Association Between Lack of Insight and Prefrontal Serotonin Transporter Availability in Antipsychotic-Free Patients with Schizophrenia: A High-Resolution PET Study with [11C]DASB.

BACKGROUND: Previous studies suggested a link between serotonergic neurotransmission and impaired insight in schizophrenia. In this study, we examined the relationship between serotonin transporter (SERT) availability in regions of the prefrontal cortex (dorsolateral, ventrolateral, ventromedial, and orbitofrontal cortices) and insight deficits in antipsychotic-free patients with schizophrenia using high-resolution positron emission tomography (PET) with [11C]DASB.
METHODS: Nineteen patients underwent [11C]DASB PET and 7-Tesla magnetic resonance imaging scans. To assess SERT availability, the binding potential with respect to non-displaceable compartment (BPND) was derived using the simplified reference tissue model. Patients' level of insight was assessed using the Insight and Treatment Attitude Questionnaire (ITAQ). The relationship between ITAQ scores and [11C]DASB BPND values was examined using the region-of-interest (ROI)- and voxel-based analyses with relevant variables as covariates. The prefrontal cortex and its four subregions were selected as a priori ROIs since the prefrontal cortex has been implicated as the critical neuroanatomical substrate of impaired insight in schizophrenia.
RESULTS: The ROI-based analysis revealed that the ITAQ illness insight dimension had significant negative correlations with the [11C]DASB BPND in the left dorsolateral, left orbitofrontal, and bilateral ventrolateral prefrontal cortices. The ITAQ treatment insight dimension had significant negative correlations with the [11C]DASB BPND in the bilateral dorsolateral, left orbitofrontal, and bilateral ventrolateral prefrontal cortices. The ITAQ total score showed significant negative correlations with the [11C]DASB BPND in the bilateral prefrontal cortex and three subregions (dorsolateral, ventrolateral, and orbitofrontal cortices). A supplementary voxel-based analysis corroborated a significant negative association between the ITAQ score and the [11C]DASB BPND in the prefrontal cortices.
CONCLUSION: Our study provides in vivo evidence of significant negative correlations between insight deficits and prefrontal SERT availability in patients with schizophrenia, suggesting significant involvement of prefrontal serotonergic signaling in impaired insight, one of the core symptoms of schizophrenia.

Introduction

Lack of insight is common among patients with schizophrenia and is significantly linked with poor antipsychotic drug adherence and frequent relapse, leading to a poor prognosis.1 Poor insight has long been recognized as a significant barrier to treatment adherence and recovery in schizophrenia.1 Although numerous investigations have been made concerning the clinical correlates of poor insight in patients with schizophrenia, the neurobiological underpinning of lack of insight is still unclear and not well understood.2

Several magnetic resonance imaging (MRI) studies on the neuroanatomical and functional correlates of poor insight in schizophrenia have been performed, which suggest that the prefrontal cortex is involved in the lack of insight in patients with schizophrenia.3–9 A meta-analysis also reported that insight deficits in patients with schizophrenia are significantly correlated with impairment in specific cognitive functioning, such as set-shifting and error monitoring,10 which is primarily subserved by the prefrontal cortex. Another meta-analysis by Nair et al11 reported significant associations between insight into illness and executive function. These findings suggest a strong link between poor insight and prefrontal cortical dysfunction in schizophrenia.

However, the neurochemical underpinning of impaired insight in schizophrenia remains poorly understood. In a previous study, platelet serotonin concentrations were significantly correlated with lack of insight in patients with schizophrenia,12 suggesting a possible involvement of serotonergic neurotransmission in insight deficits in schizophrenia. A genetic association study reported that the functional polymorphism of the serotonin 1A receptor was significantly related to the theory of mind (ToM) performance,13 which was found to be an important factor contributing to impaired insight in schizophrenia.14 In addition, genetic variations of tryptophan hydroxylase-2 (TPH2) and serotonin 2A receptors were significantly associated with social cognitive functions, particularly emotional management components,15,16 which play a substantial role in insight deficits in schizophrenia.17 Moreover, the core pathophysiology in schizophrenia is associated with altered synaptic plasticity in the prefrontal cortex,18 where serotonin plays a significant role as a neuromodulatory transmitter.19 Hence, we suppose that serotonin-related mechanisms in the prefrontal cortex could be involved in impaired insight in patients with schizophrenia. However, no in vivo molecular positron emission tomography (PET) imaging investigations have been reported to elucidate the relationship between serotonergic neurotransmission and impaired insight in schizophrenia.

