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PLOS ONE  2014 

Widespread Hypermetabolism in Symptomatic and Asymptomatic Episodes in Kleine-Levin Syndrome

DOI: 10.1371/journal.pone.0093813

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Abstract:

Background No reliable biomarkers are identified in KLS. However, few functional neuroimaging studies suggested hypoactivity in thalamic and hypothalamic regions during symptomatic episodes. Here, we investigated relative changes in regional brain metabolism in Kleine-Levin syndrome (KLS) during symptomatic episodes and asymptomatic periods, as compared to healthy controls. Methods Four drug-free male patients with typical KLS and 15 healthy controls were included. 18-F-fluorodeoxy glucose positron emission tomography (PET) was obtained in baseline condition in all participants, and during symptomatic episodes in KLS patients. All participants were asked to remain fully awake during the whole PET procedure. Results Between state-comparisons in KLS disclosed higher metabolism in paracentral, precentral, and postcentral areas, supplementary motor area, medial frontal gyrus, thalamus and putamen during symptomatic episodes, and decreased metabolism in occipital and temporal gyri. As compared to healthy control subjects, KLS patients in the asymptomatic phase consistently exhibited significant hypermetabolism in a wide cortical network including frontal and temporal cortices, posterior cingulate and precuneus, with no detected hypometabolism. In symptomatic KLS episodes, hypermetabolism was additionally found in orbital frontal and supplementary motor areas, insula and inferior parietal areas, and right caudate nucleus, and hypometabolism in the middle occipital gyrus and inferior parietal areas. Conclusion Our results demonstrated significant hypermetabolism and few hypometabolism in specific but widespread brain regions in drug-free KLS patients at baseline and during symptomatic episodes, highlighting the behavioral state-dependent nature of changes in regional brain activity in KLS.

References

[1]  Arnulf I, Lin L, Gadoth N, File J, Lecendreux M, et al. (2008) Kleine-Levin syndrome: a systematic study of 108 patients. Ann Neurol 63: 482–493. doi: 10.1002/ana.21333
[2]  Arnulf I, Rico TJ, Mignot E (2012) Diagnosis, disease course, and management of patients with Kleine-Levin syndrome. Lancet Neurol 11: 918–28. doi: 10.1016/s1474-4422(12)70187-4
[3]  The International Classification of Sleep Disorders (2005) 2nd edition: diagnostic and coding manual. Westchester, IL: American Academy of Sleep Medicine.
[4]  Billiard M, Jaussent I, Dauvilliers Y, Besset A (2011) Recurrent hypersomnia: a review of 339 cases. Sleep Med Rev 15: 247–57. doi: 10.1016/j.smrv.2010.08.001
[5]  Arnulf I, Zeitzer JM, File J, Farber N, Mignot E (2005) Kleine-Levin syndrome: a systematic review of 186 cases in the literature. Brain 128: 2763–76. doi: 10.1093/brain/awh620
[6]  Huang YS, Guilleminault C, Kao PF, Liu FY (2005) SPECT findings in the Kleine-Levin syndrome. Sleep 28: 955–60.
[7]  Huang YS, Guilleminault C, Lin KL, Hwang FM, Liu FY, et al. (2012) Relationship between Kleine-Levin syndrome and upper respiratory infection in Taiwan. Sleep 35: 123–129. doi: 10.5665/sleep.1600
[8]  Hong SB, Joo EY, Tae WS, Lee J, Han SJ, et al. (2006) Episodic diencephalic hypoperfusion in Kleine-Levin syndrome. Sleep 29: 1091e3. doi: 10.13078/jksrs.05015
[9]  Arias M, Crespo Iglesias JM, Perez J, Requena- Caballero I, Sesar-Ignacio A, et al. (2002) Kleine-Levin syndrome: contribution of brain SPECT in diagnosis. Rev Neurol 35: 531–33.
[10]  Landtblom AM, Dige N, Schwerdt K, Safstrom P, Granerus G (2002) A case of Kleine-Levin syndrome examined with SPECT and neuropsychological testing. Acta Neurol Scand 105: 318–321. doi: 10.1034/j.1600-0404.2002.1c162.x
[11]  Lo YC, Chou YH, Yu HY (2012) PET finding in Kleine-Levin syndrome. Sleep Med 13: 771–2. doi: 10.1016/j.sleep.2012.01.009
[12]  Haba-Rubio J, Prior JO, Guedj E, Tafti M, Heinzer R, et al. (2012) Kleine-Levin syndrome: functional imaging correlates of hypersomnia and behavioral symptoms. Neurology 79: 1927–9. doi: 10.1212/wnl.0b013e318271f85a
[13]  Dauvilliers Y, Mayer G, Lecendreux M, Neidhart E, Peraita-Adrados R, et al. (2002) Kleine-Levin syndrome: an autoimmune hypothesis based on clinical and genetic analyses. Neurology 59: 1739–45. doi: 10.1212/01.wnl.0000036605.89977.d0
[14]  Drummond SP, Gillin JC, Brown GG (2001) Increased cerebral response during a divided attention task following sleep deprivation. J Sleep Res 10: 85e92. doi: 10.1046/j.1365-2869.2001.00245.x
[15]  Vigren P, Tisell A, Engstr?m M, Karlsson T, Leinhard Dahlqvist O, et al. (2012) Low thalamic NAA-concentration corresponds to strong neural activation in working memory in Kleine-Levin syndrome. PLoS One 8: e56279. doi: 10.1371/journal.pone.0056279
[16]  Dauvilliers Y, Comte F, Bayard S, Carlander B, Zanca M, et al. (2010) A brain PET study in patients with narcolepsy-cataplexy. J Neurol Neurosurg Psychiatry 81: 344–8. doi: 10.1136/jnnp.2009.175786

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