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Asian Journal of Psychiatry 57 (2021) 102581

Contents lists available at ScienceDirect

Asian Journal of Psychiatry


journal homepage: www.elsevier.com/locate/ajp

Review article

A meta-analysis on the prevalence of depression in perimenopausal and


postmenopausal women in India
Vikas Yadav a, Akanksha Jain a, Deepti Dabar b, *, Akhil Dhanesh Goel c, Akanksha Sood d,
Ankur Joshi b, Sanjay S. Agarwal a, Sunil Nandeshwar e
a
Department of Community Medicine, Atal Bihari Vajpayee Government Medical College, Vidisha, India
b
Department of Community and Family Medicine, AIIMS, Bhopal, India
c
Department of Community Medicine and Family Medicine, AIIMS, Jodhpur, India
d
Department of Obstetrics and Gynaecology, St. Mary’s Hospital, Oxford Road, Manchester, UK
e
Atal Bihari Vajpayee Government Medical College, Vidisha, India

A R T I C L E I N F O A B S T R A C T

Keywords: Introduction: The mental health of perimenopausal and postmenopausal women is a relatively understudied area.
Prevalence This review formally explores the prevalence of depression in perimenopausal and postmenopausal women in
India India.
Meta-analysis
Methods: Databases like PubMed, Embase, Cochrane library, Web of Science and Scopus were systematically
Depression
Menopause
searched for cross-sectional or cohort studies, providing prevalence of depression in Indian perimenopausal and
Women postmenopausal women. Systematic study selection and data extraction procedures were followed. Quality
Climacteric assessment of individual study was done using AXIS tool. For pooling of effect sizes, the random effects model
was used. Funnel plot and Egger’s test were used to ascertain publication bias. Subgroup analyses and meta-
regression analysis were used to explore heterogeneity in the summary estimates.
Results: After a thorough search, ten studies were found to be eligible and included in this review. Pooled esti­
mate for prevalence of depression (random effects model) in perimenopausal and postmenopausal women in
India is 42.47 % (95 % CI: 28.73–57.49, I2 = 97.7 %). On visual inspection of the funnel plot and interpreting
egger’s test (bias: 3.49, SE bias: 3.68, p = 0.37), there was absence of publication bias.
Conclusion: We documented 42.47 % pooled prevalence of depression in perimenopausal and postmenopausal
women in India.

1. Introduction (Soares, 2019). Common physical symptoms during the menopausal


transition include hot flushes, night sweating, breast tenderness, vaginal
Menopause is a crucial transition in women’s lives, in which several dryness, migraine and insomnia. Anxiety, stress, mood swing and
biological and psychological changes take place (Freeman, 2015). depression are common psychological symptoms (Di et al., 2019;
Menopause is defined post hoc as a complete cessation of menstrual Freeman, 2015; Soares, 2019).
bleeding for at least one year. Perimenopause is defined as the time from Depression is often described as the loss of interest in routine life, loss
the start of irregular periods until one year after menopause of pleasure in previously pleasurable activities and depressed mood for
(Ahuja, 2016). Mean menopause age in India is 45.5 (± 5.5 SD) years more than two weeks (Bromberger and Epperson, 2018; Di et al., 2019).
(Ahuja, 2016). Perimenopausal period ranges from 2 years to 8 years Lifetime estimated prevalence of major depression is 17 %, and its
with a mean duration of 5 years (Treloar, 1981; Santoro, 2016). incidence is nearly two times in females as compared to males
Women often display clinical signs and symptoms corresponding to (Kessler et al., 1994). Depression in the female is known to be associated
hormonal, psychological and physical changes in their body with reproductive events, which is also called reproductive-related

* Correspondence author at: Department of Community and Family Medicine, AIIMS, Bhopal, India.
E-mail addresses: drvikasyadav@gmail.com (V. Yadav), dr.akanksha3186@gmail.com (A. Jain), deepti.dabar@gmail.com (D. Dabar), doc.akhilgoel.aiims@gmail.
com (A.D. Goel), drakankshasood@gmail.com (A. Sood), ankur.cfm@aiimsbhopal.edu.in (A. Joshi), agarwalsanjay8@rediffmail.com (S.S. Agarwal),
drsunilnandeshwar@gmail.com (S. Nandeshwar).