Therefore, in this study, we examined the relationship between serotonin transporter (SERT) availability in regions of the prefrontal cortex (dorsolateral, ventrolateral, ventromedial, and orbitofrontal cortices) and insight deficits in antipsychotic-free patients with schizophrenia. We employed high-resolution PET with 11C-3-amino-4-(2-dimethylaminomethylphenylthio)benzonitrile ([11C]DASB), a highly selective radioligand with high affinity and good specificity for in vivo SERT imaging in the brain including the cortical regions.20–24 In this study, the prefrontal cortex and its four subregions were chosen a priori based on the aforementioned literature, which implicates the prefrontal cortex as a critical neuroanatomical substrate of impaired insight in schizophrenia.3,6,9,25

Materials and Methods

Subjects

The study protocol was approved by the Institutional Review Board of the Gachon University Gil Medical Center, and all procedures used in the study were conducted in accordance with international ethical standards and the Declaration of Helsinki. Patients were recruited from the schizophrenia clinic at Gachon University Gil Medical Center. Written informed consent was obtained from all participants after providing a full explanation of the study procedures.

The criteria for patient recruitment were as follows: (i) a diagnosis of schizophrenia based on the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (DSM-IV),26 which was established using the Structured Clinical Interview for DSM-IV (SCID);27 (ii) age between 18 and 55 years; (iii) absence of any psychotropic medication for at least 14 days before the PET scan (with the exception of lorazepam, which was allowed at a maximal dose of 3 mg per day); and (iv) no history of receiving antidepressant medications. Patients were excluded if they (i) met the diagnostic criteria for a psychiatric diagnosis other than schizophrenia; (ii) had a concurrent diagnosis of substance abuse or dependence; (iii) had concurrent medical or neurological disorders; (iv) were acutely psychotic or suicidal/homicidal; (v) were judged to be uncooperative with regard to the study; (vi) did not fully understand the study procedures; or (vii) could not give written informed consents.

Nineteen patients were enrolled in the study (Table 1). The mean Positive and Negative Syndrome Scale (PANSS)28 total score was 84.7 ± 23.6. The mean duration of illness was 2.3 ± 1.8 years. Before the PET scans, all patients underwent urine tests to exclude substance abuse, and female patients had additional urine pregnancy tests to exclude pregnancy. None of the patients had any structural abnormalities on brain MRI, which was confirmed by a board-certified radiologist.

Table 1

Demographic/Clinical Characteristics and PET Scan Parameters

Variables		Mean ± SD/Number (%)
Demographic and clinical characteristics
Age (years)		32.6 ± 12.0
Gender	Male	12 (63.2)
	Female	7 (36.8)
Education (years)		11.4 ± 1.6
Duration of illness (years)		2.3 ± 1.8
Antipsychotic-free period (days)		136.0 ± 103.9
PANSS positive score		21.0 ± 7.4
PANSS negative score		22.5 ± 6.8
PANSS general score		41.2 ± 13.4
PANSS total score		84.7 ± 23.6
[11C]DASB PET scan information
Injected dose (MBq)		582.4 ± 53.5
Specific activity (GBq/μmol)		83.1 ± 62.6

Abbreviations: PET, positron emission tomography; SD, standard deviation; PANSS, Positive and Negative Syndrome Scale.

