- Research article
- Open Access
Alterations in white matter fractional anisotropy in subsyndromal perimenopausal depression
BMC Psychiatry volume 14, Article number: 367 (2014)
Subsyndromal depression (SSD) is considered as a predictor for future depressive disorders, however whether white matter abnormalities are involved in the high-susceptibility of women to depressive disorders during perimenopause is unknown. The purpose of this study was to investigate fractional anisotropy (FA) in the white matter of the whole brain in perimenopausal women with SSD using diffusion tensor imaging (DTI).
In a cross-sectional study, 24 perimenopausal women with SSD and 24 other age-, education-, and body mass index-matched healthy women underwent DTI. A voxel-based analysis was used to elucidate regional FA changes at a voxel threshold of p < 0.001 with an extent threshold of k > 127 voxels (p < 0.05, AlphaSim correction). Subsequently, correlation analyses were performed between mean FA values in significant brain regions and plasma estradiol level.
Compared to healthy controls, women with SSD exhibited significantly lower FA values in the left insula, while higher FA values were observed in the left ventral lateral thalamus and left and right brainstem in the midbrain. In subjects with SSD, the mean FA value in the left insula was positively correlated to plasma estradiol levels (r = 0.453, p = 0.026) (uncorrected).
Our findings indicate altered microstructures in white matter of the insula and subcortical regions may be associated with the high susceptibility of perimenopausal women to depressive disorders. Estrogen may modulate the white matter microstructure of the insula.
Numerous studies have confirmed that in women, perimenopause is a vulnerable window to depressive disorders . The probability of a high Center for Epidemiological Studies of Depression scale (CES-D) score was four times greater during perimenopause than during the premenopausal phase . One study found that perimenopausal women were twice as likely to experience significant depressive symptoms compared to premenopausal women, and major depressive disorder (MDD) occurred in 9.5% of premenopausal and 16.6% of perimenopausal women . However, the causes of perimenopausal depression remain unclear. Although multiple factors may be involved, such as vasomotor symptoms, sleep disturbance, stressful life events, personal psychosocial features, and endocrine changes ,,, few studies have focused on the structural or functional brain aberrancies of perimenopausal depression.
In addition to depressive disorders, such as MDD and dysthymia, which can be diagnosed by criteria such as the Diagnostic and Statistical Manual of Mental Disorders, fourth edition (DSM-IV, American Psychiatry Association, Washington, D.C., 1994), a quite common subsyndromal, subclinical, or subthreshold, but clinically undiagnosable, depressive condition exists in which people experience at least one depressive symptom (insufficient for diagnosis) or inadequate persistence (shorter than 2 weeks) and demonstrate significantly high scores on depressive symptom scales -. Moreover, subsyndromal depression (SSD) may be a remarkable predictor for future MDD, and people with SSD are highly susceptible to depressive disorders ,. The Zung Self-Rating Depression Scale (ZSDS) is used globally in clinical or research assessments for depressive symptoms and depression intensity. A ZSDS index score of more than 50 has been set as the significance threshold for depression . Therefore, we presumed that perimenopausal women with SSD had a higher susceptibility to perimenopausal depression than those without depressive symptoms according to ZSDS.
Distinct biological change occurring during perimenopause is the programmed aging of the hypothalamic-pituitary-gonadal axis (HPG) system. Main changes include great variations in plasma sex hormone levels, especially the fluctuation of estradiol (E2) at a higher level than in premenopause ; and effects on the central nervous system by the sex hormones such as estrogen and androgen . Therefore, sex hormones are thought to play an important role in the pathology of perimenopausal depression. The estrogen withdrawal hypothesis for perimenopausal depression associates a decline in estrogen directly with biochemical changes in the brain and postulates that the estrogen insufficiency lead to depression . However, majority of previous studies on the direct association between perimenopausal depression and plasma sex hormones have shown inconsistent results ,-.
