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Urinary incontinence and its functional anatomy in frontotemporal lobar degenerations

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European Journal of Nuclear Medicine and Molecular Imaging Aims and scope Submit manuscript

Abstract

Purpose

The frontal lobes play a crucial role in micturition control. However, no reports exist on the functional role of distinct frontal brain regions in urinary incontinence (UIC) in patients with a neurodegenerative damage of the frontal lobe. The aim of the present study was therefore to explore if functional brain lesions were associated with UIC in patients suffering from frontotemporal lobar degenerations (FTLD).

Methods

Forty-four patients, including eight incontinent subjects, underwent cranial positron emission tomography scanning with 18F-fluoro-2-deoxy-glucose (18F-FDG PET) to assess the relative metabolic rate of glucose (rCMRglc). Group comparisons of rCMRglc were conducted in SPM2 to identify brain regions where the group of incontinent patients (FTLD+UIC) had significant alterations compared with the group without UIC (FTLD−UIC).

Results

At the stringent statistical threshold of p < 0.05, corrected for multiple comparisons according to the family-wise error rate, the statistical analysis revealed two significant right-hemispheric hypometabolic clusters located in the premotor/anterior cingulate cortex and the putamen/claustrum/insula. No hypermetabolic regions were found.

Conclusions

The present study is the first to provide evidence for brain functional alterations involved in the occurrence of UIC in FTLD. These results provide an important piece of evidence to the understanding of a particularly distressing autonomic nervous system symptom of dementia.

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References

  1. Andrew J, Nathan PW. Lesions on the anterior frontal lobes and disturbances of micturition and defaecation. Brain 1964;87:233–62.

    Article  PubMed  CAS  Google Scholar 

  2. Athwal BS, Berkley KJ, Hussain I, et al. Brain responses to changes in bladder volume and urge to void in healthy men. Brain 2001;124:369–77.

    Article  PubMed  CAS  Google Scholar 

  3. Bennett DA, Gilley DW, Lee S, et al. White matter changes: neurobehavioral manifestations of Binswanger’s disease and clinical correlates in Alzheimer’s disease. Dementia 1994;5:148–52.

    Article  PubMed  CAS  Google Scholar 

  4. Blok BF, Willemsen AT, Holstege G. A PET study on brain control of micturition in humans. Brain 1997;120(Pt 1):111–21.

    Article  PubMed  Google Scholar 

  5. Boecker H, Ceballos-Baumann AO, Volk D, et al. Metabolic alterations in patients with Parkinson disease and visual hallucinations. Arch Neurol 2007;64:984–8.

    Article  PubMed  Google Scholar 

  6. Bush G, Luu P, Posner MI. Cognitive and emotional influences in anterior cingulate cortex. Trends Cogn Sci 2000;4:215–22.

    Article  PubMed  Google Scholar 

  7. Critchley HD, Wiens S, Rotshtein P, et al. Neural systems supporting interoceptive awareness. Nat Neurosci 2004;7:189–95.

    Article  PubMed  CAS  Google Scholar 

  8. Diehl-Schmid J, Grimmer T, Drzezga A, et al. Longitudinal changes of cerebral glucose metabolism in semantic dementia. Dement Geriatr Cogn Disord 2006;22:346–51.

    Article  PubMed  CAS  Google Scholar 

  9. Diehl-Schmid J, Grimmer T, Drzezga A, et al. Decline of cerebral glucose metabolism in frontotemporal dementia: a longitudinal 18F-FDG-PET-study. Neurobiol Aging 2007;28:42–50.

    Article  PubMed  CAS  Google Scholar 

  10. Drzezga A, Lautenschlager N, Siebner H, et al. Cerebral metabolic changes accompanying conversion of mild cognitive impairment into Alzheimer’s disease: a PET follow-up study. Eur J Nucl Med Mol Imaging 2003;30:1104–13.

    Article  PubMed  Google Scholar 

  11. Drzezga A, Riemenschneider M, Strassner B, et al. Cerebral glucose metabolism in patients with AD and different APOE genotypes. Neurology 2005;64:102–7.

    PubMed  CAS  Google Scholar 

  12. Dubois B, Slachevsky A, Litvan I, et al. The FAB: a Frontal Assessment Battery at bedside. Neurology 2000;55:1621–6.

    PubMed  CAS  Google Scholar 

  13. Folstein MF, Folstein SE, McHugh PR. “Mini-mental state”. A practical method for grading the cognitive state of patients for the clinician. J Psychiatr Res 1975;12:189–98.

    Article  PubMed  CAS  Google Scholar 

  14. Gorno-Tempini ML, Dronkers NF, Rankin KP, et al. Cognition and anatomy in three variants of primary progressive aphasia. Ann Neurol 2004;55:335–46.

    Article  PubMed  Google Scholar 

  15. Griffiths D. Clinical studies of cerebral and urinary tract function in elderly people with urinary incontinence. Behav Brain Res 1998;92:151–5.

    Article  PubMed  CAS  Google Scholar 

  16. Griffiths D, Tadic SD, Schaefer W, et al. Cerebral control of the bladder in normal and urge-incontinent women. Neuroimage 2007;37:1–7.

    Article  PubMed  Google Scholar 

  17. Harvey RJ, Skelton-Robinson M, Rossor MN. The prevalence and causes of dementia in people under the age of 65 years. J Neurol Neurosurg Psychiatry 2003;74:1206–9.

