Factors Affecting Recovery Following Vascular Aphasia
Transcription
Factors Affecting Recovery Following Vascular Aphasia
Mervat Mostafa et al Factors Affecting Recovery Following Vascular Aphasia Mervat Mostafa1, Hosna Mostafa2, Ibtesam Fahmy1, Manal Fahmy1, Kamel Hamouda1, Yahia Zakaria1, Nervana El-Faioumy1, Noha Abo-Krysha1 Departments of Neurology1, Nuclear Medicine2, Cairo University ABSTRACT Objective: To study the influence of some demographic, clinical and neuroimaging variables on recovery of vascular aphasia. Subjects and Methods: The study included 47 aphasic patients (27 females and 20 males), who were subjected to thorough clinical assessment, scoring of aphasia using modified Chesher test and Achen aphasia test (AAT), laboratory work-up and SPECT scan of the brain. Results: A significant negative correlation was obtained between age and the scores of the different aspects of the aphasia scales, though no significant correlation was found between age and regional cerebral blood flow (rCBF). Female patients with aphasia of more than 3 months duration showed significant higher mean scores of aphasia tests compared to males, moreover, females had a higher mean left hemispheric CBF compared to males. Literate patients had significantly higher mean scores of aphasia tests compared to illiterates, however, no significant difference was observed between literates and illiterates regarding CBF. Patients with multiple risk factors for stroke had lower mean scores of aphasia scales and lower rCBF compared to those with a single risk factor. Patients with nominal and transcortical (TCM) aphasia had significantly higher mean scores of aphasia scales compared to global and Broca’s aphasics, though no significant difference was detected between different types of aphasia regarding CBF. Patients with large sized hypoperfusion and those with cerebellar diaschesis had lower mean scores in the used aphasia tests compared to those with small sized hypoperfusion and those without diaschesis. Conclusion: Factors predicting good recovery following vascular aphasia include: young age, female gender, education, absence of risk factors for stroke, localized forms of aphasia, higher grade of motor power on the paretic side, small sized hypoperfusions and absence of cerebellar diaschesis on SPECT study. . (Egypt J. Neurol. Psychiat. Neurosurg., 2004, 41(1): 183-194). INTRODUCTION It is known that the greatest spontaneous recovery in vascular aphasia takes place within the first 6 months following stroke onset,1,2 however, other authors use a 3months as a cut off point of spontaneous recovery.3,4 Many variables tend to affect recovery of aphasia as: etiology of aphasia, type of aphasia, age and sex of the patient, handedness, intellectual and educational level of the patient and certain behavioral and social factors.5 The prognosis of aphasia is significantly different according to etiological varieties; aphasias caused by trauma have better prognosis than aphasias caused by progressive disorders and strokes.6 Moreover, patients with aphasia caused by strokes, who have had prior infarcts, show limited recovery.7 183 Egypt J. Neurol. Psychiat. Neurosurg. Mild Broca’s aphasia, transcortical motor aphasia (TCMA), and conduction aphasia usually show good recovery compared to global aphasia.8 However, severe Broca’s and Wernicke’s aphasias tend to recover along several pathways.9 Recovery from aphasia may be agerelated. Some authors documented that improvement appeared to favor younger patients.10.11 However, others found that age had a minor effect as regard recovery in aphasics.2,4 Several studies showed that gender difference had no significant effect in recovery in aphasics.6,12,13 However, other studies concluded that females recover significantly better than males in oral expression, but not in auditory verbal comprehension.14,15 Aphasia in left handers