Goal Combinatorial therapy directed at both vascular and neurodegenerative aspects of dementia may offer a promising strategy for treatment of dementia, which often has a multifactorial basis in the elderly. We investigated whether the phosphodiesterase III inhibitor cilostazol, which is often used in the prevention of stroke and peripheral artery disease, may delay cognitive decline in the elderly receiving donepezil. Methods Medical records were retrospectively surveyed to identify patients who had received donepezil for more than one year and had undergone Mini-Mental State Examination (MMSE) at least at two time points. Those with an initial MMSE score of less than 27 points were subjected to analysis (n = 156), with a cut-point of 21/22 applied to assign them to mild (n = 70) and moderate/severe (n = 86) dementia. The change of total MMSE score per year was compared between patients who had received donepezil and those given both donepezil and cilostazol. Findings In patients with mild dementia who had received donepezil and cilostazol (n = 34; 77.2±6.8 years old), the annual change in MMSE score was ?0.5±1.6 during an observational period of 28.6±11.7 months, with those receiving donepezil only (n = 36; 78.4±6.5 years old) scoring less (?2.2±4.1) during 30.4±12.8 months with a statistical intergroup difference (p = 0.022). Multivariate analysis showed that absence of cilostazol treatment was the only significant predictor of MMSE decline. A positive effect of cilostazol was found in three subscale scores of MMSE, orientation for time or place and delayed recall. By clear contrast, in patients with moderate/severe dementia, there were no intergroup differences in decrease of total or subscale MMSE scores between the two groups. Conclusions These results suggest potential for cilostazol treatment in the suppression of cognitive decline in patients receiving donepezil with mild dementia but not in those with moderate/severe dementia.
References
[1]
Gorelick PB, Scuteri A, Black SE, Decarli C, Greenberg SM, et al. (2011) Vascular contributions to cognitive impairment and dementia: a statement for healthcare professionals from the American Heart Association/American Stroke Association. Stroke 42: 2672–2713. doi: 10.1161/str.0b013e3182299496
[2]
Toledo JB, Arnold SE, Raible K, Brettschneider J, Xie SX, et al. (2013) Contribution of cerebrovascular disease in autopsy confirmed neurodegenerative disease cases in the National Alzheimer's Coordinating Centre. Brain 136: 2697–2706. doi: 10.1093/brain/awt188
[3]
Kalaria RN, Akinyemi R, Ihara M (2012) Does vascular pathology contribute to Alzheimer changes? J Neurol Sci 322: 141–147. doi: 10.1016/j.jns.2012.07.032
[4]
Kalaria RN, Ihara M (2013) Dementia: Vascular and neurodegenerative pathways-will they meet? Nat Rev Neurol. 487–488.
[5]
Liu Y, Shakur Y, Yoshitake M, Kambayashi JJ (2001) Cilostazol (pletal): a dual inhibitor of cyclic nucleotide phosphodiesterase type 3 and adenosine uptake. Cardiovasc Drug Rev 19: 369–386. doi: 10.1111/j.1527-3466.2001.tb00076.x
[6]
Kim KY, Shin HK, Choi JM, Hong KW (2002) Inhibition of lipopolysaccharide-induced apoptosis by cilostazol in human umbilical vein endothelial cells. J Pharmacol Exp Ther 300: 709–715. doi: 10.1124/jpet.300.2.709
[7]
Fujita Y, Lin JX, Takahashi R, Tomimoto H (2008) Cilostazol alleviates cerebral small-vessel pathology and white-matter lesions in stroke-prone spontaneously hypertensive rats. Brain Res 1203: 170–176. doi: 10.1016/j.brainres.2008.01.103
[8]
Tanaka K, Gotoh F, Fukuuchi Y, Amano T, Uematsu D, et al. (1989) Effects of a selective inhibitor of cyclic AMP phosphodiesterase on the pial microcirculation in feline cerebral ischemia. Stroke 20: 668–673. doi: 10.1161/01.str.20.5.668
[9]
Hiramatsu M, Takiguchi O, Nishiyama A, Mori H (2010) Cilostazol prevents amyloid β peptide(25–35)-induced memory impairment and oxidative stress in mice. Br J Pharmacol 161: 1899–1912. doi: 10.1111/j.1476-5381.2010.01014.x
[10]
Park SH, Kim JH, Bae SS, Hong KW, Lee D-S, et al. (2011) Protective effect of the phosphodiesterase III inhibitor cilostazol on amyloid β-induced cognitive deficits associated with decreased amyloid β accumulation. Biochem Biophys Res Commun 408: 602–608. doi: 10.1016/j.bbrc.2011.04.068
[11]
Arai H, Takahashi T (2009) A combination therapy of donepezil and cilostazol for patients with moderate Alzheimer disease: pilot follow-up study. Am J Geriatr Psychiatry 17: 353–354.
[12]
Sakurai H, Hanyu H, Sato T, Kume K, Hirao K, et al. (2013) Effects of cilostazol on cognition and regional cerebral blood flow in patients with Alzheimer's disease and cerebrovascular disease: a pilot study. Geriatr Gerontol Int 13: 90–97. doi: 10.1111/j.1447-0594.2012.00866.x
[13]
Taguchi A, Takata Y, Ihara M, Kasahara Y, Tsuji M, et al. (2013) Cilostazol improves cognitive function in patients with mild cognitive impairment: A retrospective analysis. Psychogeriatrics 13: 164–169. doi: 10.1111/psyg.12021
[14]
Kamiyama K, Wada A, Sugihara M, Kurioka S, Hayashi K, et al. (2010) Potential hippocampal region atrophy in diabetes mellitus type 2: a voxel-based morphometry VSRAD study. Jpn J Radiol 28: 266–272. doi: 10.1007/s11604-009-0416-2
[15]
Shinohara Y, Katayama Y, Uchiyama S, Yamaguchi T, Handa S, et al. (2010) Cilostazol for prevention of secondary stroke (CSPS 2): an aspirin-controlled, double-blind, randomised non-inferiority trial. Lancet Neurol 9: 959–968. doi: 10.1016/s1474-4422(10)70198-8
[16]
Zlokovic BV (2011) Neurovascular pathways to neurodegeneration in Alzheimer's disease and other disorders. Nat Rev Neurosci 12: 723–738. doi: 10.1038/nrn3114
[17]
Chow N, Bell RD, Deane R, Streb JW, Chen J, et al. (2007) Serum response factor and myocardin mediate arterial hypercontractility and cerebral blood flow dysregulation in Alzheimer's phenotype. Proc Natl Acad Sci U S A 104: 823–828. doi: 10.1073/pnas.0608251104
[18]
Weller RO, Djuanda E, Yow HY, Carare RO (2009) Lymphatic drainage of the brain and the pathophysiology of neurological disease. Acta Neuropathol 117: 1–14. doi: 10.1007/s00401-008-0457-0