Enhanced positive emotional reactivity in frontotemporal dementia reflects left-lateralized atrophy in the temporal and frontal lobes

Affiliations

¹ Memory and Aging Center, Department of Neurology, University of California, San Francisco, San Francisco, CA, USA; University of California, Berkeley, Department of Psychology, Berkeley, CA, USA. Electronic address: shdo@berkeley.edu.
² Memory and Aging Center, Department of Neurology, University of California, San Francisco, San Francisco, CA, USA. Electronic address: ashlin.roy@ucsf.edu.
³ Memory and Aging Center, Department of Neurology, University of California, San Francisco, San Francisco, CA, USA. Electronic address: samir.datta@ucsf.edu.
⁴ Memory and Aging Center, Department of Neurology, University of California, San Francisco, San Francisco, CA, USA. Electronic address: jsible@usc.edu.
⁵ Memory and Aging Center, Department of Neurology, University of California, San Francisco, San Francisco, CA, USA. Electronic address: sladjana.lukic@ucsf.edu.
⁶ Memory and Aging Center, Department of Neurology, University of California, San Francisco, San Francisco, CA, USA. Electronic address: david.perry@ucsf.edu.
⁷ Memory and Aging Center, Department of Neurology, University of California, San Francisco, San Francisco, CA, USA. Electronic address: katherine.rankin@ucsf.edu.
⁸ Memory and Aging Center, Department of Neurology, University of California, San Francisco, San Francisco, CA, USA. Electronic address: joel.kramer@ucsf.edu.
⁹ Memory and Aging Center, Department of Neurology, University of California, San Francisco, San Francisco, CA, USA. Electronic address: howie.rosen@ucsf.edu.
¹⁰ Memory and Aging Center, Department of Neurology, University of California, San Francisco, San Francisco, CA, USA; Department of Psychiatry and Behavioral Sciences, University of California, San Francisco, San Francisco, CA, USA. Electronic address: bruce.miller@ucsf.edu.
¹¹ Memory and Aging Center, Department of Neurology, University of California, San Francisco, San Francisco, CA, USA. Electronic address: bill.seeley@ucsf.edu.
¹² Department of Psychiatry and Behavioral Sciences, University of California, San Francisco, San Francisco, CA, USA; San Francisco State University, Department of Psychology, San Francisco, CA, USA. Electronic address: sholley@sfsu.edu.
¹³ Memory and Aging Center, Department of Neurology, University of California, San Francisco, San Francisco, CA, USA; Department of Psychiatry and Behavioral Sciences, University of California, San Francisco, San Francisco, CA, USA. Electronic address: marialuisa.gornotempini@ucsf.edu.
¹⁴ Memory and Aging Center, Department of Neurology, University of California, San Francisco, San Francisco, CA, USA; Department of Psychiatry and Behavioral Sciences, University of California, San Francisco, San Francisco, CA, USA. Electronic address: virginia.sturm@ucsf.edu.

PMID: 35930892
PMCID: PMC9867572
DOI: 10.1016/j.cortex.2022.02.018

Enhanced positive emotional reactivity in frontotemporal dementia reflects left-lateralized atrophy in the temporal and frontal lobes

Suzanne M Shdo et al. Cortex. 2022 Sep.

. 2022 Sep:154:405-420.

doi: 10.1016/j.cortex.2022.02.018. Epub 2022 Jun 28.

Authors

Affiliations

¹ Memory and Aging Center, Department of Neurology, University of California, San Francisco, San Francisco, CA, USA; University of California, Berkeley, Department of Psychology, Berkeley, CA, USA. Electronic address: shdo@berkeley.edu.
² Memory and Aging Center, Department of Neurology, University of California, San Francisco, San Francisco, CA, USA. Electronic address: ashlin.roy@ucsf.edu.
³ Memory and Aging Center, Department of Neurology, University of California, San Francisco, San Francisco, CA, USA. Electronic address: samir.datta@ucsf.edu.
⁴ Memory and Aging Center, Department of Neurology, University of California, San Francisco, San Francisco, CA, USA. Electronic address: jsible@usc.edu.
⁵ Memory and Aging Center, Department of Neurology, University of California, San Francisco, San Francisco, CA, USA. Electronic address: sladjana.lukic@ucsf.edu.
⁶ Memory and Aging Center, Department of Neurology, University of California, San Francisco, San Francisco, CA, USA. Electronic address: david.perry@ucsf.edu.
⁷ Memory and Aging Center, Department of Neurology, University of California, San Francisco, San Francisco, CA, USA. Electronic address: katherine.rankin@ucsf.edu.
⁸ Memory and Aging Center, Department of Neurology, University of California, San Francisco, San Francisco, CA, USA. Electronic address: joel.kramer@ucsf.edu.
⁹ Memory and Aging Center, Department of Neurology, University of California, San Francisco, San Francisco, CA, USA. Electronic address: howie.rosen@ucsf.edu.
¹⁰ Memory and Aging Center, Department of Neurology, University of California, San Francisco, San Francisco, CA, USA; Department of Psychiatry and Behavioral Sciences, University of California, San Francisco, San Francisco, CA, USA. Electronic address: bruce.miller@ucsf.edu.
¹¹ Memory and Aging Center, Department of Neurology, University of California, San Francisco, San Francisco, CA, USA. Electronic address: bill.seeley@ucsf.edu.
¹² Department of Psychiatry and Behavioral Sciences, University of California, San Francisco, San Francisco, CA, USA; San Francisco State University, Department of Psychology, San Francisco, CA, USA. Electronic address: sholley@sfsu.edu.
¹³ Memory and Aging Center, Department of Neurology, University of California, San Francisco, San Francisco, CA, USA; Department of Psychiatry and Behavioral Sciences, University of California, San Francisco, San Francisco, CA, USA. Electronic address: marialuisa.gornotempini@ucsf.edu.
¹⁴ Memory and Aging Center, Department of Neurology, University of California, San Francisco, San Francisco, CA, USA; Department of Psychiatry and Behavioral Sciences, University of California, San Francisco, San Francisco, CA, USA. Electronic address: virginia.sturm@ucsf.edu.