is usually milder than in right handers, regardless of the hemisphere damaged. Moreover, left handers generally recovery more quickly and more thoroughly from aphasia than do right handers.6 Intellectual and educational level influences the limits of what the patient and his environment will consider normal.6 In addition several behavioral and psychological factors were found to have significant effect on the course of recovery from aphasia.16 Studies using CBF during recovery from aphasia have produced conflicting results. Some studies found that good recovery form aphasia was associated with an increase in regional CBF in the right hemisphere.17,18 Other studies suggested that the activation of the left hemisphere was the best indictor of good recovery from aphasia.19 In addition, other researchers suggested that the initial language recovery within the first year post-stroke may be linked primarily to functional recovery in the dominant hemisphere, whereas, long-term recovery in 184 Vol. 41 (1) – Jan 2004 aphasia may be related to slow and gradual compensatory functions in the contralateral hemisphere.20 So, this study was designed to study the influence of some demographic, clinical and neuroimaging variables on the rate of recovery following vascular aphasia. PATIENTS AND METHODS This study was conducted on 47 righthanded Egyptian aphasic patients due to cerebral infarction in the domain of middle cerebral artery. Patients were recruited from the Internal Medicine and Neurology Departments, Kasr El-Aini Hospitals. Excluded from this work were: Patients with aphasia due to causes other than stroke, patients with disturbed conscious level or comatosed patients and patients with other concomitant neurologic or psychiatric diseases. Patients were submitted to the following battery of assessment: 1. Thorough clinical evaluation. 2. Clinical testing of aphasia using: a. The Arabic translated form of the modified Chesher test. b. Aachen aphasia test (AAT). 3. Laboratory test including: Complete blood picture, fasting and postprandial blood sugar, urea and creatinine levels, liver function, lipid profile, and serum uric acid. 4. Non-contrast CT and or MRI of the brain: To confirm that aphasia is due to vascular occlusion in the domain of MCA. 5. Single photon Emission computerized tomography (SPECT): SPECT scans of the brain were performed using Tc99m Hexamethyl Mervat Mostafa et al propylenamine (HMPAO). SPECT images were acquired 60 minutes postinjection of the radiopharmaceutical by a dual head gamma camera equipped with high-resolution collimators interfaced to a dedicated computer. Statistical Methods: Individual data were expressed in mean and standard deviation (SD). The Student ttest was used to test the significance of differences between the two means. The Mann-Whitney U test was used to compare the means of two independent groups. The correlation coefficient and the Chi-squared tests were used to measure the relationship between two quantitative and qualitative variables respectively. RESULTS Forty-seven right-handed aphasic patients (27 females and 20 males) were included in this study. Their ages ranged from 17 to 81 years with a mean of 46.45±12.71 years. Fourteen patients were literate (29.79%), mostly males, whereas, 33 patients were illiterate (70.21%). Forty-two patients (89.36%) were found to have multiple risk factors for cerebrovascular stroke (CVS) detected either clinically or by investigations, while 5 patients (10.64%) had only a single risk factor. The clinical risk factors for CVS encountered in our patients included: hypertension in 21 patients (44.68%), smoking in 12 patients (25.53%) and Diabetes Mellitus in 8 patients (17.02%). History of rheumatic fever was recorded in 11 patients (23.4%) and cardiac arrhythmias were found in 8 patients. Previous transient ischemic attacks (TIAs) in the domain of the carotid