Risk factors (excluding hormone therapy) for endometrial hyperplasia:

a systematic review.
Sanni, O. B., Kunzmann, A. T., Murray, L. J., McCluggage, W. G., & Coleman, H. G. (2016). Risk factors
(excluding hormone therapy) for endometrial hyperplasia: a systematic review. Epidemiology: Open Access,
6(3), [229]. DOI: 10.4172/2161- 1165.1000229

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 y: Open Sanni et al., Epidemiol 2016, 6:2
Epidemiology
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http://dx.doi.org/10.4172/2161-1165.1000229
Ac
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cess
ISSN: 2161-1165
Open Access
Review Article
Research Article OpenAccess
Open Access

Risk Factors (Excluding Hormone Replacement Therapy) for Endometrial

Hyperplasia: A Systematic Review
Omolara B Sanni1*, Andrew T Kunzmann1, Liam J Murray1, W Glenn McCluggage2 and Helen G Coleman1
1
Cancer Epidemiology & Health Services Research Group, Centre for Public Health, Queens University Belfast, Northern Ireland
2
Department of Pathology, Belfast Health and Social Care Trust, Northern Ireland

Abstract
To conduct a systematic review of risk factors associated with the development of Endometrial Hyperplasia (EH).
Data sources
Ovid MEDLINE, EMBASE and Web of Science databases were searched from inception to 30 June 2015.
Study eligibility
Fifteen observational studies that reported on EH risk in relation to lifestyle factors (n=14), medical history (n=11),
reproductive and menstrual history (n=9) and measures of socio-economic status (n=2) were identified. Pooled relative
risk estimates and corresponding 95% confidence intervals (CI) were able to be derived for EH and Body Mass Index
(BMI), smoking, diabetes and hypertension, using random effects models comparing high versus low categories.
Results
The pooled relative risk for EH when comparing women with the highest versus lowest BMI was 1.82 (95% CI
1.222.71; n=7 studies, I2=90.4%). No significant associations were observed for EH risk for smokers compared
with non-smokers (RR 0.88, 95% CI 0.66-1.17; n=3, I2=0.0%), hypertensive versus normotensive women (RR 1.51,
95% CI 0.723.15; n=5 studies, I2=79.1%), or diabetic versus non-diabetic women (RR 1.77, 95% CI 0.793.96; n=5
studies, I2=31.8%) respectively although the number of included studies was limited. There were mixed reports on the
relationship between age and risk of EH. Too few studies reported on other factors to reach any conclusions in relation
to EH risk.
Conclusions
A high BMI was associated with an increased risk of EH, providing additional rationale for women to maintain a
normal body weight. No significant associations were detected for other factors and EH risk, however relatively few
studies have been conducted and few of the available studies adequately adjusted for relevant confounders. Therefore,
further aetiological studies of endometrial hyperplasia are warranted.

Keywords: Endometrial hyperplasia; Endometrial cancer; Risk following an EH diagnosis [9]. highlight the importance of preventing
factors EH where possible. Identification of modifiable risk factors for EH
would enable women to make lifestyle changes that could reduce risk
Introduction of this condition, and subsequent cancer risk [10]. EH, especially EH
without atypia, develops as a consequence of excessive or prolonged
Endometrial Hyperplasia (EH) is a condition that is characterised
exposure to oestrogen [11-13], and an imbalance between oestrogen
by abnormal growth of the endometrium lining the uterus [1-3].
and progesterone levels which usually occur as a result of insufficient
This condition is more prevalent among peri-menopausal and post-
progesterone in comparison with oestrogen level in a womans
menopausal women [4]. While previously EH was classified into simple
system [13], For premenopausal women, the balance between these
or complex EH, with or without atypia [2], the 2014 World Health
hormones changes during a womans menstrual cycle each month.
Organisation classification simplifies this into EH without atypia and
After menopause, the ovaries stop producing these hormones, but a
atypical hyperplasia [5]. Atypical hyperplasia is less common than other
small amount of oestrogen can be synthesized from androgen by the
types, and results from observational studies suggest that it is the type
which is more associated with the risk of progression to endometrial
cancer [1-3]. The endometrial cancers which develop from EH are so- *Corresponding author: Omolara Sanni, Centre for Public Health, Institute of
called type 1 endometrial cancers of endometrioid type [6]. Clinical Sciences, Block B, Queens University Belfast, Royal Victoria Hospital,
Grosvenor Road, Belfast, Northern Ireland, Tel: 009 44 7476101022; E-mail:
The risk of progression for EH to endometrial cancer has been osanni01@qub.ac.uk
reported from a large population-based nested case-control study
Received February 15, 2016; Accepted March 04, 2016; Published March 11,
including 7,947 enrolees at a prepaid health plan in the USA. In that 2016
study, atypical EH was associated with a 14-fold increased risk of
Citation: Sanni OB, Kunzmann AT, Murray LJ, McCluggage WG, Coleman HG
endometrial cancer, while the risk of progression for simple EH and (2016) Risk Factors (Excluding Hormone Replacement Therapy) for Endometrial
complex (non-atypical) EH were significantly lower [7]. Hyperplasia: A Systematic Review. Epidemiol 6: 229. doi:10.4172/2161-
1165.1000229
Given the potential for neoplastic progression, treatment options
for EH include hysterectomy, and hormonal therapies; occasionally Copyright: 2016 Sanni OB et al., This is an open-access article distributed under
the terms of the Creative Commons Attribution License, which permits unrestricted
watchful waiting is adopted for EH without atypia [8]. The need for use, distribution, and reproduction in any medium, provided the original author and
such interventions, and potential psychological distress for women source are credited.

