Loading

Journal of Neurology and Translational Neuroscience

Right Hemisphere Dysfunction is Better Predicted by Emotional Prosody Impairments as Compared to Neglect

Research Article | Open Access | Volume 2 | Issue 1

  • 1. Departments of Neurology Johns Hopkins University School of Medicine, Baltimore, MD, USA
  • 2. Department of Epidemiology, Bloomberg School of Public Health, Johns Hopkins University; Baltimore, MD, USA
  • 3. Physical Medicine and Rehabilitation, Johns Hopkins University School of Medicine, Baltimore, MD, USA
  • 4. Department of Cognitive Science, Johns Hopkins University, Baltimore, MD, USA
+ Show More - Show Less
Corresponding Authors
Argye E. Hillis, Phipps 446; 600 N. Wolfe Street; Johns Hopkins University School of Medicine; Baltimore, Tel: 410-614-2381; Fax: 410-614-9807
Abstract

Background: Neurologists generally consider hemispatial neglect to be the primary cognitive deficit following right hemisphere lesions. However, the right hemisphere has a critical role in many cognitive, communication and social functions; for example, in processing emotional prosody (tone of voice). We tested the hypothesis that impaired recognition of emotional prosody is a more accurate indicator of right hemisphere dysfunction than is neglect.

Methods: We tested 28 right hemisphere stroke (RHS) patients and 24 hospitalized age and education matched controls with MRI, prosody testing and a hemispatial neglect battery. Emotion categorization tasks assessed recognition of emotions from prosodic cues. Receiver operating characteristic (ROC) analyses were used to compare tests in their ability to distinguish stroke patients from controls.

Results: ROC analyses revealed that the Prosody Score was more effective than the Neglect Battery Score in distinguishing stroke patients from controls, as measured by area under the curve (AUC) ; Prosody Score = 0.84; Neglect Battery Score =0.57. The Prosody Score correctly classified 78.9%, while Neglect Score correctly classified 55.8% of participants as patients versus controls. The Prosody Score was similar to the total NIH Stroke Scale in identifying RHS patients (AUC=0.86, correctly classifying 80.1% of patients versus controls), but the tests only partially overlapped in the patients identified.

Conclusions: Severe prosody impairment may be a better indicator of right hemisphere dysfunction than neglect. Larger studies are needed to determine if including a bedside test of Prosody with the NIH Stroke Scale would most efficiently and reliably identify right hemisphere ischemia.

Keywords

•    Prosody
•    Neglect
•    Emotions
•    Stroke
•    Right hemisphere
•    Communication

Citation

Dara C, Bang J, Gottesman RF, Hillis AE (2014) Right Hemisphere Dysfunction is Better Predicted by Emotional Prosody Impairments as Compared to Neglect. J Neurol Transl Neurosci 2(1): 1037

ABBREVIATIONS

ADC: Apparent Diffusion Coefficient; AUC: Area Under the Curve; DWI: Diffusion Weighted Imaging; FLAIR: fluid attenuation inversion recovery; NIHSS: National Institutes of Health Stroke Scale; RHS: right hemisphere stroke; ROC: Receiver Operating Curve; USN: Unilateral spatial neglect

INTRODUCTION

It is generally believed that the most common cognitive deficits following right hemisphere stroke are unilateral spatial neglect (USN) and extinction with double simultaneous stimulation [1]. USN is typically defined as an inability to detect, attend or respond to stimuli on the side of space contralateral to brain damage, while detecting and responding to stimuli on the ipsilesional side [2]. Approximately 25-30% of acute right hemisphere stroke patients have USN [3]. The only “right hemisphere” cognitive deficits evaluated by the NIH Stroke Scale (NIHSS) are neglect and extinction [4]. One limitation of this fact is that the NIHSS may be less sensitive to right hemisphere than left hemisphere stroke, or may underestimate the volume of right hemisphere stroke [4].

However, the right hemisphere has other cognitive functions that are less widely recognized that may be at least equally important from a functional standpoint and may provide clinical markers that are more reliable than USN for indicating the presence or severity of right hemisphere stroke (RHS). Adding evaluation of such cognitive functions could improve detection and evaluation of outcome of RHS. For example, the right hemisphere is critical for emotional prosody (expression or comprehension of emotional meaning through speech prosody, such as variations in pitch, intensity, and rate). Individuals with right hemisphere lesions have shown difficulty identifying emotions (such as happy, angry, sad, and fearful) of the speaker during human communication. The predominant role of the right hemisphere in processing emotional prosody is corroborated by studies recording event-related brain potentials [5]; fMRI studies showing right hemisphere activation in association with prosody judgments [6,7]; a left ear advantage for prosody using the dichotic listening paradigm [8,9]; and lesion studies of judging emotional meaning from prosody [10-14]. There are a number of other “right hemisphere deficits” that have clear functional consequences, such as anosognosia and apathy (see, 15, 16), integration of information to comprehend discourse, interpret metaphor, draw inferences, and so on (see, 17) for review). It is also crucial for both affective empathy (the ability to recognize and respond to affective experiences of another person; (18, 19) and cognitive empathy (the ability to take the perspective of another person). However, impairments in many of these cognitive functions are difficult to objectively quantify on a scale of more than a few points. One reason USN may have been used so frequently as the primary marker of right hemisphere cognitive function is that it is relatively easy to measure the severity with a variety of bedside pencil and paper, computer, or other standardized tests. We hypothesized that impairment in comprehension of emotional prosody, which can also be measured on a scale of 0-100% accuracy on objective and reliable tests, is even more sensitive and specific for RHS than is USN.