Clinical Assessments

Symptoms of schizophrenia were assessed using the PANSS.28 Patients’ level of clinical insight was assessed using the Insight and Treatment Attitude Questionnaire (ITAQ).29 The ITAQ is a rater-administered 11-item scale that measures clinical insight in two dimensions: awareness of illness (illness insight) and awareness of need for treatment (treatment insight).29 Each item on the ITAQ elicits responses on a Likert type scale scored 0 for no insight, 1 for partial insight and 2 for good insight.29 A higher score is indicative of good insight. A standardized Korean version of the ITAQ was used in this study.30

[11C]DASB PET and MRI Data Acquisition

All patients were scanned with the High Resolution Research Tomograph (HRRT)-PET (Siemens, Knoxville, TN, USA) using [11C]DASB. For attenuation and scatter correction, a transmission scan using a 137Cs point source was performed during the six minutes preceding the start of the PET emission recording.31 Following a mean bolus injection of 582 ± 54 MBq [11C]DASB with a mean molar activity of 83 ± 63 GBq/μmol, a dynamic emission recording lasting 90 minutes was obtained in three-dimensional (3-D) acquisition mode. Following the PET scans, structural MRI images were acquired with 7-Tesla MRI (MAGNETOM 7T, Siemens, Erlangen, Germany) using a 3-D T1-weighted magnetization-prepared rapid gradient echo (T1MPRAGE) sequence. This entailed the following parameters: repetition time = 1900 ms; echo time = 3.73 ms; inversion time = 1100 ms; flip angle = 10°; number of slices = 256; and voxel size = 0.8 × 0.8 × 0.8 mm3. To minimize the patient’s head movement during the MRI and PET scans, all patients’ heads were fixed to the sponges as comfortably as possible.

Image Analysis

The [11C]DASB PET emission data were reconstructed as 22 frames of increasing duration (4 × 30, 2 × 60, 2 × 90, 3 × 150, 3 × 210, 4 × 300, 3 × 600, and 1 × 900 s) using the 3-D ordinary Poisson ordered‐subset expectation maximization algorithm based on the symmetry and single‐instruction multiple data-based projection and back-projection.32 All reconstructed PET frames were normalized for detector efficiency and corrected for scatter, randoms, attenuation, decay, and dead time according to the procedures installed by the HRRT-PET manufacturer. These frames had a matrix size of 256 × 256 × 207 and an iso-voxel resolution of 1.22 × 1.22 × 1.22 mm3.

For reconstructed PET frames, the preprocessing steps were performed using Statistical Parametric Mapping 8 (SPM8; Wellcome Department of Imaging Neuroscience, London, UK)33 implemented in MATLAB R2014b (The MathWorks, Natick, MA, USA). For motion correction of the reconstructed PET frames, realignment was conducted according to a two-pass procedure. In the first pass realignment, each reconstructed PET frame was registered to the first frame, a reference frame with high signal-to-noise ratio in the series, after which a mean PET image was computed. In the second pass realignment, each frame from the first pass alignment was registered to the mean PET image. Next, the mean PET image was co-registered to the structural MRI image using a 12-parameter affine transformation, and the estimated transformation was applied to the corresponding reconstructed PET frames. To estimate SERT availability, the binding potential with respect to non-displaceable compartment (BPND) of [11C]DASB was calculated in the kinetic modeling tool of the PMOD software v3.2 (PMOD Technologies Ltd., Zürich, Switzerland) using the simplified reference tissue model 2 (SRTM2)34 with the cerebellum serving as the reference region, as previously used for this tracer.22,35–38 In the [11C]DASB BPND calculation process, the time-activity curves were obtained from reconstructed dynamic PET images by averaging all the voxels within each region of interest (ROI). The [11C]DASB BPND images were spatially normalized to the Montreal Neurological Institute (MNI) standard template using SPM8. The anatomical locations of the ROIs, ie, the prefrontal cortex and its subregions, were determined based on the Brodmann areas in the Talairach atlas,39 which include dorsolateral prefrontal, ventromedial prefrontal, ventrolateral prefrontal, and orbitofrontal subregions.40–42 The left and right regions were analyzed separately, given the lateralized cognitive processes and their deficits in schizophrenia.43,44

Statistical Analysis

Statistical analyses were performed using the Statistical Package for the Social Sciences (SPSS) version 23.0 (IBM Corp., Armonk, NY, USA). The relationship between the ITAQ scores and the [11C]DASB BPND values was examined using the a priori ROI-based correlation analysis with relevant variables as covariates. The statistical significance was set at a threshold of two-tailed p < 0.05.

