Literature DB >> 21180483

Intracranial (structural) changes in obsessive- compulsive disorder: A computerized tomography scan study.

Deepak Kumar Giri1, Indira Sharma.   

Abstract

OBJECTIVE: To assess intracranial structural changes in obsessive-compulsive disorder (OCD) with CT scan.
MATERIALS AND METHODS: Thirty patients of OCD between 21 and 40 years of age and fulfilling various inclusion and exclusion criteria were compared with control group. CT scans of all the patients and controls were taken and compared with regard to ventricular size, Evan's ratio and ventricular brain ratio (VBR).
RESULTS: Patients of OCD were found to have greater cortical atrophy and scored significantly higher in frontal and parietal area. Only 4 patients had enlarged ventricles, and there were none with a smaller ventricle. Mean Evan's ratio of patients was lower than that of the control group but the difference was statistically nonsignificant. The mean VBR of patients was lower than that of the control group and the difference was highly significant.
CONCLUSIONS: The evidence of neuro-radiological abnormalities in patients with OCD suggests that these disorders should not be considered merely functional in the traditional sense.

Entities:  

Keywords:  Computerized tomography scan; Intracranial structural changes; Neuro-imaging; Obsessive-compulsive disorder

Year:  2009        PMID: 21180483      PMCID: PMC2996199          DOI: 10.4103/0972-6748.62266

Source DB:  PubMed          Journal:  Ind Psychiatry J        ISSN: 0972-6748


Till 1980, obsessive-compulsive disorder (OCD) was thought to be a relatively rare disorder with poor chances of recovery. Current data estimate the lifetime prevalence of OCD to be around 2%-3% of the general population (Behar et al., 1984). Organic basis of OCD has been reported by various researchers like Guirdham (1972), Hillbom (1960) and Insel et al. (1983). With the advent of successful clinical trials with clomipramine in the treatment of OCD (Karno et al., 1988), the search for a primary biochemical abnormality increased, with the focus being on serotonin. The research on the neuroanatomical substrate for OCD has been more sparse and scattered. Current workers laid stress on the role of the basal ganglia (Khanna, 1988; Lensi et al., 1996), although some models implicate frontal lobe function (Luxenberg et al., 1988; McTavish et al., 1999). Insel et al. showed ventricular brain ratio (VBR) asymmetry and sulcal prominence measures indistinguishable from those of a matched group of nonpsychiatric control subjects. Rapoport et al. (1988) in their study on CT scans showed a mean VBR significantly higher than that of controls and showed spatial perceptual defects similar to those found in patients with frontal lobe lesions. Rasmussen et al. (1992) after analyzing brain volumes of 10 male patients found that caudate nucleus volumes in the patients with OCD were significantly less than those of control subjects; but lenticular nucleus, third ventricle and lateral ventricle volumes did not differ between these two groups and no abnormal asymmetry of bilateral structures was detected. In the available studies, there is no consistent evidence of structural etiology in patients with OCD. There is a paucity of literature as far as the CT variables in OCD are concerned, and the Indian scene is especially meager in terms of information available. Considering the fact that some intracranial structural changes may be found in OCD, we planned to carry out this study to find out any intracranial structural changes in patients of OCD.