MATERIALS AND METHODS

Participants

A series of 28 patients with acute RHS (mean age 55 years old and mean education 14 years) and 24 patients with transient ischemic attacks (TIA) admitted to Johns Hopkins Hospital, Baltimore, USA were recruited for this study. TIA participants were included as age and education matched controls without evidence of brain lesion on MRI and resolution of presenting symptoms at the time of testing, but with similar socioeconomic background as the stroke patients and same testing environment as the stroke patients. All patients were examined on the clinical and behavioral tests within 48 hours from the admission to the hospital. Exclusion criteria included: bilateral brain damage, injury to brainstem/cerebellum, history of other major neurological or psychiatric illness or previous stroke, and positive toxicology screens for drugs of abuse or alcohol.

Imaging: Lesion location for all patients was identified by the neuroradiologist and technicians on MRI sequences, which included: Axial diffusion weighted imaging (DWI) trace sequences and apparent diffusion coefficient (ADC) maps, fluid attenuation inversion recovery (FLAIR) to evaluate for old strokes, susceptibility weighted images to evaluate for hemorrhage, and T2 weighted sequences to evaluate for other lesions. Technicians masked to behavioral assessment measured volume of infarct on DWI.

EXPERIMENTAL TASKS

Emotional prosody tasks

Two categorization tasks evaluated emotional processing for prosodic features alone. In the word identification task (word ID), participants were presented utterances that were semantically neutral but communicated specific emotions through the prosody (e. g. , I am going to the other movies). In the monosyllabic identification task (monosyllabic ID), participants were presented with monosyllabic utterances that conveyed specific emotions through prosody (e. g. , ba ba ba ba ba ba ba). In word and monosyllabic ID tasks, participants listened to each utterance (from an audio file) and then identified the emotion of the speaker based on the prosodic features in a six forced-choice response format (alternatives - happy, surprise, angry, sad, disinterest, neutral) presented as a picture and as a word on a laptop or on paper. Stimuli for each of these tasks were specifically developed to assess comprehension of emotional prosody in patients as well as healthy adults and this type of stimuli has been used successfully in previous studies [14,20]. The administration time for these two tasks ranged from 5.4 to 7.6 minutes.

Neglect tasks

Hemispatial neglect tests administered as part of the Stroke Cognitive Outcomes and REcovery (SCORE) study included: [1] copy scene (copying the “Ogden scene”: a house, a fence, and two trees; there are 36 total components to the picture, so each missing component yields a percent error) ; [2] a gap detection test (identifying the gaps in small and large circles (21). In this test, a sheet of paper filled with 10 whole circles, 10 circles with gaps on the left, and 10 circles with gaps on the right was presented to the patient. Patients were instructed to cross out the circles with the gaps and to circle the full circles on the paper. This test was administered at midline of the patient’s body. For each task, the number of errors and the total number of stimuli were tabulated. Errors on each side of the page and/or stimulus were recorded in order to distinguish between viewer- and stimulus-centered neglect. The test is administered twice, once with large circles, and once with smaller circles. The administration time for these tasks ranged from 2.9 to 5.8 minutes. Error rate on the SCORE neglect tests potentially ranged from 0-100%.

Neglect and extinction as scored on the NIH Stroke Scale (NIHSS) were also recorded for each patient. The NIHSS scores were obtained by reading through the admission history and physical notes, progress notes from the first full day of admission, and discharge summaries. If NIHSS was not documented, a retrospective NIHSS was calculated using the algorithm used by Williams et al. , 2000 [22]. Neglect is assessed on the basis of describing a complex picture, reading words and sentences, and eye movements (pursuits). Extinction is assessed with double simultaneous stimulation in tactile and visual modalities. Each participant was scored as having neglect [0-1], extinction [0-1] or both (maximum of 2 possible points).

Procedure

Ethical approval of the study was obtained from the Johns Hopkins Institutional Review Board, and informed written consent was obtained from all participants prior to testing. Participants were tested in their individual rooms in the Stroke ward. Testing was carried out in one session; these tests were part of a larger battery that included assessment of prosody production and imitation, as well as other cognitive assessments. Auditory stimuli were presented by a laptop over headphones controlled by Presentation software (NeuroBehavioral Systems, USA). Stimuli within each task were randomized and then played over high quality, volume adjustable headphones at a comfortable listening level. They were instructed to listen carefully to each utterance and then make a judgment about the emotion of the speaker. Most patients responded by pressing a button on a Cedrus 730 response box. For these patients, the response alternatives (verbal labels) were presented centrally on the computer screen as well as marked on the response box. However, for the initial 18 patients, response alternatives were presented on paper, and the patient simply pointed to the emotion of the speaker. There was no time limitation for the participants and the next trial was presented only after the participant had provided a response. There was not a marked difference in the administration time for the two subtests when the paper version was used versus the computer version.