system were reported in 8 patients (17.02%) and pulseless disease was encountered in one patient (2.13 %). Contraceptive pill intake was reported in 4 female patients. Risk factors detected by laboratory workup are shown in table (1). Carotid duplex studies revealed diffuse atherosclerosis in both carotid arteries in 7 cases (14.9%), atheromatous plaques in 5 cases (10.6%), left internal carotid artery stenosis in 3 cases (6.4%), complete occlusion of left common carotid artery in 2 cases (4.3%), tortousity of left common carotid artery (CCA) and internal carotid artery (ICA) in one case (2.13%) and complete occlusion of left and right common carotid arteries, both subclavian arteries and both axillary arteries in one case (2.13%). Echocardiography studies revealed concentric left ventricular hypertrophy in 8 cases (17.02%), mitral regurge and left atrial dilatation in 7 cases (14.9%), aortic regurge in 5 cases (10.6%), diastolic dysfunction in 4 cases (8.5%), mitral valve prolapse, dilated cardiomyopathy and sclerosed aortic valve, each detected in 2 cases (4.3%) and pulmonary hypertension, interventricular hypertrophy and dilatation of right atrium and ventricle, each detected in one case (2.1%). Age: A significant negative correlation was found between the age of the patient with the repetition subtest of modified Chesher test (p=0.02); total score of spontaneous speech ratings, repetition and token subtests of AAT (p= 0.009, 0.01 and 0.02 respectively). However, no significant correlation was found between age and the CBF of the left or right hemispheres (p= 0.91, 0.63 respectively). Sex: No significant difference was found between male and female patients as regards the mean scores of aphasia subtests. 185 Egypt J. Neurol. Psychiat. Neurosurg. However, comparison between male and female patients with aphasia of more than 3 months duration showed that female patients had significantly higher total score of modified Chesher test and higher articulation score of AAT, (p= 0.02, 0.01 respectively). As regard CBF, there was a trendwise higher mean left hemispheric CBF in female patients compared to males (p= 0.07). Moreover, the mean left temporal and left parietal CBF were significantly higher in female patients compared to males, (p= 0.001, 0.04 respectively). Table (2) Literacy State: Literate patients showed significantly higher mean scores in nearly all subtests of the used aphasia scales. Table (3). However, comparison between literate and illiterate patients as regard CBF revealed no significant difference between both groups. Table (4). Grade of motor power on the hemiparetic side: The grade of motor power in upper limb showed significant positive correlation with comprehension score and the total score of modified Chesher test (p= 0.04, 0.03 respectively); and with articulation and comprehension scores of AAT (p= 0.04, 0.006 respectively). The grade of motor power in lower limb was also positively correlated with repetition; comprehension, and the total scores of modified Chesher test (p= 0.007, 0.003 and 0.002 respectively), and with total spontaneous speech rating score; naming, repetition; comprehension and token test scores of AAT (p= 0.005, 0.05, 0.02, 0.000 and 0.020 respectively). A significant positive correlation was also found between the grade of motor power of upper limb and the rCBF of both right and 186 Vol. 41 (1) – Jan 2004 left frontal lobes (p= 0.01,0.003 respectively). Moreover, the grade of motor power of upper and lower limbs showed significant negative correlation with the size of hypoperfusion lesion (p= 0.004, 0.02, respectively). Clinical type of aphasia: The types of aphasia found in our patients are shown in table (5). Global and Broca's aphasics showed significantly lower mean scores in almost all subtests of the used aphasia scales compared to TCM aphasics and anomics. Table (6). However, comparison