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Journal of Neurology, Neurosurgery, and Psychiatry logoLink to Journal of Neurology, Neurosurgery, and Psychiatry
. 2001 Sep;71(3):334–339. doi: 10.1136/jnnp.71.3.334

Cerebral metabolic impairment in patients with obstructive sleep apnoea: an independent association of obstructive sleep apnoea with white matter change

M Kamba 1, Y Inoue 1, S Higami 1, Y Suto 1, T Ogawa 1, W Chen 1
PMCID: PMC1737534  PMID: 11511706

Abstract

OBJECTIVES—To determine the relation between severity of obstructive sleep apnoea (OSA) and degree of cerebral metabolic impairment.
METHODS—Fifty five patients with habitual snoring and excessive daytime sleepiness underwent standard overnight polysomnography and magnetic resonance spectroscopy separately. Proton MR spectra were measured with two dimensional chemical shift imaging (repetition time; 1500 ms, echo time; 135 ms). Severity of cerebral metabolic impairment was assessed by the N-acetylaspartate (NAA)/choline ratios for the cerebral cortex and white matter. Severity of OSA was assessed by the apnoea-hypopnoea index (AHI) and the minimum value of peripheral oxyhaemoglobin saturation. All patients were evaluated for the presence or absence of comobidities including hypertension, cardiac disease, diabetes mellitus, and hyperlipidaemia. Univariate analysis of variance (ANOVA) and mulitple linear regression analysis were used for statistical analyses.
RESULTS—Univariate ANOVA disclosed significant effects of AHI, age, and the presence or absence of hypertension on the NAA/choline ratio for cerebral white matter (p=0.011, p=0.028, p=0.0496, respectively). The AHI had a significant negative association with the NAA/choline ratio for cerebral white matter, independent of age and the presence or absence of cardiac disease, in the final multivariate regression model (standardised partial regression coefficient=−0.417, p<0.001). No significant relation was found between severity of OSA and the NAA/choline ratio for the cerebral cortex. Age alone had a significant effect on the NAA/choline ratio for the cerebral cortex on univariate ANOVA (p<0.001) and a significant negative association with the NAA/choline ratio for the cerebral cortex in the regression model (r=−0.552, p<0.001).
CONCLUSIONS—A significant relation exists between AHI and the degree of metabolic impairment in cerebral white matter in patients with OSA.