Epidemiol
ISSN: 2161-1165 Epidemiol, an open access journal Volume 6 Issue 2 1000229
Citation: Sanni OB, Kunzmann AT, Murray LJ, McCluggage WG, Coleman HG (2016) Risk Factors (Excluding Hormone Replacement Therapy) for
Endometrial Hyperplasia: A Systematic Review. Epidemiol 6: 229. doi:10.4172/2161-1165.1000229

Page 2 of 15

enzyme aromatase [14]. Given the predominant role of hormones held between three reviewers (LJ, HC, OS) to resolve any discrepancies.
in the development of EH, a Cochrane review on hormone therapy The full protocol for this review can be found at http://www.crd.
in postmenopausal women which included 45 trials and 38,702 york.ac.uk/PROSPERO/display_record.asp?ID=CRD42015016569#.
participants found that unopposed oestrogen is associated with an VRfpRJMe5ME. Relevant information about study design, number of
increased risk of EH with relative risks of 3.20 (95% CI 2.02 5.26) and cases, controls or cohort size, menopausal status of the study population,
10.09 (95% CI 4.90 20.80) for moderate and high doses of oestrogen age, and method used to diagnose EH, control definition, method used
respectively, although this increased risk was not observed with low to measure exposure and adjusted confounders were extracted from
doses of hormone replacement therapy (HRT) use [13]. full text articles. The Newcastle Ottawa Scale coding manual was used
to assess quality of each study. Some studies reported EH risk as part
Similar to known risk factors for endometrial cancer [15], it is
of a combined EH and endometrial cancer risk estimate, and were
possible that demographic and modifiable factors such as age, parity,
retained for inclusion in the systematic review, and sensitivity analysis
oral contraceptive use, body fatness, physical activity, smoking and
conducted removing such studies from overall pooled estimates.
co-morbidities may play an aetiological role in the development of EH
Studies that compared risk between different types of EH, and not
[1,12,16]. The aim of this systematic review and meta-analyses is to
in comparison with a true control group that did not have EH, were
quantify the association between risk factors (excluding HRT, since this
excluded. Attempts were made to retrieve additional information where
is incorporated in a Cochrane review 13 and development of EH.
required from a number of authors via e-mail contact [17-22].
Materials and Methods Statistical analysis
Search strategy Statistical analyses were conducted with STATA version 13
Three electronic databases namely MEDLINE (US National Library (StataCorp, College Station, TX, USA). Unadjusted and maximally
of Medicine, Bethesda, Maryland), EMBASE (Reed Elsevier PLC, adjusted relative risk (RR) estimates and corresponding 95% confidence
Amsterdam, Netherlands), and Web of Science (Thomson Reuters, intervals (CI) were extracted from published articles where possible.
USA) were systematically searched from inception up to 30 June 2015 Random-effects models were used to derive pooled RRs [23] and CI.
for relevant studies that included one or more keyword(s) or Medical It was decided a priori to perform meta-analyses where at least three
Subject Heading from each of the following groups of terms: studies had reported risk estimates for a particular risk factor. When
applying these criteria we were able to conduct meta-analyses of EH
(i) endometrial hyperplasia, simple endometrial hyperplasia, risk comparing high versus low for body mass index (BMI), smoking,
complex endometrial hyperplasia, complex hyperplasia with atypia, hypertension, and diabetes.
simple hyperplasia with atypia, complex atypical endometrial
hyperplasia, simple atypical endometrial hyperplasia; Sensitivity analyses were conducted for EH risk in relation to BMI
and diabetes removing individual studies; this was not possible for
(ii) risk factor(s), causality, association, predisposing factor(s), pre- other risk factors as too few studies reported these. Sub-group analysis
disposing factor(s), parity, obesity, history of diabetes, ethnicity, race, was performed where possible for EH with or without atypia in relation
socio-economic status, occupation, education, oral contraceptive use, to BMI, diabetes and hypertension. We also assessed heterogeneity
tamoxifen use, NSAID use, aspirin use, age at first birth, miscarriage of studies included in meta-analyses using the I2 statistic [24,25]; I2
history, age at menarche, alcohol, smoking, PCOS, polycystic ovarian values of 25%, 50% and 75% are typically interpreted as low, moderate
syndrome, family history of cancer, personal history of cancer, and high heterogeneity respectively. We investigated the likelihood
medications, BMI, body mass index, waist circumference, body weight, of publication bias using the Eggers test [26,27]. Combined RR were
diet, body fatness, waist-hip ratio, physical activity, use of fertility calculated before entry into final meta-analyses for studies that reported
treatments. separate EH risk estimates only by different types of EH or different age
Review articles and animal studies were excluded and no language categories. Specifically, one study reported separate EH risk estimates
restriction was applied. for complex EH and atypical EH [28].

