 |
|
Reduced Hippocampal Volumes Associated With the Long Variant of the Serotonin Transporter Polymorphism in Major Depression
Thomas Frodl, MD;
Eva M. Meisenzahl, MD;
Peter Zill, MD;
Thomas Baghai, MD;
Dan Rujescu, MD;
Gerda Leinsinger, MD;
Ronald Bottlender, MD;
Cornelius Schüle, MD;
Peter Zwanzger, MD;
Rolf R. Engel, MD;
Rainer Rupprecht, MD;
Brigitta Bondy, MD;
Maximilian Reiser, MD;
Hans-Jürgen Möller, MD
Arch Gen Psychiatry. 2004;61:177-183.
ABSTRACT
| |
Background Substantial evidence supports a role for dysfunction of the serotonin transporter in the pathogenesis of major depression. Several studies have found reciprocal interactions between the serotonergic system and both brain-derived neurotrophic factor and glutamate, which are known to modulate or affect hippocampal morphologic characteristics.
Objective To examine the influence of a polymorphism (5-HTTLPR) in the promoter region of the serotonin transporter gene on hippocampal volumes in patients with major depression and healthy controls.
Design Baseline investigation of a prospective magnetic resonance imaging study with a 4-year follow-up period.
Patients We examined 40 inpatients with major depression as well as 40 healthy controls matched for age, sex, and handedness.
Main Outcome Measures Subjects underwent high-resolution magnetic resonance imaging. Furthermore, genotyping for the 5-HTTLPR biallelic polymorphism was performed, which consists of a 44–base pair insertion (L allele) or deletion (S allele).
Results Patients with the L/L homozygous genotype had significantly smaller hippocampal gray matter (left hemisphere: P = .003; right hemisphere: P = .01) and white matter volumes (left hemisphere: P = .001; right hemisphere: P = .002) than controls with this genotype. No significant differences were found between patients and controls with the L/S or S/S genotype. Moreover, patients with the L/L genotype had significantly smaller hippocampal white matter volumes than those with the L/S or S/S genotype (P = .03).
Conclusions These findings suggest that homozygosity for the L allele is associated with decreased hippocampal volumes in patients with major depression but not in healthy controls. A possible explanation is that the interaction between the serotonergic system and neurotrophic factors as well as excitatory amino acid neurotransmission may affect hippocampal morphologic characteristics.
INTRODUCTION
One of the major biological substrates in the pathogenesis of major depression is the serotonergic system.1 Serotonin is a widespread neurotransmitter in the central nervous system. Serotonergic neurons are mainly found in different raphe nuclei, from which they project to numerous brain regions such as cortical areas, the hippocampus, and the basal ganglia.2 The fine-tuning of serotonin neurotransmission seems to be critically influenced by the serotonin transporter (5-HTT) via clearing synaptic serotonin.
A polymorphism (5-HTTLPR) in the promoter region of the 5-HTT gene on chromosome 17q11.2 was identified with a 44–base pair insertion (L allele) or deletion (S allele).3 The relationship of this polymorphism to major depression is unequivocal; one study found a relationship,4 whereas others did not.5-6 Cultured human lymphoblast cell lines homozygous for the L allele were associated with nearly 2-fold increased 5-HTT expression and increased serotonin reuptake.3 Moreover, in mice with targeted inactivation (knockout) of the 5-HTT gene, the modulation of serotonergic system activity was found to depend on the 5-HTTLPR genotype.7 In vivo studies also support these findings. A significant association between the L/L genotype and the depressive response to tryptophan depletion showed that patients homozygous for the L/L genotype who were in remission from a major depressive episode had rapid serotonin reuptake combined with decreased brain serotonin availability.8 Furthermore, in 8 healthy controls homozygous for the L allele, a significant association with increased iodine 123–labeled 2 -carbomethoxy-3-(4-iodophenyl) tropane ([123I]-CIT)binding to 5-HTT was seen, which may indicate a greater amount of 5-HTT.9 However, these findings need clarification because 16 healthy controls did not show a relationship between the 5-HTTLPR polymorphism and [123I]-CIT binding.10
Interestingly, it has been demonstrated that serotonergic signaling is an important regulator of both early central nervous system development11 and adult neurogenesis.12 In addition, because a high density of 5-HTT has been found in the hippocampus by autoradiographic13-14 and immunocytochemical investigations,15 there may be a relationship between serotonergic function and hippocampal morphologic characteristics.
Aside from the well-documented contribution to learning and memory, the hippocampal formation plays a critical role in the regulation of motivation and emotion.16 The hippocampus is a core region in the limbic system and has widespread connections to diverse cortical areas such as the prefrontal cortex, anterior thalamic nuclei, amygdala, basal ganglia, and hypothalamus,17 all of which constitute the neuroanatomical network of mood regulation.18 Investigations of patients with recurrent depressive episodes have demonstrated structural changes in the hippocampal formation,19-22 which may decline with longer illness duration.19 One study investigating first-episode patients and those with multiple episodes found that only patients with multiple episodes had hippocampal volume reduction, which was associated with the duration of their illness.22 These findings extend those of experimental studies that suppose stress toxicity23 or a lack of neurotrophic factors24 to be the cause of these well-known structural abnormalities of the hippocampus. However, postmortem analysis of the human hippocampus in patients with major depression and in glucocorticoid-treated patients did not show any major morphologic changes associated with neuronal cell death,25 so it remains unclear whether and to what extent hippocampal changes occur in major depression.