Magnetic resonance imaging (MRI) is a noninvasive detection technique that has been successfully used in investigations of brain structure and function in vivo in both healthy people and people with illnesses. DTI, an MRI technique used to study water diffusion in tissue, can provide microstructural information on nerve fiber connectivity and integrity in the white matter of the brain. Fractional anisotropy (FA) of the directionally preferential water molecule diffusivity is usually used to assess the overall white matter integrity . Voxel-based analysis (VBA) is a common whole-brain analytic technique that is used to explore the local FA differences between groups, with the advantage of having less investigator bias from region-of-interest (ROI) selection . Ma et al.  reported significantly decreased FA in the right middle frontal gyrus, left lateral occipitotemporal gyrus, and subgyral and angular gyri of the right parietal lobe in young adults with MDD. Other DTI studies also revealed brain locations of decreased FA in MDD patients, namely the white matter fascicles connecting the prefrontal cortex within cortical (frontal, temporal, and occipital lobes) and subcortical areas (amygdala and hippocampus) -. These findings were consistent with previous structural and functional MRI studies that identified brain abnormalities in patients with MDD; for example, an abnormal emotion processing and regulation system centered on the medial prefrontal-limbic network including the amygdala, hippocampus, anterior cingulate gyrus, subgenual cortex, and medial prefrontal cortex . However, a study with a larger sample size (134 patients with MDD vs. 54 healthy controls) showed that patients with MDD had no significant differences in FA, radial diffusivity (RD), mean diffusivity, and axonal diffusivity compared to healthy controls . Even so, a preliminary research using DTI on subjects with subclinical depression (9 men and 12 women, aged 37–71 years, CES-D score of more than 16, without a history of neurological or psychiatric illness) performed voxel-based morphometry (VBM) to calculate gray matter volume and tract-specific analyses based on VBM. This study showed decreased volumes in the bilateral anterior cingulate gyri and right rectal gyrus, and a positive correlation between the RD value of the right anterior cingulum and the CES-D score in the subclinically depressed women . In another study on 810 community-dwelling adult participants by the same authors, they found a reduction in FA in the right dorsal anterior cingulate region and a positive correlation between the RD value in the same region and CES-D scores in 271 women from 24 to 81 years old .
The present study investigated the mechanisms underlying the high susceptibility of certain perimenopausal women to depressive disorders. We used diffusion tensor imaging of the brain in combination with correlation analyses between abnormal brain regions and plasma E2 level. We hypothesized that the increase vulnerability to depression of certain perimenopausal women would be related to aberrant white matter microstructure, and these alterations would be associated with plasma E2 levels. Thus, we compared the FA values in the white matter of the whole brain between perimenopausal women with SSD and healthy controls, and performed correlation analyses between the mean FA values of aberrant brain regions and plasma E2 in women with SSD. The results of this study provide important clues for etiological and neuroimaging research on depressive disorders in the future.
Subjects and depressive symptom assessment
The study was approved by the Ethics Committee of the Second Xiangya Hospital of Central South University. All subjects were recruited by placing advertisements in the Third Affiliated Hospital of Sun Yat-sen University and in some nearby communities from October 2012 to July 2013. Forty-eight volunteers participated in this study, and they all had signed informed consent forms (ICF) before the study. The inclusion criteria were as follows: (1) women from 45 to 55 years old; (2) meeting the criteria of perimenopause according to the Stages of Reproductive Aging Workshop system ; (3) with an education level of more than 5 years in elementary school in case of failure to complete the self-report scale and ICF; and (4) Han Chinese and right-handed. Exclusion criteria included: (1) a history of medical events that may significantly affect the study outcome, such as metabolic or endocrine disease; (2) a personal or family history of mental disorders, or presence of metal implants or metal objects in the body that cannot be removed (e.g., implanted ceramic dentals); and (3) recent notable negative life events, such as divorce, loss of job, fortune and/or important relatives.
Firstly, we used the ZSDS, a 20-item self-report questionnaire, to assess depression symptoms and the depressive severity in all participants . A cut-off index score of 50 was used to determine if there were the depression symptoms . Secondly, we used the Chinese version of the Mini-International Neuropsychiatric Interview (MINI) , for clinical assessment of depressive disorders in participants with ZSDS index score more than or equal to 50. Twenty-four participants with ZSDS scores more than or equal to 50 and not met the criteria for MDD according to MINI were assigned in the SSD group. Twenty-four other age-, education-, and body mass index (BMI)-matched participants with ZSDS score less than 50 were assigned in the group of healthy controls (HC).