Data extraction Results

Titles and abstracts for potentially relevant articles were After application of our search strategy in the three databases,
independently screened by two of three reviewers (OS, LM and HC). and removal of duplicates, a total of 2,890 titles and abstracts were
Then two reviewers (OS and HC) independently screened full text reviewed in the first instance to determine potentially relevant studies
articles for the remaining studies to identify relevant studies that meet for inclusion. After title and abstract review, 79 full text articles and
the pre-set inclusion criteria for the systematic review: abstracts were reviewed, and 15 full text articles were retained in the
review (Figure 1). Included articles assessed lifestyle factors, menstrual
(i) Participants: Women aged 18 and above. history, age, medical history, reproductive history and socio-economic
(ii) Interventions: Measurement of risk factors (excluding HRT) factors and their relationship with risk of developing EH.
in the study population. Lifestyle factors
(iii) Comparators: Women without a diagnosis of EH. BMI
(iv) Outcome: Risk of EH. Eight studies examined BMI and risk of EH [12,28-34]. Four were
The full text of the remaining articles were independently screened case-control studies [12,28,30,32], two were cohort studies [31,34]
by two reviewers (OS and HC) to identify relevant studies that meet the and two were cross-sectional studies [29,33]. Characteristics of these
pre-set inclusion criteria for the systematic review. Articles reporting on studies are fully described in Table 1.
less than 10 cases of EH were excluded from the review. Meetings were Six studies [12,28,29,32-34] provided or allowed unadjusted RRs

Epidemiol
ISSN: 2161-1165 Epidemiol, an open access journal Volume 6 Issue 2 1000229
Citation: Sanni OB, Kunzmann AT, Murray LJ, McCluggage WG, Coleman HG (2016) Risk Factors (Excluding Hormone Replacement Therapy) for
Endometrial Hyperplasia: A Systematic Review. Epidemiol 6: 229. doi:10.4172/2161-1165.1000229

Page 3 of 15

Potentially relevant papers identified Potentially relevant papers identified Potentially relevant papers identified through
through search of MEDLINE (n = 926) through search of EMBASE (n = 1721) search of WEB OF SCIENCE (n = 1350)

Number of titles and abstracts assessed for eligibility, after removal of duplicates
(n= 2890 )

Number of full text articles assessed for eligibility (n=79)

Reasons for exclusion (n=64):

Less than 10 cases of EH = 9
Review article = 2
Duplicate report = 3
EH risk not assessed = 31
No comparison/control group = 15
Only HRT use assessed as risk factor = 1
Article could not be retrieved = 3

Number of articles included in systematic review after application of exclusion criteria

(n= 15); comprising
Lifestyle factors (n=14)*
BMI = 8
Body weight = 1
Quetelet index = 1
Smoking = 3
Physical activity = 1
Medical history (n = 8)*
Diabetes = 5
Hypertension = 4
History of cancer = 2
Reproductive factors and Menstrual history (n = 8)*
Oral contraceptives use = 2
Parity = 4
Menopausal status = 2
Intermenstrual interval = 1
Other
Education and Income = 2
Age = 2

Figure 1: Flow diagram of study selection.