A voxel-based analysis was also performed with the same data using SPM8 to supplement and corroborate the ROI-based results on the relationship between the ITAQ total scores and the [11C]DASB BPND values in the prefrontal cortex. The significance threshold was set at false discovery rate (FDR)-corrected p < 0.05. However, considering the exploratory perspective of the voxel-based analysis in our study, when no significant correlations were found at the FDR-corrected threshold, significant results were further investigated at an uncorrected p < 0.005 with an extent threshold of 50 voxels, which was considered statistically significant in previous PET imaging studies.45,46

Results

The mean ITAQ total score was 13.6 ± 6.6. The mean scores of the illness insight and treatment insight dimensions were 6.0 ± 3.2 and 7.6 ± 3.6, respectively. The ITAQ scores did not significantly correlate with age (r = 0.12 to 0.20, p > 0.05), gender (t = 0.65 to 1.35, p > 0.05), or the duration of antipsychotic-free period (r = 0.17 to 0.28, p > 0.05). The ITAQ scores had significant positive correlations with the duration of illness (illness insight dimension score: r = 0.48, p = 0.04; treatment insight dimension score: r = 0.64, p = 0.003; total score: r = 0.59, p = 0.008). Additionally, the ITAQ illness insight dimension score had a significant positive correlation with the PANSS positive score (r = 0.47, p = 0.045), and both the ITAQ treatment insight dimension score and ITAQ total score had significant positive correlations with the PANSS total score (treatment insight dimension score: r = 0.50, p = 0.029; total score: r = 0.49, p = 0.033).

The ROI-based correlation analysis with relevant PANSS scores and duration of illness as covariates revealed that the ITAQ total score had significant negative correlations with the [11C]DASB BPND values in the bilateral prefrontal cortex (left: p = 0.012; right: p = 0.035), dorsolateral prefrontal cortex (left: p = 0.015; right: p = 0.036), orbitofrontal cortex (left: p = 0.006; right: p = 0.039), and ventrolateral prefrontal cortex (left: p = 0.001; right: p = 0.008) (Table 2). The ITAQ illness insight dimension score had significant negative correlations with the [11C]DASB BPND values in the left prefrontal cortex (p = 0.034), left dorsolateral prefrontal cortex (p = 0.041), left orbitofrontal cortex (p = 0.021), and bilateral ventrolateral prefrontal cortex (left: p = 0.005; right: p = 0.034) (Table 2). The ITAQ treatment insight dimension score had significant negative correlations with the [11C]DASB BPND values in the left prefrontal cortex (p = 0.028), bilateral dorsolateral prefrontal cortex (left: p = 0.028; right: p = 0.048), left orbitofrontal cortex (p = 0.013), and bilateral ventrolateral prefrontal cortex (left: p = 0.002; right: p = 0.020) (Table 2). Representative scatter plots showing the relationship between the ITAQ scores and the [11C]DASB BPND values in the prefrontal cortex and its subregions are presented in Figure 1.

Table 2

Mean [11C]DASB BPND Values and Their Correlation Coefficients with the ITAQ Scores in the Prefrontal Cortex and Its Subregions