Sex hormone examination
Every subject meeting the inclusion criteria had an appointment scheduled specifically according to her menstrual cycle: one of the first 6 days of menstruation for women with identifiable menstrual cycles, and any day at their convenience for women with irregular menstrual cycles, i.e. the period interval more than 2 months. During their appointments, subjects were tested for plasma E2 levels. The plasma concentrations of E2 were measured using the Siemens ADVIA Centaur XP Immunoassay System (ADVIA Centaur XP, Siemens Healthcare Diagnostics Inc., New York, USA) in the Department of Clinical Laboratories in the Third Affiliated Hospital of Sun Yat-sen University.
MRI Data acquisition and processing
Images were acquired using a 3.0-Tesla Philips Achieva MR scanner (PHILIPS Achieva X-series, Philips Medical, Best, Netherlands). A single-shot, spin echo-echo planar imaging sequence (repetition time = 8,500 ms, echo time = 70 ms, slice thickness = 2.0 mm, no gap, 75 coronal slices, voxel size = 2 × 2 × 2 mm3, field of view = 256 mm × 256 mm, scan matrix = 128 × 128, flip angle = 90°) was used to acquire the DTI images. Diffusion-sensitizing gradients were applied along 33 non-collinear directions (b = 1000 s/mm2), and one non-diffusion weighted image (b = 0) was acquired. Subjects were given soft earplugs, positioned comfortably in the coil, and instructed to relax and remain still. Head motion was minimized with foam pads. High-resolution three-dimensional (3D) T1-weighted images were acquired using a fast field echo-3D T1 sequence (repetition time = 8 ms, echo time = 4 ms, 188 sagittal slices, slice thickness = 1.0 mm, no gap, flip angle = 7°, voxel size = 1 × 1 × 1 mm3).
Diffusion tensor images were pre-processed using previously published methods . The diffusion dataset was pre-aligned to correct for head motion and the effects of gradient coil eddy currents using software tools from the FMRIB software library (FSL; http://www.fmrib.ox.ac.uk/fsl). After these steps, the diffusion tensor at each voxel was calculated using the FMRIB diffusion toolbox in FSL. The resulting FA images were transformed into Montreal Neurological Institute (MNI) standard space with Statistical Parametric Mapping (SPM8) software (Wellcome Department of Cognitive Neurology, London, UK) by means of the following steps: the b = 0 images were coregistered with the 3D T1 image of the individual, the same coregistration parameters were applied to the FA maps (in the same space as the b = 0 images). Each individual’s T1 image was then normalized to the SPM T1 template (in MNI standard space), and the same normalization parameters were then applied to the coregistered FA images using the "Preserve Concentration" option. Subsequently, FA images were smoothed with an 8 mm full-width at half-maximum Gaussian kernel in order to decrease spatial noise and compensate for the inexact nature of normalization. Finally, all images were re-sampled with a voxel size of 2 × 2 × 2 mm3. For using in the two-sample t test, a binary white matter mask was made by calculating a mean FA image with a threshold FA value of 0.25 from FA images of all participants.
VBA was performed using SPM8 software. FA maps were compared between the SSD and HC groups using two-sample t-tests. The white matter mask made in processing was used to restrict the search volume for analysis. The statistical threshold for each voxel was set at p < 0.001 with an extent threshold of k > 127 voxels (1016 mm3), which yield a corrected threshold of p < 0.05, determined by the Resting-State fMRI Data Analysis Toolkit (REST) (http://restfmri.net/forum) AlphaSim program (parameters were: FWHM = 9.9 mm, 10.6 mm, 9.9 mm, rmm = 5, number of Monte Carlo simulations = 5000) . To quantify the changes in the affected regions, we constructed the ROIs mask by setting the peak coordinate of each significant cluster in the group comparison as the center of a sphere with the radius = 6 mm, respectively. For further correlation analyses, the mean FA value of each ROI was extracted from the FA maps of every subject in the SSD group using the utility for ROI time course extraction in the REST .
The Shapiro-Wilk test showed that data of the plasma E2 (W = 0.927, p = 0.083), FA values in the left insula (W = 0.965, p = 0.543), midbrain (W = 0.980, p = 0.898), and left thalamus (W = 0.962, p = 0.480) were probably normally distributed. Thus, the Pearson correlation was used in the correlation analyses between E2 and FA values of significant regions within SSD subjects. The two-sample t-test was performed to compare the age, education level, BMI, ZSDS scores, and plasma concentration of E2 between the SSD and HC groups, respectively. All statistics in this section were carried out using the Statistical Package for the Social Sciences (SPSS 16.0; SPSS Inc., Chicago, IL) with a significance level of p < 0.05 (uncorrected).
