This Article Abstract Full Text (PDF) All Versions of this Article: 36/12/2554    most recent 01.STR.0000190832.17620.25v1 Alert me when this article is cited Alert me if a correction is posted Citation Map Services Email this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Request Permissions Citing Articles Citing Articles via HighWire Citing Articles via Google Scholar Google Scholar Articles by Rufa, A. Articles by Federico, A. Search for Related Content PubMed PubMed Citation Articles by Rufa, A. Articles by Federico, A. Related Collections Autonomic, reflex, and neurohumoral control of circulation Other diagnostic testing Risk Factors Cerebral Lacunes Genetics of Stroke Computerized tomography and Magnetic Resonance Imaging

(Stroke. 2005;36:2554.)
© 2005 American Heart Association, Inc.

Original Contributions

Systemic Blood Pressure Profile in Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy

Alessandra Rufa, MD; Maria Teresa Dotti, MD; Massimo Franchi, MD; Maria Laura Stromillo, MD; Gabriele Cevenini, PhD; Silvia Bianchi, PhD; Nicola De Stefano, MD Antonio Federico, MD

From the Dipartimento di Scienze Neurologiche e del Comportamento (A.R., M.T.D., M.L.S., S.B., N.D., A.F.), Università di Siena, Italy; Dipartimento di Medicina Clinica e Scienze Immunologiche Applicate (M.F.), Università di Siena, Italy; and Dipartimento di Chirurgia e Bioingegneria (G.C.), Università di Siena, Italy.

Correspondence to Maria Teresa Dotti, MD, Dipartimento di Scienze Neurologiche e del Comportamento, Università di Siena, Viale Bracci, 53100 Siena, Italy. E-mail dotti{at}unisi.it

	Abstract

Top Abstract Introduction Materials and Methods Results Discussion References

 
Background and Purpose— Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a genetic form of subcortical ischemic vascular dementia (SIVD). The most common vascular risk factors are unremarkable in CADASIL; however, studies on systemic blood pressure (BP) changes over time are substantially lacking. Because BP instability is a relevant risk factor for developing or worsening white matter changes in sporadic SIVD, we aimed to study the BP profile of CADASIL to investigate its relationship with cognitive decline and white matter injury.

Methods— Twenty-four–hour ambulatory BP monitoring was performed in a group of 14 CADASIL patients (12 males and 2 females) and in a group of 15 healthy age-matched control subjects. The following BP variables were compared between the 2 groups: mean daytime and nighttime systolic, diastolic, and mean arterial BP (SABP_day, DABP_day, and MABP_day, and SABP_night, DABP_night, and MABP_night) and nocturnal percentage decline in arterial BP (%MABP reduction). Cognitive performances were tested by mini mental status examination (MMSE), and brain MRI was performed to extrapolate the T2-weighted lesion volume (LV) in each CADASIL patient. The 24-hour arterial BP variables were compared between CADASIL and controls. In addition, for CADASIL patients only, MMSE, LV, and age were compared with each pressure variable.

Results— Patients with CADASIL showed a significant reduction (P<0.05) of SABP_day, DABP_day, MABP_day and %MABP decline with respect to controls. In addition, MMSE of CADASIL subjects correlated significantly (P<0.0001) with daytime MABP.

Conclusions— The low systemic BP profile observed in CADASIL patients was specifically attributable to reduced diurnal BP values. This may further affect cerebral hemodynamics and increase the risk of cognitive impairment in these patients. The pathogenesis of abnormal BP profile in CADASIL remains to be clarified. It is likely that central and peripheral mechanisms controlling BP variations are involved.