to be calculated, and the pooled RR for EH when comparing women Smoking

with the highest versus lowest BMI was 1.84 (95%CI: 1.18-2.88) with
Two population-based [28,37,38] and one hospital-based 12 case-
I2 62.9%. Results from seven studies [12,28-31,33,34] were pooled to
control studies examined the relationship between smoking and risk of
derive maximally adjusted EH risk estimates for the highest versus
EH. Descriptions of study characteristics are shown in Table 4.
the lowest category of BMI. As shown in Figure 2, high BMI was
significantly associated with an increased EH risk (RR 1.82, 95%CI: Results from these three studies were pooled to derive an unadjusted
1.22-2.71) with an I2 of 90.4%. Eggers test showed no significant EH risk estimate of 0.98 (95%CI 0.64-1.49) with I2 45.7% for smokers
evidence of publication bias (p=0.18). Heterogeneity remained compared with non-smokers. Adjusted pooled risk estimate was 0.88
consistently high after removal of individual studies, this may be due (95%CI 0.66-1.17) with 0% heterogeneity for smokers when compared
to the variability of adjusted confounders across studies (Table 2). Only with non-smokers (Figure 3).
the exclusion of Balbi et al. [30] reduced heterogeneity somewhat and
The moderate heterogeneity among studies disappeared after
markedly affected results. This study investigated simple EH risk only,
adjusting for confounders. However, only one study adjusted for HRT,
and sub-group analysis between BMI and EH without atypia resulted
and two adjusted for BMI as shown in Table 4.
in a non-significant positive association (RR 1.27, 95%CI 0.49-3.59)
(Table 3). Physical activity
Other body fatness measures One Italian hospital-based case-control study 30 reported non-
significant increased risk of EH (OR 1.38 95%CI 0.503.77) among
Two studies have investigated other body fatness measures and EH
women who reported high levels of physical activity (60 minutes 3
risk, as summarised in Tables 1 and
times/week) when compared with those who reported lower levels of
One study among premenopausal women with abnormal menstrual physical activity (Tables 1 and 4).
bleeding reported a significant 7fold increased risk for complex
Medical history
atypical EH and endometrial carcinoma combined (OR 7.3, 95%CI
3.216.8), comparing body weight >90kg versus <90kg [35]. Diabetes
In a further study, the Quetelet index was reported to be significantly Five studies evaluated the relationship between diabetes and EH
higher in postmenopausal EH cases, compared with controls, leading to risk. Three were hospital-based case-control [12,30,34], one was a
an increased risk (OR 3.8, 95%CI 1.2711.40) when comparing >2.9 population-based case-control,28 and one was a prospective cohort
versus 2.9. In contrast, a protective effect for premenopausal women study [39]. Characteristics of the studies are shown in Table 5.
was noted (OR 0.25, 95% CI 0.070.95) [36]. Three studies [12,28,38] were included in meta-analysis in order
to derive unadjusted pooled EH risk estimate for diabetic versus

Epidemiol
ISSN: 2161-1165 Epidemiol, an open access journal Volume 6 Issue 2 1000229
 No. Age, years
Author, Year, No. Controls/ Menopausal (range) Case definition Method of
Study design Method of Adjusted Quality scale
Location Cases cohort status Cases/ Control definition measuring
including EH type diagnosis confounders score (max. 9)

Epidemiol
size Controls body fatness

Body Mass Index

Women attending
Balbi et al. Interview,
Hospital-based gynaecologic unit Age, hypertension,
(2012) [29], 167 282 Pre-menopausal Confirmed by 1 medical history,
case-control 40-55 Simple EH of 2 hospitals diabetes, physical 7
Italy pathologist general physical
for menstrual activity
examination
irregularities
Age, endometrial
Cheung et al. Consecutive thickness, average
Simple or complex Histologically
(2001) [30], Case-control 45 36 Pre-menopausal 23-41/21-39 women with PCOS inter-menstrual
EH with or without confirmed by Not reported 5
Canada and infertility due interval, menses
atypia pathologist
to anovulation biopsy interval, last
OC use.

ISSN: 2161-1165 Epidemiol, an open access journal

Obese
Cymbaluk et postmenopausal
Hospital-based Curettage or
al.(2006) [31], 14 46 Post -menopausal 56.3/54.8[1] EH with atypia women referred for Not reported Not reported 4
case-control hysteroscopy
Poland post-menopausal
bleeding
Epplein et Population- Randomly selected
Pre- and post- Histologically
al.(2008) [27], based case- 45 Complex EH or EH from the same Menopausal status,
446 18 confirmed by 3 Not reported 7
USA menopausal with atypia health plan as parity
control pathologists
cases
Non
Ricci et hysterectomized
Hospital-based Pre- and post- Histologically women selected Self-reported,
al.(2002) [12] 129 258 35-74 Complex EH Age, education 5
case-control menopausal confirmed form hospitals Questionnaire
Italy
covering the same
area as cases