between different clinical types of aphasia as regard CBF; revealed no significant difference. Table (7) Comparison between patients with a single risk factor and those with multiple risk factors: The mean scores of aphasia scales were compared between patients with a single risk factor and those with multiple risk factors, those with multiple risk factors had lower mean scores. Moreover, patients with multiple risk factors showed lower mean CBF in the left hemisphere compared to those with a single risk factor. However, as there is a big difference in the number of patients between the two groups (42 versus 5), the significance of these differences could not be tested. Size of cerebral infarction causing aphasia: The mean scores of aphasia tests were compared among patients with small, medium and large infarcts. Statistically significant differences in the mean scores of naming and comprehension subtests of AAT were found between the three groups (p= 0.02, 0.03 respectively), being higher in patients with small sized lesions followed by medium sized then large sized lesions. The mean CBF in different lobes of both brain hemispheres was also compared Mervat Mostafa et al between patients with small, medium and large infarcts. The means of CBF were significantly better in the left frontal, parietal and temporal lobes in the small sized lesions. Small sized infarcts also showed significantly higher CBF in the right frontal lobe. Table (8) Comparison between patient with and without cerebellar diaschesis: Patients with cerebellar diaschesis showed significantly lower mean scores in the comprehension, articulation subtests and the Token test of AAT (p=0.01, 0.05, 0.04 respectively). They also had lower mean scores in the other subtests of AAT and modified Chesher test, as compared to patients without diaschesis, however, the differences were not statistically significant (p> 0.05). Comparison between patients with cerebellar diaschesis and those without as regard CBF was biased by the presence of hyperperfusion lesions in a considerable number of patients with cerebellar diaschesis, which led to a false impression of being of better perfusion than those without diaschesis, hence, this comparison was omitted. Table 1. Laboratory risk factors detected in 47 stroke patients. Laboratory risk factors Hyperuricemia Hypercholesterolemia Hypertriglyceridemia Low HDL High LDL Positive Rheumatoid factor No. (%) 21 9 7 12 6 1 44.68 19.15 14.89 22.53 12.77 2.13 Table 2. Comparison between male and female patients as regard mean CBF in different lobes of both hemispheres. Lobe Side Male (n=20) Female (n=27) Mean ± SD Mean ± SD Frontal Left 93.77 ± 18.69 88.57 ± 16.92 Right 96.7 ± 9.04 93.66 ± 11.49 Parietal Left 71.73 ± 12.93 87.69 ± 13.72 Right 84.36 ± 7.41 87.48 ± 8.59 Temporal Left 73.9 ± 15.22 83.63 ± 10.75 Right 86.22 ± 7.32 88.93 ± 7.49 Occipital Left 84.22 ± 12.56 86.03 ± 9.35 Right 87.86 ± 7 88.57 ± 5.88 Hemispheres Left 69.3 ± 12.27 75.84 ± 13.45 Right 83.49 ± 7.88 87.3 ± 9 *Statistically significant. ** Highly significant ~ Trendwise higher P value 0.2 0.15 0.04* 0.17 0.001** 0.19 0.50 0.68 0.07~ 0.1 187 Vol. 41 (1) – Jan 2004 Egypt J. Neurol. Psychiat. Neurosurg. Table 3. Comparison between literate and illiterate patients as regard the mean scores of aphasia scales. Aphasia scales I. Modified Chesher test 1) Naming 2) Repetition 3) Comprehension a) Spoken words b) Pantomime 4) Total II. AAT 1- Spontaneous speech - Articulation - Automatic - Communication - Phonology - Semantic - Syntactic - Total 2-Naming 3-Repetition 4-Comprehension 5-Token test *Statistically significant. Literate patient N= 14 Illiterate patients N= 33 P-value 78.10 ± 25.99 88.04 ± 28.39 36.62 ± 40.36 52.61 ± 46.44 0.001** 0.01* 93.53 ± 13.07 98.3 ± 4.13 84.21 ± 20.88 83.69 ± 32.82 85.02 ± 32.34 63.75 ± 30.44 0.2 0.01* 0.02* 4.46 ± 0.877 4.77 ± 0.83 3.85 ± 1.21 4.38 ± 1.19 4 ± 1.22 3.69 ± 1.38 25.15 ± 5.92 94.23 ± 30.68 116.15 ± 43.11 104.61 ± 32.56 43.07 ± 11.64 ** Highly significant. 