Key Words: blood pressure • CADASIL • dementia • magnetic resonance imaging

	Introduction

Top Abstract Introduction Materials and Methods Results Discussion References

 
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a generalized small- and medium-sized arteriopathy attributable to mutations in the Notch3 gene,¹ which causes repeated strokes, MRI evidence of diffuse white matter (WM) changes, and progressive cognitive impairment.² Although the nature of Notch3 mutations is highly stereotyped, the phenotypic expression of the disease is extremely variable,³ suggesting a possible modulating role of other genetic or acquired factors, including cardiovascular risk factors.^4,5 Vascular smooth muscle cells are thought to be targeted by the disease.⁶ Their degeneration presumably leads to loss of systemic arteriolar wall tone and failure of cerebral autoregulation with chronic hypoperfusion or abrupt lack of perfusion.⁷ Unlike in other forms of sporadic subcortical ischemic vascular dementia (SIVD), arteriolar occlusions were rarely observed in autopsied cases.⁸ However, the exact mechanism of how the alterations of the deep small penetrating arteries cause WM changes and lacunar infarcts characteristic of CADASIL are still debated.^9,10 Cerebral WM abnormalities similar to those observed in CADASIL patients, are frequently seen on MRI of elderly individuals, particularly in those with vascular risk factors and with cognitive impairment.¹¹ Blood pressure (BP) instability is a serious risk factor for developing or worsening WM changes in sporadic SIVD because prolonged hypertensive or conversely hypotensive state is associated with increased risk of cerebral WM changes and dementia.^12–14

Unlike SIVD, the common vascular risk factors are unremarkable in CADASIL; nevertheless, studies on systemic BP changes over time are lacking. The aim of the present study was to determine the BP profile in 14 CADASIL patients and to investigate its relationship with cognitive decline and MRI evidence of WM changes.

	Materials and Methods

Top Abstract Introduction Materials and Methods Results Discussion References

 
Subjects
Fourteen CADASIL patients (12 males and 2 females; mean age 48.1; range 25 to 70) from 10 families were recruited. None of them experienced acute vascular events or migraine with aura in the 3 months preceding and during the study. No cardiac disease was reported in their clinical history. The following clinical features were recorded: first symptom and age of onset, global cognitive performance evaluated by mini mental status examination (MMSE;¹⁵ dementia defined as MMSE <23), and functional ability at the time of investigation by Rankin scale.

CADASIL patients underwent complete general and laboratory assessment, including vascular risk factors (smoking history, cholesterol, triglycerides, glucose, homocysteine, complete blood cell count, electrocardiography, echocardiography, and carotid Doppler sonography). Three patients were taking aspirin at the time of enrollment. All patients underwent neuropsychological evaluation and conventional MRI examination.

Control subjects were white, nonsmoking, healthy age-matched volunteers (5 females and 10 males; mean age 46.2; range 25 to 73). Exclusion criteria for controls included obesity, history of cerebral or heart disease, and personal or family history of risk factors for vascular disease. All subjects gave informed consent, and the study was approved by the regional ethics committee.

BP Profile Assessment
Basal BP was measured with a mercury sphygmomanometer either in the right or left arm in the seated position after 5 minutes of rest.

Twenty-four–hour ambulatory BP monitoring was performed in the right arm in 2 sessions separated by a 3-month interval in each subject using Novacor Dyasis Integra equipment to assess circadian pattern, and the values of the 2 measurements were averaged. The instrument is a noninvasive portable automatic ambulatory BP recorder operating in each standard auscultatory and oscillomatic mode. Recordings were performed in auscultatory mode based on detection of appearance and disappearance of Korotkoff sounds. Systolic and diastolic arterial BP (SABP and DABP, respectively) and heart rate were averaged over successive 20-minute intervals through the day (from 7 AM to 12 PM) and 30-minute intervals at night (from 12 PM to 7 AM). Mean arterial BP (MABP) was computed automatically by the equipment; overall diurnal and nocturnal values and percentage nocturnal dipping of MABP (%MABP reduction) [(BP_day–BP_night/BP_day)x100], were also calculated by the instrument. Only effective records (85% of probes and measurements per hour) were examined for each patient. On the basis of nocturnal MABP dipping, patients were classified as extreme dippers (MABP reduction 20%); dippers (10% but <20%), nondippers (<10% but 0%), and inverted dippers (<0%). Hypertension was defined as persistent baseline SABP 160 mm Hg or DABP 95 mm Hg or current treatment with antihypertensive drugs. Conversely, hypotension was considered SABP 110 mm Hg and DABP 70 mm Hg (subcommittee of World Health Organization/International Society of Hypertension Mild Hypertension Liaison Committee 1993).