Statistical analyses

Firstly, to examine the performance of the two participant groups (RHS, TIA), two 2 x 2 ANOVAs were conducted separately for prosody identification and neglect tasks. Secondly, Receiver Operating Characteristic (ROC) analyses were conducted to identify a more accurate cut-off point that could help identify the probability of disease in individual participants [23]. ROC curves were created by plotting the range of sensitivity and specificity pairs for each participant’s error rate, with case status (stroke versus TIA) as the classifier variable. A global assessment of the performance of the test is given by the area under the ROC curve (AUC). That is, AUC provides an estimate of the accuracy of the diagnostic test in discriminating between the patients and controls. AUC’s were compared for different tests in their characteristics relative to case status. In addition to the AUC, when evaluating the usefulness of a screening measure to identify those individuals with cognitive impairment, the cut-off point would be chosen to ensure that most cases were detected (high sensitivity; >80% is desirable) but not at the cost of many false positives (goal specificity; >60% is acceptable; 24). Therefore, cut-offs were selected that maximized the sensitivity (>80%) of the tests while maintaining an acceptably low false positive rate (specificity > 60%).

RESULTS AND DISCUSSION

Results

A 2 x 2 ANOVA with factors of Group (RHS, TIA) and Prosody (word ID, monosyllabic ID) revealed a significant main effect of Group, F [1,50] = 29.22, p < 0.00001 and a main effect of Prosody, F [1,50] = 8.51, p < 0.01. Post-hoc Tukey’s (HSD) inspection of the group effect revealed that the RHS patients (M=0.49% errors) made significantly more errors than the TIA group (M=0.25% errors). Also, the prosody main effect showed that both the groups tend to make more errors in the prosody word ID task (M=0.43% errors) as compared to the monosyllabic ID task (M=0.33% errors). A 2 x 2 ANOVA with factors of Group (RHS, TIA) and SCORE Neglect (viewer-centered, stimulus-centered) did not reveal any main or significant effects. The neglect scores from the NIHSS were also similar. Out of 28 patients, 3 patients showed signs of neglect, 5 patients showed signs of extinction, and 2 patients had both neglect and extinction. All individuals with neglect on either test also had impaired prosody. A summary of the mean error rate for the prosody and SCORE neglect tasks is shown in the table 1.

Table 1: Demographics and mean error rates on the prosody and neglect tasks for RHS and control participants.

Participants

Age

Education

Sex

Prosody ID

Neglect

       

word

monosyllabic

Viewer Centered

Stimulus Centered

RHS (n=28)

55.93

13.62

12 female

0.54

0.43

0.01

0.02

SD

11.69

2.94

 

0.19

0.22

0.06

0.07

Controls(n=24)

51.71

13.33

16 female

0.30

0.21

0.00

0.00

SD

10.11

3.95

 

0.22

0.12

0.00

0.00

Abbreviations: SD: standard deviation

The ROC analysis showed that the Prosody Score was more effective than the SCORE Neglect Score in distinguishing stroke patients from controls, as measured by the ROC curve (AUC for the overall Prosody Score = 0.84; AUC for the overall Neglect Score = 0.57). The overall Prosody score of >31% error correctly classified 78.9% of the participants versus controls. For the overall Prosody score, the sensitivity was 92.9% and the specificity was 62.5%. For the prosody word ID task, an error rate of > 37% had a sensitivity of 82.1% and specificity of 66.7% (correctly classifying 75% of participants as patients versus controls). An error rate of > 33% on the prosody monosyllabic ID task had a sensitivity of 78.6% and specificity of 79.2% (correctly classifying 78.9% of participants as patients versus controls) ; ROC curves are shown in Figure 1.

ROC curve plots for the prosody and neglect tasks. Panel A) This graph shows the ROC curve for the error rates for prosody word ID task with an area under  the ROC curve = 0.78. Panel B) This graph shows the ROC curve for the error rates for prosody monosyllabic ID task with an area under the ROC curve = 0.78. Panel C)  This graph shows the ROC curve for the stimulus-centered neglect measure with an area under the ROC curve = 0.55. Panel D) This graph shows the ROC curve for the  viewer-centered neglect measure with an area under the ROC curve = 0.55.

Figure 1 ROC curve plots for the prosody and neglect tasks. Panel A) This graph shows the ROC curve for the error rates for prosody word ID task with an area under the ROC curve = 0.78. Panel B) This graph shows the ROC curve for the error rates for prosody monosyllabic ID task with an area under the ROC curve = 0.78. Panel C) This graph shows the ROC curve for the stimulus-centered neglect measure with an area under the ROC curve = 0.55. Panel D) This graph shows the ROC curve for the viewer-centered neglect measure with an area under the ROC curve = 0.55.

In contrast, the AUC for SCORE neglect summary score was 0.55 for both viewer-centered and stimulus-centered neglect measures. At most, the SCORE Neglect Score could classify 55.8% of patients vs. controls. Of 28 RHS patients, only 5 (17.9%) patients made fewer errors than the cut-off point on the prosody word ID task and 6 (21.4%) patients made fewer errors than the cut-off point on the prosody monosyllabic ID task; whereas 24 (85.7%) patients made 0% errors on the SCORE Neglect tests. The possible range of cut-off points for the sensitivity and specificity for prosody scores on the two ID tasks and neglect measures are shown in Figure 1.

