2021, Number 4
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Medicina & Laboratorio 2021; 25 (4)
Detection of isocitrate dehydrogenase enzyme mutation in grades II, III and IV diffuse gliomas
Naranjo-Botero P, Medina-Zuluaica LA, Muñetón-Peña CM, Arango-Viana JC, Ospina-Ospina S
Language: Spanish
References: 31
Page: 709-719
PDF size: 966.49 Kb.
ABSTRACT
Introduction. Gliomas are the most common primary malignancies of the
central nervous system, associated with high mortality and morbidity. Mutations in
the isocitrate dehydrogenase (IDH) enzyme IDH1 and IDH2 genes, are key in tumorigenesis,
and are considered an important prognostic factor in these neoplasms.
This study aimed to determine the presence of IDH1 and IDH2 gene mutations in
patients diagnosed with diffuse glioma in different degrees, and their correlation
with survival.
Methodology. A descriptive, prospective and retrospective study was
conducted. The study population consisted of patients between the ages of 18 and
45 with a diagnosis of grade II, III and IV diffuse glioma, treated at the Hospital San
Vicente Fundación in Medellín, between 2012 and 2017, in whom an analysis of
IDH1 and IDH2 gene mutations was performed by Sanger sequencing and immunohistochemical
staining.
Results. Fourteen patients with a mean age of 37 years
were included, 57% were male. Glioblastoma was the most frequent neoplasm,
diagnosed in 42.9% of the cases. By immunohistochemistry, 10 of the 14 (71.4%)
patients had a mutation of the IDH1 enzyme, while 1 of the 11 (9%) patients in
whom IDH2 gene sequencing was achieved showed a mutation. In general, 78.6%
had IDH enzyme mutations, with an average survival of 48 months.
Conclusion.
These findings suggest that gliomas are a heterogeneous group of tumors, with
great genetic variability that impacts their prognosis and behavior.
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