MRI Examination and Analysis
All patients were examined using the same magnetic resonance protocol, which included combined proton MRI of the brain obtained in a single session of 50 minutes for each examination using a Philips Gyroscan operating at 1.5 T (Philips Medical Systems). A transverse dual-echo, turbo spin-echo sequence (repetition time/echo time 1/echo time 2=2075/30/90 ms, 256x256 matrix, 1 signal average, 250 mm field of view) yielding proton density (PD) and T2-weighted (T2W) images with 50 contiguous 3-mm slices was acquired parallel to the line connecting the anterior and posterior commissures.

Classification of T2W lesion volume (LV) was performed in each patient by a single observer (M.L.S.) using a segmentation technique based on user-supervised local thresholding unaware of subject identity. Lesion borders were determined primarily on PD-weighted images, but information from T2W and T1W images was also considered because the software (Jim 3.0; Xinapse System) offered the possibility of switching between PD, T2W, and T1W images, providing the operator with convenient access to the information in both data sets while defining lesions and facilitating discrimination of cerebrospinal fluid and periventricular plaque. Total brain LV was calculated by multiplying lesion area by slice thickness and was reproducible to 5% in serial measurements.

Statistical Analysis
All the pressure variables (SABP_day, DABP_day, MABP_day, SABP_night, DABP_night, and MABP_night) and nocturnal percentage decline in arterial BP (% MABP reduction) were compared between CADASIL and controls using Student t test for equal or unequal group variance. The Mann–Whitney U test was also applied to reinforce the t test statistical results. Equality of group variances was first tested by Levene statistics.

For CADASIL patients only, paired association between MMSE, LV, and all pressure variables was evaluated by the Pearson correlation coefficient r. Correlation was also tested between MMSE and LV.

A probability error P<0.05, corresponding to a significance level >95%, was chosen for the significance of all statistical computing. Statistical analysis was performed with the SPSS computer package

	Results

Top Abstract Introduction Materials and Methods Results Discussion References

 
Clinical Characteristics and Risk Factors (Table 1)
The age at onset of the first symptom ranged from 17 to 66 years. Only 1 patient was currently asymptomatic (25 years of age). Symptoms at onset were: acute ischemic cerebrovascular episodes in 9 subjects (presenting as ocular manifestations in 4 of them), migraine with or without aura in 2, and depression in 2. The following cardiovascular risk factors were found: hyperhomocysteinemia in 5 of 14, hypercholesterolemia in 3 of 14, current smokers 2 of 14, and ex-smokers 2 of 14. No diabetes, hypertension, significant heart disease, or carotid stenosis was found. At recruitment, stroke/TIA had occurred in 11 of 14 patients, migraine in 2 of 14, and dementia (MMSE corrected for age, socioeconomic, and educational variables <23) in 8 of 14. Only 2 patients were moderately disabled (Rankin score 3), whereas the majority of patients mildly disabled (11 patients; Rankin score 1 to 2), or normal (1 patient; Rankin score 0).

View this table: [in this window] [in a new window]   TABLE 1. Phenotypic and Genetic Profile

BP Profile
No significant differences were observed on basal conditions between left and right brachial BP measurements.

Among all the measured parameters, a statistically significant difference (P<0.05) was observed between CADASIL and controls for: MABP_day, SABP_day, DABP_day, and %MABP reduction. Nocturnal BP variables did not show any statistical differences (Table 2).

View this table: [in this window] [in a new window]   TABLE 2. Statistical Comparison of Differences Between CADASIL Patients and Control Subjects

