Hostname: page-component-745bb68f8f-b95js Total loading time: 0 Render date: 2025-02-10T13:33:43.345Z Has data issue: false hasContentIssue false
  • English
  • Français

Posttraumatic stress disorder symptom severity is associated with left hippocampal volume reduction: a meta-analytic study

Published online by Cambridge University Press:  19 December 2016

Michael D. Nelson  and
Alecia M. Tumpap
Michael D. Nelson*
Affiliation:
Department of Psychology, Gonzaga University, Spokane, Washington, USA
Alecia M. Tumpap
Affiliation:
Department of Psychology, Gonzaga University, Spokane, Washington, USA
*
*Address for correspondence: Michael D. Nelson, Assistant Professor, Department of Psychology, Gonzaga University, 502 East Boone Avenue, AD Box 54, Spokane, WA 99258, USA. (Email: nelsonm2@gonzaga.edu)
Rights & Permissions [Opens in a new window]

Abstract

Objective

Many studies have reported hippocampal volume reductions associated with posttraumatic stress disorder (PTSD), while others have not. Here we provide an updated meta-analysis of such reductions associated with PTSD and evaluate the association between symptom severity and hippocampal volume.

Methods

A total of 37 studies met the criteria for inclusion in the meta-analysis. Mean effect sizes (Hedges’ g) and 95% confidence intervals (CI95%) were computed for each study and then averaged to obtain an overall mean effect size across studies. Meta-regression was employed to examine the relationship between PTSD symptom severity and hippocampal volume.

Results

Results showed that PTSD is associated with significant bilateral reduction of the hippocampus (left hippocampus effect size=–0.400, p<0.001, 5.24% reduction; right hippocampus effect size=–0.462, p<0.001, 5.23% reduction). Symptom severity, as measured by the Clinician-Administered PTSD Scale (CAPS), was significantly associated with decreased left, but not right, hippocampal volume.

Conclusions

PTSD was associated with significant bilateral volume reduction of the hippocampus. Increased symptom severity was significantly associated with reduced left hippocampal volume. This finding is consistent with the hypothesis that PTSD is more neurotoxic to the left hippocampus than to the right. However, whether the association between PTSD and lower hippocampal volume reflects a consequence of or a predisposition to PTSD remains unclear. More prospective studies are needed in this area.

Keywords

Posttraumatic stress disorderhippocampusmagnetic resonance imagingmeta-analysissymptom severity
Type
Original Research
Information
CNS Spectrums , Volume 22 , Issue 4 , August 2017 , pp. 363 - 372
Copyright
© Cambridge University Press 2016 

Introduction

Posttraumatic stress disorder (PTSD) is a severe and debilitating mental illness that may develop after experiencing a traumatic event. The Diagnostic and Statistical Manual of Mental Disorders (DSM–5) defines a traumatic event as an experience that possesses the threat of death or serious injury to the self or others. 1 The event also induces feelings of intense fear, helplessness, or terror. Some events that frequently precede PTSD include physical assault, sexual assault, motor vehicle accidents, and combat experience.Reference Villarreal, Hamilton and Petropoulus 2 PTSD is characterized by symptoms of increased arousal, intrusive reexperiencing, avoidant behaviors, and negative changes in mood and/or cognition. 1 The National Comorbidity Survey Replication (NCS–R) estimated lifetime prevalence of PTSD among U.S. adults to be 6.8%.Reference Kessler, Berglund, Delmer, Jin, Merikangas and Walters 3 Current PTSD prevalence (within 12 months) was estimated at 3.5%.Reference Kessler, Chiu, Demler, Merikangas and Walters 4

Improving technology has caused a surge of interest in studying the neuroanatomic correlates of PTSD using magnetic resonance imaging (MRI). One structure that has received substantial research is the hippocampus. It has been shown to play a role in learning, memory storage, and retrieval.Reference Squire and Zola-Morgan 5 – Reference van Strien, Cappaert and Witter 7 Furthermore, the hippocampus specifically facilitates emotional memory storage and recall.Reference Vermetten and Bremner 8 As a result, it is likely a significant component involved in remembering traumatic memories and events. Moreover, PTSD has been linked to a variety of memory disturbances, such as an increased ability or an inability to recall aspects of a traumatic event. Meta-analytic studies of memory function in PTSD show impairments in both verbalReference Brewin, Kleiner, Vasterling and Field 9 , Reference Johnsen and Asbjørnsen 10 and visual memory.Reference Brewin, Kleiner, Vasterling and Field 9 These disruptions may result from hippocampal pathology.Reference Burgess, Maguire and O’Keefe 11 – Reference Weiss 14 Indeed, hippocampal volume has been shown to be inversely correlated with verbal memory in PTSD.Reference Bremner, Randall and Scott 15 – Reference Tischler, Brand and Stavitsky 17 In a recent study, bilateral hippocampal volume reduction was significantly associated with overgeneralization of negative contexts in an associative learning paradigm,Reference Levy-Gigi, Szabo, Richter-Levin and Kéri 18 which could be related to the triggering of intrusive “flashbacks” in this population. Moreover, the hippocampus and ventromedial prefrontal cortex (vmPFC) have been implicated in conditioned fear extinction,Reference Milad, Wright, Orr, Pitman, Quirk and Rauch 19 , Reference Milad, Orr, Lasko, Chang, Rauch and Pitman 20 which is abnormal in this population.Reference Milad, Orr, Lasko, Chang, Rauch and Pitman 20

It has been theorized that dysregulation of the hypothalamus–pituitary–adrenal (HPA) axis may contribute to hippocampal pathology.Reference Weiss 14 , Reference Höschl and Hajek 21 For example, it has been proposed that changes in hippocampal structure and function might result from chronic exposure to corticosteroids and glutamate (stress-related chemicals).Reference Vermetten and Bremner 22 Furthermore, decreased hippocampal volume might stem from a reduction in hippocampal activity following a traumatic event.Reference Teicher, Tomoda and Andersen 23 This decreased activity may result from, and further potentiate, diminished neuron density, reduced neuron branching, and the degeneration of neurons at synaptic terminals.Reference Duman, Malberg and Nakagawa 24 Additionally, PTSD is associated with decreased hippocampal N-acetylaspartate:creatine (NAA/Cr) ratios,Reference Li, Chen, Liu, Zhang, He and Lin 25 – Reference Shu, Xue and Liu 28 thought to reflect neuronal integrity. These findings suggest a link between responses to traumatic stress and structural changes in the hippocampus.