https://doi.org/10.1016/j.ajp.2021.102581
Received 21 November 2020; Received in revised form 20 January 2021; Accepted 24 January 2021
Available online 5 February 2021
1876-2018/© 2021 Elsevier B.V. All rights reserved.
V. Yadav et al. Asian Journal of Psychiatry 57 (2021) 102581

depressive episodes. The premenstrual dysphoric disorder (PMDD) is 4) Case reports and reviews
linked with the menstrual cycle, and incidence of depression is more in 5) Studies, not using any standard scale for assessing depression
the postpartum period and perimenopausal period (Soares, 2019). This 6) Studies reporting the prevalence of subjective or self-perceived
occurs due to changes in the hormonal environment in the luteal phase depression
of the cycles, in the postpartum period and the menopause transition
(Soares, 2019). 2.2. Information sources
In the perimenopausal period, women with no history of depression
may experience depressed mood two to four times as compared to pre­ We searched for relevant articles using online databases like
menopausal women, and this risk is even higher in women with a history PubMed, Embase, Cochrane library, Web of Science and Scopus. Search
of depression (Bromberger and Kravitz, 2011; Freeman, 2010). This queries were done on 10th of June 2020, and articles published up to
debilitating depression in perimenopausal period could impair func­ this date were included. While conducting these searches, any date or
tional outcomes and can also deteriorate their quality of life language restrictions were not applied. Bibliographies of selected arti­
(Ho et al., 2017; Park and Kim, 2018). cles were also explored to find additional relevant studies. The themes of
Various prevalence studies conducted worldwide reported that the search items were menopausal status, geographic area (i.e. India),
prevalence of depression in perimenopausal and postmenopausal depression, women, and prevalence. The detailed search strategy used
women is exceptionally high (Afshari et al., 2015; Chedraui et al., 2009; on PubMed is provided in Table 1.
Gonçalves et al., 2013; Onya and Otorkpa, 2018; Yen et al., 2009).
Psychiatric health of menopausal women has not been add 2.3. Study selection
ressed separately in the National Mental Health Prog
ramme (of India) and India’s National Mental Health Policy (2014) All search results were uploaded to Rayyan QCRI
(Gupta and Sagar, 2018; Wig and Murthy, 2015). (https://rayyan.qcri.org), an online citation screening tool
It has also been documented in previous studies that the prevalence of (Ouzzani et al., 2016). A reviewer (VY) identified and removed
depression in this group is enormously influenced by economic and socio- duplicate citations and ‘switched on’ the ‘blind mode’ to ensure an
cultural circumstances; hence prevalence estimates of other countries are independent selection of relevant studies. In the first stage, two re­
not an accurate proxy for India (Compton et al., 2006; Kleinman, 2004). viewers (ADG and DD) independently screened titles and abstracts of
Though national level survey to assess the burden of mental illnesses all the included studies in search results considering eligibility criteria.
among various age categories was conducted in India in 2015− 16; still, it In the second stage, full-text copies of all selected studies were ob­
did not provide the prevalence of psychiatric illnesses in perimenopausal tained, and exclusions of more articles were done based on the eligi­
or postmenopausal women (Gautham et al., 2020). For that reason, there bility criteria. Reasons for exclusions were also documented for each
is still a scarcity of nationally representative data for depression preva­ excluded article explored as full text. In the third stage, the third
lence in this group of women. Therefore, we planned to conduct this reviewer (VY) identified discrepancies among selected articles by
systematic review and meta-analysis with the aim to explore the preva­ ‘switching off’the ‘blind mode’. Differences were discussed and
lence of depression in perimenopausal and postmenopausal women in resolved by building consensus among reviewers (ADG, DD and VY).
India. The current study is an attempt to investigate the prevalence and Finally, we arrived at the list of studies fulfilling all the inclusion and
hence highlighting the case of depression in perimenopausal and post­ exclusion criteria.
menopausal women. This calls for informed policy decisions towards
better management of the situation.
2.4. Data extraction
2. Methods
From all the selected eligible studies, two reviewers (ADG and DD)
independently extracted relevant information. Data were extracted
This review is reported according to the ‘Preferred Reporting Items for
regarding author, year of publication, age of participants, the screening/
Systematic Reviews and Meta-Analyses’ (PRISMA) statement
diagnostic instrument used, population (menopausal or perimenopausal
(Liberati et al., 2009), and this review is registered with the PROSPERO
women or both), residence (district, state), area (urban or rural or both),
database (ID: CRD42020191934).
setting (hospital or community based), type of sampling and prevalence
data (total participants included, number of participants found
2.1. Eligibility criteria
depressed). Inconsistencies were again resolved by building consensus
among reviewers (ADG, DD and VY).
We included all the studies reporting the prevalence of depression in
perimenopausal and postmenopausal women in India.
2.5. Quality assessment of the studies
2.1.1. Inclusion criteria
To ascertain the quality of the included studies for their mathemat­
ical rigour, ‘Critical appraisal tool to assess the quality of cross-sectional
1) Studies Type: Cross-sectional or Cohort studies
2) Studies conducted in perimenopausal and postmenopausal women
3) Studies reported the prevalence of depression/ Depressive symp­ Table 1
toms/ Depressive Disorders Search strategy used in PubMed.
4) Studies conducted in Indian population Themes Keywords
5) Studies in which depression assessed using any one of the depression 1 Menopausal menopausal OR postmenopaus* OR post-menopaus* OR
screening (or diagnostic) scale status premenopaus* OR pre-menopaus* OR perimenopaus* OR
peri-menopaus* OR “midlife” OR climacteric
2 Geographic area India*
2.1.2. Exclusion criteria
3 Depression psychiatric OR depressi* OR mental
4 Women “women” or “female”
1) Studies conducted in a specific sub-set (i.e. studies conducted in 5 Prevalence prevalence OR epidemiology
women suffering from a particular disease etc.) Note: • We used the Boolean operator ‘AND’ to combine all themes
2) Studies,not providing relevant data for the prevalence of depression in search.
• Any date or language restrictions were not applied.
3) Studies reporting sub-category of depression