The demographic characteristics and clinical data of the two groups are shown in Table 1. The SSD group had a mean ZSDS score of 55.33 (standard deviation [SD], 4.72) and included 16 mild and 8 moderate to severe depressive cases. The HC group had a mean ZSDS score of 37.38 (SD, 5.19; t = 12.546, p < 0.0001). There were no significant differences in age, education level, BMI, or E2 between the two groups (p > 0.05).
FA values differ between SSD and HC subjects
Brain regions with altered FA in white matter are shown in Figure 1 and Table 2. Compared to the HCs, perimenopausal women with SSD had decreased FA values in the left anterior insula (Brodmann area [BA] 13) . Meanwhile, women with SSD showed increased FA values in the left ventral lateral thalamus extending to the extra-nuclear area, and left and right brainstem in the midbrain.
Correlation analyses between the mean FA values of altered brain regions and plasma E2 level within SSD subjects
Pearson bivariate correlation analyses showed a positive relationship between the mean FA value of the left insula and plasma E2 levels (r = 0.453, p = 0.026) (Figure 2). There were no significant correlations between plasma E2 and mean FA values in the midbrain (r = −0.284, p = 0.178) or left thalamus (r = −0.071, p = 0.741)(Figure 2).
In this study, we focused on women during the perimenopause, which has been considered as a vulnerable window to depressive disorders. Women with SSD were thought more susceptible to depressive disorders than those without depressive symptoms. To investigate regional abnormalities of the white matter in perimenopausal women with SSD, DTI was used and FA was calculated and statistically analyzed. We found decreased FA values in the insula and increased FA values in the thalamus and midbrain. Meanwhile, FA values in the insula were in concordance with plasma estradiol level in subjects with SSD. These findings suggest that alterations in the white matter of emotion-related brain regions and subcortical regions may be involved in the high-susceptibility of perimenopausal women to depressive disorders.
Reduced FA has been considered to be a clue to impaired myelin fiber integrity in the white matter . In the present study, we found decreased FA in the left anterior insula (Figure 1 and Table 2). The insula, especially the anterior insula, has been considered as an integral hub for mediating dynamic interactions between other large-scale brain networks, such as the default mode network, salient network, and central executive network. Therefore, the insula is thought to be involved in emotional processing, cognitive control, self-awareness, and homeostasis, based on its structural and functional connectivity with the limbic system, prefrontal lobe, and subcortical structures (e.g., the thalamus and the midbrain) . In patients with MDD, reduced gray matter volume has been noted in the insula -, but few studies have reported abnormal FA values in the white matter of this region. Our finding indicates that the microstructure of white matter in the insula maybe was abnormal in perimenopausal women with even depressive symptoms. Whether structural or functional abnormalities in the insula are the early pathological changes of perimenopausal depression, still needs to be validated in future studies.
Moreover, the present study showed a positive relationship between mean FA value in the left insula and plasma E2 levels (r = 0.453, p = 0.026) (uncorrected) (Figure 2). Estrogen has widespread effects on the human brain, especially the emotional circuitry , and may have neuroprotective and antidepressant roles in MDD ,. Additionally, Berent-Spillson et al. reported that long-term exposure to exogenous estrogen maybe affect the functional activity of the insula. They found that menopausal women using conjugated equine estrogens for more than ten continuous years had increased activation in the frontal and parietal cortices, insula, hippocampus, and cingulate during the visual work memory task compared to never-users . Until recently, few studies have focused on the association between alterations in the structure or function of brain regions and endogenous E2 level in patients with depressive disorders. Our finding suggest that circulating E2 level may act on the microstructure of the white matter in emotion-related brain regions, and to an extent, support the estrogen withdrawal hypothesis for perimenopausal depression .