While many structural MRI studies have found smaller hippocampal volumes in participants with PTSD,Reference Villarreal, Hamilton and Petropoulus 2 , Reference Bremner, Randall and Scott 15 , Reference Levy-Gigi, Szabo, Richter-Levin and Kéri 18 , Reference Bossini, Tavanti and Calossi 29 – Reference Winter and Irle 45 others have not.Reference Schuff, Neylan and Lenoci 27 , Reference Bonne, Brandes and Giboa 46 – Reference Yehuda, Golier and Bierer 59 However, previous meta-analyses on the neuroanatomic correlates of PTSD demonstrate that it is associated with reduced volume of the hippocampus bilaterally in adults.Reference Kitayama, Vaccarino, Kutner, Weiss and Bremner 60 – Reference O’Doherty, Chitty, Saddiqui, Bennett and Lagopoulos 66

The severity of PTSD symptoms is often assessed using the Clinician-Administered Posttraumatic Stress Disorder Scale (CAPS),Reference Blake, Weathers and Nagy 67 which has three subscales: reexperiencing (CAPS–B), avoidance (CAPS–C), and hyperarousal (CAPS–D). Some data suggest that PTSD symptom severity may moderate the relationship between PTSD and reduced hippocampal volume.Reference Karl, Schaefer, Malta, Dorfel, Rohleder and Werner 62 For example, hippocampal volume has been found to vary inversely with intrusive reexperiencingReference Lindauer, Vlieger and Jalink 36 , Reference Lindauer, Olff, van Meijel, Carlier and Gersons 68 and total PTSD symptoms.Reference Villarreal, Hamilton and Petropoulus 2 , Reference Shu, Xue and Liu 28 , Reference Bossini, Tavanti and Calossi 29 , Reference Bremner, Vythilingam and Vermetten 31 , Reference Admon, Milad and Hendler 69 , Reference Apfel, Ross and Hlavin 70 However, others found no such relationships.Reference Bremner, Randall and Scott 15 , Reference Schuff, Neylan and Lenoci 27 , Reference Bossini, Tavanti and Calossi 29

Meta-analysis provides a systematic quantitative method for integrating results across studies. This not only dramatically increases sample size (and therefore statistical power) but also allows the researcher to specify moderator variables that may help account for differences in results between studies. When assessing volumetric differences in brain structures between groups, the mean volumes and standard deviations for each group are used to compute an effect size (Cohen’s d, for example), which is the difference between group means divided by the pooled standard deviation. Values of Cohen’s d of 0.20 are considered small, 0.50 medium, and 0.80 large.Reference Cohen 71 Here we provide an updated meta-analysis regarding hippocampal volume deficits in PTSD and evaluate the relationship between symptom severity and hippocampal volume by conducting a meta-regression with symptom severity (total CAPS score) as a continuous moderator variable.

Methods

Study selection

Searches for the terms “posttraumatic stress disorder,” “stress,” “hippocampus,” “hippocampal volume,” “MRI,” and “magnetic resonance imaging” were entered into the PsycINFO, MEDLINE, and ProQuest databases. Cited reference searches (both forward and backward) for relevant articles were performed using the Web of Science. The reference sections of previous meta-analyses were also examined. From these results, 89 articles published between 1995 and 2016 were retrieved. To be included in the meta-analysis, studies must have (1) used human adults (minimum age≥18 years) as participants, (2) a group diagnosed with PTSD, (3) a non-PTSD comparison group, (4) reported means and standard deviations for left and right hippocampal volumes separately, (5) not included participants from another study used in the meta-analysis, and (6) reported a mean CAPS score of 45 or greater (if the CAPS was employed). The last criterion was utilized because a psychometric study found that a total CAPS score of 45 represents a reasonable threshold for PTSD diagnosis.Reference Weathers, Ruscio and Keane 72 From the initial group of studies, 37 studies met the inclusion criteria. Mean volumetric data from Wang and colleaguesReference Wang, Neylan and Mueller 57 were obtained from the corresponding author. One studyReference Schuff, Marmar and Weiss 26 reported volume for the right hippocampus only. When studies reported volumes for both traumatized and nontraumatized control groups, data from the nontraumatized control group were utilized in the interest of sample homogeneity. If a study reported volumes separately for PTSD participants with and without comorbidities, volumes for the PTSD-only (no comorbidity) group were used.