PMID: 35930892
PMCID: PMC9867572
DOI: 10.1016/j.cortex.2022.02.018

Abstract

In frontotemporal dementia (FTD), left-lateralized atrophy patterns have been associated with elevations in certain positive emotions. Here, we investigated whether positive emotional reactivity was enhanced in semantic variant primary progressive aphasia (svPPA), an FTD syndrome that targets the left anterior temporal lobe. Sixty-one participants (16 people with svPPA, 24 people with behavioral variant FTD, and 21 healthy controls) viewed six 90-sec trials that were comprised of a series of photographs; each trial was designed to elicit a specific positive emotion, negative emotion, or no emotion. Participants rated their positive emotional experience after each trial, and their smiling behavior was coded with the Facial Action Coding System. Results indicated that positive emotional experience and smiling were elevated in svPPA in response to numerous affective and non-affective stimuli. Voxel-based morphometry analyses revealed that greater positive emotional experience and greater smiling in the patients were both associated with smaller gray matter volume in the left superior temporal gyrus (p_FWE < .05), among other left-lateralized frontotemporal regions. Whereas enhanced positive emotional experience related to atrophy in middle superior temporal gyrus and structures that promote cognitive control and emotion regulation, heightened smiling related to atrophy in posterior superior temporal gyrus and structures that support motor control. Our results suggest positive emotional reactivity is elevated in svPPA and offer new evidence that atrophy in left-lateralized emotion-relevant systems relates to enhanced positive emotions in FTD.

Keywords: Elation; Euphoria; Mood; Neurodegeneration; Semantic dementia.

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Conflict of interest statement

Declaration of competing interest The authors report no competing interests.

Figures

**Figure 1.. Mean positive emotional experience across trials in each diagnostic group**
*= p<.05, **=p<.001. Separate ANCOVAs (controlling for age and sex) were run for each trial to decompose the significant diagnosis by trial interaction that was detected in our primary analysis on total positive emotional experience. Tukey-adjusted pairwise comparisons were conducted to correct for multiple comparisons. Error bars represent the standard error. These analyses revealed that people with svPPA reported significantly higher levels of total positive emotional experience during the awe (p<.001), love (p<.05), and neutral (p<.05) trials than the bvFTD and healthy control groups. People with svPPA also reported significantly higher levels of positive emotional experience during the fear trial than healthy controls (p<.05).

**Figure 2.. Mean smiling behavior across trials in each diagnostic group.**
*=p<.05. Separate ANCOVAs (controlling for age and sex) were run for each trial to decompose the significant diagnosis by trial interaction that was detected in our primary analysis on smiling behavior. Tukey-adjusted pairwise comparisons were used to correct for multiple comparisons. People with svPPA had a higher total smiling score during the fear (p<.05) and sadness (p<.05) trials than those with bvFTD. People with bvFTD had a greater total smiling score during the amusement trial than the healthy controls (p<.05).

**Figure 3.. Distinct and overlapping atrophy patterns in svPPA and bvFTD.**
Whole-brain voxel-based morphometry analyses (controlling for age, sex, and TIV) confirmed that the A) svPPA and (B) bvFTD groups had smaller gray matter volume than the healthy controls in frontotemporal and subcortical regions typically atrophied in these syndromes (p_FWE<.05). (C) In svPPA and bvFTD, there was some overlapping atrophy, but the people with svPPA tended to have more left lateralized atrophy than those with bvFTD, whose atrophy was more bilateral (p_FWE<.05). Statistical maps are superimposed on the Montreal Neurological Institute template.

**Figure 4.. Left-lateralized atrophy related to greater total positive emotional experience and greater total smiling behavior.**
Voxel-based morphometry analyses (controlling for age, sex, diagnosis, MMSE, and TIV) revealed that (A) smaller gray matter volume in left superior temporal gyrus was associated with greater total positive emotional experience (p_FWE<.05) and greater total smiling behavior (p_FWE<.05). (B) Greater total positive emotional experience was associated with smaller gray matter volume in the left superior temporal gyrus, left dorsal anterior insula, and left orbitofrontal cortex (p<.001), and (C) greater total smiling behavior was associated with smaller gray matter volume in the left temporal lobe and middle frontal gyrus. Color bars represent T-scores at p<.001. Statistical maps are superimposed on the Montreal Neurological Institute template.

**Figure 5.. Linear association between total positive emotional experience and gray matter volume across the clinical groups.**
A regression model (controlling for age, sex, diagnosis, TIV, and MMSE) confirmed that total positive emotional experience had a linear association across the clinical groups with gray matter volume in the left superior temporal gyrus and left dorsal anterior insula clusters that emerged in the VBM analyses. These results suggest the neuroimaging results reflected linear brain-emotion associations and were not driven by one diagnostic group.

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Enhanced positive emotional reactivity in frontotemporal dementia reflects left-lateralized atrophy in the temporal and frontal lobes

Affiliations

Enhanced positive emotional reactivity in frontotemporal dementia reflects left-lateralized atrophy in the temporal and frontal lobes

Authors

Affiliations

Abstract

Conflict of interest statement

Figures

References

Publication types

MeSH terms

Grants and funding

LinkOut - more resources

Full Text Sources