The AUC for NIHSS Neglect was 0.63 and for Extinction was 0.57, and for both was 0.66. Again, prosody was significantly better than NIHSS neglect/extinction in distinguishing stroke patients from controls in this study. Using quintile scores for Prosody Recognition (so that they would have similar scales, rather than comparing a 100 point continuous scale to a 3 point scale), the AUC for Prosody was significantly higher than the NIHSS neglect/extinction score of 0-2 (χ2 = 4.0; p= 0.047).

The SCORE neglect tests identified three stroke patients with neglect who were not identified by the NIHSS as having neglect, but two were identified as having extinction on the NIHSS. The NIHSS identified 7 participants as having extinction, but one was a control.

The AUC for the total NIHSS score was 0.86; it classified 80.8% of patients. Three patients were detected with prosody who were not detected with NIHSS; both had cortical strokes (two parietal, one frontal). Two patients were detected with NIHSS who were not detected with the prosody summary score; one had a subcortical infarct and one had an in infarct in the motor strip. Therefore, the most effective classification of right hemisphere stroke patients versus controls was with the NIHSS score combined with the Prosody Score, yielding an AUC of 0.89 (CI 0.81-0.98). Together, they classified 82.7% of patients. Table 2

Table 2: Comparison of sensitivity and specificity of SCORE Neglect, NIHSS, and Prosody tests.

Test

Sensitivity

Specificity

% Correctly classified

SCORE Neglect Test

14.30%

100.00%

55.80%

NIHSS Extinction 

17.90%

95.80%

53.90%

NIHSS Neglect+Extinction 

35.70%

95.80%

63.50%

Total NIHSS Score

75.00%

87.50%

80.80%

Prosody

92.90%

62.50%

78.90%

Abbreviations: SCORE: Stroke Cognitive Outcome and Recovery; NIHSS: National Institutes of Health Stroke Scale

summarizes the sensitivity and specificity of each test.

Discussion

The current study investigated whether deficits in emotional prosody comprehension are more sensitive than neglect for identifying acute stroke in the right hemisphere. The ROC analysis shows that RHS patients have a higher probability of showing significant impairment in processing emotional prosody than showing significant neglect or extinction. The overall Prosody Score could classify 78.9% of patients vs. controls. In contrast, the SCORE Neglect tests could classify only 55.8% of patients vs. controls, and NIHSS neglect/extinction could classify 63.5 of patients vs controls. The SCORE neglect tests detected three additional stroke patients beyond those detected by NIHSS neglect test, but two of those three were also detected by the NIHSS extinction test. NIHSS extinction identified 7 participants with extinction, but one of these was a control. Still, NIHSS neglect plus extinction was slightly better in detecting right hemisphere stroke than the SCORE neglect tests alone (without extinction). Nevertheless, testing prosody detected 15 more patients with right hemisphere stroke than the NIHSS neglect plus extinction. The two prosody subtests took minimally more time (5.4-7.6 minutes) compared to neglect subtests (2.9-5.8 minutes) and slightly more equipment. Although we presented the audiofiles on a laptop, they could as easily be presented from a smart phone, i-pod, or other electronic storage device. We have also presented the response alternatives on either paper or laptop. The neglect tests were “paper and pencil” tests, but laptop versions could be created, particularly for the gap detection test.

Cancellere and Kertsez, 1990 proposed that impairments in recognition of emotions from prosodic cues in patients with right hemisphere lesions may be due to attentional difficulties [12]. The current study does not provide clear support for this hypothesis. In spite of spared performance on neglect tasks, many RHS patients were profoundly impaired on the prosody tasks. Our study indicates that neglect (one type of spatial attention) and emotional prosody impairment are independent deficits caused by a stroke in the right hemisphere. There is other evidence that RHS patients have significant difficulty in comprehension of emotions from prosody without visual neglect [13]. However, such findings do not rule out that other types of attentional deficits may underlie both prosodic impairments and neglect.

Some brain regions have been identified that can result in both emotional prosody comprehension impairment and neglect. Using multivariate pattern analysis of activation during a gender recognition task during event-related functional MRI of young healthy adults, Ethofer and colleagues [2009] observed that each emotion category had a different localization of activation. However, all emotion categories activated voxels in bilateral mid superior temporal gyrus (STG; (25), implicating the role of mid STG in processing prosodic features irrespective of the emotion category. Right STG has been associated with left USN [1,26-28] or at least left stimulus-centered neglect [29]. Several studies have implicated the right inferior frontal gyrus in evaluative judgments of emotional prosody [30,31] and inferior frontal lobe in neglect tasks [32,33]. Patients in our study as well had lesions in frontal, temporal and parietal regions. An overlay of lesions of all the patients is shown in Figure 2.

Lesions overlay of the RHS patients. An overlay of the lesions of the  28 patients with the right hemisphere stroke (RHS). Nine slices are presented  with all strokes from all the patients overlaid.

Figure 2 Lesions overlay of the RHS patients. An overlay of the lesions of the 28 patients with the right hemisphere stroke (RHS). Nine slices are presented with all strokes from all the patients overlaid.

One account of the rare neglect in RHS patients in this study is that we might not have used adequately sensitive tests of USN. However, the NIHSS also demonstrated that only 18% patients had neglect. Additionally, we have previously used these tests along with more traditional tests such as line bisection, line cancellation, reading, clock drawing, and have found that these two tests identified virtually all patients with neglect [34].