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Selected References

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  1. Birken D. L., Oldendorf W. H. N-acetyl-L-aspartic acid: a literature review of a compound prominent in 1H-NMR spectroscopic studies of brain. Neurosci Biobehav Rev. 1989 Spring;13(1):23–31. doi: 10.1016/s0149-7634(89)80048-x. [DOI] [PubMed] [Google Scholar]
  2. Bålfors E. M., Franklin K. A. Impairment of cerebral perfusion during obstructive sleep apneas. Am J Respir Crit Care Med. 1994 Dec;150(6 Pt 1):1587–1591. doi: 10.1164/ajrccm.150.6.7952619. [DOI] [PubMed] [Google Scholar]
  3. Carskadon M. A., Dement W. C., Mitler M. M., Roth T., Westbrook P. R., Keenan S. Guidelines for the multiple sleep latency test (MSLT): a standard measure of sleepiness. Sleep. 1986 Dec;9(4):519–524. doi: 10.1093/sleep/9.4.519. [DOI] [PubMed] [Google Scholar]
  4. Chimowitz M. I., Estes M. L., Furlan A. J., Awad I. A. Further observations on the pathology of subcortical lesions identified on magnetic resonance imaging. Arch Neurol. 1992 Jul;49(7):747–752. doi: 10.1001/archneur.1992.00530310095018. [DOI] [PubMed] [Google Scholar]
  5. Diomedi M., Placidi F., Cupini L. M., Bernardi G., Silvestrini M. Cerebral hemodynamic changes in sleep apnea syndrome and effect of continuous positive airway pressure treatment. Neurology. 1998 Oct;51(4):1051–1056. doi: 10.1212/wnl.51.4.1051. [DOI] [PubMed] [Google Scholar]
  6. Findley L. J., Barth J. T., Powers D. C., Wilhoit S. C., Boyd D. G., Suratt P. M. Cognitive impairment in patients with obstructive sleep apnea and associated hypoxemia. Chest. 1986 Nov;90(5):686–690. doi: 10.1378/chest.90.5.686. [DOI] [PubMed] [Google Scholar]
  7. Fischer A. Q., Chaudhary B. A., Taormina M. A., Akhtar B. Intracranial hemodynamics in sleep apnea. Chest. 1992 Nov;102(5):1402–1406. doi: 10.1378/chest.102.5.1402. [DOI] [PubMed] [Google Scholar]
  8. Furuta A., Ishii N., Nishihara Y., Horie A. Medullary arteries in aging and dementia. Stroke. 1991 Apr;22(4):442–446. doi: 10.1161/01.str.22.4.442. [DOI] [PubMed] [Google Scholar]
  9. Gastaut H., Tassinari C. A., Duron B. Etude polygraphique des manifestations épisodiques (hypniques et respiratoires), diurnes et nocturnes, du syndrome de Pickwick. Rev Neurol (Paris) 1965 Jun;112(6):568–579. [PubMed] [Google Scholar]
  10. Greenberg G. D., Watson R. K., Deptula D. Neuropsychological dysfunction in sleep apnea. Sleep. 1987 Jun;10(3):254–262. doi: 10.1093/sleep/10.3.254. [DOI] [PubMed] [Google Scholar]
  11. Guilleminault C., Tilkian A., Dement W. C. The sleep apnea syndromes. Annu Rev Med. 1976;27:465–484. doi: 10.1146/annurev.me.27.020176.002341. [DOI] [PubMed] [Google Scholar]
  12. Kales A., Caldwell A. B., Cadieux R. J., Vela-Bueno A., Ruch L. G., Mayes S. D. Severe obstructive sleep apnea--II: Associated psychopathology and psychosocial consequences. J Chronic Dis. 1985;38(5):427–434. doi: 10.1016/0021-9681(85)90138-9. [DOI] [PubMed] [Google Scholar]
  13. Kamba M., Suto Y., Ohta Y., Inoue Y., Matsuda E. Cerebral metabolism in sleep apnea. Evaluation by magnetic resonance spectroscopy. Am J Respir Crit Care Med. 1997 Jul;156(1):296–298. doi: 10.1164/ajrccm.156.1.9611063. [DOI] [PubMed] [Google Scholar]
  14. Katsumata K., Okada T., Miyao M., Katsumata Y. High incidence of sleep apnea syndrome in a male diabetic population. Diabetes Res Clin Pract. 1991 Aug;13(1-2):45–51. doi: 10.1016/0168-8227(91)90032-9. [DOI] [PubMed] [Google Scholar]
  15. Kim H. C., Young T., Matthews C. G., Weber S. M., Woodward A. R., Palta M. Sleep-disordered breathing and neuropsychological deficits. A population-based study. Am J Respir Crit Care Med. 1997 Dec;156(6):1813–1819. doi: 10.1164/ajrccm.156.6.9610026. [DOI] [PubMed] [Google Scholar]
  16. Larsson H. B., Christiansen P., Jensen M., Frederiksen J., Heltberg A., Olesen J., Henriksen O. Localized in vivo proton spectroscopy in the brain of patients with multiple sclerosis. Magn Reson Med. 1991 Nov;22(1):23–31. doi: 10.1002/mrm.1910220104. [DOI] [PubMed] [Google Scholar]