    Article  PubMed  CAS  Google Scholar 

  18. Herholz K, Salmon E, Perani D, et al. Discrimination between Alzheimer dementia and controls by automated analysis of multicenter FDG PET. Neuroimage 2002;17:302–16.

    Article  PubMed  CAS  Google Scholar 

  19. Hirono N, Kitagaki H, Kazui H, et al. Impact of white matter changes on clinical manifestation of Alzheimer's disease: a quantitative study. Stroke 2000;31:2182–8.

    PubMed  CAS  Google Scholar 

  20. Holstege G, Griffiths D, de Wall H, et al. Anatomical and physiological observations on supraspinal control of bladder and urethral sphincter muscles in the cat. J Comp Neurol 1986;250:449–61.

    Article  PubMed  CAS  Google Scholar 

  21. Hughes CP, Berg L, Danziger WL, et al. A new clinical scale for the staging of dementia. Br J Psychiatry 1982;140:566–72.

    Article  PubMed  CAS  Google Scholar 

  22. Kavia RB, Dasgupta R, Fowler CJ. Functional imaging and the central control of the bladder. J Comp Neurol 2005;493:27–32.

    Article  PubMed  Google Scholar 

  23. Kertesz A, Davidson W, Fox H. Frontal behavioral inventory: diagnostic criteria for frontal lobe dementia. Can J Neurol Sci 1997;24:29–36.

    PubMed  CAS  Google Scholar 

  24. Kitta T, Kakizaki H, Furuno T, et al. Brain activation during detrusor overactivity in patients with Parkinson’s disease: a positron emission tomography study. J Urol 2006;175:994–8.

    Article  PubMed  Google Scholar 

  25. Kono AK, Ishii K, Sofue K, et al. Fully automatic differential diagnosis system for dementia with Lewy bodies and Alzheimer’s disease using FDG-PET and 3D-SSP. Eur J Nucl Med Mol Imaging 2007;34:1490–7.

    Article  PubMed  Google Scholar 

  26. Minoshima S, Foster NL, Sima AA, et al. Alzheimer’s disease versus dementia with Lewy bodies: cerebral metabolic distinction with autopsy confirmation. Ann Neurol 2001;50:358–65.

    Article  PubMed  CAS  Google Scholar 

  27. Neary D, Snowden JS, Gustafson L, et al. Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria. Neurology 1998;51:1546–54.

    PubMed  CAS  Google Scholar 

  28. Nour S, Svarer C, Kristensen JK, et al. Cerebral activation during micturition in normal men. Brain 2000;123(Pt 4):781–9.

    Article  PubMed  Google Scholar 

  29. Perneczky R, Diehl-Schmid J, Pohl C, et al. Non-fluent progressive aphasia: Cerebral metabolic patterns and brain reserve. Brain Res 2007;1133:178–85.

    Article  PubMed  CAS  Google Scholar 

  30. Perneczky R, Wagenpfeil S, Komossa K, et al. Mapping scores onto stages: mini-mental state examination and clinical dementia rating. Am J Geriatr Psychiatry 2006;14:139–44.

    Article  PubMed  Google Scholar 

  31. Pool JL, Ransohoff J. Autonomic effects on stimulating rostral portion of cingulate gyri in man. J Neurophysiol 1949;12:385–92.

    PubMed  CAS  Google Scholar 

  32. Ratnavalli E, Brayne C, Dawson K, et al. The prevalence of frontotemporal dementia. Neurology 2002;58:1615–21.

    PubMed  CAS  Google Scholar 

  33. Reitan R. Validity of the Trail Making Test as an indicator of organic brain damage. Percept Mot Skills 1985;8:271–6.

    Article  Google Scholar 

  34. Sakakibara R, Uchida Y, Uchiyama T, et al. Reduced cerebellar vermis activation during urinary storage and micturition in multiple system atrophy: 99mTc-labelled ECD SPECT study. Eur J Neurol 2004;11:705–8.

    Article  PubMed  CAS  Google Scholar 

  35. Talairach J, Tournoux P. Co-planar stereotactical atlas of the human brain: 3-dimensional proportional system - an approach to cerebral imaging. Thieme Medical Publishers, New York, 1988.

    Google Scholar 

  36. Thalmann B, Monsch A, CERAD. The Consortium to Establish a Registry for Alzheimer’s Disease. Neuropsychologische Testbatterie. Memory Clinic Basel, Basel, 1997.

    Google Scholar 

  37. Walters K, Iliffe S, Tai SS, et al. Assessing needs from patient, carer and professional perspectives: the Camberwell Assessment of Need for Elderly people in primary care. Age Ageing 2000;29:505–10.

    Article  PubMed  CAS  Google Scholar 

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Acknowledgements

Dr. Diehl-Schmid received KKF and HWP-II grants from the Technical University Munich. However, the sponsor did neither play a role in design and conduct of the study, collection, management, analysis and interpretation of the data nor in the preparation, review or approval of the manuscript.

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Correspondence to Robert Perneczky.

Additional information

Robert Perneczky and Janine Diehl-Schmid contributed equally.

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Perneczky, R., Diehl-Schmid, J., Förstl, H. et al. Urinary incontinence and its functional anatomy in frontotemporal lobar degenerations. Eur J Nucl Med Mol Imaging 35, 605–610 (2008). https://doi.org/10.1007/s00259-007-0626-8

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  • DOI: https://doi.org/10.1007/s00259-007-0626-8

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