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V. Yadav et al. Asian Journal of Psychiatry 57 (2021) 102581

studies’ (AXIS tool) was used (Downes et al., 2016). This tool consists of investigate the source of heterogeneity. Subgroup analyses were con­
20 questions, which needs to be responded to as ‘yes’, ‘no’ or ‘don’t ducted for screening instrument (HAM-D or other), population (meno­
know’. Two reviewers (ADG and DD) critically appraised each study pausal or perimenopausal women or both), Zonal council administrative
independently using this critical appraisal tool. Discrepancies found division of India (Northern or Southern or Central or Western or
during the critical appraisal were resolved by the discussion with the Eastern), (Government of India, 2014) year of publication (before the
third reviewer (VY). Studies having thirteen or more score (out of 20) year 2016 or year 2016 and after), residence (urban or rural or both),
were considered as good quality studies. setting (hospital or community) and sampling method (random or
non-random). Sensitivity analysis was done to exclude studies with
2.6. Data synthesis and analyses lower quality (AXIS score of less than 13).

The effect sizes for current meta-analysis are prevalence estimates of 3. Results
depression in perimenopausal and postmenopausal women of India,
which were calculated based on prevalence estimates obtained from From all the databases, a total of 332 articles were identified. After
each selected research article. After that, the pooled estimate of removing duplicates, exclusions were made by reviewing titles and ab­
depression prevalence was calculated. stracts. Full texts of 96 articles were screened. Total of 10 cross-sectional
Generalised Linear Mixed Models (GLMMs) Logit transformation studies fulfilled eligibility criteria and were thus eligible for inclusion in
methods for transforming single proportion were used to calculate effect this systematic review and meta-analysis (Aaron et al., 2002; Ahlawat
sizes for each study, as these methods are preferred in calculating effect et al., 2019; Bansal et al., 2015; Dutta et al., 2018; Jagtap et al., 2016;
size in such a situation (Schwarzer et al., 2019). Nayak et al., 2019; Ps et al., 2017; Santwani et al., 2010; Singh and
I squared (I2) statistic and Cochran’s Q test were used to examine Pradhan, 2014; Tamaria et al., 2013). We did not find any eligible cohort
heterogeneity between studies. Due to considerable heterogeneity (I2 = study for our review. Fig. 1 depicts the study selection process.
97.7 %, Cochran’s Q = 174.24, df = 9, p-value < 0.0001) between the Most (5 studies) of the studies were published in the year 2016 and
studies, random effects model was used in analysis later. Among the included studies, the most frequently used depression
(Higgins and Thompson, 2002). Tau squared was calculated using screening instrument was the Hamilton Depression Rating Scale (HAM-
Restricted Maximum-Likelihood Estimator (REML) method. D, 4 studies). Remaining five studies used Screening for Depression
Clopper-Pearson method was used to calculate confidence intervals of Questionnaire-9 (SDQ-9, 1 study), Zung Self-Rating Depression Scale
effect sizes of individual studies. All effect sizes and pooled estimates are (ZSDS, 1 study), Mini International Neuropsychiatric Interview (MINI, 1
reported as proportions with 95 % confidence intervals. Visual inspection study), Inventory of Depressive Symptomatology Self Report (IDS-SR, 1
of funnel plots and egger’s test provided evidence for publication bias if study), Patient Health Questionnaire (PHQ-9, 1 study) and Center for
any (Egger et al., 1997). Data extraction was done in Microsoft excel Epidemiologic Studies Depression Scale (CES-D, 1 study) for screening