  17. Miller B. L. A review of chemical issues in 1H NMR spectroscopy: N-acetyl-L-aspartate, creatine and choline. NMR Biomed. 1991 Apr;4(2):47–52. doi: 10.1002/nbm.1940040203. [DOI] [PubMed] [Google Scholar]
  18. Montplaisir J., Bédard M. A., Richer F., Rouleau I. Neurobehavioral manifestations in obstructive sleep apnea syndrome before and after treatment with continuous positive airway pressure. Sleep. 1992 Dec;15(6 Suppl):S17–S19. doi: 10.1093/sleep/15.suppl_6.s17. [DOI] [PubMed] [Google Scholar]
  19. Moody D. M., Bell M. A., Challa V. R. Features of the cerebral vascular pattern that predict vulnerability to perfusion or oxygenation deficiency: an anatomic study. AJNR Am J Neuroradiol. 1990 May;11(3):431–439. [PMC free article] [PubMed] [Google Scholar]
  20. Netzer N., Werner P., Jochums I., Lehmann M., Strohl K. P. Blood flow of the middle cerebral artery with sleep-disordered breathing: correlation with obstructive hypopneas. Stroke. 1998 Jan;29(1):87–93. doi: 10.1161/01.str.29.1.87. [DOI] [PubMed] [Google Scholar]
  21. Pantoni L., Garcia J. H. Pathogenesis of leukoaraiosis: a review. Stroke. 1997 Mar;28(3):652–659. doi: 10.1161/01.str.28.3.652. [DOI] [PubMed] [Google Scholar]
  22. Peker Y., Kraiczi H., Hedner J., Löth S., Johansson A., Bende M. An independent association between obstructive sleep apnoea and coronary artery disease. Eur Respir J. 1999 Jul;14(1):179–184. doi: 10.1034/j.1399-3003.1999.14a30.x. [DOI] [PubMed] [Google Scholar]
  23. Poceta J. S., Timms R. M., Jeong D. U., Ho S. L., Erman M. K., Mitler M. M. Maintenance of wakefulness test in obstructive sleep apnea syndrome. Chest. 1992 Apr;101(4):893–897. doi: 10.1378/chest.101.4.893. [DOI] [PubMed] [Google Scholar]
  24. Rumbach L., Krieger J., Kurtz D. Auditory event-related potentials in obstructive sleep apnea: effects of treatment with nasal continuous positive airway pressure. Electroencephalogr Clin Neurophysiol. 1991 Sep-Oct;80(5):454–457. doi: 10.1016/0168-5597(91)90094-e. [DOI] [PubMed] [Google Scholar]
  25. Sangal R. B., Sangal J. M. P300 latency: abnormal in sleep apnea with somnolence and idiopathic hypersomnia, but normal in narcolepsy. Clin Electroencephalogr. 1995 Jul;26(3):146–153. doi: 10.1177/155005949502600305. [DOI] [PubMed] [Google Scholar]
  26. Schmidt R., Fazekas F., Offenbacher H., Dusek T., Zach E., Reinhart B., Grieshofer P., Freidl W., Eber B., Schumacher M. Neuropsychologic correlates of MRI white matter hyperintensities: a study of 150 normal volunteers. Neurology. 1993 Dec;43(12):2490–2494. doi: 10.1212/wnl.43.12.2490. [DOI] [PubMed] [Google Scholar]
  27. Valencia-Flores M., Bliwise D. L., Guilleminault C., Cilveti R., Clerk A. Cognitive function in patients with sleep apnea after acute nocturnal nasal continuous positive airway pressure (CPAP) treatment: sleepiness and hypoxemia effects. J Clin Exp Neuropsychol. 1996 Apr;18(2):197–210. doi: 10.1080/01688639608408275. [DOI] [PubMed] [Google Scholar]
  28. Walsleben J. A., Squires N. K., Rothenberger V. L. Auditory event-related potentials and brain dysfunction in sleep apnea. Electroencephalogr Clin Neurophysiol. 1989 Jul-Aug;74(4):297–311. doi: 10.1016/0168-5597(89)90060-9. [DOI] [PubMed] [Google Scholar]
  29. Ylikoski R., Ylikoski A., Erkinjuntti T., Sulkava R., Raininko R., Tilvis R. White matter changes in healthy elderly persons correlate with attention and speed of mental processing. Arch Neurol. 1993 Aug;50(8):818–824. doi: 10.1001/archneur.1993.00540080029009. [DOI] [PubMed] [Google Scholar]
  30. Young T., Peppard P., Palta M., Hla K. M., Finn L., Morgan B., Skatrud J. Population-based study of sleep-disordered breathing as a risk factor for hypertension. Arch Intern Med. 1997 Aug 11;157(15):1746–1752. [PubMed] [Google Scholar]
  31. van der Grond J., Balm R., Kappelle L. J., Eikelboom B. C., Mali W. P. Cerebral metabolism of patients with stenosis or occlusion of the internal carotid artery. A 1H-MR spectroscopic imaging study. Stroke. 1995 May;26(5):822–828. doi: 10.1161/01.str.26.5.822. [DOI] [PubMed] [Google Scholar]

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