Regions of Interest		Mean (SD)	Correlation Coefficients† (p-value)
			ITAQ Illness Insight Score	ITAQ Treatment Insight Score	ITAQ Total Score
Prefrontal cortex	rt	0.22 (0.07)	−0.433 (0.083)	−0.465 (0.060)	−0.513 (0.035)*
	lt	0.19 (0.06)	−0.517 (0.034)*	−0.531 (0.028)*	−0.596 (0.012)*
Dorsolateral prefrontal cortex	rt	0.11 (0.03)	−0.425 (0.089)	−0.486 (0.048)*	−0.510 (0.036)*
	lt	0.10 (0.03)	−0.501 (0.041)*	−0.532 (0.028)*	−0.579 (0.015)*
Orbitofrontal cortex	rt	0.33 (0.12)	−0.405 (0.107)	−0.453 (0.068)	−0.503 (0.039)*
	lt	0.26 (0.10)	−0.555 (0.021)*	−0.587 (0.013)*	−0.639 (0.006)**
Ventrolateral prefrontal cortex	rt	0.23 (0.08)	−0.515 (0.034)*	−0.558 (0.020)*	−0.619 (0.008)**
	lt	0.13 (0.05)	−0.645 (0.005)**	−0.697 (0.002)**	−0.739 (0.001)**
Ventromedial prefrontal cortex	rt	0.35 (0.12)	−0.379 (0.134)	−0.362 (0.154)	−0.425 (0.089)
	lt	0.38 (0.14)	−0.410 (0.102)	−0.390 (0.121)	−0.475 (0.054)

Notes: †Correlation coefficients were obtained using partial correlation analysis with Positive and Negative Syndrome Scale (PANSS) scores and duration of illness as covariates. Asterisks and bolds indicate statistical significance at p < 0.05* and p < 0.01**.

Abbreviations: BPND, binding potential with respect to non-displaceable compartment; ITAQ, Insight and Treatment Attitude Questionnaire; SD, standard deviation; rt, right; lt, left.

Figure 1

Representative scatter plots of the correlations between the ITAQ scores and the [11C]DASB BPND in the PFC. (A and B) The ITAQ illness insight and treatment insight scores had significant negative correlations with the [11C]DASB BPND in the left VLPFC (illness insight: r = −0.645, p = 0.005; treatment insight: r = −0.697, p = 0.002). (C) The ITAQ total score had significant negative correlations with the [11C]DASB BPND in the left OFC (r = −0.639, p = 0.006) and bilateral VLPFC (left: r = −0.739, p = 0.001; right: r = −0.619, p = 0.008). The solid and dotted lines indicate the regression lines and 95% confidence intervals, respectively.

In addition, voxel-based correlation analysis with the PANSS total score and duration of illness as covariates revealed significant negative correlations between the ITAQ total score and [11C]DASB BPND values in the right orbitofrontal cortex (p = 0.0004), left ventromedial prefrontal cortex (p = 0.001), left dorsolateral prefrontal cortex (p = 0.002), and right ventrolateral prefrontal cortex (p = 0.003), which did not survive FDR correction for multiple correlations (FDR-corrected p = 0.320). These results are shown in Figure 2.

Figure 2

Voxel-based analysis of the correlation between the ITAQ total score and [11C]DASB BPND in the prefrontal cortex (uncorrected p < 0.005). The ITAQ total score had significant negative correlations with the [11C]DASB BPND in the right OFC (peak MNI coordinate: 38, 28, 2; cluster size = 332 voxels; p = 0.0004), left VMPFC (peak MNI coordinate: −2, 50, −12; cluster size = 52 voxels; p = 0.001), left DLPFC (peak MNI coordinate: −54, 24, 20; cluster size = 62 voxels; p = 0.002), and right VLPFC (peak MNI coordinate: 38, 26, −18; cluster size = 100 voxels; p = 0.003).

Discussion

In this study, we identified significant negative correlations between the level of insight measured by the ITAQ and the prefrontal SERT availability quantified by the [11C]DASB BPND in antipsychotic-free patients with schizophrenia, suggesting a significant involvement of serotonergic neurotransmission in insight deficits in schizophrenia. To the best of our knowledge, this is the first molecular PET study reporting the relationship between in vivo serotonin parameter and insight in schizophrenia.

It is unclear whether there is a simple competition model between SERT radiotracer and extracellular serotonin for SERT binding sites; however, it has been reported that lower SERT functioning is associated with greater extracellular serotonin.24 Ginovart et al47 reported that significantly decreased [11C]DASB binding was observed in cat brains under conditions in which tranylcypromine, a monoamine oxidase inhibitor, was administered to increase serotonin levels. In addition, Yamamoto et al48 also reported that increased endogenous serotonin using 5-hydroxy-L-tryptophan significantly decreased the binding potential of [11C]DASB in several brain regions in the conscious nonhuman primate. In contrast, Milak et al49 reported a decreased [11C]DASB binding under the rapid tryptophan depletion paradigm in the brains of baboons, suggesting the internalization of SERT. The effects of anesthesia on SERT and [11C]DASB radioligands and the interval between tryptophan depletion and [11C]DASB PET scan may be factors involved in these discrepancies.