An alternative account of the rare neglect in RHS patients in our study is the relatively small lesions (0.2 cc to 98.8 cc range; mean = 53.79 cm3 ). Severity of extinction and neglect correlates with the volume of infarct [35] and volume of hypoperfusion [36] in acute stroke. Moreover, the patients were relatively young compared to some previous studies (range= 33-75; mean=55.25 years), although the age was average age of stroke patients for our hospital. Previous studies have shown that neglect is more common and more severe after right hemisphere stroke in older individuals [37,38]. Therefore, spared performance of many of our RHS patients on neglect tasks suggests that either [1] the spatial attention network is intact in the majority of our patients, or [2] hemispatial neglect requires “two hits”: damage to one component of the spatial attention work, and damage to a more general attentional system for vigilance. This latter hypothesis is consistent with the model of Corbetta and Schulman [39], which accounts for neglect in large right MCA strokes as damage to both the bilateral dorsal spatial attention network and the right-dominant, nonspatial ventral attention network. It may be that comprehension of emotional prosody is a better marker of right hemisphere stroke than neglect in unselected, diverse stroke patients (many of whom have small strokes, and now have average age of 55), while neglect remains a strong marker of large right MCA stroke. The important point is that neglect is not the only cortical function that is impaired after RHS. The addition of test of other right hemisphere cortical functions, such as prosody, would improve detection of RHS.

CONCLUSION

The important finding of our study is that impairments in comprehension of emotional prosody is a common indicator of acute right hemisphere dysfunction – even more common than hemispatial neglect or extinction in some populations. These results indicate that acute stroke assessment could be improved by including a test (perhaps a downloadable audio file for a mobile phone) of prosodic comprehension. Furthermore, the addition of evaluation of prosody comprehension may improve our measures of effectiveness of interventions to salvage right cortical function, such as reperfusion therapies. However, the effectiveness, reliability, and efficiency of testing prosody comprehension at bedside (e. g. in an Emergency Department setting, which might require headphones) would need to be tested in a much larger study with an independent population.

ACKNOWLEDGEMENTS

This work was supported by: National Institute of Neurological Disorders and Stroke, RO1NS47691 (to AEH)

REFERENCES

1. Karnath HO, Rorden C. The anatomy of spatial neglect. Neuropsychologia. 2012; 50: 1010-1017.

2. Bowers D, Bauer RM, Heilman KM. The nonverbal affect lexicon: Theoretical perspectives from neuropsychological studies of affect perception. Neuropsychology.1993; 7:433-444.

3. Ringman JM, Saver JL, Woolson RF, Clarke WR, Adams HP. Frequency, risk factors, anatomy, and course of unilateral neglect in an acute stroke cohort. Neurology. 2004; 63: 468-474.

4. Lee M, Saver JL, Alger JR, Hao Q, Salamon N, Starkman S, et al. Association of laterality and size of perfusion lesions on neurological deficit in acute supratentorial stroke. Int J Stroke. 2012; 7: 293-297.

5. Pihan H, Altenmüller E, Hertrich I, Ackermann H. Cortical activation patterns of affective speech processing depend on concurrent demands on the subvocal rehearsal system. A DC-potential study. Brain. 2000; 123 : 2338-2349.

6. Beaucousin V, Lacheret A, Turbelin MR, Morel M, Mazoyer B, Tzourio-Mazoyer N. FMRI study of emotional speech comprehension. Cereb Cortex. 2007; 17: 339-352.

7. Buchanan TW, Lutz K, Mirzazade S, Specht K, Shah NJ, Zilles K, et al. Recognition of emotional prosody and verbal components of spoken language: an fMRI study. Brain Res Cogn Brain Res. 2000; 9: 227-238.

8. Grimshaw GM, Kwasny KM, Covell E, Johnson RA. The dynamic nature of language lateralization: effects of lexical and prosodic factors. Neuropsychologia. 2003; 41: 1008-1019.

9. Ley RG, Bryden MP. A dissociation of right and left hemisphere effects for recognizing emotional tone and verbal content. Brain Cogn. 1982; 1: 3-9.

10. dolphs R. Neural systems for recognizing emotion. Curr Opin Neurobiol. 2002; 12: 169-177.

11. Blonder LX, Bowers D, Heilman KM. The role of the right hemisphere in emotional communication. Brain. 1991; 114 : 1115-1127.

12. Cancelliere AE, Kertesz A. Lesion localization in acquired deficits of emotional expression and comprehension. Brain Cogn. 1990; 13: 133- 147.

13. ell MD. Cerebral mechanisms for understanding emotional prosody in speech. Brain Lang. 2006; 96: 221-234.

14. Ross ED, Monnot M. Neurology of affective prosody and its functionalanatomic organization in right hemisphere. Brain Lang. 2008; 104: 51-74.

15. Barrett AM, Buxbaum LJ, Coslett HB, Edwards E, Heilman KM, Hillis AE, et al. Cognitive rehabilitation interventions for neglect and related disorders: moving from bench to bedside in stroke patients. J Cogn Neurosci. 2006; 18: 1223-1236.

16. Kortte K, Hillis AE. Recent advances in the understanding of neglect and anosognosia following right hemisphere stroke. Curr Neurol Neurosci Rep. 2009; 9: 459-465.