Recently, studies have begun to address the issue that structural changes may predispose patients to depression; hippocampal size has been found to be strongly genetically determined,26 and even first-episode patients with major depression showed a diminished volume of 6% in the left side of the hippocampus.27 An association between heritability and brain size is supported by twin studies28 and by studies from our laboratory showing that methionine homozygosity at codon 129 on the prion protein was associated with white matter reduction as well as enlargement of cerebrospinal fluid volume in healthy controls,29 and that the allele 2 within the promoter region of the interleukin 1 gene was related to bifrontal temporal gray matter volume deficits and reduced overall white matter in patients with schizophrenia.30 A genetic influence on brain volumes was also found in patients with geriatric depression, in whom at least 1 APOE  4 allele showed significant decline in the right hippocampus.31
The aim of our study was to investigate the influence of functional polymorphisms in the 5-HTT gene on hippocampal morphologic characteristics in patients with major depression and healthy controls.
METHODS
SUBJECTS
We recruited 40 inpatients with major depression from the Department of Psychiatry at Ludwig-Maximilians-University, Munich, Germany (age range, 18-65 years; mean ± SD age, 44.4 ± 11.7 years) (Table 1). Psychiatric diagnoses based on DSM-IV criteria and on the Structured Clinical Interview for DSM-IV were determined by a consensus of at least 2 psychiatrists. Mean ± SD illness duration was 7.9 ± 10.1 years, and number of hospitalizations was 2.2 ± 3.0. Moreover, mean ± SD cumulative illness duration as described by Sheline et al19 (27.7 ± 35.2 months) and total previous duration of antidepressant medication use (25.5 ± 55.8 months) were obtained retrospectively according to the anamnesis. Clinical variables were documented using the 21-item Hamilton Depression Rating Scale. Fourteen patients received selective serotonin reuptake inhibitors (4 sertraline hydrochloride, 7 citalopram, 2 paroxetine, and 1 fluvoxamine maleate), 7 were taking tricyclic antidepressants (2 amitriptyline hydrochloride, 2 doxepin hydrochloride, and 1 trimipramine), and 16 received other new antidepressants (5 venlafaxine hydrochloride, 4 reboxetine, and 7 mirtazapine). Four patients were not taking antidepressant medication at the time of magnetic resonance imaging.
|
|
|
|
Table 1. Demographic and Clinical Data of Patients With Major Depression and Healthy Controls*
|
|
|
For comparison, 40 healthy control subjects were matched with respect to age (age range, 19-58 years; mean ± SD age, 41.7 ± 12.1 years), sex, and handedness. A structured interview was used to assess medical history, trauma, and other exclusion criteria. Neither the healthy controls nor their first-degree relatives had a history of neurologic or mental illness. Exclusion criteria for patients and controls were previous head injury with loss of consciousness, cortisol medication use in the medical history, previous alcohol or substance abuse, or neurologic diseases. Comorbidity with other mental illnesses or personality disorders was also excluded. No subject had received previous electroconvulsive therapy. Hypertension was excluded using blood pressure measures, and handedness was determined with the Edinburgh inventory.32
After an extensive description of the study to the patients with major depression and healthy controls, written informed consent was obtained. The study design was approved by the local ethics committee and was prepared in accordance with the ethical standards in the Declaration of Helsinki.
MAGNETIC RESONANCE IMAGING PROCEDURES
Magnetic resonance images were obtained (1.5-T Magnetom Vision; Siemens, Erlangen, Germany) using a coronal T2- and proton density–weighted dual echo sequence (repetition time, 3710 milliseconds; echo time, 22/90 ms; total acquisition time, 9 minutes; number of acquisitions, 1; field of view, 230 mm; matrix, 240 x 256; section thickness, 3 mm) and a 3-dimensional magnetization prepared rapid acquisition gradient-echo sequence (repetition time, 11.6 milliseconds; echo time, 4.9 milliseconds; total acquisition time, 9 minutes; number of acquisitions, 1; field of view, 230 mm; matrix, 512 x 512; section thickness, 1.5 mm). A commercial software package was used (Analyze; Biomedical Imaging Resource, Mayo Foundation, Rochester, Minn) for further image processing, with size reduction from 16 to 8 bit and transformation to a uniform matrix of 256 x 256 on 192 sections each 1.0 mm thick. All datasets were realigned and resampled 3-dimensionally for the anterior commissure to posterior commissure line according to Talairach coordinates with the software program BRAINS (Brain Research: Analysis of Images, Networks and Systems; developed by Andreasen et al).33 This program allowed control of the regions of interest for the sagittal and transverse sections simultaneously as well as of the segmentation for calculating the intracranial content and the gray and white matter volumes (cubic centimeters) within the defined region of interest.