Meta-analytic techniques

All meta-analyses were performed using Comprehensive Meta-Analysis version 2.2.064 (Biostat, Englewood, New Jersey), a commercially available software package designed for meta-analysis and meta-regression. Hippocampal mean volumes and standard deviations from each study were entered directly into the software, which then computed Cohen’s d, which in this context is the mean difference between patient and control hippocampal volumes divided by the pooled within-group standard deviation. Cohen’s d was then transformed to Hedges’ g with correction for potential bias due to sample size.Reference Borenstein, Hedges, Higgins and Rothstein 73 Hedges’ g and 95 percent confidence intervals (CI 95%) were then computed for each study. A mean effect size across studies was then calculated, with each study weighted inversely according to its variance.Reference Borenstein, Hedges, Higgins and Rothstein 73 A random-effects model was used for all analyses. Meta-regression is conceptually similar to multiple regression, except that the study becomes the unit of analysis. The reader interested in further details regarding meta-analysis is referred to the work of Borenstein and colleagues,Reference Borenstein, Hedges, Higgins and Rothstein 73 Hedges and Olkin,Reference Hedges and Olkin 74 and Cooper and coworkers.Reference Cooper, Hedges and Valentine 75

Results

After the initial meta-analyses, two studiesReference Gurvits, Shenton and Hokama 34 , Reference Hedges, Allen and Tate 35 were identified as outliers, as they had very large effect sizes, high standard errors, and small sample sizes. Therefore, they were excluded from further consideration. Demographic information from the remaining 35 studies is provided in Table 1. Mean hippocampal volumes are given in Table 2. Total n for the left hippocampus was 1354 (PTSD=654, controls=700) and 1368 for the right hippocampus (PTSD=661, controls=707). The results of the overall meta-analysis showed significant volumetric reductions for both the left (g=–0.400; CI 95%=[–0.563, –0.237]; p<0.001; see Figure 1) and right (g=–0.462; CI 95%=[–0.621, –0.302]; p<0.001; see Figure 2) hippocampi in participants with PTSD compared to non-PTSD controls. These results correspond to a volumetric reduction of 5.24% for the left hippocampus and 5.23% for the right hippocampus. Secondary meta-analyses conducted only on those studies that reported CAPS scores again showed significant, but smaller, reductions in both the left (g=–0.307; CI 95%=[–0.546, –0.069]; p=0.012) and right hippocampus (g=–0.243; CI 95%=[–0.465, –0.022]; p=0.031). These results correspond to a volumetric reduction of 4.02% for the left hippocampus and 2.55% for the right hippocampus. However, only 19 studies reported CAPS scores (see Table 1). The meta-regression of CAPS scores on Hedges’ g for the left hippocampus (slope=–0.024; intercept=1.20; Z=–2.92, p<0.004; see Figure 3) was significant, but the meta-regression for the right hippocampus (slope=–0.010; intercept=0.38; Z=–1.26, p<0.21; see Figure 4) was not. In other words, increased symptom severity was significantly associated with decreased volume of the left, but not the right, hippocampus.

Figure 1 Forest plot showing overall left hippocampal volume effect sizes (Hedges’ g) and 95% confidence intervals (CI 95%) for comparisons of PTSD and control groups. Negative effect sizes (Hedges’ g) indicate smaller hippocampal volume in the PTSD participant group. Square size indicates relative study weight in the meta-analysis. Mean effect size and confidence interval across studies are indicated by the solid diamond.

Figure 2 Forest plot showing overall right hippocampal volume effect sizes (Hedges’ g) and 95% confidence intervals (CI 95%) for comparisons of PTSD and control groups. Negative effect sizes (Hedges’ g) indicate smaller hippocampal volume in the PTSD participant group. Square size indicates relative study weight in the meta-analysis. Mean effect size and confidence interval across studies is indicated by the solid diamond.

Figure 3 Meta-regression of participants’ CAPS scores on Hedges’ g for the left hippocampus. Circle size indicates relative study weight in the meta-regression. Slope=–0.024; intercept=1.20; Z=–2.92, p<0.004.

Figure 4 Meta-regression of participants’ CAPS scores on Hedges’ g for the right hippocampus. Circle size indicates relative study weight in the meta-regression. Slope=–0.010; intercept=0.38; Z=–1.26, p<0.21.

Table 1 Demographic information for PTSD and control participants in studies that reported mean hippocampal volumes.

* Gender breakdown not reported. CAPS=Clinician-Administered PTSD Scale; DSM=Diagnostic and Statistical Manual of Mental Disorders; DTS=Davidson Trauma Scale; F=number of female participants; ICD=International Classification of Diseases; M=number of male participants; M–PTSD=Mississippi Scale for Combat-Related PTSD; NR=not reported; SCID=Structured Clinical Interview for DSM–IV; SI–PTSD=Structured Interview for Posttraumatic Stress Disorder.

Table 2 Hippocampal means (M)/standard deviations (SD), and scanning parameters for studies included in the meta-analysis

Volumes not originally reported in mm3 have been converted to mm3 for ease of comparison, with the exception of one studyReference Fennema-Notestine, Stein, Kennedy, Archibald and Jernigan 48 for which this was not possible, as voxel dimensions were not reported. mm=millimeter; mm3=cubic millimeter; NR=not reported; T=tesla.

Discussion

This meta-analytic study produced two main findings. First, PTSD in adults was associated with significant bilateral volumetric reduction of the hippocampus, as has been reported in previous meta-analyses.Reference Kitayama, Vaccarino, Kutner, Weiss and Bremner 60 – Reference O’Doherty, Chitty, Saddiqui, Bennett and Lagopoulos 66 Second, increased PTSD symptom severity was associated with decreased left hippocampal volume. No association was found between symptom severity and right hippocampal volume. This conclusion, however, must be viewed with caution, as studies that reported CAPS scores had lower mean effect sizes than those in the overall meta-analysis. Therefore, the relationship between symptom severity and right hippocampal volume may have been underestimated.