17. Tompkins CA, Lehman MT. Interpreting intended meanings after right hemisphere brain damage: An analysis of evidence, potential accounts, and clinical implications. Topics in Stroke Rehabilitation.1998; 5: 29- 47.

18. Decety J, Jackson PL. A social-neuroscience perspective on empathy. Current Directions in Psychological Science. 2006; 15: 54-58.

19. Leigh R, Oishi K, Hsu J, Lindquist M, Gottesman RF, Jarso S, et al. Acute lesions that impair affective empathy. Brain. 2013; 136: 2539-2549.

20. Ross ED, Thompson RD, Yenkosky J. Lateralization of affective prosody in brain and the callosal integration of hemispheric language functions. Brain Lang. 1997; 56: 27-54.

21. Ota H, Fujii T, Suzuki K, Fukatsu R, Yamadori A. Dissociation of body-centered and stimulus-centered representations in unilateral neglect. Neurology. 2001; 57: 2064-2069.

22. Williams LS, Yilmaz EY, Lopez-Yunez AM. Retrospective assessment of initial stroke severity with the NIH Stroke Scale. Stroke. 2000; 31: 858-862.

23. Zweig MH, Campbell G. Receiver-operating characteristic (ROC) plots: a fundamental evaluation tool in clinical medicine. Clin Chem. 1993; 39: 561-577.

24. Altman DG, Bland JM. Diagnostic tests 3: receiver operating characteristic plots. BMJ. 1994; 309: 188.

25. Ethofer T, Van De Ville D, Scherer K, Vuilleumier P. Decoding of emotional information in voice-sensitive cortices. Curr Biol. 2009; 19: 1028-1033.

26. Committeri G, Galati G, Paradis AL, Pizzamiglio L, Berthoz A, LeBihan D. Reference frames for spatial cognition: Different brain areas are involved in viewer-, object-, and landmark-centered judgments about object location. J Cogn Neurosci. 2004; 16: 1517-1535.

27. Galati G, Lobel E, Vallar G, Berthoz A, Pizzamiglio L, Le Bihan D. The neural basis of egocentric and allocentric coding of space in humans: a functional magnetic resonance study. Exp Brain Res. 2000; 133: 156- 164.

28. Karnath HO, Fruhmann Berger M, Küker W, Rorden C. The anatomy of spatial neglect based on voxelwise statistical analysis: A study of 140 patients. Cereb Cortex. 2004; 14: 1164-1172.

29. Hillis AE, Newhart M, Heidler J, Barker PB, Herskovits EH, Degaonkar M. Anatomy of spatial attention: insights from perfusion imaging and hemispatial neglect in acute stroke. J Neurosci. 2005; 25: 3161-3167.

30. Wildgruber D, Ethofer T, Grandjean D, Kreifelts B. A cerebral network model of speech prosody comprehension. International Journal of Speech-Language Pathology. 2009; 11: 277-281.

31. Wildgruber D, Riecker A, Hertrich I, Erb M, Grodd W, Ethofer T, et al. Identification of emotional intonation evaluated by fMRI. Neuroimage. 2005; 24: 1233-1241.

32. Husain M, Kennard C. Visual neglect associated with frontal lobe infarction. J Neurol. 1996; 243: 652-657.

33. Rengachary J, He BJ, Shulman GL, Corbetta M. A behavioral analysis of spatial neglect and its recovery after stroke. Front Hum Neurosci. 2011; 5: 29.

34. Medina J, Kannan V, Pawlak MA, Kleinman JT, Newhart M, Davis C, et al. Neural substrates of visuospatial processing in distinct reference frames: evidence from unilateral spatial neglect. J Cogn Neurosci. 2009; 21: 2073-2084.

35. Gottesman RF, Kleinman JT, Davis C, Heidler-Gary J, Newhart M, Hillis AE. The NIHSS-plus: improving cognitive assessment with the NIHSS. Behav Neurol. 2010; 22: 11-15.

36. Hillis AE, Wityk RJ, Barker PB, Ulatowski JA, Jacobs MA. Change in perfusion in acute nondominant hemisphere stroke may be better estimated by tests of hemispatial neglect than by the National Institutes of Health Stroke Scale. Stroke. 2003; 34: 2392-2396.

37. Gottesman RF, Kleinman JT, Davis C, Heidler-Gary J, Newhart M, Kannan V, et al. Unilateral neglect is more severe and common in older patients with right hemispheric stroke. Neurology. 2008; 71: 1439- 1444

38. evine DN. Unilateral neglect is more severe and common in older patients with right hemispheric stroke. Neurology. 2009; 73: 489.