Unlike previous studies on DTI in patients with depressive disorders, we also discovered two subcortical regions with higher FA values in subjects with SSD compared to healthy controls, including the left and right brainstem in the midbrain and the left thalamus (Figure 1 and Table 2). In patients with euthymic bipolar disorder and attention deficit/hyperactivity disorder (ADHD), elevated FA in white matter has been commonly reported ,, and Silk et al.  suggested that the greater FA values observed in patients with ADHD may represent an abnormal reduction in the degree of neuronal branching within significant areas. Human midbrain contains several important nerve tracts involved in up or down transmissions of sensory or motor information, reticular formation and critical nuclei producing monoamine neurotransmitters such as the dopamine, norepinephrine, and serotonin . The monoamine-deficiency hypothesis presumes that norepinephrine and serotonin have critical roles in the mechanisms of the pathogeny and treatment of depression . Meanwhile, the thalamus is generally believed to act as a relay between different subcortical areas and the cerebral cortex. Previous studies have found increased thalamic functional connectivity in the default-mode network of depressed subjects , and increased thalamic metabolism during depression episodes ,. Collectively, our findings of increased FA values suggest that aberrant white matter microstructures in the midbrain and thalamus in SSD subjects may be involved in perimenopausal depression.
The sample size of this study was relatively small to determine the alteration in the white matter of brain and the relationship between plasma sex hormone levels and significant brain regions. This study focused on perimenopausal women with SSD and healthy controls; however, we did not include perimenopausal women with MDD or premenopausal women with depressive disorders for comparison. Future research using a larger sample size and a more comprehensive range of participants is needed to validate our findings. In addition, other methods for the microstructural analysis in the brain white matter, such as TBSS, maybe offer more informative, precise, and inspiring details about the brain mechanism of the subsyndromal perimenopausal depression.
In conclusion, the results of the present study indicate that the altered microstructures in white matter of the insula and subcortical regions may be associated with the high-susceptibility of perimenopausal women to depressive disorders. Meanwhile, estrogen may modulate the white matter microstructure of the insula.
Parry BL: Perimenopausal Depression. Am J Psychiatry. 2008, 165 (1): 23-27. 10.1176/appi.ajp.2007.07071152.
Freeman EW, Sammel MD, Lin H, Nelson DB: Associations of hormones and menopausal status with depressed mood in women with no history of depression. Arch Gen Psychiatry. 2006, 63 (4): 375-382. 10.1001/archpsyc.63.4.375.
Cohen LS, Soares CN, Vitonis AF, Otto MW, Harlow BL: Risk for new onset of depression during the menopausal transition: the Harvard study of moods and cycles. Arch Gen Psychiatry. 2006, 63 (4): 385-390. 10.1001/archpsyc.63.4.385.
Gibbs Z, Lee S, Kulkarni J: Factors associated with depression during the perimenopausal transition. Womens Health Issues. 2013, 23 (5): e301-307. 10.1016/j.whi.2013.07.001.
Maartens L, Knottnerus J, Pop V: Menopausal transition and increased depressive symptomatology: a community based prospective study. Maturitas. 2002, 42 (3): 195-200. 10.1016/S0378-5122(02)00038-5.
Li Y, Yu Q, Ma L, Sun Z, Yang X: Prevalence of depression and anxiety symptoms and their influence factors during menopausal transition and postmenopause in Beijing city. Maturitas. 2008, 61 (3): 238-242. 10.1016/j.maturitas.2008.09.002.
Phillips MR, Zhang J, Shi Q, Song Z, Ding Z, Pang S, Li X, Zhang Y, Wang Z: Prevalence, treatment, and associated disability of mental disorders in four provinces in China during 2001–05: an epidemiological survey. Lancet. 2009, 373 (9680): 2041-2053. 10.1016/S0140-6736(09)60660-7.
Rodríguez MR, Nuevo R, Chatterji S, Ayuso-Mateos JL: Definitions and factors associated with subthreshold depressive conditions: a systematic review. BMC Psychiatry. 2012, 12 (1): 181-10.1186/1471-244X-12-181.
Klein DN, Shankman SA, Lewinsohn PM, Seeley JR: Subthreshold depressive disorder in adolescents: predictors of escalation to full-syndrome depressive disorders. J Am Acad Child Adolesc Psychiatry. 2009, 48 (7): 703-710. 10.1097/CHI.0b013e3181a56606.
Keenan K, Hipwell A, Feng X, Babinski D, Hinze A, Rischall M, Henneberger A: Subthreshold symptoms of depression in preadolescent girls are stable and predictive of depressive disorders. J Am Acad Child Adolesc Psychiatry. 2008, 47 (12): 1433-1442. 10.1097/CHI.0b013e3181886eab.
Butler L, Santoro N: The reproductive endocrinology of the menopausal transition. Steroids. 2011, 76 (7): 627-635. 10.1016/j.steroids.2011.02.026.