Histologically Pregnancy, severe

Shan et al. Simple or complex Height and infection, CVD, breast
(2014) [28] Cross-sectional 194 39 Pre-menopausal confirmed
18-35 EH with or without Not reported weight measured cancer, reproductive 7
China by at least 2
atypia to calculate BMI cancers , HRT use,
pathologists
age, menopause
Topcu et
Retrospective Pre- and EH with or without Histologically
al.(2014) [33], 13 203 41-69/ 40-84 Not reported Not reported Not reported 7
cohort postmenopausal atypia confirmed
Turkey
Steroid hormone
Viola et al. Simple or complex use, tamoxifen use,
Pre- and Weight and
(2007) [32], Cross-sectional 10 177 18-70 EH with or without Not reported history of ovarian
Not reported height measured 6
Endometrial Hyperplasia: A Systematic Review. Epidemiol 6: 229. doi:10.4172/2161-1165.1000229

Brazil postmenopausal or endometrial

atypia to calculate BMI
tumour, history of
endometriosis
Quetelet Index
Kreiger et al. Population- Randomly selected
(1986) [35], Pre- and post- Adenomatous Confirmed by 3 from same
based case- 149 248 40-74 Not reported Menopausal status 6
Canada menopausal hyperplasia pathologists neighbourhood as
control
cases
Body weight
Farquhar et Simple or complex Histologically
Retrospective Patient record
al. (1999) [34], 46 1033 Pre-menopausal 17-50 EH with or without confirmed by Not reported Not reported 4
cohort review
New Zealand atypia pathologist

Table 1: Characteristics of studies included in the systematic review of Endometrial Hyperplasia and risk factor: body fatness.

Volume 6 Issue 2 1000229

Page 4 of 15
Citation: Sanni OB, Kunzmann AT, Murray LJ, McCluggage WG, Coleman HG (2016) Risk Factors (Excluding Hormone Replacement Therapy) for
Citation: Sanni OB, Kunzmann AT, Murray LJ, McCluggage WG, Coleman HG (2016) Risk Factors (Excluding Hormone Replacement Therapy) for
Endometrial Hyperplasia: A Systematic Review. Epidemiol 6: 229. doi:10.4172/2161-1165.1000229

Page 5 of 15

Number of studies included References Pooled risk estimate (95% CI) I-squared (%) p-value
Body mass index
Unadjusted 6 (12,27-30,32) 1.84 (1.18 2.88) 62.9 0.02
Adjusted, excluding Balbi et al. [29] 6 (12,27,28,30,32,33) 1.20 (0.97 1.49) 60.8 0.03
Adjusted, excluding Ricci et al. [12] 6 (27-30,32,33) 1.88 (1.21 2.93) 91.9 0
Adjusted, excluding Epplein et al. [27] 6 (12,28-30,32,33) 1.78 (1.16 2.74) 91.6 0
Adjusted, excluding Cheung et al. [30] 6 (12,27-29,32,32) 2.29 (1.10 4.74) 88.6 0
Adjusted, excluding Shan et al. [28] 6 (12,27,29,30,32,33) 2.21 (0.96 5.07) 91.8 0
Adjusted, excluding Viola et al. [32] 6 (12,27-30,33) 1.78 (1.19 2.67) 91.9 0
Adjusted excluding Topcu et al. [33] 6 (12,27-30,32) 1.80 (1.19 2.71) 91.9 0
EH without atypia only 3 (12,27,28) 1.27 (0.49 3.59) 0 0.9
Smoking
Unadjusted 3 (12,27,36) 0.98 (0.64 1.49) 45.7 0.16
Diabetes
Unadjusted 3 (12,27,38) 1.43 (0.79 2.57) 0 0.96
Adjusted, excluding Ricci et al. [12] 4 (27,29,33,38) 1.48 (0.47 4.64) 46.3 0.13
Adjusted, excluding Balbi et al. [29] 4 (12,27,33,38) 1.89 (0.82 4.37) 40.6 0.17
Adjusted, excluding Epplein et al. [27] 4 (12,29,33,38) 2.31 (1.10 4.85) 11.6 0.34
Adjusted, excluding Gol et al. [38] 4 (12,27,29,33) 1.89 (0.64 5.52) 43.8 0.15
Adjusted, excluding Topcu et al. [33] 4 (12,27,29,38) 1.37 (0.66 2.82) 0 0.43
EH without atypia only 3 (12,27,38) 1.32 (0.31 5.70) 0 0.78
Hypertension
Unadjusted 3 (12,27,39) 1.33 (0.76 2.30) 68.5 0.04
Atypical EH only 3 (27,38,39) 1.92 (0.57 6.53) 70.3 0.04
EH without atypia only 3 (12,27,38) 1.17 (0.39 3.45) 0 0.96
Table 2: Summary of unadjusted, subgroup and sensitivity analyses excluding individual studies from meta-analyses.

