PMID- 22914832 OWN - NLM STAT- MEDLINE DCOM- 20130321 LR - 20220316 IS - 1526-632X (Electronic) IS - 0028-3878 (Print) IS - 0028-3878 (Linking) VI - 79 IP - 10 DP - 2012 Sep 4 TI - Metabolic profile of PML lesions in patients with and without IRIS: an observational study. PG - 1041-8 LID - 10.1212/WNL.0b013e318268465b [doi] AB - OBJECTIVE: To characterize progressive multifocal leukoencephalopathy (PML) lesions by contrast-enhanced MRI and evaluate their metabolism using proton magnetic resonance spectroscopy ((1)H- MRS) in the setting of immune reconstitution inflammatory syndrome (IRIS). METHODS: A total of 42 patients with PML underwent a clinical evaluation as well as brain MRI and (1)H-MRS at baseline and 3, 6, and 12 months later. The presence of IRIS was determined based on clinical and laboratory criteria. Ratios of N-acetylaspartate (NAA), choline (Cho), myo-inositol (mI), and lipid/lactate (Lip1 and Lip2) to creatine (Cr) were measured and correlated with the presence of contrast enhancement (CE) in PML lesions. RESULTS: IRIS occurred in 16 of 28 (57.1%) PML survivors (PML-S) and 1 of 14 (7.1%) PML progressors (PML-P). Lesions of patients with PML-IRIS showed significantly higher Cho/Cr (p = 0.0001), mI/Cr (p = 0.02), Lip1/Cr (p < 0.0001), and Lip2/Cr (p = 0.002) ratios and lower NAA/Cr (p = 0.02) ratios than patients with PML who did not have IRIS. An elevated Cho/Cr ratio was associated with CE within the (1)H-MRS voxel, whereas lipid/Cr ratios were elevated in PML-IRIS lesions independently of CE. Follow-up until 33 months from PML onset showed persistent elevation of the mI/Cr ratio in lesions of patients with PML-IRIS. A Lip1/Cr ratio greater than 1.5 combined with the presence of CE yielded a 79% probability of IRIS compared with 13% in the absence of these criteria. CONCLUSION: (1)H-MRS is a valuable tool to recognize and track IRIS in PML and may prove useful in the clinical management of these patients. FAU - Gheuens, Sarah AU - Gheuens S AD - Division of Neurovirology, Department of Neurology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA., USA. FAU - Ngo, Long AU - Ngo L FAU - Wang, Xiaoen AU - Wang X FAU - Alsop, David C AU - Alsop DC FAU - Lenkinski, Robert E AU - Lenkinski RE FAU - Koralnik, Igor J AU - Koralnik IJ LA - eng GR - T32 AI007387/AI/NIAID NIH HHS/United States GR - NS047029/NS/NINDS NIH HHS/United States GR - MH077073/MH/NIMH NIH HHS/United States GR - AG028076,/AG/NIA NIH HHS/United States GR - DC008796/DC/NIDCD NIH HHS/United States GR - MH80729/MH/NIMH NIH HHS/United States GR - AG031720/AG/NIA NIH HHS/United States GR - K24-NS060950/NS/NINDS NIH HHS/United States GR - CA115745/CA/NCI NIH HHS/United States GR - EB004582/EB/NIBIB NIH HHS/United States GR - R01 NS047029/NS/NINDS NIH HHS/United States GR - DK084463)/DK/NIDDK NIH HHS/United States GR - CA101942/CA/NCI NIH HHS/United States GR - T32-AI07387-21/AI/NIAID NIH HHS/United States GR - R56-NS041198/NS/NINDS NIH HHS/United States GR - R01-NS047029/NS/NINDS NIH HHS/United States PT - Journal Article PT - Research Support, N.I.H., Extramural PT - Research Support, Non-U.S. Gov't DEP - 20120822 PL - United States TA - Neurology JT - Neurology JID - 0401060 SB - IM MH - Adult MH - Aged MH - Brain/*metabolism/pathology MH - Female MH - HIV Seropositivity/complications/metabolism/pathology MH - Humans MH - Immune Reconstitution Inflammatory Syndrome/complications/*metabolism/pathology MH - Leukoencephalopathy, Progressive Multifocal/complications/*metabolism/pathology MH - Magnetic Resonance Spectroscopy MH - Male MH - Middle Aged PMC - PMC3430711 EDAT- 2012/08/24 06:00 MHDA- 2013/03/22 06:00 PMCR- 2013/09/04 CRDT- 2012/08/24 06:00 PHST- 2012/08/24 06:00 [entrez] PHST- 2012/08/24 06:00 [pubmed] PHST- 2013/03/22 06:00 [medline] PHST- 2013/09/04 00:00 [pmc-release] AID - WNL.0b013e318268465b [pii] AID - WNL204103 [pii] AID - 10.1212/WNL.0b013e318268465b [doi] PST - ppublish SO - Neurology. 2012 Sep 4;79(10):1041-8. doi: 10.1212/WNL.0b013e318268465b. Epub 2012 Aug 22.