Because of the cross-sectional nature of the studies reviewed here, the observed volume differences in the overall meta-analysis could either indicate that PTSD produces hippocampal volume deficits or that they are a predisposing factor. A recent model of PTSD suggests that a hyperresponsive amygdala and dorsal anterior cingulate cortex (dACC) are predisposing factors to the development of the disorder, while reduced hippocampal connectivity with the vmPFC is a consequence of it.Reference Admon, Milad and Hendler 69 Additional research demonstrates that current, but not lifetime, PTSD symptomatology predicts hippocampal volume deficits.Reference Apfel, Ross and Hlavin 70 If smaller hippocampal volume were a predisposing factor to PTSD, one would expect that both current and lifetime symptom severity would be associated with volumetric deficits.Reference Apfel, Ross and Hlavin 70 Furthermore, in an 18-month prospective study of Israeli Defense Force soldiers pre- and postcombat, increased PTSD symptomatology postcombat was associated with reduced hippocampal volume.Reference Admon, Leykin and Lubin 76 Additionally, in a study of veterans with brain lesions, the vmPFC and amygdala were found to be critical in the etiology of PTSD, while the hippocampus was not.Reference Koenigs, Huey and Raymont 77 These findings suggest that the hippocampal volume changes observed in PTSD are a result of the disease rather than its cause. However, a study of monozygotic twins (one with and one without PTSD) found that PTSD symptom severity in the affected twin was inversely associated with hippocampal volume in both PTSD and non-PTSD twins.Reference Gilbertson, Shenton and Ciszewski 50 This suggests that reduced hippocampal volume constitutes a predisposition to PTSD.Reference Gilbertson, Shenton and Ciszewski 50 A more recent study also suggested that left hippocampal volume reduction is a risk factor for the persistence of PTSD.Reference van Rooij, Kennis, Sjouwerman, van den Heuvel, Kahn and Geuze 78 Clearly, more prospective studies are necessary to determine the reasons for these hippocampal volume differences.

The finding that left hippocampal volume was significantly and inversely associated with symptom severity is consistent with the results of several previous studies. For example, total CAPS score and CAPS–B score significantly predicted left hippocampal volume deficits in a civilian PTSD sample, while time since trauma, illness duration, and age did not.Reference Villarreal, Hamilton and Petropoulus 2 Another study also found a significant correlation between CAPS total and CAPS–C score and left, but not right, hippocampal volume.Reference Shu, Xue and Liu 28 Additionally, CAPS–B score was inversely correlated with left hippocampal volume in a sample of Dutch police officers.Reference Lindauer, Vlieger and Jalink 36 , Reference Lindauer, Olff, van Meijel, Carlier and Gersons 68 Furthermore, in a study of survivors of a Chinese coal-mining disaster using both voxel-based morphometry (VBM) and region of interest (ROI) approaches, reduced gray matter volume in the left hippocampus and left parahippocampal gyrus were observed.Reference Zhang, Tan and Yin 79 There was also reduced gray matter density in the left hippocampus. While there was no correlation between left hippocampal volume and total CAPS score, a significant inverse correlation (r=–0.49) was found between left hippocampal gray matter density and total CAPS score.Reference Zhang, Tan and Yin 79 These findings suggest that increased PTSD symptom severity may be associated with hippocampal pathology in ways that are not always observable using traditional volumetric MRI techniques. Similarly, in a study of civilians with recent-onset PTSD, significant inverse correlations were found between left hippocampus NAA/Cr ratio and total CAPS (r=–0.939), CAPS–B (r=–0.829), CAPS–C (r=–0.743), and CAPS–D (r=–0.635) scores.Reference Shu, Xue and Liu 28 No such relationships between NAA/Cr ratio and symptom severity were observed for the right hippocampus.Reference Shu, Xue and Liu 28 However, other studies examining the effects of PTSD on the hippocampus have not found any effects of symptom severity on hippocampal volume.Reference Bremner, Randall and Scott 15 , Reference Schuff, Neylan and Lenoci 27 , Reference Bossini, Tavanti and Calossi 29 Taken together with the current results, these findings suggest that PTSD damages the left hippocampus more than the right hippocampus and that this relationship may manifest itself in additional ways other than those observable with MRI volumetry.

Study limitations

There are several factors that limited this study. Not all studies investigating hippocampal volume reduction in PTSD reported mean CAPS scores, and those that did had smaller effect sizes than those that did not. This may have led to the underestimation of the relationship between symptom severity and hippocampal volume, especially for the right hippocampus. Furthermore, we were unable to account for some potentially important moderator variables, such as illness duration (only seven studies in this sample reported illness duration), psychiatric comorbidity (which is high in this population), MRI scanning parameters, and substance abuse, all of which may affect reported hippocampal volume. There was also substantial variance in the anatomical boundaries used to delineate the hippocampus. This variance may at least partially explain the wide range in hippocampal volumes reported in the studies included in this meta-analysis. Finally, as the majority of studies examined were cross-sectional designs, rather than longitudinal, we cannot unequivocally state whether or not the observed differences in hippocampal volume were consequences of the disorder or predisposing factors.

Conclusions

In conclusion, the studies reviewed in this meta-analysis indicate that PTSD is associated with moderate bilateral volumetric reduction of the hippocampal formation in adults. Increased symptom severity appears to be associated with reduced left, but not right, hippocampal volume in this group of studies. More prospective studies are needed to clarify the etiology of the differences in hippocampal volume associated with PTSD.

Acknowledgments

The authors wish to thank Anna Marie Medina, PhD, and Gary L. Thorne, PhD, for helpful comments concerning this manuscript, and Norbert Schuff, PhD, for providing hippocampal volumes not included in a published article.

Disclosures

Michael Nelson and Alecia Tumpap hereby state that they have no conflicts of interest to disclose.