2.95 ± 2.12 2.69 ± 2.28 1.67 ± 1.86 2.26 ± 2.23 2.11 ± 2.05 1.83 ± 1.95 13.52 ± 11.49 40.36 ± 45.74 61.9 ± 58.36 91.42 ± 37.26 23.23 ± 17.22 0.016* 0.002** 0.000** 0.002** 0.003** 0.002** 0.001** 0.001** 0.003** 0.26 0.001** Table 4. Comparison between literate and illiterate patients as regard CBF of different lobes of both brain hemispheres. Site Frontal Parietal Temporal Occipital Hemisphere 188 Left Right Left Right Left Right Left Right Left Right Literate N=14 94.23 ± 17.16 98 ± 11.3 73 ± 12.33 83.61 ± 9.19 76.61 ± 14.23 85.69 ± 8.03 85 ± 12.24 89.92 ± 2.66 71.89 ± 11.29 82.98 ± 8.92 Illiterate N=33 89.54 ± 17.87 95.5 ± 10.85 76.02 ± 14.04 87.04 ± 7.82 80.71 ± 13.26 88.52 ± 7.26 85.4 ± 10.31 87.78 ± 7.01 73.58 ± 13.94 86.63 ± 8.54 P value 0.4 0.47 0.48 0.19 0.34 0.23 0.9 0.29 0.69 0.18 Mervat Mostafa et al Table 5. Clinical types of aphasia in our patients. Clinical type of aphasia *Aphasia with repetitive disorder: - Broca’s - Global - Conduction - Wernicke’s *Aphasia without repetitive disorder: - TCM - Mixed TC - Nominal * Alexia with agraphia No. Percent 12 7 2 2 25.5 14.7 4.2 4.2 14 2 7 1 29.4 4.2 14.7 2.1 Table 6. Comparison between different types of aphasia as regards the mean scores of aphasia scales. Subtests I. Modified chesher test 1) Naming 2) Repetition 3) Comprehension - Spoken words - Pantomime Total II. AAT 1) Spontaneous speech - Articulation - Automatic - Communication - Phonology - Semantic - Syntactic - Total 2) Naming 3) Repetition 4) Comprehension 5) Token test Global N=7 Broca’s N=12 TCM N=14 Nominal N=7 P 17.6±32.5 15.1 ± 37.5 13.4 ± 24.4 22.13 ± 35.7 71.08 ± 35.9 94.81 ± 20.75 71.3 ± 32.7 99.2 ± 2.1 0.001** 0.001** 34.85 ± 44.5 38.85 ± 49.4 24.15 ± 37.2 96 ± 7.43 94.06 ± 7.6 56.7 ± 14.25 93.06 ± 24.96 93.75 ± 25 86.7 ± 24.2 100 ± 0 100 ± 0 91.3 ± 8.4 0.002** 0.007** 0.001** 1.4 ± 1.9 1.7 ± 2.4 0.86 ± 1.46 0.86 ± 1.5 0.86 ± 1.5 0.43 ± 0.8 6.1 ± 9.1 21.42 ± 36.3 17.14 ± 41.1 34.3 ± 41.2 8.6 ± 16.5 1.9 ± 2.2 1.4 ± 2.03 0.59 ± 0.94 1.29 ± 1.96 0.94 ± 1.51 0.64 ± 0.79 6.8 ± 8.47 14.11 ± 24.25 22.35 ± 35.79 102.35 ± 22.22 23.3 ± 14.9 4.5 ± 0.73 4.3 ± 1.6 3 ± 1.8 3.8 ± 1.93 3.75 ± 1.65 3.18 ± 1.79 22.56 ± 8.39 85 ± 43.32 120.63 ± 36.6 106.25 ± 31.6 34.7 ± 16.5 4.5 ± 0.5 4.7 ± 0.5 4.43 ± 0.9 4.7 ± 0.5 4.6 ± 0.5 4.6 ± 0.5 27.57 ± 2.9 75.7 ± 46.1 132.9 ± 26.3 114.3 ± 15.1 40.29 ± 16.6 0.001** 0.001** 0.001** 0.001** 0.001** 0.001** 0.001** 0.001** 0.001** 0.002** 0.001** ** Highly significant. 189 Vol. 41 (1) – Jan 2004 Egypt J. Neurol. Psychiat. Neurosurg. Table 7. Comparison between clinical types of aphasia as regard CBF. Site 1-Left hemisphere 2- Left frontal 3- Left parietal 4- Left Temporal 5- Left occipital 6-Right hemisphere 7- Right frontal 8- Right parietal 9- Right Temporal 10- Right occipital Global N=7 Mean±SD 69.6 ± 5.3 90.4 ± 18.4 69.5 ± 5.7 73.3 ± 8.9 86.3 ± 9.8 82.9 ± 9.4 97.1 ± 10.5 82.9 ± 9.5 84.1 ± 9.8 88.7 ± 3.4 Mean CBF in different types of aphasia Broca’ TCM Nominal N=12 N=14 N=7 Mean±SD Mean±SD Mean±SD 75.4 ± 17.07 77.87 ± 12.3 67±10.1 91.7 ± 17.19 86 ± 17.9 94 ± 19.3 77.94 ± 16.33 78.68 ± 11.8 69.1 ± 13.22 79.7 ± 15.5 83.12 ±12.8 84.14 ± 11.4 83.05 ± 12.9 90 ±0 82.6 ± 12.9 88.53 ± 7.5 87.9 ± 8.2 83.4 ± 8.9 96.9 ± 9.16 92.9 ± 11.01 99.14 ± 10.33 88.5 ± 6.2 88.2 ± 7.9 85.3 ± 8.7 90.5 ± 6.3 88.8 ± 6.06 89.4 ± 5.5 85.7 ± 10.12 90 ± 0 89.1 ± 5.4 P 0.2 0.7 0.2 0.4 0.1 0.3 0.5 0.3 0.2 0.3 Table 8. Comparison between patients with small, medium and large infarcts as regard means of CBF. Left frontal Left parietal Left temporal Left occipital Left hemisphere Right frontal Right parietal Small infarct Mean ± SD 105 ± 0 81.63 ± 11.8 83.72 ± 12.4 87.54 ± 7.2 72.96 ± 12.27 105 ± 0 87.09 ± 8.65 Medium infarct Mean ± SD 94.1 ± 15.55 72.94 ± 12.47 81.47 ± 12.49 82.42 ± 13.09 72.2 ± 11.62 98 ± 9.97 