39. Corbetta M, Shulman GL. Spatial neglect and attention networks. Annu Rev Neurosci. 2011; 34: 569-599

Dara C, Bang J, Gottesman RF, Hillis AE (2014) Right Hemisphere Dysfunction is Better Predicted by Emotional Prosody Impairments as Compared to Neglect. J Neurol Transl Neurosci 2(1): 1037

Received : 16 Dec 2013
Accepted : 20 Jan 2014
Published : 28 Jan 2014
Journals
Annals of Otolaryngology and Rhinology
ISSN : 2379-948X
Launched : 2014
JSM Schizophrenia
Launched : 2016
Journal of Nausea
Launched : 2020
JSM Internal Medicine
Launched : 2016
JSM Hepatitis
Launched : 2016
JSM Oro Facial Surgeries
ISSN : 2578-3211
Launched : 2016
Journal of Human Nutrition and Food Science
ISSN : 2333-6706
Launched : 2013
JSM Regenerative Medicine and Bioengineering
ISSN : 2379-0490
Launched : 2013
JSM Spine
ISSN : 2578-3181
Launched : 2016
Archives of Palliative Care
ISSN : 2573-1165
Launched : 2016
JSM Nutritional Disorders
ISSN : 2578-3203
Launched : 2017
Annals of Neurodegenerative Disorders
ISSN : 2476-2032
Launched : 2016
Journal of Fever
ISSN : 2641-7782
Launched : 2017
JSM Bone Marrow Research
ISSN : 2578-3351
Launched : 2016
JSM Mathematics and Statistics
ISSN : 2578-3173
Launched : 2014
Journal of Autoimmunity and Research
ISSN : 2573-1173
Launched : 2014
JSM Arthritis
ISSN : 2475-9155
Launched : 2016
JSM Head and Neck Cancer-Cases and Reviews
ISSN : 2573-1610
Launched : 2016
JSM General Surgery Cases and Images
ISSN : 2573-1564
Launched : 2016
JSM Anatomy and Physiology
ISSN : 2573-1262
Launched : 2016
JSM Dental Surgery
ISSN : 2573-1548
Launched : 2016
Annals of Emergency Surgery
ISSN : 2573-1017
Launched : 2016
Annals of Mens Health and Wellness
ISSN : 2641-7707
Launched : 2017
Journal of Preventive Medicine and Health Care
ISSN : 2576-0084
Launched : 2018
Journal of Chronic Diseases and Management
ISSN : 2573-1300
Launched : 2016
Annals of Vaccines and Immunization
ISSN : 2378-9379
Launched : 2014
JSM Heart Surgery Cases and Images
ISSN : 2578-3157
Launched : 2016
Annals of Reproductive Medicine and Treatment
ISSN : 2573-1092
Launched : 2016
JSM Brain Science
ISSN : 2573-1289
Launched : 2016
JSM Biomarkers
ISSN : 2578-3815
Launched : 2014
JSM Biology
ISSN : 2475-9392
Launched : 2016
Archives of Stem Cell and Research
ISSN : 2578-3580
Launched : 2014
Annals of Clinical and Medical Microbiology
ISSN : 2578-3629
Launched : 2014
JSM Pediatric Surgery
ISSN : 2578-3149
Launched : 2017
Journal of Memory Disorder and Rehabilitation
ISSN : 2578-319X
Launched : 2016
JSM Tropical Medicine and Research
ISSN : 2578-3165
Launched : 2016
JSM Head and Face Medicine
ISSN : 2578-3793
Launched : 2016
JSM Cardiothoracic Surgery
ISSN : 2573-1297
Launched : 2016
JSM Bone and Joint Diseases
ISSN : 2578-3351
Launched : 2017
JSM Bioavailability and Bioequivalence
ISSN : 2641-7812
Launched : 2017
JSM Atherosclerosis
ISSN : 2573-1270
Launched : 2016
Journal of Genitourinary Disorders
ISSN : 2641-7790
Launched : 2017
Journal of Fractures and Sprains
ISSN : 2578-3831
Launched : 2016
Journal of Autism and Epilepsy
ISSN : 2641-7774
Launched : 2016
Annals of Marine Biology and Research
ISSN : 2573-105X
Launched : 2014
JSM Health Education & Primary Health Care
ISSN : 2578-3777
Launched : 2016
JSM Communication Disorders
ISSN : 2578-3807
Launched : 2016
Annals of Musculoskeletal Disorders
ISSN : 2578-3599
Launched : 2016
Annals of Virology and Research
ISSN : 2573-1122
Launched : 2014
JSM Renal Medicine
ISSN : 2573-1637
Launched : 2016
Journal of Muscle Health
ISSN : 2578-3823
Launched : 2016
JSM Genetics and Genomics
ISSN : 2334-1823
Launched : 2013
JSM Anxiety and Depression
ISSN : 2475-9139
Launched : 2016
Clinical Journal of Heart Diseases
ISSN : 2641-7766
Launched : 2016
Annals of Medicinal Chemistry and Research
ISSN : 2378-9336
Launched : 2014
JSM Pain and Management
ISSN : 2578-3378
Launched : 2016
JSM Women's Health
ISSN : 2578-3696
Launched : 2016
Clinical Research in HIV or AIDS
ISSN : 2374-0094
Launched : 2013
Journal of Endocrinology, Diabetes and Obesity
ISSN : 2333-6692
Launched : 2013
Journal of Substance Abuse and Alcoholism
ISSN : 2373-9363
Launched : 2013
JSM Neurosurgery and Spine
ISSN : 2373-9479
Launched : 2013
Journal of Liver and Clinical Research
ISSN : 2379-0830
Launched : 2014
Journal of Drug Design and Research
ISSN : 2379-089X
Launched : 2014