DEFINITION OF THE HIPPOCAMPAL FORMATION
We used the definition of the hippocampus (Figure 1) according to Niemann et al.34 The hippocampal-amygdala border was detected using the description by Convit et al35; in addition, Frodl et al27 provide a detailed description of this area. The evaluation staff was blind to each subject's status. On each magnetic resonance image, we started with the most posterior coronal section where the hippocampus was clearly detectable. The posterior hippocampal body and intralimbic sulcus can be seen in Figure 1A. In Figure 1B, the shape of the hippocampus may be compared with that of a rabbit with the head directed vertically; the medial ambient cistern is separated from the temporal horn of the lateral ventricles. The amygdala-hippocampal transition zone appears as a diffuse area of gray matter between the anterior portion of the hippocampus and the posterior portion of the amygdala. This structure can be identified most reliably in the axial plane. The boundary between the hippocampus and amygdala is clearly detectable in the sagittal plane (Figure 1C). The anterior part of the hippocampus ends where the cornu inferius of the lateral ventricle becomes vertically oriented.
|
|
|
|
Figure 1. Magnetic resonance image of coronal sections running in the occipitorostral direction. A, The hippocampal body. B, The shape of the hippocampus may be compared with that of a rabbit with the head directed vertically. C, The amygdala-hippocampal transition area.
|
|
|
For determination of interrater reliability, 10 brains were randomly chosen, and regions of interest were independently determined by 2 raters. The intraclass correlations for the interrater reliability of hippocampal gray matter (r9 = 0.97; P<.001) and hippocampal white matter (r9 = 0.82; P = .008) were high. For the intrarater reliability, 10 brains were obtained 4 weeks apart by 1 rater (T.F.) (hippocampal gray matter: r9 = 0.96; P<.001; hippocampal white matter: r9 = 0.93; P<.001).
LABORATORY METHOD
The DNA was extracted from of a 5-mL blood sample using a kit (QIAamp Blood Isolation Kit; QIAGEN GmbH, Hilden, Germany) following the prescription of the supplier. Genotyping was carried out applying polymerase chain reaction amplification using the primers and methods described earlier by Heils et al.36 The final volume was 25 µL consisting of 50 ng of DNA, l µmol/L of each primer, 200µM of deoxynucleotide triphosphate, 100µM of 7-deaza–guanosine triphosphate, 5% dimethyl sulfoxide, 10mM of Tris hydrochloride (pH, 8.3), 50mM of potassium chloride, 1.5mM of magnesium chloride, and 2.5 U of DNA polymerase (AmpliTaq Gold; PerkinElmer, Langen, Germany). The polymerase chain reaction products were separated on a 3% agarose gel (FMC NuSieve, 3:1; Biozym Diagnostic GmbH, Oldendorf, Germany) and visualized with ethidium bromide staining.
STATISTICAL ANALYSES
Morphometric measurements in both groups were tested for normal distribution and homogeneity of variance. All statistical tests were considered to be significant at P<.05. We used t tests and analysis of variance to test for differences in demographic variables between patients and controls as well as between genotypes. We used  2 tests to compare the genotype frequencies between patients and controls. Hippocampal volumes underwent analysis of covariance (ANCOVA) assessing the main and interaction effects of the within-subject factor of hemisphere (left or right) and the between-subject factors of diagnosis (patients with depression or controls) and genotype (L/L, L/S, or S/S) using total cranial volume as the cofactor. Brain lobe volumes also underwent ANCOVA with the within-subject factors of hemisphere (left or right) and region (frontal, temporal, parietal, or occipital) and the between-subject factors of diagnosis (patients with depression or controls) and genotype (L/L, L/S, or S/S). Furthermore, hippocampal volumes of individuals homozygous for the L/L genotype were compared with those carrying the L/S or S/S genotype in each diagnostic group by ANCOVA design. Posthoc analyses were carried out with ANCOVA and t tests to test hippocampal volumes for differences between genotypes. Effect sizes regarding the association between genotype and hippocampal volumes were presented as Pearson correlation coefficients according to a method described by Rosenthal.37
RESULTS
Patients and controls did not differ with regard to demographic variables (Table 1), and these variables were not different between genotypes (L/L, L/S, and S/S). Illness duration (F2,39 = 0.15; P = .86), age at onset (F2,39 = 0.40; P = .67), number of hospitalizations (F2,39 = 0.98; P = .39), and depression severity measured with the Hamilton Depression Rating Scale (F2,39 = 0.27; P = .77) did not differ between genotypes (L/L, L/S, and S/S). Furthermore, antidepressant medication use (selective serotonin reuptake inhibitors, tricyclic antidepressants, and other antidepressants; 238 = 3.4; P = .50) and total previous duration of antidepressant treatment (F2,39 = 0.68; P = .51) were not significantly different between genotypes. The allele and genotype frequencies are indicated in Table 1; they did not differ between patients and controls (239 = 0.56; P = .76).