86.57 ± 8.28 Large infarct Mean ± SD 76.35 ± 16.10 68.6 ± 9.19 72.25 ± 12.48 85.65 ± 10.83 68.61 ± 9.18 90.35 ± 11.23 85.55 ± 9.09 0.00** 0.012* 0.025* 0.44 0.46 0.006** 0.87 Right temporal Right occipital Right hemisphere 87.9 ± 4.78 90.09 ± 2.02 83.96 ± 9.5 89.47 ± 7.91 86.26 ± 9.57 87.37 ± 8.86 86.6 ± 8.93 88.8 ± 4.11 85.56 ± 9.08 0.522 0.26 0.6 Site **Highly significant *Statistically significant DISCUSSION This study was conducted on 47 aphasic patients in an attempt to throw light on the factors which may affect recovery following vascular aphasia including: age, sex, literacy state, risk factors, type of aphasia and size of the vascular lesions. In our study, no significant correlation was observed between age of the patient and 190 P value the rCBF. However, a significant negative correlation was obtained between age and the scores of the different aspects of the used aphasia scales, i.e. the younger the patient, the higher the score of aphasia scales. This observation agreed with previous studies,6,21,22,23,24 that reported that age and rate of recovery from aphasia showed a trend of negative correlation; but there were exceptions, depending on other factors; as the initial severity of aphasia. However, Mervat Mostafa et al Ogrezeanu et al.4, and Pedreson et al.25, reported that the influence of age was minimal on the recovery of aphasia. Comparison between male and female patients in the scores of the used aphasia scales revealed no significant difference. However, female patients with aphasia of more than 3 months duration had significant higher mean scores of aphasia scales compared to males. This finding suggests that during the recovery period (i.e. 3 months following the onset of aphasia), female patients achieve better performance than males. The same conclusion was documented by Basso et al.12, Schehter et al.14, and Elias et al.23, who reported that females recovered significantly better than males in oral expression. It was suggested that the bilateral or diffuse representation of language function in the female brain may account for the greater improvement of aphasia in females.15 However, other studies reported no significant sex difference in the recovery of aphasia.4,6,13,25,26 In our study, female patients showed a higher left hemispheric mean CBF compared to males, especially the mean left temporal and parietal CBF. Our results confirmed with that of Hatazawa et al.27, who reported that women have higher rates of CBF than men, however, after the sixth decade, men and women have similar flow rates. Regland et al.28, also reported that women have better verbal memory and higher rates of resting regional CBF compared to men. Intellectual and educational levels influence the limit of what the aphasic and his environment will consider normal; as those with premorbid superior IQ and high environment expectations may score within the normal range of aphasia scales.6 In our study, literate patients have significantly higher mean scores in the used aphasic tests than illiterate patients. This is in agreement with Elias et al.23, who reported that patients who had the fewest years of formal education had the lowest performance levels, with lower levels of performance for men than women among the least educated patients. Moreover, Connor et al.29, also found that early severity of aphasia to be significantly greater for subjects in the lower educational and occupational groups, however, rate of recovery was the same regardless of educational and occupational status. To our knowledge there is no published data studying the effect of literacy on CBF. In our study, no significant difference was found between literate and illiterate patients as regard CBF. Different risk factors for CVS were detected among our studied patients. Most of our patients, 42, had multiple risk factors (89.36%), those with a single risk factors were only 