Studd J, Panay N: Hormones and depression in women. Climacteric. 2004, 7 (4): 338-346. 10.1080/13697130400012262.
Avis NE: Depression During the Menopausal Transition. Psychol Women Q. 2003, 27 (2): 91-100. 10.1111/1471-6402.00089.
Daly RC, Danaceau MA, Rubinow DR, Schmidt PJ: Concordant restoration of ovarian function and mood in perimenopausal depression. Am J Psychiatry. 2003, 160 (10): 1842-1846. 10.1176/appi.ajp.160.10.1842.
Schmidt P, Murphy J, Haq N, Danaceau M, St Clair LS: Basal plasma hormone levels in depressed perimenopausal women. Psychoneuroendocrinology. 2002, 27 (8): 907-920. 10.1016/S0306-4530(02)00004-5.
Alpay N, Kivanc ZE, Ulasoglu C: The relationship between hormonal profile and depressive symptoms in menopausal women. Dusunen Adam. 2013, 26 (2): 171-176.
Le Bihan D, Mangin JF, Poupon C, Clark CA, Pappata S, Molko N, Chabriat H: Diffusion tensor imaging: concepts and applications. J Magn Reson Imaging. 2001, 13 (4): 534-546. 10.1002/jmri.1076.
Thomason ME, Thompson PM: Diffusion imaging, white matter, and psychopathology. Annu Rev Clin Psychol. 2011, 7: 63-85. 10.1146/annurev-clinpsy-032210-104507.
Ma N, Li L, Shu N, Liu J, Gong G, He Z, Li Z, Tan L, Stone W, Zhang Z: White matter abnormalities in first-episode, treatment-naive young adults with major depressive disorder. Am J Psychiatry. 2007, 164 (5): 823-826. 10.1176/ajp.2007.164.5.823.
Liao Y, Huang X, Wu Q, Yang C, Kuang W, Du M, Lui S, Yue Q, Chan RC, Kemp GJ, Gong Q: Is depression a disconnection syndrome? Meta-analysis of diffusion tensor imaging studies in patients with MDD. J Psychiatry Neurosci. 2013, 38 (1): 49-56. 10.1503/jpn.110180.
Sexton CE, Mackay CE, Ebmeier KP: A Systematic Review of Diffusion Tensor Imaging Studies in Affective Disorders. Biol Psychiatry. 2009, 66 (9): 814-823. 10.1016/j.biopsych.2009.05.024.
Guo W, Liu F, Xun G, Hu M, Guo X, Xiao C, Chen H, Chen J, Zhao J: Disrupted white matter integrity in first-episode, drug-naive, late-onset depression. J Affect Disord. 2014, 163: 70-75. 10.1016/j.jad.2014.03.044.
Guo WB, Liu F, Chen JD, Xu XJ, Wu RR, Ma CQ, Gao K, Tan CL, Sun XL, Xiao CQ, Chen HF, Zhao JP: Altered white matter integrity of forebrain in treatment-resistant depression: a diffusion tensor imaging study with tract-based spatial statistics. Prog Neuro-Psychopharmacol Biol Psychiatry. 2012, 38 (2): 201-206. 10.1016/j.pnpbp.2012.03.012.
Zhu X, Wang X, Xiao J, Zhong M, Liao J, Yao S: Altered white matter integrity in first-episode, treatment-naive young adults with major depressive disorder: a tract-based spatial statistics study. Brain Res. 2011, 1369: 223-229. 10.1016/j.brainres.2010.10.104.
Kupfer DJ, Frank E, Phillips ML: Major depressive disorder: new clinical, neurobiological, and treatment perspectives. Lancet. 2012, 379 (9820): 1045-1055. 10.1016/S0140-6736(11)60602-8.
Choi KS, Holtzheimer PE, Franco AR, Kelley ME, Dunlop BW, Hu XP, Mayberg HS: Reconciling Variable Findings of White Matter Integrity in Major Depressive Disorder. Neuropsychopharmacology 2014:1–8.
Hayakawa YK, Sasaki H, Takao H, Mori H, Hayashi N, Kunimatsu A, Aoki S, Ohtomo K: Structural brain abnormalities in women with subclinical depression, as revealed by voxel-based morphometry and diffusion tensor imaging. J Affect Disord. 2013, 144 (3): 263-268. 10.1016/j.jad.2012.10.023.