The analysis of variance for frontal, temporal, parietal, and occipital lobes did not show significant effects. There were neither significant main effects for diagnosis and genotype nor significant interactions of diagnosis and genotype; genotype and region; genotype, diagnosis, and region; or genotype, diagnosis, hemisphere, and region.
The results of ANCOVA for the gray and white matter of the hippocampus appear in Table 2. A significant main diagnosis effect was found, indicating smaller hippocampal gray and white matter volumes in patients with major depression as compared with healthy controls. Moreover, there was a significant association between genotype and hippocampal volumes, with a significant diagnosis and genotype interaction for hippocampal white matter (F2,73 = 3.0; P = .05) but not hippocampal gray matter (F2,73 = 0.88; P = .42).
|
|
|
|
Table 2. Repeated-Measures Analysis of Covariance for Hippocampal Gray and White Matter*
|
|
|
Post hoc ANCOVA revealed a significant effect of genotype for hippocampal white matter in patients (F2,36 = 3.8; P = .03) (Figure 2), whereas no significant effect was found for healthy controls (F2,36 = 0.58; P = .56). Furthermore, significantly smaller right hippocampal white matter volumes (F1,39 = 8.0; P = .008; r39 = 0.42) and a trend toward smaller left hippocampal white matter volumes (F1,39 = 3.7; P = .06; r39 = 0.30) were found in patients with the L/L genotype as compared with those who carried the L/S or S/S genotype.
|
|
|
|
Figure 2. Scattergrams of left and right hippocampal white matter showing serotonin transporter polymorphisms in patients with depression. Bars depict the mean for each group.
|
|
|
Post hoc t tests showed significantly smaller right hippocampal white matter volumes in patients homozygous for the L/L genotype compared with the L/S (t30 = 2.6; P = .02; effect size: r29 = 0.41) and S/S (t22 = 2.7; P = .01; r21 = 0.43) genotypes, as well as smaller left hippocampal white matter volumes compared with the S/S genotype (t22 = 2.3; P = .03; effect size: r21 = 0.36) but not compared with the L/S genotype (t30 = 1.5; P = .15; effect size: r29 = 0.24).
The results of ANCOVA to assess differences between patients and controls in each genotype group are presented in Table 3. Significantly smaller hippocampal gray matter (Figure 3) and white matter volumes were detected in patients homozygous for the L/L genotype as compared with controls who carried this genotype. On the other hand, no significant differences were observed between patients heterozygous for the L/S genotype and controls with this genotype or between those homozygous for the S/S genotype and controls who carried that genotype.
|
|
|
|
Table 3. Analysis of Covariance for Hippocampal Gray and White Matter*
|
|
|
|
|
|
|
Figure 3. Scattergrams of left and right hippocampal gray matter for subjects with the L/L genotype. Patients and healthy controls did not differ significantly in age, sex, or handedness. The sample size was 16 patients and 13 controls. Bars depict the mean for each group.
|
|
|
There were no significant correlations between hippocampal volumes and illness duration (left hippocampal gray matter: r29 = -0.17; P = .30; right hippocampal gray matter: r29 = -0.17; P = .29; left hippocampal white matter: r29 = -0.18; P = .26; right hippocampal white matter: r29 = 0.06; P = .73). There was also no significant correlation between severity of depression as measured by the Hamilton Depression Rating Scale and hippocampal volumes (left hippocampal gray matter: r29 = -0.17; P = .30; right hippocampal gray matter: r29 = -0.17; P = .29; left hippocampal white matter: r29 = -0.18; P = .26; right hippocampal white matter: r29 = 0.06; P = .73). Furthermore, including illness duration as a cofactor in the ANCOVA did not change the effect of genotype on hippocampal volumes.
When we excluded from analysis the patient and control subject who appeared to be outliers in the scattergrams, these results did not change. Because 1 study reported brain abnormalities in psychotic depression as compared with nonpsychotic depression,38 the analysis was also conducted without the 5 patients who had psychotic features, but again the results did not change.
COMMENT
Our study investigates the contribution of functional genetics to hippocampal volumes in patients with major depression and healthy controls. In line with previous results,20, 25-27 hippocampal volumes were found to be significantly smaller in patients as compared with healthy controls. The main new finding of this study was that the L/L genotype was associated with reduced gray and white matter of the hippocampal formation in patients vs healthy controls.
To our knowledge, this is the first study of the relationship between the 5-HTTLPR polymorphism and hippocampal volumes in major depression. Therefore, our findings deserve discussion, particularly with respect to limitations. The study was not designed to test an association of the 5-HTTLPR polymorphism with major depression because the sample size was too small to detect modest contributions. Nevertheless, this result was similar to that in recent investigations with larger samples.5-6
Case-control associations are known to be sensitive to population stratification. Patients who have recurrent depression may have a longer duration of exposure to antidepressant medication as compared with those with a first episode. However, because patients and controls with the 5-HTTLPR genotype did not differ with respect to age, sex, illness duration, age at onset, medication use, or national origin, the population stratification in this study was likely not a problem.