References

1. American Psychiatric Association (APA). Diagnostic and Statistical Manual of Mental Disorders, 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
2. Villarreal, G, Hamilton, DA, Petropoulus, H, et al. Reduced hippocampal volume and total white matter volume in posttraumatic stress disorder. Biol Psychiatry. 2002; 52(2): 119–125.CrossRefGoogle ScholarPubMed
3. Kessler, RC, Berglund, P, Delmer, O, Jin, R, Merikangas, KR, Walters, EE. Lifetime prevalence and age-of-onset distributions of DSM–IV disorders in the National Comorbidity Survey Replication. Arch Gen Psychiatry. 2005; 62(6): 593–602. http://jamanetwork.com/journals/jamapsychiatry/fullarticle/208678.Google Scholar
4. Kessler, RC, Chiu, WT, Demler, O, Merikangas, KR, Walters, EE. Prevalence, severity, and comorbidity of 12-month DSM–IV disorders in the National Comorbidity Survey Replication. Arch Gen Psychiatry. 2005; 62(6): 617–627. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2847357/pdf/nihms176704.pdf.CrossRefGoogle ScholarPubMed
5. Squire, LR, Zola-Morgan, S. The medial temporal lobe memory system. Science. 1991; 253(5026): 1380–1386.Google Scholar
6. Treves, A, Rolls, ET. Computational analysis of the role of the hippocampus in memory. Hippocampus. 1994; 4(3): 374–391.Google Scholar
7. van Strien, NM, Cappaert, NLM, Witter, MP. The anatomy of memory: an interactive overview of the parahippocampal-hippocampal network. Nat Rev Neurosci. 2009; 10(4): 273–282.CrossRefGoogle ScholarPubMed
8. Vermetten, E, Bremner, JD. Circuits and systems in stress: applications to neurobiology and treatment in posttraumatic stress disorder. Depress Anxiety. 2002; 16(1): 14–38.Google Scholar
9. Brewin, CR, Kleiner, JS, Vasterling, JJ, Field, AP. Memory for emotionally neutral information in posttraumatic stress disorder: a meta-analytic investigation. J Abnorm Psychol. 2007; 116(3): 448–463.Google Scholar
10. Johnsen, GE, Asbjørnsen, AE. Consistent impaired verbal memory in PTSD: a meta-analysis. J Affect Disord. 2008; 111(1): 74–82. Epub ahead of print Apr 2.CrossRefGoogle ScholarPubMed
11. Burgess, N, Maguire, EA, O’Keefe, J. The human hippocampus and spatial and episodic memory. Neuron. 2002; 35(4): 625–641. http://www.cell.com/neuron/fulltext/S0896-6273(02)00830-9.Google Scholar
12. Giap, BT, Jong, CN, Ricker, JH, Cullen, NK, Zafonte, RD. The hippocampus: anatomy, pathophysiology, and regenerative capacity. J Head Trauma Rehabil. 2000; 15(3): 875–894.CrossRefGoogle ScholarPubMed
13. Squire, LR. Memory and the hippocampus: a synthesis from findings with rats, monkeys, and humans. Psychol Rev. 1992; 99(2): 195–231. Erratum in Psychol Rev. 1992; 99(3): 582.Google Scholar
14. Weiss, SJ. Neurobiological alterations associated with traumatic stress. Perspect Psychiatr Care. 2007; 43(3): 114–122.CrossRefGoogle ScholarPubMed
15. Bremner, JD, Randall, P, Scott, TM, et al. MRI-based measurement of hippocampal volume in patients with combat-related posttraumatic stress disorder. Am J Psychiatry. 1995; 152(7): 973–981. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3233767/pdf/nihms-340189.pdf.Google ScholarPubMed
16. Bremner, JD. Neuroimaging of posttraumatic stress disorder. Psychiatr Ann. 1998; 28(8): 445–450.Google Scholar
17. Tischler, L, Brand, SR, Stavitsky, K, et al. The relationship between hippocampal volume and declarative memory in a population of combat veterans with and without PTSD. Ann N Y Acad Sci. 2006; 1071(1): 405–409.Google Scholar
18. Levy-Gigi, E, Szabo, C, Richter-Levin, G, Kéri, S. Reduced hippocampal volume is associated with overgeneralization of negative context in individuals with PTSD. Neuropsychology. 2015; 29(1): 151–161. Epub ahead of print Jul 28, 2014.Google Scholar
19. Milad, MR, Wright, CI, Orr, SP, Pitman, RK, Quirk, GJ, Rauch, SL. Recall of fear extinction in humans activates the ventromedial prefrontal cortex and hippocampus in concert. Biol Psychiatry. 2007; 62(5): 446–454. Epub ahead of print Jan 9.CrossRefGoogle ScholarPubMed
20. Milad, MR, Orr, SP, Lasko, NP, Chang, Y, Rauch, SL, Pitman, RK. Presence and acquired origin of reduced recall for fear extinction in PTSD: results of a twin study. J Psychiatr Res. 2008; 42(7): 515–520; Epub ahead of print Feb 29. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2377011/pdf/nihms46966.pdf.Google Scholar
21. Höschl, C, Hajek, T. Hippocampal damage mediated by corticosteroids: a neuropsychiatric research challenge. Eur Arch Psychiatry Clin Neurosci. 2001; 251(Suppl 2): II81–II88.Google Scholar
22. Vermetten, E, Bremner, JD. Circuits and systems in stress, I: preclinical studies. Depress Anxiety. 2002; 15(3): 126–147.CrossRefGoogle ScholarPubMed
23. Teicher, M, Tomoda, A, Andersen, S. Neurobiological consequences of early stress and childhood maltreatment: are results from human and animal studies comparable? Ann N Y Acad Sci. 2006; 1071(1): 313–323.CrossRefGoogle ScholarPubMed
24. Duman, RS, Malberg, J, Nakagawa, S. Regulation of adult neurogenesis by psychotropic drugs and stress. J Pharmacol Exp Ther. 2001; 299(2): 401–407. http://jpet.aspetjournals.org/content/299/2/401.long.Google Scholar
25. Li, L, Chen, S, Liu, J, Zhang, J, He, Z, Lin, X. Magnetic resonance imaging and magnetic resonance spectroscopy study of deficits in hippocampal structure in fire victims with recent-onset posttraumatic stress disorder. Can J Psychiatry. 2006; 51(7): 431–437.Google Scholar
26. Schuff, N, Marmar, CR, Weiss, DS, et al. Reduced hippocampal volume and N-acetyl aspartate in posttraumatic stress disorder. Ann N Y Acad Sci. 1997; 821(1): 516–520.Google Scholar
27. Schuff, N, Neylan, TC, Lenoci, MA, et al. Decreased hippocampal N-acetylaspartate in the absence of atrophy in posttraumatic stress disorder. Biol Psychiatry. 2001; 50(12): 952–959. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2733624/pdf/nihms125448.pdf.CrossRefGoogle ScholarPubMed
28. Shu, XJ, Xue, L, Liu, W, et al. More vulnerability of left than right hippocampal damage in right-handed patients with post-traumatic stress disorder. Psychiatry Res. 2013; 212(3): 237–244. Epub ahead of print Nov 11, 2012.CrossRefGoogle ScholarPubMed