Hayakawa YK, Sasaki H, Takao H, Hayashi N, Kunimatsu A, Ohtomo K, Aoki S: Depressive symptoms and neuroanatomical structures in community-dwelling women: A combined voxel-based morphometry and diffusion tensor imaging study with tract-based spatial statistics. NeuroImage: Clinical. 2014, 4: 481-487. 10.1016/j.nicl.2014.03.002.
Harlow SD, Gass M, Hall JE, Lobo R, Maki P, Rebar RW, Sherman S, Sluss PM, de Villiers TJ, Group SC: Executive summary of the Stages of Reproductive Aging Workshop +10: addressing the unfinished agenda of staging reproductive aging. Climacteric. 2012, 15 (2): 105-114. 10.3109/13697137.2011.650656.
Zung WW, Richards CB, Short MJ: Self-rating depression scale in an outpatient clinic: further validation of the SDS. Arch Gen Psychiatry. 1965, 13 (6): 508-10.1001/archpsyc.1965.01730060026004.
Si T, Shu L, Dang W, Su Y, Chen J, Dong W, Kong Q, Zhang W: Evaluation of the reliability and validity of Chinese version of the Mini-International Neuropsychiatric Interview in patients with mental disorders. Chin Ment Health J. 2009, 23 (7): 493-497,503.
Sheehan DV, Lecrubier Y, Sheehan KH, Amorim P, Janavs J, Weiller E, Hergueta T, Baker R, Dunbar GC: The Mini-International Neuropsychiatric Interview (M.I.N.I.): the development and validation of a structured diagnostic psychiatric interview for DSM-IV and ICD-10. J Clin Psychiatry. 1998, 59 (Suppl 20): 22-33.
Liao Y, Tang J, Ma M, Wu Z, Yang M, Wang X, Liu T, Chen X, Fletcher PC, Hao W: Frontal white matter abnormalities following chronic ketamine use: a diffusion tensor imaging study. Brain. 2010, 133 (7): 2115-2122. 10.1093/brain/awq131.
Song XW, Dong ZY, Long XY, Li SF, Zuo XN, Zhu CZ, He Y, Yan CG, Zang YF: REST: a toolkit for resting-state functional magnetic resonance imaging data processing. PLoS One. 2011, 6 (9): e25031-10.1371/journal.pone.0025031.
Jakab A, Molnár P, Bogner P, Béres M, Berényi E: Connectivity-based parcellation reveals interhemispheric differences in the insula. Brain Topogr. 2012, 25 (3): 264-271. 10.1007/s10548-011-0205-y.
Menon V, Uddin LQ: Saliency, switching, attention and control: a network model of insula function. Brain Struct Funct. 2010, 214 (5–6): 655-667. 10.1007/s00429-010-0262-0.
Sprengelmeyer R, Steele JD, Mwangi B, Kumar P, Christmas D, Milders M, Matthews K: The insular cortex and the neuroanatomy of major depression. J Affect Disord. 2011, 133 (1–2): 120-127. 10.1016/j.jad.2011.04.004.
Mutschler I, Ball T, Wankerl J, Strigo IA: Pain and emotion in the insular cortex: evidence for functional reorganization in major depression. Neurosci Lett. 2012, 520 (2): 204-209. 10.1016/j.neulet.2012.03.095.
Ansell EB, Rando K, Tuit K, Guarnaccia J, Sinha R, Hamilton JP, Furman DJ, Chang C, Thomason ME, Dennis E, Gotlib IH: Cumulative Adversity and Smaller Gray Matter Volume in Medial Prefrontal, Anterior Cingulate, and Insula Regions. Biol Psychiatry. 2012, 72 (1): 57-64. 10.1016/j.biopsych.2011.11.022.
van Wingen GA, Ossewaarde L, Backstrom T, Hermans EJ, Fernandez G: Gonadal hormone regulation of the emotion circuitry in humans. Neuroscience. 2011, 191: 38-45. 10.1016/j.neuroscience.2011.04.042.
Schule C, Eser D, Baghai TC, Nothdurfter C, Kessler JS, Rupprecht R: Neuroactive steroids in affective disorders: target for novel antidepressant or anxiolytic drugs?. Neuroscience. 2011, 191: 55-77. 10.1016/j.neuroscience.2011.03.025.