5 patients (10.64%). patients with multiple risk factors were found to have lower scores in aphasia scales and lower rCBF compared to patients with a single risk factor, however, the significance of these findings could not be tested due to the big difference in number of patients. Moreover, we could not be able to correlate between a certain risk factor as hypertension or DM and rCBF as the majority of our patients had multiple risk factors, so the effect of each risk factor per se on CBF could not be assessed. In our study, a statistically significant difference was observed between the mean scores of the used aphasia scales in the different clinical types of aphasia. Generally speaking, patients with nominal and TCM aphasia had significantly higher mean scores as compared to global and Broca’s aphasics. Our finding confirmed the previous impressions of Kertesz and McCabe6 and Hojo et al.22, who concluded that global aphasics usually have poor recovery, while 191 Vol. 41 (1) – Jan 2004 Egypt J. Neurol. Psychiat. Neurosurg. anomics, conduction and TCM aphasics have a uniformly good prognosis whereas Broca’s and Wernicke’s aphasia usually have heterogeneous outcome depending on the initial severity. A significant negative correlation was observed between the size of cerebral infarcts and mean scores of aphasia tests and this is reflected on the significant positive correlation between grade of motor power on the hemiparetic side and the scores of aphasia tests (i.e. patients with smaller lesions had better motor power and scored better than those with larger ones). This is in agreement with Hojo et al.22, who studied the relation between the size of lesions detected by CT brain in 127 aphasic patients and recovery rates depending on the Standard Language Test of Aphasia (SLTA) scores (initial and 3 months later). They found a negative correlation between the size of lesions and the initial SLTA score, i.e., the larger the lesions, the more severe the aphasia. They also found a negative correlation between the size of lesions and the recovery rate. Moreover, Goldenberg and Spatt30, found that the size of lesion had a negative influence on recovery of aphasia in all phases. In our study, a significant negative correlation was also detected between the size of infarcts and rCBF i.e., patients with large sized infarcts had the lowest rCBF compared to those with medium and small sized infarcts. Crossed cerebellar diaschesis (CCD) is a SPECT finding that may be seen following stroke, it is one of the most important functional derangements that represent a disconnection or deafferentation phenomenon that occur following stroke.31 In our study, patients with cerebellar diaschesis (14 patients) were found to have lower mean scores in the used aphasia scales as compared to those without diaschesis, 192 especially the mean scores of the articulation, comprehension and Token test of AAT. Moreover, we observed that cerebellar diaschesis is more frequent in patients having large sized lesions involving mainly the frontal and parietal lobes. This also explains the observation that patients with CCD had lower grades of motor power on the paretic side, especially the power in the upper limb, which was significantly lower in those with CCD as compared to those without CCD. This may lead us to consider that the presence of CCD may be a predictor of poor recovery in aphasic patients.32 In our study, the association of CCD with the large sized lesion involving the left frontal and parietal lobes conformed with Marien et al.33, who said that the occurrence of a CCD in aphasic syndromes support the pathophysiological hypothesis for the deactivation of the left hemispheric language areas (especially the left frontal area) due to the loss of excitatory impulses through cerebello-ponto-thalamo cortical pathways. 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