29. Bossini, L, Tavanti, M, Calossi, S, et al. Magnetic resonance imaging volumes of the hippocampus in drug-naïve patients with post-traumatic stress disorder without comorbidity conditions. J Psychiatr Res. 2008; 42(9). 752–762. Epub ahead of print Sep 24, 2007.Google Scholar
30. Bremner, JD, Randall, P, Vermetten, E, et al. Magnetic resonance imaging-based measurement of hippocampal volume in posttraumatic stress disorder related to childhood physical and sexual abuse: a preliminary report. Biol Psychiatry. 1997; 41(1): 23–32. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3229101/pdf/nihms-340184.pdf.Google Scholar
31. Bremner, JD, Vythilingam, M, Vermetten, E, et al. MRI and PET study of deficits in hippocampal structure and function in women with childhood sexual abuse and posttraumatic stress disorder. Am J Psychiatry. 2003; 160(5): 924–932. http://ajp.psychiatryonline.org/doi/full/10.1176/appi.ajp.160.5.924.Google Scholar
32. Chalavi, S, Vissia, EM, Giesen, ME, et al. Abnormal hippocampal morphology in dissociative identity disorder and post-traumatic stress disorder correlates with childhood trauma and dissociative symptoms. Hum Brain Mapp. 2015; 36(5): 1692–1704. Epub ahead of print Dec 29, 2014. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4400262/pdf/nihms-673286.pdf.Google Scholar
33. Emdad, R, Bonekamp, D, Sondergaard, HP, et al. Morphometric and psychometric comparisons between non-substance-abusing patients with posttraumatic stress disorder and normal controls. Psychother Psychosom. 2006; 75(2): 122–132.CrossRefGoogle ScholarPubMed
34. Gurvits, TV, Shenton, ME, Hokama, H, et al. Magnetic resonance imaging study of hippocampal volume in chronic, combat-related posttraumatic stress disorder. Biol Psychiatry. 1996; 40(11): 1091–1099. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2910907/pdf/nihms170395.pdf.CrossRefGoogle ScholarPubMed
35. Hedges, DW, Allen, S, Tate, DF, et al. Reduced hippocampal volume in alcohol and substance naïve Vietnam combat veterans with posttraumatic stress disorder. Cogn Behav Neurobiol. 2003; 16(4): 219–224.Google Scholar
36. Lindauer, RJL, Vlieger, EJ, Jalink, M, et al. Smaller hippocampal volume in Dutch police officers with posttraumatic stress disorder. Biol Psychiatry. 2004; 56(5): 356–363.CrossRefGoogle ScholarPubMed
37. Morey, RA, Gold, AL, Labar, KS, et al. Amygdala volume changes in posttraumatic stress disorder in a large case-controlled veterans group. Arch Gen Psychiat. 2012; 69(11): 1169–1178. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3647246/pdf/nihms452834.pdf.Google Scholar
38. Pavić, L, Gregurek, R, Rados, M, et al. Smaller right hippocampus in war veterans with posttraumatic stress disorder. Psychiatry Res. 2007; 154(2): 191–198; Epub ahead of print Jan 26.Google Scholar
39. Schmahl, C, Berne, K, Krause, A, et al. Hippocampus and amygdala volumes in patients with borderline personality disorder with or without posttraumatic stress disorder. J Psychiatry Neurosci. 2009; 34(4): 289–295. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2702446/pdf/0340289.pdf.Google Scholar
40. Shin, LM, Shin, PS, Heckers, S, et al. Hippocampal function in posttraumatic stress disorder. Hippocampus. 2004; 14(3): 292–300.CrossRefGoogle ScholarPubMed
41. Starčević, A, Dimitrijević, I, Aksić, M, et al. Brain changes in patients with posttraumatic stress disorder and associated alcoholism: MRI-based study. Psychiatr Danub. 2015; 27(1): 78–83. http://www.hdbp.org/psychiatria_danubina/pdf/dnb_vol27_no1/dnb_vol27_no1_78.pdf.Google Scholar
42. Vythilingam, M, Luckenbaugh, DA, Lam, T, et al. Smaller head of the hippocampus in Gulf War–related posttraumatic stress disorder. Psychiatry Res. 2005; 139(2): 89–99.Google Scholar
43. Weniger, G, Lange, C, Sachsse, U, Irle, E. Amygdala and hippocampal volumes and cognition in adult survivors of childhood abuse with dissociative disorders. Acta Psychiatr Scand. 2008; 118(4): 281–290.CrossRefGoogle ScholarPubMed
44. Wignall, EL, Dickson, JM, Vaughan, P, et al. Smaller hippocampal volume in patients with recent-onset posttraumatic stress disorder. Biol Psychiatry. 2004; 56(11): 832–836.Google Scholar
45. Winter, H, Irle, E. Hippocampal volume in adult burn patients with and without posttraumatic stress disorder. Am J Psychiatry. 2004; 161(12): 2194–2200.Google Scholar
46. Bonne, O, Brandes, D, Giboa, A, et al. Longitudinal MRI study of hippocampal volume in trauma survivors with PTSD. Am J Psychiatry. 2001; 158(8): 1248–1251. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2819102/pdf/nihms170397.pdf.CrossRefGoogle ScholarPubMed
47. Eckart, C, Kaufmann, J, Kanowski, M, et al. Magnetic resonance volumetry and spectroscopy of hippocampus and insula in relation to severe exposure of traumatic stress. Psychophysiology. 2012; 49(2): 261–270. Epub ahead of print Oct 21, 2011.CrossRefGoogle ScholarPubMed
48. Fennema-Notestine, C, Stein, MB, Kennedy, CM, Archibald, SL, Jernigan, TL. Brain morphometry in female victims of intimate partner violence with and without posttraumatic stress disorder. Biol Psychiatry. 2002; 52(11): 1089–1101.CrossRefGoogle ScholarPubMed
49. Freeman, T, Kimbrell, T, Booe, L, et al. Evidence of resilience: neuroimaging in former prisoners of war. Psychiatry Res. 2006; 146(1): 59–64; Epub ahead of print Dec 19, 2005.Google Scholar
50. Gilbertson, MW, Shenton, ME, Ciszewski, A, et al. Smaller hippocampal volume predicts pathologic vulnerability to psychological trauma. Nat Neurosci. 2002; 5(11): 1242–1247. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2819093/pdf/nihms170404.pdf.Google Scholar
51. Golier, JA, Yehuda, R, De Santi, S, Segal, S, Dolan, S, de Leon, MJ. Absence of hippocampal volume differences in survivors of the Nazi Holocaust with and without posttraumatic stress disorder. Psychiatry Res. 2005; 139(1): 53–64.Google Scholar
52. Hara, E, Matsuoka, Y, Hakamata, Y, et al. Hippocampal and amygdalar volumes in breast cancer survivors with posttraumatic stress disorder. J Neuropsychiatry Clin Neurosci. 2008; 20(3): 302–308. http://neuro.psychiatryonline.org/doi/full/10.1176/jnp.2008.20.3.302.CrossRefGoogle ScholarPubMed
53. Jatzko, A, Rothenhofer, S, Schmitt, A, et al. Hippocampal volume in chronic posttraumatic stress disorder (PTSD): MRI study using two different evaluation methods. J Affect Disord. 2006; 94(1–3): 121–126. Epub ahead of print May 15.Google Scholar