Our patients were currently receiving medication. We are aware of no studies on the influence of antidepressants on brain structures in depressed patients, so the medications' effects are unknown. A preliminary investigation in 10 pediatric patients with obsessive-compulsive disorder showed enlarged thalamic volumes before treatment and a decrease in thalamic volumes after 12 weeks of treatment with paroxetine hydrochloride; it is unclear if this effect is due to the medication or to changes in symptoms during treatment.39 In neural cell lines, tricyclic antidepressants and selective serotonin reuptake inhibitors were found to be neurotoxic.40 In the future, it would be interesting to study patients with no previous medication use to overcome the bias that hippocampal volumes are influenced by medication.
Because the L allele is more common in the population than the S allele, it could be argued that an equal number of individuals for each genetic subtype should have been sampled. However, this would have meant including an extremely large number of patients and controls.
The results of our study indicate that hippocampal volume is genetically determined.19Concerning the functional importance of the neurotransmitter serotonin on brain morphologic characteristics, it has been demonstrated that serotonergic signaling is an important regulator of early central nervous system development.11 Hippocampal volumes were already found to be reduced early in the disease20; thus, reduced hippocampal volumes in patients with the L/L genotype might be a risk factor rather than a consequence of major depression.
The effects we saw of genotype on the hippocampus could also be linked to central nervous system development, modulation of certain effects of the illness, different vulnerability to stress, or different response to antidepressant treatment. If the higher reuptake of serotonin in subjects with the L/L genotype modulates the course of the disease, the hippocampal volumes might be affected as a result of depression or stress-related neurotoxic processes. The L/L genotype might cause a distinct vulnerability to the stress reaction. A hypothesis is that stress and increased glucocorticoids may contribute to hippocampal volume loss via glutamatergic toxic effects.29 Stress decreases the expression of brain-derived neurotrophic factor in the hippocampus,41 which was found to have trophic effects on serotonergic neurons.42 Brain-derived neurotrophic factor and the serotonergic system may regulate reciprocal functions; the 5-HTT function is modulated by brain-derived neurotrophic factor,43 which in turn was found to be elevated in the hippocampus and frontal cortex after antidepressant treatment.42 However, our study did not show a significant correlation between the hippocampus and illness duration in contrast to that by Sheline et al,19 who investigated elderly patients. Thus, a hippocampal decline during the course of depression must be further evaluated in prospective studies.
Furthermore, the short variant of the 5-HTTLPR polymorphism was associated with a poor response to antidepressant treatment.44 Therefore, particular patients with the L/L genotype may benefit from antidepressant drugs. Adaptation of the cyclic adenosine monophosphate second-messenger pathway, including up-regulation of the cyclic adenosine monophosphate response element binding protein as a result of therapy, increases the expression of brain-derived neurotrophic factor,45 which has neurotrophic and possibly protective effects on hippocampal neurons.
In summary, this is the first study that investigates genetic contributions of the 5-HTTLPR polymorphism to hippocampal volume reduction in major depression. Patients with the L/L genotype may have a higher vulnerability to hippocampal changes. It is unclear whether these changes occur before the beginning of the disease or are triggered from a variety of factors, such as stress or emotional trauma during the depressive episode. We hope that our study may stimulate further research into the influence of functional genetics on brain structure in major depression.
AUTHOR INFORMATION
| |
Corresponding author: Eva M. Meisenzahl, MD, head, imaging laboratory, Department of Psychiatry, Ludwig-Maximilians-University of Munich, Nussbaumstr 7, Munich 80336, Germany (e-mail: emeisen{at}psy.med.uni-muenchen.de).
Submitted for publication July 24, 2002; final revision received July 14, 2003; accepted July 21, 2003.
This study was supported by the German Federal Research Ministry (Berlin) within the German Research Networks in Medicine promotion as part of the German Research Network on Depression project.
We thank Nancy C. Andreasen, MD, PhD, and her staff, who provided generous support with the BRAINS segmentation program, and Anton Strauss, MD, and Bernhard Burgermeister, who provided technical support.
From the Departments of Psychiatry (Drs Frodl, Meisenzahl, Zill, Baghai, Rujescu, Bottlender, Schüle, Zwanzger, Engel, Rupprecht, Bondy, and Möller) and Radiology (Drs Leinsinger and Reiser), Ludwig-Maximilians-University of Munich, Munich, Germany.
REFERENCES
1. Owens MJ, Nemeroff CB. The role of serotonin in the pathophysiology of depression: focus on the serotonin transporter. Clin Chem. 1994;40:288-295.