JSM Clinical Oncology and Research
ISSN : 2373-938X
Launched : 2013
JSM Bioinformatics, Genomics and Proteomics
ISSN : 2576-1102
Launched : 2014
JSM Chemistry
ISSN : 2334-1831
Launched : 2013
Journal of Trauma and Care
ISSN : 2573-1246
Launched : 2014
JSM Surgical Oncology and Research
ISSN : 2578-3688
Launched : 2016
Annals of Food Processing and Preservation
ISSN : 2573-1033
Launched : 2016
Journal of Radiology and Radiation Therapy
ISSN : 2333-7095
Launched : 2013
JSM Physical Medicine and Rehabilitation
ISSN : 2578-3572
Launched : 2016
Annals of Clinical Pathology
ISSN : 2373-9282
Launched : 2013
Annals of Cardiovascular Diseases
ISSN : 2641-7731
Launched : 2016
Journal of Behavior
ISSN : 2576-0076
Launched : 2016
Annals of Clinical and Experimental Metabolism
ISSN : 2572-2492
Launched : 2016
Clinical Research in Infectious Diseases
ISSN : 2379-0636
Launched : 2013
JSM Microbiology
ISSN : 2333-6455
Launched : 2013
Journal of Urology and Research
ISSN : 2379-951X
Launched : 2014
Journal of Family Medicine and Community Health
ISSN : 2379-0547
Launched : 2013
Annals of Pregnancy and Care
ISSN : 2578-336X
Launched : 2017
JSM Cell and Developmental Biology
ISSN : 2379-061X
Launched : 2013
Annals of Aquaculture and Research
ISSN : 2379-0881
Launched : 2014
Clinical Research in Pulmonology
ISSN : 2333-6625
Launched : 2013
Journal of Immunology and Clinical Research
ISSN : 2333-6714
Launched : 2013
Annals of Forensic Research and Analysis
ISSN : 2378-9476
Launched : 2014
JSM Biochemistry and Molecular Biology
ISSN : 2333-7109
Launched : 2013
Annals of Breast Cancer Research
ISSN : 2641-7685
Launched : 2016
Annals of Gerontology and Geriatric Research
ISSN : 2378-9409
Launched : 2014
Journal of Sleep Medicine and Disorders
ISSN : 2379-0822
Launched : 2014
JSM Burns and Trauma
ISSN : 2475-9406
Launched : 2016
Chemical Engineering and Process Techniques
ISSN : 2333-6633
Launched : 2013
Annals of Clinical Cytology and Pathology
ISSN : 2475-9430
Launched : 2014
JSM Allergy and Asthma
ISSN : 2573-1254
Launched : 2016
Journal of Neurological Disorders and Stroke
ISSN : 2334-2307
Launched : 2013
Annals of Sports Medicine and Research
ISSN : 2379-0571
Launched : 2014
JSM Sexual Medicine
ISSN : 2578-3718
Launched : 2016
Annals of Vascular Medicine and Research
ISSN : 2378-9344
Launched : 2014
JSM Biotechnology and Biomedical Engineering
ISSN : 2333-7117
Launched : 2013
Journal of Hematology and Transfusion
ISSN : 2333-6684
Launched : 2013
JSM Environmental Science and Ecology
ISSN : 2333-7141
Launched : 2013
Journal of Cardiology and Clinical Research
ISSN : 2333-6676
Launched : 2013
JSM Nanotechnology and Nanomedicine
ISSN : 2334-1815
Launched : 2013
Journal of Ear, Nose and Throat Disorders
ISSN : 2475-9473
Launched : 2016
JSM Ophthalmology
ISSN : 2333-6447
Launched : 2013
Journal of Pharmacology and Clinical Toxicology
ISSN : 2333-7079
Launched : 2013
Annals of Psychiatry and Mental Health
ISSN : 2374-0124
Launched : 2013
Medical Journal of Obstetrics and Gynecology
ISSN : 2333-6439
Launched : 2013
Annals of Pediatrics and Child Health
ISSN : 2373-9312
Launched : 2013
JSM Clinical Pharmaceutics
ISSN : 2379-9498
Launched : 2014
JSM Foot and Ankle
ISSN : 2475-9112
Launched : 2016
JSM Alzheimer's Disease and Related Dementia
ISSN : 2378-9565
Launched : 2014
Journal of Addiction Medicine and Therapy
ISSN : 2333-665X
Launched : 2013
Journal of Veterinary Medicine and Research
ISSN : 2378-931X
Launched : 2013
Annals of Public Health and Research
ISSN : 2378-9328
Launched : 2014
Annals of Orthopedics and Rheumatology
ISSN : 2373-9290
Launched : 2013
Journal of Clinical Nephrology and Research
ISSN : 2379-0652
Launched : 2014
Annals of Community Medicine and Practice
ISSN : 2475-9465
Launched : 2014
Annals of Biometrics and Biostatistics
ISSN : 2374-0116
Launched : 2013
JSM Clinical Case Reports
ISSN : 2373-9819
Launched : 2013
Journal of Cancer Biology and Research
ISSN : 2373-9436
Launched : 2013
Journal of Surgery and Transplantation Science
ISSN : 2379-0911
Launched : 2013
Journal of Dermatology and Clinical Research
ISSN : 2373-9371
Launched : 2013
JSM Gastroenterology and Hepatology
ISSN : 2373-9487
Launched : 2013
Annals of Nursing and Practice
ISSN : 2379-9501
Launched : 2014
JSM Dentistry
ISSN : 2333-7133
Launched : 2013
Author Information X