MATERIALS AND METHODS

The present study was conducted at the Department of Psychiatry, Institute of Medical Sciences, BHU, Varanasi, from January 2001 to August 2002. The sample consisted of 30 patients of OCD from the outpatient and inpatient sections of the university hospital. Only those who fulfilled the DSM-IV criteria and were between 21 and 40 years of age were included in the study. Patients below 21 or above 40 years, having past history of head injury causing unconsciousness, having history of any significant physical illness, substance abuse and who had used oral steroid medication in the past 3 months prior to onset of psychiatric illness were excluded from the study. Informed consent was taken from each patient. All 30 patients were interviewed with the help of a pro forma sheet covering identification data, socio-demographic details, precipitating factors, age, total duration of illness, chief complaints, family history, past history of mental illness and pre-morbid personality. Physical and mental illness examinations were carried out in detail and information was recorded. After initial assessment, patients were examined by G.E. Syted 4000i CT scanner; 5-mm contiguous axial sections of brain were obtained from Reid’s baseline to the vertex. The pertinent slices for measurements of VBR and Evan’s ratio and evaluation of sulcal widening for 5 areas were recorded on the imaging film for analysis. Radiologists blindly rated ventricular size as small, normal or enlarged, and the VBR was estimated by measuring width of lateral ventricle most prominent in the CT slice and the maximum diameter of brain at the same level. It was expressed as percentage. Cortical atrophy (sulcal widening) was rated on a 4-point scale for 5 cortical areas (frontal, temporal, parietal, insular and occipital), and a cumulative cortical atrophy score for the separate regions was obtained. Evan’s ratio was measured as the ratio of the maximum width between the frontal horns of lateral ventricle to maximum internal skull diameter. Thirty normal CT scans of age- and sex-matched controls were screened and collected to compare the parameters (e.g., cortical atrophy, Evan’s ratio and VBR) with those of OCD patients.

RESULTS

There were 18 men and 12 women in the study group in comparison to 11 men and 19 women in the control group. Sex distribution did not differ significantly [Table 1]. Majority of the patients in the study group were in the age range of 21-25 years with mean age of 26.73 ± 6.49 years [Table 2]. In the study group, cortical atrophy score between 0 and 2 was found in 16 men and 8 women, and a score between 3 and 5 was found in 2 men and 4 women. These were statistically nonsignificant.
Table 1

Sex distribution in study and control groups

Study group n = 30Control group n = 30χ2P
No.%No.%
Male18601136.73.268>0.05
Female12401963.3
Table 2

Age distribution in study and control groups

Age group (in years)Study group n = 30Control group n = 30χ2P
No.%No.%
21-2519631446.74.413>0.10
26-3027723.3
31-35620413.3
36-40310516.6
Sex distribution in study and control groups Age distribution in study and control groups The cumulative cortical atrophy score of frontal area of 30 patients in the study group was found to be 12; and in the parietal area, it was 23 — both these values were highly significant in comparison to those of the control group [Table 3].
Table 3

Comparisons of cumulative cortical atrophy score in different areas of brain between study and control groups

Cortical atrophy score in different areas of brainStudy group n = 30Control group n = 30χ2P
Cumulative scoreMean ± SDCumulative scoreMean ± SD
Frontal120.4 ± 0.34270.07 ± 0.203.07<0.001[**]
Parietal230.76 ± 0.62160.03 ± 0.125.40<0.001[**]
Insular30.1 ± 0.0810.00 ± 0.002.00>0.05NS
Temporal40.166 ± 0.1520.066 ± 0.051.24>0.1NS
Occipital20.066 ± 0.051.65>0.12NS

Highly significant; NS - Not significant

Comparisons of cumulative cortical atrophy score in different areas of brain between study and control groups Highly significant; NS - Not significant The number of patients in the study group having normal ventricular size was 26; enlarged, 4; and none of them had small ventricular size in comparison to 27, 2 and 1, respectively, in the control group [Table 4].
Table 4

Comparison of ventricle size between study and control groups

Ventricle sizeStudy group n = 30Control group n = 30
No.%No.%
Normal2686.72790
Small13.3
Enlarged413.326.7
Comparison of ventricle size between study and control groups Mean ventricular size of 19 patients in the 21-25 years age group was 2.64, which was highly significant statistically in comparison with that of control group. The data was also highly significant for age groups 26-30 years and 31-35 years, where ventricle size was 2.43 ± 0.04 and 2.41 ± 0.39, respectively [Table 5].
Table 5

Comparison of mean ventricle size between study and control groups

Age group (in years)Study group n = 30Control group n = 30tP
No.Mean ± SDNo.Mean ± SD
21-25192.64 ± 0.34143.04 ± 0.293.53<0.01[**]
26-3022.43 ± 0.0473.13 ± 0.394.37<0.01[**]
31-3562.41 ± 0.3942.97 ± 0.223.11<0.05[*]
36-4032.73 ± 0.0952.89 ± 0.130.84>0.1NS

Highly significant

Significant; NS - Not significant

Comparison of mean ventricle size between study and control groups Highly significant Significant; NS - Not significant Mean Evan’s ratio was statistically nonsignificant in different age groups [Table 6].
Table 6