FREE FULL TEXT
2. Parent A, Descarries L, Beaudet A. Organization of ascending serotonin systems in the adult rat brain: a radioautographic study after intraventricular administration of [3H]5-hydroxytryptamine. Neuroscience. 1981;6:115-138.
FULL TEXT
|
WEB OF SCIENCE
| PUBMED
3. Lesch KP, Bengel D, Heils A, Sabol SZ, Greenberg BD, Petri S, Benjamin J, Muller CR, Hamer DH, Murphy DL. Association of anxiety-related traits with a polymorphism in the serotonin transporter gene regulatory region. Science. 1996;274:1527-1531.
FREE FULL TEXT
4. Collier DA, Stober G, Li T, Heils A, Catalano M, Di Bella D, Arranz MJ, Murray RM, Vallada HP, Bengel D, Muller CR, Roberts GW, Smeraldi E, Kirov G, Sham P, Lesch KP. A novel functional polymorphism within the promoter of the serotonin transporter gene: possible role in susceptibility to affective disorders. Mol Psychiatry. 1996;1:453-460.
WEB OF SCIENCE
| PUBMED
5. Minov C, Baghai TC, Schule C, Zwanzger P, Schwarz MJ, Zill P, Rupprecht R, Bondy B. Serotonin-2A-receptor and -transporter polymorphisms: lack of association in patients with major depression. Neurosci Lett. 2001;303:119-122.
FULL TEXT
|
WEB OF SCIENCE
| PUBMED
6. Seretti A, Lilli R, Lorenzi C, Lattuada E, Cusin C, Smeraldi E. Serotonin transporter gene (5-HTTLPR) and major psychoses. Mol Psychiatry. 2002;7:95-99.
FULL TEXT
|
WEB OF SCIENCE
| PUBMED
7. Bengel D, Murphy DL, Andrews AM, Wichems CH, Feltner D, Heils A, Mossner R, Westphal H, Lesch KP. Altered brain serotonin homeostasis and locomotor insensitivity to 3, 4-methylenedioxymethamphetamine ("Ecstasy") in serotonin transporter-deficient mice. Mol Pharmacol. 1998;53:649-655.
FREE FULL TEXT
8. Moreno FA, Rowe DC, Kaiser B, Chase D, Michaels T, Gelernter J, Delgado PL. Association between a serotonin transporter promoter region polymorphism and mood response during tryptophan depletion. Mol Psychiatry. 2002;7:213-216.
FULL TEXT
|
WEB OF SCIENCE
| PUBMED
9. Heinz A, Jones DW, Mazzanti C, Goldman D, Ragan P, Hommer D, Linnoila M, Weinberger DR. A relationship between serotonin transporter genotype and in vivo protein expression and alcohol neurotoxicity. Biol Psychiatry. 2000;47:643-649.
FULL TEXT
|
WEB OF SCIENCE
| PUBMED
10. Willeit M, Stastny J, Pirker W, Praschak-Rieder N, Neumeister A, Asenbaum S, Tauscher J, Fuchs K, Sieghart W, Hornik K, Aschauer HN, Brucke T, Kasper S. No evidence for in vivo regulation of midbrain serotonin transporter availability by serotonin transporter promoter gene polymorphism. Biol Psychiatry. 2001;50:8-12.
FULL TEXT
|
WEB OF SCIENCE
| PUBMED
11. Lauder JM. Neurotransmitters as growth regulatory signals: role of receptors and second messengers. Trends Neurosci. 1993;16:233-240.
FULL TEXT
|
WEB OF SCIENCE
| PUBMED
12. Gould E. Serotonin hippocampal neurogenesis. Neuropsychopharmacology. 1999;21:46S-51S.
PUBMED
13. D'Amato RJ, Largent BL, Snowman AM, Snyder SH. Selective labeling of serotonin uptake sites in rat brain by [3H]citalopram contrasted to labeling of multiple sites by [3H]imipramine. J Pharmacol Exp Ther. 1987;242:364-371.
FREE FULL TEXT
14. Hrdina PD, Foy B, Hepner A, Summers RJ. Antidepressant binding sites in brain: autoradiographic comparison of [3H]paroxetine and [3H]imipramine localization and relationship to serotonin transporter. J Pharmacol Exp Ther. 1990;252:410-418.
FREE FULL TEXT
15. Sur C, Betz H, Schloss P. Immuncytochemical detection of the serotonin transporter in rat brain. Neuroscience. 1996;73:217-231.
FULL TEXT
|
WEB OF SCIENCE
| PUBMED
16. Gray JA, McNaughton N. Comparison between the behavioural effects of septal and hippocampal lesions: a review. Neurosci Biobehav Rev. 1983;7:119-188.
FULL TEXT
|
WEB OF SCIENCE
| PUBMED
17. Rosene DL, Van Hoesen GW. The hippocampal formation of the primate brain: a review of some comparative aspects of cytoarchitecture and connections. In: Jones EG, Peters A, eds. Cerebral Cortex. Vol 6. New York, NY: Plenum Press; 1987:345-456.