Since a higher ITAQ score is indicative of good insight, we suppose that a low endogenous extracellular serotonin levels in the prefrontal cortex may be associated with low levels of insight in schizophrenia. The higher density of SERT could also increase serotonin clearance24 and the conditions of higher SERT density may lead to greater extracellular serotonin decrease, thereby accounting for an inverse association between SERT functioning and extracellular serotonin levels. Thus, based on this additional model as well as the model noted above,24,47,48 we may explain our results as being an association between more severe lack of insight assessed by the ITAQ and lower endogenous extracellular serotonin levels in the prefrontal cortex. Further studies with pharmacological challenge paradigms may be required. Moreover, since we cannot directly measure in vivo extracellular serotonin levels in the human brain,50 the interpretation regarding the relationship between insight deficits and SERT levels should be validated using a multitracer imaging method, combining both SERT and postsynaptic serotonergic markers.

Previous studies using clinical assessments including cognitive tests have implicated the prefrontal cortex in insight deficits in schizophrenia.10,11 In a structural MRI study, the left frontal pole volume was a significant predictor of the self-reflectiveness in schizophrenia.51 In a functional MRI study, the activation in the bilateral ventrolateral prefrontal cortex was significantly correlated with the self-reflective capacity in schizophrenia.6 The prefrontal cortex is also a critical brain region for self-reflective processes in the healthy human brain.52 It is also involved in critical functions, such as metacognition, which is associated with identifying and correcting erroneous beliefs and misinterpretations and is impaired in schizophrenia.53,54 Our study corroborates the importance of the prefrontal cortex underlying the lack of insight in schizophrenia and suggests the prefrontal SERT as the important neurochemical correlate.

In our study, the duration of illness was significantly positively associated with insight, particularly, treatment insight. This finding is in line with previous reports that insight impairment modestly improves over the course of the illness,55 and that patients in the chronic phase of schizophrenia have better insight than those in the first episode of psychosis or with a shorter duration of illness.56,57 Our finding along with previous reports may reflect the acceptance of the illness, more knowledge of the illness, or effects of a longer treatment period in patients with a longer duration than in those with a shorter duration of illness.55

The strengths of our study include the use of high-resolution PET imaging techniques. Compared with conventional PET systems, the HRRT-PET system used in our study has been reported to improve the quantification of monoamine neurotransmission parameters owing to reduced partial volume effects by enhanced spatial resolution.58,59 This enabled more accurate measurements of prefrontal SERT availability in our study. Another strength of this study is that all patients were antipsychotic-free and had not been taking psychotropic medications for at least 14 days before the PET scans. In addition, all patients had no history of taking antidepressant medications. All these aspects evidently minimized the confounding effects of psychotropic medications on the quantification of SERT availability.

The interpretation of the results of the present study should be considered in light of some limitations. The [11C]DASB BPND was quantified using the reference tissue model34,60 rather than using the metabolite-corrected arterial input function model. However, quantification using a metabolite-corrected arterial input function is invasive due to the requirement for cannulation of a radial artery, and consequent discomfort might be a confounding factor. Moreover, imprecision in determining the metabolite-corrected input function can be a source of variance in estimation of the endpoint.61 In our study, we used the [11C]DASB radiotracer. Additional research using other SERT tracers, such as [11C]MADAM62 and [11C]AFM63 may be required to confirm our findings. In addition, our study is considered preliminary as the results did not survive FDR correction for multiple correlations.

Conclusion

Our study provides in vivo evidence of significant negative correlations between insight deficits and prefrontal SERT availability in antipsychotic-free patients with schizophrenia, suggesting a significant involvement of cortical serotonergic signaling in impaired insight, one of the core symptoms of schizophrenia.