBIDITY
dc.subjectWEIGHT
dc.subjectADOLESCENTS
dc.subjectSURGERY
dc.subjectTHERAPY
dc.subjectHEIGHT
dc.titleRisk factors for mortality caused by hypothalamic obesity in children with hypothalamic tumours
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage388
oaire.citation.issue5
oaire.citation.startPage383
oaire.citation.titlePEDIATRIC OBESITY
oaire.citation.volume11

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