2019 software. Meta and Metafor packages of R software were used to depression. Total 7 studies conducted over postmenopausal women, 1
conduct all the statistical analyses (Schwarzer, 2007; Viechtbauer, 2010). was conducted over perimenopausal women and 2 studies covered both.
Subgroup analyses and meta-regression analysis were performed to An equal number (4 studies each) of studies were from Northern and

Fig. 1. PRISMA Flowchart of study selection.

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V. Yadav et al. Asian Journal of Psychiatry 57 (2021) 102581

Southern India, and only two studies were conducted in Western India. 21.91− 82.13) but the difference is not statisticallysignificant (p = 0.42).
We did not find any study conducted in Eastern or Central India. Most (7 India is administratively divided into five zonal councils, i.e.
studies) of the studies were conducted in the community-based setting, Northern, Southern, Central, Western and Eastern. In our review, we did
and rest (3 studies) were conducted in the hospital-based setting. Most of not find any study conducted in Eastern or Central zonal council. Pooled
the studies were from rural areas (5 studies), followed by urban (4 prevalence was highest in Western zonal council (2 studies, 56.28 %; 95
studies) and mixed (1 study) areas. Random sampling was the most % CI: 22.49− 85.10) followed by Northern (4 studies, 53.17 %; 95 % CI:
commonly employed sampling procedure (8 studies) and 2 studies did 29.70− 75.33) and Southern (4 studies, 27.35 %; 95 % CI: 22.80–32.43)
not report sampling methods. Total 8 studies were found to be of high zonal council and difference was significant (p = 0.03).
quality (AXIS score 13 or more), and 2 studies were of low quality (score Studies published before the year 2016had estimated pooled preva­
less than 13) on methodological quality assessment (Table 2). lence of 56.35 % (5 studies, 95 % CI: 32.29− 77.75), which was higher
than the studies published in the year 2016 or later (5 studies, 30.57 %;
95 % CI: 24.62− 37.25) and the difference was significant (p = 0.04).
3.1. The pooled prevalence of depression
Studies conducted in urban (4 studies, 46.85 %; 95 % CI:
27.64− 67.03) areas exhibited higher pooled prevalence of depression as
Pooled estimate for depression (random effects model) in perimen­
compared to studies conducted in rural (5 studies, 41.28 %;
opausal and postmenopausal women in India was 42.47 % (95 % CI:
20.90− 65.16) or both, rural and urban (1 study, 31.48 %; 95 % CI:
28.73–57.49, Tou2: 0.9166, I2 = 97.7 %, Cochran’s Q = 174.24, df = 9,
23.43− 40.81) areas (difference non-significant, p = 0.1286).
p-value < 0.0001) (Fig. 2).
Studies conducted in hospital setting (3 studies, 51.87 %; 95 % CI:
28.61− 74.34) recorded higher pooled prevalence as compared to the
3.2. Subgroup analyses studies conducted in community setting (7 studies, 38.60 %; 95 % CI:
23.43− 56.37) but this difference was statistically non-significant (p =
Studies used HAM-D (4 studies, 43.58 %; 95 % CI: 24.25− 65.08) for 0.39).
screening depression showed higher estimates of depression prevalence Studies carried out with random sampling methods (8 studies, 37.64
as compared to studies using other screening (6 studies, 41.67; 95 % CI: %; 95 % CI: 24.27–53.21) were documented lower prevalence as
23.99− 61.79) scales but the difference was not statistically significant compared to studies without reporting of sampling methods (2 studies,
(p = 0.90). 62.37 %; 95 % CI: 35.65− 83.22) but the difference was statistically non-
The pooled prevalence of depression in postmenopausal women (7 significant with a p-value of 0.12.
studies, 37.83 %; 95 % CI: 25.83− 51.53) is lower as compared peri­
menopausal women or mixed population (3 studies, 53.17 %; 95 % CI:

Table 2
Characteristics of the studies included in Meta-analysis.
S. Study Location Area Study Setting Diagnostic Population type Sampling Age Sample No. Quality
No. design scale used size Depression score

1 Aaron Vellore, Tamil rural cross- community SDQ-9 postmenopausal Multistage 40− 49 100 29 15
et al. Nadu, sectional based sampling years
(2002) Southern
2 Ahlawat Delhi, Delhi, urban cross- community HAM-D postmenopausal Systematic 41− 60 580 241 (mild 15
et al. Northern sectional based random years = 222,
(2019) sampling moderate
= 19)
3 Bansal Ludhiana, rural cross- community ZSDS perimenopausal PPS 40− 60 136 118 (mild 14
et al. Punjab, sectional based and years = 39,
(2015) Northern postmenopausal moderate
= 67,
severe =
12)
4 Dutta Chennai, urban cross- community HAM-D postmenopausal All eligible 41− 60 171 42 (mild = 13
et al. Tamil Nadu, sectional based women of years 36,
(2018) Southern area moderate
included = 6)
5 Jagtap Loni, urban cross- hospital MINI perimenopausal Consecutive 45− 55 108 34 11
et al. Maharashtra, and sectional based eligible years
(2016) Western rural women in
OPD
6 Nayak Udupi, rural cross- community IDS-SR postmenopausal Multistage 51.68 290 65 (mild = 16
et al. Karnataka, sectional based sampling ± 4.2 60,
(2019) Southern years moderate
= 5)
7 PS et al. Alappuzha, rural cross- community PHQ9 perimenopausal Cluster 40-60 477 159 16
(2017) Kerala, sectional based and sampling years
Southern postmenopausal
8 Santwani Jamnagar, urban cross- hospital HAM-D postmenopausal Not 40− 50 48 38 10
et al. Gujarat, sectional based Reported years
(2010) Western
9 Singh Delhi, Delhi, rural cross- community HAM-D postmenopausal Multistage 40− 54 252 81 (mild = 13
et al. Northern sectional based sampling years 78,
(2014) moderate
= 3)
10 Tamaria Delhi, Delhi, urban cross- hospital CES-D postmenopausal Not 46.8 ± 200 89 13
et al. Northern sectional based Reported 2.9
(2013) years

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V. Yadav et al. Asian Journal of Psychiatry 57 (2021) 102581

Fig. 2. Forest plot of the prevalence of depression in perimenopausal and postmenopausal women in India.