Based on percentage nocturnal fall in MABP, 9 CADASIL patients were nondippers (%MABP decline was respectively: 4% in 2, 5% in 2, 6% in 3, and 8% in 2), 3 dippers (respectively 10%, 12%, and 14%), 1 extreme dipper (21%), and 1 was an inverted dipper (+2%). Among normal subjects: 11 were dippers (%MABP reduction was respectively: 19% in 1, 18% in 3, 17% in 3, 16% in 2, and 15% in 2); 3 extreme dippers (20%, 22%, and 27%, respectively), and 1 nondipper (10%). Comparison of mean, SABP_day, DABP_day, and MABP_day revealed a significantly lower daily BP profile (SABP_day 111.7 mm Hg range 102 to 118; DABP_day 74.4 mm Hg range 68 to 76; MABP_day 86.5 mm Hg range 80 to 97) in CADASIL patients than normal subjects (SABP_day 126.4 mm Hg range 118 to 133; DABP_day 82.2 mm Hg range 76 to 86 and MABP_day 96.9 mm Hg, range 91 to 103). Figure 1 shows the 24-hour differences in MABP_day and percentage reduction in MABP between CADASIL and controls. Average 24-hour MABP values revealed a reduced BP variability, mostly because of lower daily MABP values in CADASIL patients than controls (Figure 2). By comparing each BP variable with global cognitive performances and magnetic resonance volume of tissue damage, a positive correlation was found between MMSE score and MABP_day (r=0.834; P<0.0001). No correlations were observed between pressure variables or MMSE and T2W MRI LV.

View larger version (10K): [in this window] [in a new window]   Figure 1. Bidimensional plot showing differences in MABPday and percentage reduction in MABP between CADASIL () and controls (). CADASIL patients have lower values of percentage of MABP decline (CADASIL range –21%; +2%; control range –27%; –10%) and MABPday (CADASIL range 80 to 97 mm Hg; control range 91 to 103 mm Hg).

View larger version (17K): [in this window] [in a new window]   Figure 2. Average of 24-hour MABP variation in CADASIL (dotted line) and controls (unbroken line). Note the reduced BP circadian variability, mostly attributable to lower MABP daily in CADASIL than in controls.

	Discussion

Top Abstract Introduction Materials and Methods Results Discussion References

 
Studies on BP profile are substantially lacking in CADASIL. Here, we demonstrated for the first time a significant reduction in mean diurnal systolic and diastolic BP in CADASIL patients with respect to age- and sex-matched healthy controls. We also confirmed the reduced nocturnal BP decline observed previously in a few cases.¹⁶

CADASIL is an inherited form of SIVD attributable to small artery disease. As in sporadic SIVD, MRI studies of CADASIL patients have revealed a microangiopathic pattern of signal abnormalities, including diffuse WM hyperintensities in T2 signal sequences and circumscribed subcortical lesions.¹⁷ Unlike sporadic SIVD, the most common cardiovascular risk factors were unremarkable in a large sample of CADASIL patients except for smoke and hyperhomocysteinemia which, in a previous study, significantly correlated with increased risk of stroke and migraine.⁴ The mechanisms leading to WM hyperintensities and lacunar infarcts in CADASIL are still debated. Decreasing or loss of cerebral vasoreactivity is commonly considered the pathophysiological key, primarily responsible for the hemodynamic changes leading to subcortical chronic hypoperfusion and ischemic lacunar lesions.^18,19,20 This would make the WM more susceptible to decline in blood flow during systemic hypotension.

In this study, we found an atypical systemic BP profile with reduced 24-hour variability in BP in 14 CADASIL patients in different stages of the disease and a reduced percentage of MABP decline with respect to controls. The differences in the average of circadian MABP variation between the 2 groups were mostly attributable to MABP daily values, which were lower in CADASIL (Figure 2). In fact, no significant differences were observed during nighttime. Probably, reduced daily BP values may be contributing to a lower percentage of nocturnal MABP decline in our CADASIL patients.

The pathogenesis of abnormal BP profile in CADASIL remains to be clarified. It is likely that central and peripheral mechanisms controlling BP variations are involved. Peripheral compensatory mechanisms of BP regulation may be impaired in CADASIL. Systemic peripheral small vessels show the characteristic pathological features of the disease consisting of degeneration of vascular smooth muscle cells and accumulation of granular osmiophilic material,^21,8 which may result in hemodynamic consequences on peripheral resistance arteries. In this respect, early damage of resistance artery responses to flow and pressure has been shown in a mouse model of CADASIL.²² In vivo, a selective systemic microvascular vasoconstrictor abnormality and severe weakness of the arteriolar wall were also reported.²³ One interpretation might be that reduced BP variability, found in our patients with respect to controls, reflects an abnormal responsiveness of peripheral resistance arteries during daily life, when the mechanisms of BP regulation are more stressed. The difference is unremarkable during nighttime. Alternatively, the low BP profile may be attributable to functional failure of brain structures and connections controlling circadian BP variations, secondary to the extensive WM damage observed in most cases. The latter cannot be excluded by the present study. An alternative hypothesis is the involvement of peripheral and central mechanisms controlling BP variability in different stages of the disease.