54. Landré, L, Destrieux, C, Baudry, M, et al. Preserved subcortical volumes and cortical thickness in women with sexual abuse-related PTSD. Psychiatry Res. 2010; 183(3): 181–186; Epub ahead of print Aug 4.CrossRefGoogle ScholarPubMed
55. Pederson, CL, Maurer, SH, Kaminski, PL, et al. Hippocampal volume and memory performance in a community-based sample of women with posttraumatic stress disorder secondary to child abuse. J Trauma Stress. 2004; 17(1): 37–40.CrossRefGoogle Scholar
56. Starčević, A, Srdjan, P, Radojicic, Z, et al. Volumetric analysis of amygdala, hippocampus, and prefrontal cortex in therapy-naïve PTSD participants. BioMed Res Int. 2014; 2014: 1–6. Article ID 968495.CrossRefGoogle ScholarPubMed
57. Wang, Z, Neylan, TC, Mueller, SG, et al. Magnetic resonance imaging of hippocampal subfields in posttraumatic stress disorder. Arch Gen Psychiatry. 2010; 67(3): 296–303. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2848481/pdf/nihms184801.pdf.Google Scholar
58. Yehuda, R, Golier, JA, Tischler, L, et al. Hippocampal volume in aging combat veterans with and without post-traumatic stress disorder: relation to risk and resilience factors. J Psychiatr Res. 2007; 41(5): 435–445; Epub ahead of print Jan 30, 2006.Google Scholar
59. Yehuda, R, Golier, JA, Bierer, LM, et al. Hydrocortisone responsiveness in Gulf War veterans with PTSD: Effects on ACTH, declarative memory hippocampal [18F]FDG uptake on PET. Psychiatry Res. 2010; 184(2). 117–127. Epub ahead of print Oct 8.Google Scholar
60. Kitayama, N, Vaccarino, V, Kutner, M, Weiss, P, Bremner, JD. Magnetic resonance imaging (MRI) measurement of hippocampal volume in posttraumatic stress disorder: a meta-analysis. J Affect Disord. 2005; 88(1): 79–86.Google Scholar
61. Smith, ME. Bilateral hippocampal volume reduction in adults with post-traumatic stress disorder: a meta-analysis of structural MRI studies. Hippocampus. 2005; 15(6): 798–807.CrossRefGoogle ScholarPubMed
62. Karl, A, Schaefer, M, Malta, LS, Dorfel, D, Rohleder, N, Werner, A. A meta-analysis of structural brain abnormalities in PTSD. Neurosci Biobehav Rev. 2006; 30(7): 1004–1031. Epub ahead of print May 26.Google Scholar
63. Woon, FL, Sood, S, Hedges, DW. Hippocampal volume deficits associated with exposure to psychological trauma and posttraumatic stress disorder in adults: a meta-analysis. Prog Neuropsychopharmacol Biol Psychiatry. 2010; 34(7): 1181–1188. Epub ahead of print Jun 21.Google Scholar
64. Woon, FL, Hedges, DW. Hippocampal and amygdala volumes in children and adults with childhood maltreatment-related posttraumatic stress disorder: a meta-analysis. Hippocampus. 2008. 18(8): 729–736.Google Scholar
65. Woon, F, Hedges, DW. Gender does not moderate hippocampal volume deficits in adults with posttraumatic stress disorder: a meta-analysis. Hippocampus. 2011; 21(3): 243–252. Epub ahead of print Sep 29, 2010.CrossRefGoogle Scholar
66. O’Doherty, DC, Chitty, KM, Saddiqui, S, Bennett, MR, Lagopoulos, J. A systematic review and meta-analysis of magnetic resonance imaging measurement of structural volumes in posttraumatic stress disorder. Psychiatry Res. 2015; 232(1): 1–33. Epub ahead of print Jan 30.CrossRefGoogle ScholarPubMed
67. Blake, DD, Weathers, FW, Nagy, LM, et al. The development of a clinician-administered PTSD scale. J Trauma Stress. 1995; 8(1): 75–90.Google Scholar
68. Lindauer, RJ, Olff, M, van Meijel, EP, Carlier, IV, Gersons, BP. Cortisol, learning, memory, and attention in relation to smaller hippocampal volume in police officers with posttraumatic stress disorder. Biol Psychiatry. 2006; 59(2): 171–177.Google Scholar
69. Admon, R, Milad, M R, Hendler, T. A causal model of post-traumatic stress disorder: Disentangling predisposed from acquired neural abnormalities. Trends Cogn Sci. 2013; 17(7): 337–347. Epub ahead of print Jun 12.Google Scholar
70. Apfel, BA, Ross, J, Hlavin, J, et al. Hippocampal volume differences in Gulf War veterans with current versus lifetime posttraumatic stress disorder symptoms. Biol Psychiatry. 2011; 69: 541–548. Epub ahead of print Nov 20, 2010. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3259803/pdf/nihms291995.pdf.Google Scholar
71. Cohen, J. Statistical Power Analysis for the Behavioral Sciences, 2nd ed. Hillsdale, NJ: Lawrence Erlbaum; 1988.Google Scholar
72. Weathers, FW, Ruscio, AM, Keane, TM. Psychometric properties of nine scoring rules for the Clinician-Administered Posttraumatic Stress Disorder Scale. Psychol Assess. 1999; 11(2): 124–133.CrossRefGoogle Scholar
73. Borenstein, M, Hedges, LV, Higgins, JPT, Rothstein, HR. Introduction to Meta-Analysis. West Sussex, UK: Wiley; 2009. https://www.meta-analysis-workshops.com/download/bookChapterSample.pdf.Google Scholar
74. Hedges, LV, Olkin, I. Statistical Methods for Meta-Analysis. New York: Academic Press; 1985.Google Scholar
75. Cooper, H, Hedges, LV, Valentine, JC, eds. The Handbook of Research Synthesis and Meta-Analysis, 2nd ed. New York: The Russell Sage Foundation; 2009.Google Scholar
76. Admon, R, Leykin, D, Lubin, G, et al. Stress-induced reduction in hippocampal volume and connectivity with the ventromedial prefrontal cortex are related to maladaptive responses to stressful military service. Hum Brain Mapp. 2013; 34(11): 2808–2816. Epub ahead of print Jul 17, 2012.Google Scholar
77. Koenigs, M, Huey, ED, Raymont, V, et al. Focal brain damage protects against post-traumatic stress disorder in combat veterans. Nat Neurosci. 2008; 11(2): 232–237. Epub ahead of print Dec 23, 2007. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2693133/pdf/nihms-108233.pdf.CrossRefGoogle ScholarPubMed
78. van Rooij, SJ, Kennis, M, Sjouwerman, R, van den Heuvel, MP, Kahn, RS, Geuze, E. Smaller hippocampal volume as a vulnerability factor for the persistence of post-traumatic stress disorder. Psychol Med. 2015; 45(13): 2737–2746. Epub ahead of print May 4.CrossRefGoogle ScholarPubMed
79. Zhang, J, Tan, Q, Yin, H, et al. Decreased gray matter volume in the left hippocampus and bilateral calcarine cortex in coal mine flood disaster survivors with recent-onset PTSD. Psychiatry Res. 2011; 192(2): 84–90.Google Scholar
Figure 0