3.3. Quality assessment funnel plot, it looks reasonably symmetrical, which also supports the
findings of egger’s test. (Fig. 3)
AXIS Quality score of included studies ranges from 10 to 16 with a
median of 13.5. There was a total of 8 high quality studies and two low 4. Discussion
quality studies included in this review.
Quality scores for each study are provided in Table 2. With this meta-analysis, we have estimated pooled prevalence of
perimenopausal and postmenopausal depression from 10 studies. We
3.4. Sensitivity analysis found that pooled estimate for depression (random effects model) in
perimenopausal and postmenopausal women in India was 42.47 % (95
On sensitivity analysis, omitting lower quality studies (AXIS score % CI: 28.73–57.49). Various small and large studies conducted in other
less than 13) pooled prevalence declined to 39.29 % with 95 % CI of parts of the world also documented a remarkably high prevalence of
25.64–54.86 (Tou2: 0.7996, I2 = 97.8 %, Cochran’s Q = 144.99, df = 10, depression in this group (Afshari et al., 2015; Chedraui et al., 2009;
p-value < 0.0001), which is lower than the overall pooled prevalence Gonçalves et al., 2013; Onya and Otorkpa, 2018; Yen et al., 2009).
(42.47 %) (Table 3). Zeng et al. (2019) conducted a meta-analysis of studies of Chinese
population documented 36.3 % prevalence of depression in menopausal
3.5. Meta-regression analysis women (Zeng et al., 2019). On sensitivity analysis, after omitting lower
quality studies, we documented the estimated pooled prevalence of
On meta-regression analysis, we found that meta-analysis results are 39.29 %, which is very similar to results found by Zeng et al. (2019).
not associated with quality of studies (B = − 0.19, z = − 1.25, p-value = Risk factors for depression in these women can be divided into three
0.21). major categories. First, biological factors, i.e. fatigue, sleep disturbances,
vasomotor symptoms, obesity, and chronic medical condition (Brom­
berger et al., 2007; Dennerstein et al., 2000, 1999; Woods et al., 2009).
3.6. Influential analysis
Second, behaviour and social factors, i.e., physical inactivity, relationship
issues, financial issues, unemployment, retirement, social isolation, and
On influential analysis, pooled results of the meta-analysis are not
poor social support (Bromberger et al., 2007; Dennerstein et al., 1999;
significantly affected by data of any single study.
Freeman et al., 2004; Sternfeld et al., 2014; Woods et al., 2009, 2008).
Third, psychological factors, i.e. previous history of depression or anxiety
3.7. Publication bias and stressful life event (Bromberger et al., 2009; Dennerstein et al., 2000;
Woods et al., 2009). The data also suggest that depressed mood in the
The results of egger’s test (bias: 3.49, SE bias: 3.68, p = 0.37) did not menopausal transition is multifactorial and not merely due to menopausal
provide any evidence of publication bias. On visual inspection of the

Table 3
Subgroup analysis of prevalence of depression in menopausal women in India.
Subgroup Categories (no. of studies) Prevalence in % 95 % CI in % I2 in % Between group Q (p value)

Instrument HAM-D (4) 43.58 24.25− 65.08 97.1 0.02 (0.90)


Other (6) 41.67 23.99− 61.79 97.6
Population type Postmenopausal (7) 37.83 25.83− 51.53 96.0 0.66 (0.42)
Perimenopausal or mixed (3) 53.17 21.91− 82.13 97.9
Zone Northern (4) 53.17 29.70− 75.33 98.2 6.81 (0.03)
Southern (4) 27.36 22.80− 32.44 62.4
Western (2) 56.28 22.49− 85.10 92.7
Year of publication Before 2016 (5) 56.35 32.29− 77.75 97.1 4.11 (0.04)
2016 and later (5) 30.57 24.62− 37.25 85.7
Area Rural (5) 41.28 20.90− 65.16 98.2 2.21 (0.33)
Urban (4) 46.85 27.64− 67.03 96.7
Mixed (1) 31.48 23.43− 40.81 –
Setting Community (7) 38.60 23.43− 56.37 98.1 0.74 (0.39)
Hospital (3) 51.87 28.61− 74.34 93.8
Sampling Random (8) 37.64 24.27− 53.20 97.6 2.45 (0.12)
Not Reported (2) 62.37 35.65− 83.22 88.3

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V. Yadav et al. Asian Journal of Psychiatry 57 (2021) 102581

Fig. 3. Funnel plot with transformed prevalence on the x-axis and standard error of transformed proportions on the y-axis.