18. Soares JC, Mann JJ. The anatomy of mood disorders: review of structural neuroimaging studies. Biol Psychiatry. 1997;41:86-106.
FULL TEXT
|
WEB OF SCIENCE
| PUBMED
19. Sheline YI, Sanghavi M, Mintun MA, Gado MH. Depression duration but not age predicts hippocampal volume loss in medically healthy women with recurrent major depression. J Neurosci. 1999;19:5034-5043.
FREE FULL TEXT
20. Steffens DC, Byrum CE, McQuoid DR, Greenberg DL, Payne ME, Blitchington TF, MacFall JR, Krishnan KR. Hippocampal volume in geriatric depression. Biol Psychiatry. 2000;48:301-309.
FULL TEXT
|
WEB OF SCIENCE
| PUBMED
21. Bremner JD, Narayan M, Anderson ER, Staib LH, Miller HL, Charney DS. Hippocampal volume reduction in major depression. Am J Psychiatry. 2000;157:115-118.
FREE FULL TEXT
22. MacQueen GM, Campbell S, McEwen BS, Macdonald K, Amano S, Joffe RT, Nahmias C, Young LT. Course of illness, hippocampal function, and hippocampal volume in major depression. Proc Natl Acad Sci U S A. 2003;100:1387-1392.
FREE FULL TEXT
23. Sapolsky RM. Glucocorticoids and hippocampal atrophy in neuropsychiatric disorders. Arch Gen Psychiatry. 2000;57:925-935.
FREE FULL TEXT
24. Nestler EJ, Barrot M, DiLeone RJ, Eisch AJ, Gold SJ, Monteggia LM. Neurobiology of depression. Neuron. 2002;34:13-25.
FULL TEXT
|
WEB OF SCIENCE
| PUBMED
25. Müller MB, Lucassen PJ, Yassouridis A, Hoogendijk WJG, Holsboer F, Swaab DF. Neither major depression nor glucocorticoid treatment affects the cellular integrity of the human hippocampus. Eur J Neurosci. 2001;14:1603-1612.
FULL TEXT
|
WEB OF SCIENCE
| PUBMED
26. Schatzberg AF. Major depression: causes or effects? Am J Psychiatry. 2002;159:1077-1079.
FREE FULL TEXT
27. Frodl T, Meisenzahl EM, Zetzsche T, Born C, Groll C, Jäger M, Leinsinger G, Bottlender R, Hahn K, Möller H-J. Hippocampal changes in patients with a first episode of major depression. Am J Psychiatry. 2002;159:1112-1118.
FREE FULL TEXT
28. Bartley AJ, Jones DW, Weinberger DR. Genetic variability of human brain size and cortical gyral patterns. Brain. 1997;120:257-269.
FREE FULL TEXT
29. Rujescu D, Meisenzahl EM, Giegling I, Kirner A, Leinsinger G, Hegerl U, Hahn K, Möller H-J. Methionine homozygosity at codon 129 in the prion protein is associated with white matter reduction and enlargement of CSF compartments in healthy volunteers and schizophrenic patients. Neuroimage. 2002;15:200-206.
FULL TEXT
|
WEB OF SCIENCE
| PUBMED
30. Meisenzahl EM, Rujescu D, Kirner A, Giegling I, Kathmann N, Leinsinger G, Maag K, Hegerl U, Hahn K, Moller HJ. Association of an interleukin-1beta genetic polymorphism with altered brain structure in patients with schizophrenia. Am J Psychiatry. 2001;158:1316-1319.
FREE FULL TEXT
31. Kim DH, Payne ME, Levy RM, MacFall JR, Steffens DC. APOE genotype and hippocampal volume change in geriatric depression. Biol Psychiatry. 2002;51:426-429.
FULL TEXT
|
WEB OF SCIENCE
| PUBMED
32. Oldfield RC. The assessment and analysis of handedness: the Edinburgh inventory. Neuropsychologia. 1971;9:97-113.
FULL TEXT
|
WEB OF SCIENCE
| PUBMED
33. Andreasen NC, Cohen G, Harris G, Cizadlo T, Parkkinen J, Rezai K, Swayze VW. Image processing for the study of brain structure and function: problems and programs. J Neuropsychiatry Clin Neurosci. 1992;4:125-133.
FREE FULL TEXT
34. Niemann K, Hammers A, Coenen VA, Thron A, Klosterkotter J. Evidence of a smaller left hippocampus and left temporal horn in both patients with first episode schizophrenia and normal control subjects. Psychiatry Res. 2000;99:93-110.
WEB OF SCIENCE
| PUBMED
35. Convit A, McHugh P, Wolf OT, de Leon MJ, Bobinski M, De Santi S, Roche A, Tsui W. MRI volume of the amygdala: a reliable method allowing separation from the hippocampal formation. Psychiatry Res. 1999;90:113-123.
