2011
DOI: 10.4103/0972-3919.90255
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Spectrum of neurocognitive dysfunction in Indian population on FDG PET/CT imaging

Abstract: Background:A variety of neurodegenerative disorders produce significant abnormal brain function which can be detected using fluorodeoxyglucose positron emission tomography (FDG PET) scan even when structural changes are not detected on CT or MRI Scan. A study was undertaken at our institute to evaluate the FDG PET/CT findings in Indian population suffering from mild cognitive impairment (MCI), Alzheimer's disease (AD), fronto-temporal dementia (FTD), dementia with lewy body disease (DLBD) and other miscellaneo… Show more

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Cited by 5 publications
(3 citation statements)
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“…[48] AD has been found to be the most frequent form of dementia. However, a significantly higher proportion of frontal lobe involvement was noted in the Indian population, as compared to global literature.…”
Section: Neuroimagingmentioning
confidence: 99%
“…[48] AD has been found to be the most frequent form of dementia. However, a significantly higher proportion of frontal lobe involvement was noted in the Indian population, as compared to global literature.…”
Section: Neuroimagingmentioning
confidence: 99%
“…One-hundred and twenty-nine papers were identified and screened by the referent panelist (ZW), but only 29 were selected as adequate for assessment and sent to the methodology team (see Figure 1 -PICO 8). Of these, 16 papers were excluded because i) one did not include the population of interest [26]; ii) eight did not compare DLB and AD patients [27][28][29][30][31][32][33][34]; iii) one was an epidemiologic study [35]; iv) two were methodological studies for quantitative analyses of FDG-PET [36,37]; v)…”
Section: Pico 8: Fdg-pet To Differentiate Between Dlb and Admentioning
confidence: 99%
“…A total of 101 patients were included in the final analysis. Sixty of the patients included in this study had been included in a previous analysis by our group 10 . The final diagnosis of dementia type was based on longitudinal clinical follow-up of at least 18 months at the CDM clinic, after the preliminary diagnosis of dementia by a specialist neurologist.…”
Section: Final Diagnosismentioning
confidence: 99%