status alone (Freeman, 2015). The association of menopause and depres­ (Gautham et al., 2020). Modern lifestyle, competitive work environ­
sion is possibly due to the changes in the level of reproductive hormone ments, poverty, nuclear families, migration and poor living conditions in
alter neuroregulatory system responsible for mood and behaviour slums of urban areas could be an explanation for the higher prevalence
(Rubinow et al., 1998; Schmidt and Rubinow, 2009); still, the actual of depression in urban areas (Gautham et al., 2020).
reason for depression in menopausal transition is not yet known In our meta-analysis, studies, carried out with random sampling
(Freeman, 2015; Soares, 2019). methods, documented lower prevalence as compared to studies not
In the current meta-analysis, we found that studies used HAM-D for reporting sampling methods. Studies with random sampling methods
screening depression are reporting slightly higher estimates of depres­ may be more representative of the population and have lesser selection
sion prevalence as compared to studies using other screening, but the bias. Those studies, which have not reported sampling methods, might
difference was not significant. Various scales for screening depression have used convenient sampling methods and overestimated the
has been developed and validated to use in different settings and pop­ prevalence.
ulation. Sensitivity and specificity of depression screening scales may In this review, studies conducted in the hospital setting, recorded
vary; hence their results may also come out different from each other higher pooled prevalence as compared to studies conducted in the
(Behera et al., 2017). community setting, but these differences were statistically non-
In the current meta-analysis, we have documented that pooled preva­ significant. Most (2 out of 3) of the hospital-based studies in the cur­
lence of depression in postmenopausal women is lesser as studies comprise rent review have not reported sampling methods, and selection bias is a
of perimenopausal or both as participants. These results are in accordance probable explanation for higher prevalence. Participants from the hos­
with previous studies in which the prevalence of depression is more in pital setting are at higher risk of developing depression due to illness, for
perimenopausal women than postmenopausal women which they have visited the hospital, so getting a higher prevalence of
(Dennerstein et al., 2004; Tangen and Mykletun, 2008). In perimenopausal depression in them is likely.
women, due to the hormonal transition, vasomotor symptom, negative
attitude towards menopause, ageing and poor health due to other diseases, 5. Conclusion
depression may precipitate more often (Freeman, 2015).
In our review, we have found that pooled prevalence was higher in This meta-analysis reports that 42.47 % (95 % CI: 28.73–57.49) of
Western and Northern zonal councils, and it is comparatively low in perimenopausal and postmenopausal women have some form of depres­
Southern zonal council. In previous studies, it has been reported that lower sion. There is no separate mention of mental health in menopausal women
socioeconomic status and lack of education increases the chances of having in India’s National Mental Health Programme and the National Mental
depression (Rai et al., 2013). The lower prevalence of depression in the Health Policy (2014) (Gupta and Sagar, 2018; Wig and Murthy, 2015).
Southern zone may be due to higher education level and less of poverty in Considering this high burden of depression in perimenopausal and post­
these states (Chandramouli, 2011; Ministry of Statistics and Programme menopausal women, India should assign a higher priority to menopausal
Implementation, 2011). mental health and include the screening of depression for this group in
In the current research, we reported that study published before the routine care.
year 2016 were having a higher prevalence than the studies published in
the year 2016 or later. India framed the National Mental Health Policy of 6. Limitation
India in 2014 (Wig and Murthy, 2015). Since then, several initiatives
have been taken to incorporate mental health in routine health care, and We found only ten suitable studies from a country of 1.3 billion
this might be the reason for improved indicators found in studies pub­ population, so publication bias is likely. Many of the included studies
lished in 2016 or later years in the current review (Sharma, 2014). have not provided a detailed explanation regarding employed methods;
In the current review, studies conducted in urban area were exhib­ therefore, selection bias is also possible. Depression prevalence provided
iting higher pooled prevalence of depression as compared to studies by screening tools cannot be considered as the prevalence of clinical
conducted in rural or both, rural and urban areas. National Mental depression. Nevertheless, participants found positive on screening
Health Survey of India (2015− 16) also found that the prevalence of scales, can be referred to a psychiatrist or monitored for deterioration of
almost all mental disorders, including depression in the adult popula­ the condition.
tion, were high in the urban areas as compared to rural areas

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V. Yadav et al. Asian Journal of Psychiatry 57 (2021) 102581

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