WEB OF SCIENCE
| PUBMED
36. Heils A, Teufel A, Petri S, Stöber G, Riederer P, Bengel D, Lesch KP. Allelic variation of human serotonin transporter gene expression. J Neurochem. 1996;66:2621-2624.
WEB OF SCIENCE
| PUBMED
37. Rosenthal R. Meta-Analytic Procedures for Social Research. 2nd ed. New York, NY: Sage Publications; 1991.
38. Salokangas RK, Cannon T, Van Erp T, Ilonen T, Taiminen T, Karlsson H, Lauerma H, Leinonen KM, Wallenius E, Kaljonen A, Syvalahti E, Vilkman H, Alanen A, Hietala J. Structural magnetic resonance imaging in patients with first-episode schizophrenia, psychotic and severe non-psychotic depression and healthy controls: results of the schizophrenia and affective psychoses (SAP) project. Br J Psychiatry Suppl. 2002;43:S58-S65.
39. Gilbert AR, Moore GJ, Keshavan MS, Paulson LA, Narula V, Mac Master FP, Steward CM, Rosenberg DR. Decrease in thalamic volumes of pediatric patients with obsessive-compulsive disorder who are taking paroxetine. Arch Gen Psychiatry. 2000;57:449-459.
FREE FULL TEXT
40. Post A, Crochemore C, Uhr M, Holsboer F, Behl C. Differential induction of NF-kappaB activity and neural cell death by antidepressants in vitro. Eur J Neurosci. 2000;12:4331-4337.
FULL TEXT
|
WEB OF SCIENCE
| PUBMED
41. Vollmayr B, Keck S, Henn FA, Schloss P. Acute stress decreases serotonin transporter mRNA in the raphe pontis but not in other raphe nuclei of the rat. Neurosci Lett. 2000;290:109-112.
FULL TEXT
|
WEB OF SCIENCE
| PUBMED
42. Nibuya M, Morinobu S, Duman RS. Regulation of BDNF and trkB mRNA in rat brain by chronic electroconvulsive seizure and antidepressant drug treatments. J Neurosci. 1995;15:7539-7547.
ABSTRACT
43. Mössner R, Daniel S, Albert D, Heils A, Okladnova O, Schmitt A, Lesch K-P. Serotonin transporter function is modulated by brain-derived neurotrophic factor (BDNF) but not nerve growth factor (NGF). Neurochem Int. 2000;36:197-202.
FULL TEXT
|
WEB OF SCIENCE
| PUBMED
44. Smeraldi E, Zanardi R, Benedetti F, Dibella D, Perez J, Catalano M. Polymorphism within the promotor of the serotonin transporter gene and antidepressant efficacy of fluvoxamine. Mol Psychiatry. 1998;3:508-511.
FULL TEXT
|
WEB OF SCIENCE
| PUBMED
45. Duman RS, Malberg J, Nakagawa S, D'Sa C. Neuronal plasticity and survival in mood disorders. Biol Psychiatry. 2000;48:732-739.
FULL TEXT
|
WEB OF SCIENCE
| PUBMED
 CiteULike  Connotea  Del.icio.us  Digg  Reddit  Technorati  Twitter
What's this?
THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES
|
Association of GSK3{beta} Polymorphisms With Brain Structural Changes in Major Depressive Disorder
Inkster et al.
Arch Gen Psychiatry 2009;66:721-728.
ABSTRACT
| FULL TEXT
Regional Brain Abnormalities Associated With Long-term Heavy Cannabis Use
Yucel et al.
Arch Gen Psychiatry 2008;65:694-701.
ABSTRACT
| FULL TEXT
Hippocampal Morphology and Distinguishing Late-Onset From Early-Onset Elderly Depression
Ballmaier et al.
Am. J. Psychiatry 2008;165:229-237.
ABSTRACT
| FULL TEXT
Cerebral Cortical Gray Matter Overgrowth and Functional Variation of the Serotonin Transporter Gene in Autism
Wassink et al.
Arch Gen Psychiatry 2007;64:709-717.
ABSTRACT
| FULL TEXT
Association of the Brain-Derived Neurotrophic Factor Val66Met Polymorphism With Reduced Hippocampal Volumes in Major Depression
Frodl et al.
Arch Gen Psychiatry 2007;64:410-416.
ABSTRACT
| FULL TEXT
Neural correlates of epigenesis
Canli et al.
Proc. Natl. Acad. Sci. USA 2006;103:16033-16038.
ABSTRACT
| FULL TEXT
Influence of Serotonin Transporter Promoter Region Polymorphisms on Hippocampal Volumes in Late-Life Depression
Taylor et al.
Arch Gen Psychiatry 2005;62:537-544.
ABSTRACT
| FULL TEXT
Recent Studies of the Biology and Treatment of Depression
Schatzberg
Focus 2005;3:14-24.
ABSTRACT
| FULL TEXT
5-HT1A Receptors, Gene Repression, and Depression: Guilt by Association
Albert and Lemonde
Neuroscientist 2004;10:575-593.
ABSTRACT
|