The low daytime MABP significantly correlated with global cognitive impairment (MMSE) in our patients. As extensively reported in previous studies, a lower BP profile increases the risk of leukoaraiosis and dementia in elderly people.^24,25 The BP profile seems to be relevant for different outcomes of patients with SIVD, tending to elevate over time in patients with a fair outcome and to decrease in those with lacunar infarcts and diffuse WM changes who developed dementia and symptomatic infarcts.^26,27

We cannot draw final conclusions about the mechanism underlying the correlation between MMSE and MABP daily. Systemic BP below a critical threshold could result in cerebral hypoperfusion in CADASIL patients who already have impaired cerebral hemodynamics and impaired cerebral vasoreactivity.¹⁸ We hypothesize on this basis that dementia may be worsened by a low BP profile, not only in terms of WM changes but probably also in terms of hippocampal and cortical damage. Recent data on SIVD²⁸ and CADASIL patients showing the presence of cortical damage seem to support this hypothesis. In CADASIL, some evidences suggest a cortical damage: (1) cortical vessel structural abnormalities,⁹ (2) cortical functional impairment,²⁹ and (3) cortical atrophy.³⁰

In conclusion, our results suggest that low BP profile may be part of the clinical features in patients with CADASIL and that may be a further risk factor for global cognitive deterioration. The mechanism by which abnormal BP profile modulates the clinical course of disease needs to be further investigated in longitudinal studies.

	Acknowledgments

 
The research for this work was supported in part by a grant from Regione Toscana to A.F.

Received April 19, 2005; revision received September 19, 2005; accepted September 30, 2005.

	References

Top Abstract Introduction Materials and Methods Results Discussion References

 