Comparison of mean evan’s ratio in relation to age between study and control groups

Age group (in years)Evan’s ratiotP
Study group (n = 30)Control group (n = 30)
No.Mean ± SDNo.Mean ± SD
21-251923.21 ± 6.11425.86 ± 1.61.81>0.05NS
26-30225.45 ± 0.04725.43 ± 2.30.022>0.1NS
31-35625.35 ± 1.61426.50 ± 3.10.682>0.1NS
36-40326.7 ± 1.0526.40 ± 2.280.255>0.1NS

NS - Not significant

Comparison of mean evan’s ratio in relation to age between study and control groups NS - Not significant Mean VBR of 22.05 ± 3.11 was also statistically significant in comparison to that of control group [Table 7].
Table 7

Comparison of mean ventricular brain ratio between study and control groups

Study group (n = 30)Control group (n = 30)tP
Mean VBR22.05 ± 3.126.00 ± 3.014.98<0.001**
Comparison of mean ventricular brain ratio between study and control groups The difference in mean VBR of 21-25 years age group between study group (22.19 ± 3.05) and control group (26.07 ± 2.09) was highly significant. The difference was also highly significant in age group 26-30 years, where mean VBR of study group was 20.30 ± 0.00 and that of control group was 27.43 ± 3.57 [Table 8].
Table 8

Comparison of ventricular brain ratio between study and control groups in relation to age

Age group (in years)Ventricular brain ratiotP
Study group n = 30Control group n = 30
No.Mean ± SDNo.Mean ± SD
21-251922.19 ± 3.051426.07 ± 2.094.32,0.01**
26-30220.30 ± 0.00627.43 ± 3.574.88,0.01**
31-35621.55 ± 3.11525.75 ± 1.692.837,0.05*
36-40323.30 ± 2.7524.80 ± 1.290.901.0.05NS
Comparison of ventricular brain ratio between study and control groups in relation to age

DISCUSSION

With the introduction of CT scan in 1971, revolution suddenly took place in the field of research in psychiatric disorders. In recent years, psychiatrists have employed CT scan as a tool to investigate possible intracranial (structural) changes in brain associated with major psychiatric illnesses. In the present study, an attempt has been made to assess intracranial (structural) changes in obsessive-compulsive disorder. The mean age in the study group was 26.76 ± 6.49 years, while it was 28.63 ± 7.99 years in the control group. This finding is consistent with the finding of Schilder (1938). Majority of the patients had duration of illness more than 18 months. For adult patients who came for treatment, OCD appeared to be a chronic condition. This finding is supported by findings of Weissman et al. (1994). They reported that 85% of 560 patients in their series had a continuous course with waxing and waning symptom; 10%, a deteriorative course; and 2%, an episodic course. Lensi et al. (1996) reported in their study that 65% had chronic course; 26%, episodic course; and 9% had deteriorative course. The difference in mean cortical atrophy score between study and control groups was found to be statistically nonsignificant. McTavish et al. (1999) also showed that VBR asymmetry and sulcal prominence measures in their study were indistinguishable from those of a matched group of nonpsychiatric control subjects. In the study group, cumulative cortical atrophy score in frontal and parietal areas was highly significant in comparison to that of the control group. A perusal of literature could not reveal any study that stressed atrophy of specific areas of cerebral hemisphere. The mean ventricle size was statistically highly significant in the age group 21-25 years and was significant in the age group 31-35 years. No definite pattern of association between the duration of illness and ventricular size could be observed. Findings of the present study are in accordance with those of the study by Rapoport et al. (1988), in which they found that children with severe primary OCD had higher-than-expected frequency of relative brain ventricular enlargement, and ventricular size did not correlate with sex, onset age or duration of illness. The mean Evan’s ratio in the study group (24.94 ± 0.52) was smaller than that in the control group (26.00 ± 0.36). However, the difference was statistically nonsignificant. On comparing mean Evan’s ratio between study and control groups in relation to age, findings suggested that in the study group, mean Evan’s ratio was either lower or equal to that of the control group; however, the difference was statistically nonsignificant. On reviewing literature, in any study that had a mention of Evan’s ratio, its relation with duration of illness of OCD could not be found. One study conducted by Behar et al. (1984) reported that when Evan’s ratios of patients and controls were compared, a significant difference was found between patients (mean ± SD, 0.31 ± 0.3) and controls (mean ± SD, 0.27 ±0.05). The mean VBR in patients showed a continuous increase as the duration of illness increased. This finding suggested that as the duration of illness increases, the VBR also increases in OCD. The findings are inconsistent with the findings from the study by Behar et al. (1984). They showed that patients had a mean VBR significantly higher than that of the controls and showed spatial-perceptual deficits similar to those found in patients with frontal lobe lesions. When the results of the present study were compared with those of normal CT scans of controls, intracranial structural changes were found particularly in VBR, ventricular enlargement and Evan’s ratio. Observations about some aspects in this study could not be compared with those of other studies because none of them have mentioned about these aspects of the present study. Correlation of these changes may throw light on etiological significance, course and prognosis.