Study Comparison OR (95% CI) Weight

Epplein et al, 2008 Current vs Never 0.72 (0.42, 1.22) 28.93

Ricci et al, 2002 Ever vs Never 1.11 (0.70, 1.73) 39.87

Weir et al, 1994 Ever vs Never 0.80 (0.48, 1.34) 31.20

Overall (I-squared = 0.0%, p = 0.435) 0.88 (0.66, 1.17) 100.00

.5 .75 1 1.5 2

Figure 2: Adjusted meta-analysis for highest versus lowest category of BMI and EH risk.

when the study by Epplein et al. [28] was excluded. Heterogeneity

non-diabetic women (RR 1.43, 95%CI 0.792.57; I2=0%). Five studies
however ranged from low to moderate throughout. Sub-group analysis
[12,28,30,34,38] were included in meta-analyses to derive adjusted pooled
by EH type showed non-significant positive association between EH
EH risk estimate (RR 1.77, 95%CI 0.793.96; I2=31.8%), as shown in Figure
without atypia and diabetes (RR 1.32, 95%CI 0.31-5.70) (Table 2). Two
4. Eggers test showed no significant evidence of publication bias (p=0.34).
studies reported adjusting for BMI while none adjusted for HRT use as
While risk estimates remained non-significant for the most part shown in Table 5.
of sensitivity analyses, a significant positive association was observed

Epidemiol
ISSN: 2161-1165 Epidemiol, an open access journal Volume 6 Issue 2 1000229
Citation: Sanni OB, Kunzmann AT, Murray LJ, McCluggage WG, Coleman HG (2016) Risk Factors (Excluding Hormone Replacement Therapy) for
Endometrial Hyperplasia: A Systematic Review. Epidemiol 6: 229. doi:10.4172/2161-1165.1000229

Page 6 of 15

No. of
Risk factor References Study design Summary of results
studies
n=1 study reported increased risk of complex EH with atypia amongst women weighing 90kg when
Body weight 1 34 Retrospective cohort
compared with women weighing <90kg.
Population-based
Quetelet index 1 35 n=1 study reported significant higher waist-hip ratio in EH cases when compared with controls.
case-control
Hospital-based case- n=1 study reported non-significant increased risk of EH amongst women who reported higher levels
Physical activity 1 29
control of physical activity.
1 hospital-based n=1 study reported non-significant 20% reduced risk of EH amongst women with a family history of
History of cancer 2 12,34 case-control, EC.
1 retrospective n=1 study reported significant increased risk of EH amongst women with a family history of EC or
cohort study colon cancer
1 population-based
n=1 study reported a reduced risk of complex and atypical EH amongst women used OC 6months
Oral contraceptive case-control, 1
2 12,27 prior to abnormal vaginal bleeding.
use hospital-based case-
n=1 study reported non-significant increased risk of EH amongst women who had ever used OC
control
compared with never-users.

1 population-based
n=1 study reported significant reduced risk of EH amongst women who had given birth to 3 or more
case-control, 1
Parity 2 12,27 children in comparison with women who had never given birth.
hospital-based case-
n=1 study reported non-significant increase in risk of EH amongst women who had given birth to 2
control
or more children in comparison with nulliparous women.

1 hospital-based
n=1 study reported significant increased risk of EH or EC amongst nulliparous women in
case-control, 1
Nulliparity 2 34,37 comparison with multiparous women.
retrospective cohort
n=1 study reported significant increased risk of EH amongst nulliparous women in comparison with
study
multiparous women

n=1 study reported a non-significant reduced risk of non-atypical EH among post-menopausal

1 hospital-based
women when compared with pre-menopausal women but non-significant increased risk of atypical
Menopausal status 2 12,28 case-control, 1
EH was reported for postmenopausal women compared with pre-menopausal women.
cross-sectional study
n=1 study reported a significant reduced risk of complex amongst post-menopausal women in

comparison with pre- and peri-menopausal women.