1. Joutel A, Corpechot C, Ducros A, Vahedi K, Chabriat H, Mouton P, Alamowitch S, Domenga V, Cecillion M, Marechal E, Maciazek J, Vayssiere C, Cruaud C, Cabanis EA, Rouchoux MM, Wessenbach J, Bach JF, Bousser M-G. Notch 3 mutation in CADASIL, a hereditary adult-onset condition causing stroke and dementia. Nature. 1996; 383: 707–710.[CrossRef][Medline] [Order article via Infotrieve]
2. Chabriat H, Vahedi K, Iba-Zizen MT, Joutel A, Nibbio A, Nagy TG, Krebs MO, Julien J, Dubois B, Ducrocq X, Levasseur M, Homeyer P, Mas JL, Lyon-Caen O, Tournier-Lasserve E, Bousser MG. Clinical spectrum of CADASIL: a study of seven families: cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. Lancet. 1995; 346: 934–939.[CrossRef][Medline] [Order article via Infotrieve]
3. Dichgans M, Mayer M, Uttner I, Bruning R, Muller-Hocker J, Rungger G, Ebke M, Klockgether T, Gasser T. The phenotypic spectrum of CADASIL: clinical findings in 102 cases. Ann Neurol. 1998; 44: 731–739.[CrossRef][Medline] [Order article via Infotrieve]
4. Singhal S, Bevan S, Barrick, Rich P, Markus HS. The influence of genetic and cardiovascular risk factors on the CADASIL phenotype. Brain. 2004; 127: 2031–2038.[Abstract/Free Full Text]
5. Peters N, Herzog J, Opherk C, Dichgans M. A two-year clinical follow-up study in 80 CADASIL subjects: progression patterns and implications for clinical trials. Stroke. 2004; 35: 1603–1608.[Abstract/Free Full Text]
6. Ruchoux MM, Guerouaou D, Vandenhaute B, Pruvo JP, Vermersch P, Leys D. Systemic vascular smooth muscle cell impairment in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. Acta Neuropathol. 1995; 89: 500–512.[Medline] [Order article via Infotrieve]
7. Kalimo H, Rouchoux MM, Viitanen M, Kalarla RN. CADASIL: a common form of hereditary arteriopathy causing brain infarcts and dementia. Brain Pathol. 2002; 12: 371–384.[Medline] [Order article via Infotrieve]
8. Brulin P, Godfraind C, Leteurtre E, Ruchoux MM. Morphometric analysis of ultrastructural vascular changes in CADASIL: analysis of 50 skin biopsy specimens and pathogenetic implications. Acta Neuropathol. 2002; 104: 241–248.[Medline] [Order article via Infotrieve]
9. Miao Q, Paloneva T, Tuominen S, Poyhonen M, Tuisku S, Viitanen M, Kalimo H. Fibrosis and stenosis of the long penetrating cerebral arteries: the cause of white matter pathology in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. Brain Pathol. 2004; 14: 358–364.[Medline] [Order article via Infotrieve]
10. Okeda R, Arima K, Kawai M. Arterial changes in cerebral autosomaldominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) in relation to pathogenesis of diffuse myelin loss of cerebral white matter. Stroke. 2002; 33: 2565–2569.[Abstract/Free Full Text]
11. Soderlund H, Nyberg L, Adolfsson R, Nilsson LG, Launer L. High prevalence of white matter hyperintensities in normal aging: relation to blood pressure and cognition. Cortex. 2003; 39: 1093–1105.[Medline] [Order article via Infotrieve]
12. Roman GC. Senile dementia of the Binswanger type. J Am Med Assoc. 1987; 258: 1782–1788.[Abstract]
13. Roman GC, Erkinjuntti T, Wallin A, Pantoni L, Chui HC. Subcortical ischaemic vascular dementia. Lancet Neurol. 2002; 1: 426–436.[CrossRef][Medline] [Order article via Infotrieve]
14. Pantoni L. Pathophysiology of age related cerebral white matter changes. Cerebrovasc Dis. 2002; 13: 7–10.
15. Cockrell JR, Folstein MF. Mini-mental state examination (MMSE). Psychopharmacol Bull. 1988; 24: 689–692.16.[Medline] [Order article via Infotrieve]
16. Manabe Y, Murakami T, Iwatsuki K, Narai H, Warita H, Hayashi T, Shoji M, Imai Y, Abe K. Nocturnal blood pressure dip in CADASIL. J Neurol. Sci. 2001; 193: 13–16.[CrossRef][Medline] [Order article via Infotrieve]
17. Chabriat H, Pappata S, Poupon C, Clark CA, Vahedi K, Poupon P, Mangin JF, Pacheot-Clouard M, Jobert A, Le Blhan D, Bousser MG. Clinical severity in CADASIL related to ultrastructural damage in white matter: in vivo study with diffusion tensor MRI. Stroke. 1999; 30: 2637–2643.[Abstract/Free Full Text]
18. Chabriat H, Pappata S, Ostergaard L, Clark CA, Pachot-Clouard M, Vahedi K, Jobert A, Le Bihan D, Bousser MG. Cerebral hemodynamics in CADASIL before and after acetazolamide challenge assessed with MRI bolus tracking. Stroke. 2000; 31: 1904–1912.[Abstract/Free Full Text]
19. Liebetrau M, Herzog J, Kloss CUA, Harmann GF, Dichgans M. Prolonged cerebral transit time in CADASIL. A transcranial ultrasound study. Stroke. 2002; 33: 509–512.[Abstract/Free Full Text]
20. Van den Boom R, Lesnik Oberstein SA, Spilt A, Behloul F, Ferrari MD, Haan J, Westendorp RG, van Buchem MA. Cerebral hemodynamics and white matter hyperintensities in CADASIL. J Cereb Blood Flow Metab. 2003; 23: 599–604.[CrossRef][Medline] [Order article via Infotrieve]
21. Mayer M, Straube A, Bruening R, Uttner I, Pongrazt D, Gasser T, Dichgans M, Muller-Hocker J. Muscle and skin biopsies are a sensitive diagnostic tool in the diagnosis of CADASIL. J Neurol. 1999; 246: 526–532.[CrossRef][Medline] [Order article via Infotrieve]
22. Dubroca C, Lacombe P, Domenga V, Maciazek J, Levy B, Tournier-Lasserve E, Joutel A, Henrion D. Impaired vascular mechanotransduction in transgenic mouse model of CADASIL arteriopathy. Stroke. 2005; 35: 113–117.
23. Hussain MB, Singhal S, Markus H, Singer DR. Abnormal vasocontrictor responses to angiotensin II and noradrenaline in isolated small arteries from patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). Stroke. 2004; 35: 853–858.[Abstract/Free Full Text]
24. Guo Z, Viitanen M, Fratiglioni L, Winblad B. Low blood pressure and dementia in elderly people: the Kungsholmen project. BMJ. 1996; 312: 805–808.[Abstract/Free Full Text]
25. Verghese J, Lipton RB, Hall C, Kuslanky G, Katz MG. Low blood pressure and risk of dementia in very old individuals. Neurology. 2003; 61: 667–672.
26. Yamamoto Y, Akiguchi I, Oiwa K, Hayashi M, Imai K. Twenty-four hour blood pressure changes in the course of lacunar disease. Cerebrovasc Dis. 2001; 11: 100–106.
27. Skoog I, Lernfelt B, Landahl S, Palmertz B, Andreasson L, Nilsson L, Persson G, Oden A, Svanborg. 15-year longitudinal study of blood pressure and dementia. Lancet. 1996; 347: 1141–1145.[CrossRef][Medline] [Order article via Infotrieve]
28. Fein G, Di Sclafani V, Tanabe J, Cardenas V, Weiner MW, Jagust WJ, Reed BR, Norman D, Schuff N, Kusdra L, Greenfield T, Chui H. Hippocampal and cortical atrophy predict dementia in subcortical ischemic vascular disease. Neurology. 2000; 55: 1626–1635.[Abstract/Free Full Text]
29. Mesulam M, Siddique T, Cohen B. Cholinergic denervation in a pure multi-infarct state. Observation on CADASIL. Neurology. 2003; 60: 1183–1185.[Abstract/Free Full Text]
30. De Stefano N, Smith SM, Dotti MT, Bianchi S, Stromillo ML, Mortilla M, Passero S, Malandrini A, Federico A. Quantitative MRI evidence of cortical brain atrophy in CADASIL patients. Neurology. 2003; 60 (suppl 1): A304.