Figure 1 Forest plot showing overall left hippocampal volume effect sizes (Hedges’ g) and 95% confidence intervals (CI 95%) for comparisons of PTSD and control groups. Negative effect sizes (Hedges’ g) indicate smaller hippocampal volume in the PTSD participant group. Square size indicates relative study weight in the meta-analysis. Mean effect size and confidence interval across studies are indicated by the solid diamond.

Figure 1

Figure 2 Forest plot showing overall right hippocampal volume effect sizes (Hedges’ g) and 95% confidence intervals (CI95%) for comparisons of PTSD and control groups. Negative effect sizes (Hedges’ g) indicate smaller hippocampal volume in the PTSD participant group. Square size indicates relative study weight in the meta-analysis. Mean effect size and confidence interval across studies is indicated by the solid diamond.

Figure 2

Figure 3 Meta-regression of participants’ CAPS scores on Hedges’ g for the left hippocampus. Circle size indicates relative study weight in the meta-regression. Slope=–0.024; intercept=1.20; Z=–2.92, p<0.004.

Figure 3

Figure 4 Meta-regression of participants’ CAPS scores on Hedges’ g for the right hippocampus. Circle size indicates relative study weight in the meta-regression. Slope=–0.010; intercept=0.38; Z=–1.26, p<0.21.

Figure 4

Table 1 Demographic information for PTSD and control participants in studies that reported mean hippocampal volumes.

Figure 5

Table 2 Hippocampal means (M)/standard deviations (SD), and scanning parameters for studies included in the meta-analysis