Neufang S, Specht K, Hausmann M, Güntürkün O, Herpertz-Dahlmann B, Fink GR, Konrad K: Sex differences and the impact of steroid hormones on the developing human brain. Cereb Cortex. 2009, 19 (2): 464-473. 10.1093/cercor/bhn100.
Berent-Spillson A, Persad CC, Love T, Tkaczyk A, Wang H, Reame NK, Frey KA, Zubieta JK, Smith YR: Early menopausal hormone use influences brain regions used for visual working memory. Menopause. 2010, 17 (4): 692-699.
Wessa M, Houenou J, Leboyer M, Chanraud S, Poupon C, Martinot J-L, Paillère-Martinot M-L: Microstructural white matter changes in euthymic bipolar patients: a whole-brain diffusion tensor imaging study. Bipolar Disord. 2009, 11 (5): 504-514. 10.1111/j.1399-5618.2009.00718.x.
van Ewijk H, Heslenfeld DJ, Zwiers MP, Buitelaar JK, Oosterlaan J: Diffusion tensor imaging in attention deficit/hyperactivity disorder: A systematic review and meta-analysis. Neurosci Biobehav Rev. 2012, 36 (4): 1093-1106. 10.1016/j.neubiorev.2012.01.003.
Silk TJ, Vance A, Rinehart N, Bradshaw JL, Cunnington R: White-matter abnormalities in attention deficit hyperactivity disorder: a diffusion tensor imaging study. Hum Brain Mapp. 2009, 30 (9): 2757-2765. 10.1002/hbm.20703.
Meyer JH: Imaging the serotonin transporter during major depressive disorder and antidepressant treatment. J Psychiatry Neurosci. 2007, 32 (2): 86-
Belmaker R, Agam G: Major depressive disorder. N Engl J Med. 2008, 358 (1): 55-68. 10.1056/NEJMra073096.
Greicius MD, Flores BH, Menon V, Glover GH, Solvason HB, Kenna H, Reiss AL, Schatzberg AF: Resting-state functional connectivity in major depression: abnormally increased contributions from subgenual cingulate cortex and thalamus. Biol Psychiatry. 2007, 62 (5): 429-437. 10.1016/j.biopsych.2006.09.020.
Holthoff V, Beuthien‐Baumann B, Zündorf G, Triemer A, Lüdecke S, Winiecki P, Koch R, Füchtner F, Herholz K: Changes in brain metabolism associated with remission in unipolar major depression. Acta Psychiatr Scand. 2004, 110 (3): 184-194. 10.1111/j.1600-0447.2004.00351.x.
Neumeister A, Nugent AC, Waldeck T, Geraci M, Schwarz M, Bonne O, Bain EE, Luckenbaugh DA, Herscovitch P, Charney DS: Neural and Behavioral Responses to Tryptophan Depletion in Unmedicated Patients With Remitted Major Depressive Disorder and Controls. Arch Gen Psychiatry. 2004, 61: 765-773. 10.1001/archpsyc.61.8.765.
We thank Dr. Yong Liu and Haixia Long from Brainnetome Center, Institute of Automation, Chinese Academy of Sciences for their kindly help in MRI data processing; Prof. Guimao Huang from Department of Radiology of Guangzhou Brain Hospital for his strong support on MRI scanning; and Drs. Weihui Li and Mei Liao from Mental Health Institute of the Second Xiangya Hospital of Central South University for their constructive suggestions on this work. We acknowledgement support from grant from the National Natural Science Foundation of China (81171286 & 91232714 to Lingjiang Li), National Basic Research Program of China (+2013CB835100 and 2009CB918303 to Lingjiang Li), the Science and Technology Program of Guangdong, China (2010B031600309 to Xianglan Wang).
The authors declare that they have no competing interests.
Authors LL, JZ and XW designed the study and wrote the protocol. Author XW managed the literature searches and analyses. Authors TJ and XW undertook the MRI data processing and the statistical analysis, and author XW wrote the first draft of the manuscript. All authors have contributed to and approved the final manuscript.
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Wang, X., Tao, J., Li, L. et al. Alterations in white matter fractional anisotropy in subsyndromal perimenopausal depression. BMC Psychiatry 14, 367 (2014). https://doi.org/10.1186/s12888-014-0367-8
- White matter
- Fractional anisotropy
- Depressive disorders