CONCLUSION

The evidence of neuro-radiological abnormalities in patients with obsessive-compulsive disorders suggests that these disorders should not be considered merely functional in the traditional sense. An important task for researchers is to find out all specific structural abnormalities associated with these conditions and try to correlate them with various important variables like age, duration of illness, clinical presentation and prognosis.
  11 in total

1.  After-effects of brain-injuries. Research on the symptoms causing invalidism of persons in Finland having sustained brain-injuries during the wars of 1939-1940 and 1941-1944.

Authors:  E HILLBOM
Journal:  Acta Psychiatr Scand Suppl       Date:  1960

Review 2.  Obsessive-compulsive disorder: evidence for basal ganglia dysfunction.

Authors:  J L Rapoport; S P Wise
Journal:  Psychopharmacol Bull       Date:  1988

3.  Neuroanatomical abnormalities in obsessive-compulsive disorder detected with quantitative X-ray computed tomography.

Authors:  J S Luxenberg; S E Swedo; M F Flament; R P Friedland; J Rapoport; S I Rapoport
Journal:  Am J Psychiatry       Date:  1988-09       Impact factor: 18.112

4.  The epidemiology of obsessive-compulsive disorder in five US communities.

Authors:  M Karno; J M Golding; S B Sorenson; M A Burnam
Journal:  Arch Gen Psychiatry       Date:  1988-12

5.  Neurological and neuropsychological studies of patients with obsessive-compulsive disorder.

Authors:  T R Insel; E F Donnelly; M L Lalakea; I S Alterman; D L Murphy
Journal:  Biol Psychiatry       Date:  1983-07       Impact factor: 13.382

Review 6.  Obsessive-compulsive disorder: is there a frontal lobe dysfunction?

Authors:  S Khanna
Journal:  Biol Psychiatry       Date:  1988-09       Impact factor: 13.382

7.  Obsessive-compulsive disorder. Familial-developmental history, symptomatology, comorbidity and course with special reference to gender-related differences.

Authors:  P Lensi; G B Cassano; G Correddu; S Ravagli; J L Kunovac; H S Akiskal
Journal:  Br J Psychiatry       Date:  1996-07       Impact factor: 9.319

8.  Computerized tomography and neuropsychological test measures in adolescents with obsessive-compulsive disorder.

Authors:  D Behar; J L Rapoport; C J Berg; M B Denckla; L Mann; C Cox; P Fedio; T Zahn; M G Wolfman
Journal:  Am J Psychiatry       Date:  1984-03       Impact factor: 18.112

Review 9.  The epidemiology and clinical features of obsessive compulsive disorder.

Authors:  S A Rasmussen; J L Eisen
Journal:  Psychiatr Clin North Am       Date:  1992-12

10.  The cross national epidemiology of obsessive compulsive disorder. The Cross National Collaborative Group.

Authors:  M M Weissman; R C Bland; G J Canino; S Greenwald; H G Hwu; C K Lee; S C Newman; M A Oakley-Browne; M Rubio-Stipec; P J Wickramaratne
Journal:  J Clin Psychiatry       Date:  1994-03       Impact factor: 4.384

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