1 hospital-based
Education and
2 12,35 case-control, 1 n=1 study reported higher level of education amongst EH cases compared with controls.
Income
population-based n=1 study reported higher income for EH cases compared with controls.

case-control study

n=1 study reported significant increased risk of EH or EC amongst women 70 years compared
2 hospital-based
Age 2 12,37 with women 49-59 years old.
case-control studies
n=1 study reported non-significant reduced risk of EH amongst women 65years in comparison with

women <45years old.

Table 3: Summary of results for risk factors for EH for which meta-analyses were not possible.

Hypertension Women with a family history of endometrial cancer were reported

Four studies [12,28,30,39] reported on hypertension in relation to by Ricci et al. [12] to have around 20 percent reduced risk of developing
EH risk. Characteristics of the studies are shown in Table 5. EH , although not statistically significant (OR 0.8 95% CI 0.2 2.6).
Another study found women with abnormal bleeding who had a family
Three studies [12,28,39] were included in meta-analysis to derive an history of colon cancer or endometrial cancer to be more likely to
unadjusted pooled risk estimate of OR 1.33 (95%CI 0.762.30; I2=68.5%), develop endometrial cancer or complex EH with atypia (OR 9.1, 95%CI
and four studies [12,28,30,39] were included in meta-analysis to derive 2.2 37.1;OR 5.8, 1.1 28.6, respectively) [35]. (Tables 1 and 5). None
adjusted pooled risk estimate of OR 1.51 (95%CI 0.723.15; I2=79.1%) for of the studies reported adjusting for BMI or HRT use as shown in Table
hypertensive versus normotensive women (Figure 5). Eggers test showed 5.
no significant evidence of publication bias (p=0.28).
Reproductive factors
Sub-group analyses showed non-significant positive associations
between atypical EH (RR 1.92 95%CI 0.57-6.53) and EH without atypia Oral contraceptive use
(RR 1.17 95%CI 0.39-3.45) (Table 2) and hypertension status; only the Two studies [12,40] examined the relationship between oral
latter showed reduced heterogeneity. Two studies adjusted for BMI contraceptive use and the risk of developing EH (Table 6). One
while one reported adjusting for HRT as shown in Table 5. population-based case-control study reported a reduced risk of
Family History of cancer complex and atypical EH among women who had used OC 6 months
before presenting with abnormal bleeding (OR 0.2, 95%CI 0.00.6) after

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ISSN: 2161-1165 Epidemiol, an open access journal Volume 6 Issue 2 1000229
Citation: Sanni OB, Kunzmann AT, Murray LJ, McCluggage WG, Coleman HG (2016) Risk Factors (Excluding Hormone Replacement Therapy) for
Endometrial Hyperplasia: A Systematic Review. Epidemiol 6: 229. doi:10.4172/2161-1165.1000229

Page 7 of 15

Age, Quality
No. Case
Author, years Method of scale
Study No. Controls/ Menopausal definition Method of Adjusted
Year, (range) Control definition measuring score
design Cases cohort status including EH diagnosis confounders
Location Cases/ body fatness (max.
size type
Controls 9)
Smoking
Epplein
Population- Histologically
et Pre- and Complex EH Randomly selected Menopausal
based confirmed Medical record
al.(2008) 45 446 post- 18 or EH with from the same health status, BMI, 7
case- by 3 review
[27], menopausal atypia plan as cases parity
control pathologists
USA
Ricci et Hospital- Non hysterectomized
Pre- and
al.(2002) based Histologically women selected form Self-reported,
129 258 post- 35-74 Complex EH Age, education 5
[12], case- confirmed hospitals covering the Questionnaire
menopausal
Italy control same area as cases
Weir et Population- Histologically Randomly selected
Pre- and
al.(1994) based Adenomatous confirmed from same Age, obesity,
177 530 post- 40-74 Interview 6
[36], case- hyperplasia by 3 neighbourhood as oestrogen use
menopausal
Canada control pathologists cases
Physical activity
Balbi et Hospital- Women attending Interview,
Age,
al.(2012) based Pre- Confirmed by gynaecologic unit of 2 medical history,
167 282 40-55 Simple EH hypertension, 7
[29], case- menopausal 1 pathologist hospitals for menstrual general physical
BMI, diabetes
Italy control irregularities examination
Table 4: Characteristics of studies included in the systematic review of Endometrial Hyperplasia and risk factor: smoking and physical activity.