This article has been cited by other articles:

				A. Stenborg, H. Kalimo, M. Viitanen, A. Terent, and L. Lind Impaired Endothelial Function of Forearm Resistance Arteries in CADASIL Patients Stroke, October 1, 2007; 38(10): 2692 - 2697. [Abstract] [Full Text] [PDF]

				A. Rufa, F. Guideri, M. Acampa, G. Cevenini, S. Bianchi, N. De Stefano, M. L. Stromillo, A. Federico, and M. T. Dotti Cardiac Autonomic Nervous System and Risk of Arrhythmias in Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy (CADASIL) Stroke, February 1, 2007; 38(2): 276 - 280. [Abstract] [Full Text] [PDF]

				J. Choi, K. H. Kim, J. Jeong, H.-s. Cho, C. H. Lee, and M. S. Kook Circadian Fluctuation of Mean Ocular Perfusion Pressure Is a Consistent Risk Factor for Normal-Tension Glaucoma Invest. Ophthalmol. Vis. Sci., January 1, 2007; 48(1): 104 - 111. [Abstract] [Full Text] [PDF]

This Article Abstract Full Text (PDF) All Versions of this Article: 36/12/2554    most recent 01.STR.0000190832.17620.25v1 Alert me when this article is cited Alert me if a correction is posted Citation Map Services Email this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Request Permissions Citing Articles Citing Articles via HighWire Citing Articles via Google Scholar Google Scholar Articles by Rufa, A. Articles by Federico, A. Search for Related Content PubMed PubMed Citation Articles by Rufa, A. Articles by Federico, A. Related Collections Autonomic, reflex, and neurohumoral control of circulation Other diagnostic testing Risk Factors Cerebral Lacunes Genetics of Stroke Computerized tomography and Magnetic Resonance Imaging