Study Comparison OR (95% CI) Weight

Epplein et al, 2008 Current vs Never 0.72 (0.42, 1.22) 28.93

Ricci et al, 2002 Ever vs Never 1.11 (0.70, 1.73) 39.87

Weir et al, 1994 Ever vs Never 0.80 (0.48, 1.34) 31.20

Overall (I-squared = 0.0%, p = 0.435) 0.88 (0.66, 1.17) 100.00

.5 .75 1 1.5 2

Figure 3: Adjusted meta-analysis for highest versus lowest category of smoking and EH risk.

adjusting for BMI. However, a non-significant increased risk of EH was with nulliparous women, Ricci et al. [12] found an almost significant
found in another study among women who had ever used OC versus 2-fold (OR 1.8, 95%CI 0.93.6) increase in risk of complex EH (Table
those who had never used OC (OR 1.6, 95%CI 0.92.8) [12] (Table 1). 1) after adjusting for age and education [12]. In contrast, Epplein et
The authors further assessed OC use and EH risk by duration of use and al. [28], found significant reduced risk (OR 0.29, 95% CI 0.070.51) of
consistently found non-significant increased risks when they compared EH among women who had given birth to three or more babies when
women who had used OC for more than 5 years, 1360 months, 12 compared with nulliparous women, after adjusting for BMI [28].
years or less with never users (OR 1.2, 95%CI 0.43.4;OR 1.4, 95%CI
Two studies which compared nulliparous women with multiparous
0.53.6; and OR 2.0, 0.94.3, respectively). It should however be noted
women found a significant increased risk of EH in nulliparous women
that BMI or HRT use was not adjusted for in the latter as shown in Table 6.
(OR 3.7, 95%CI 1.2-10.9) 35 and (OR 2.8, 95% CI 1.3-6.1) (after
Parity adjusting for prior use of oestrogen) [41], respectively. Meta-analysis
was not performed for these four studies, summarised in Table 6, due
When comparing women who had given birth to two or more babies

Epidemiol
ISSN: 2161-1165 Epidemiol, an open access journal Volume 6 Issue 2 1000229
 No. Age, years Quality
Case definition
Author, Year, No. Controls/ (range) Method of Method of measuring Adjusted scale
Study design Menopausal status including EH Control definition
Location Cases cohort Cases/ diagnosis medical history confounders score
type

Epidemiol
size Controls (max. 9)
Diabetes

Women attending
Balbi et
Hospital-based Confirmed by gynaecologic unit of 2 Interview, medical history, Age, BMI, physical
al.(2012) 167 282 Pre-menopausal 40-55 Simple EH 7
case-control 1 pathologist hospitals for menstrual general physical examination activity
[29], Italy
irregularities

Epplein et Population- Histologically Randomly selected from

Pre- and post- Complex EH or Menopausal status,
al.27 (2008) based case- 45 446 18 confirmed by the same health plan as Medical record review 7
menopausal EH with atypia BMI, parity
[27], USA control 3 pathologists cases
Gol et
EH with or Confirmed by
al.(2001) Cohort 30 556 Post-menopausal 52.56.6 Not reported Not reported Not reported 5
without atypia pathologist

ISSN: 2161-1165 Epidemiol, an open access journal

[38], Turkey
Non hysterectomized
Ricci et
Hospital-based Pre- and post- Histologically women selected form
al.(2002) 129 258 35-74 Complex EH Self-reported, Questionnaire Age, education 5
case-control menopausal confirmed hospitals covering the
[12], Italy
same area as cases
Topcu et
Retrospective Pre- and EH with or Histologically
al.(2014) 13 203 41-69/ 40-84 Not reported Not reported Not reported 7
cohort postmenopausal without atypia confirmed
[33], Turkey
Hypertension
Women attending
Balbi et
Hospital-based Confirmed by gynaecologic unit of 2 Interview, medical history, Age, BMI, physical
al.(2012) 167 282 Pre-menopausal 40-55 Simple EH 7
case-control 1 pathologist hospitals for menstrual general physical examination activity
[29], Italy
irregularities
Epplein et Population- Histologically Randomly selected from
Pre- and post- Complex EH or Menopausal status,
al.(2008) based case- 45 446 18 confirmed by the same health plan as Medical record review 7
menopausal EH with atypia BMI, parity
[27], USA control 3 pathologists cases
Non hysterectomized
Ricci et al.
Hospital-based Pre- and post- Histologically women selected form
(2002) [12], 129 258 35-74 Complex EH Self-reported, Questionnaire Age, education 5
case-control menopausal confirmed hospitals covering the
Italy
same area as cases
Vorgias et al. Women who underwent Blood pressure 150/100
Hospital-based Dilatation and HRT use, obesity,
(2005) [39], 60 45 Post-menopausal 48-83 Not reported D&C at a tertiary cancer mmHg, or daily use of 5
case-control curettage tamoxifen use
Greece hospital antihypertensive medications
Endometrial Hyperplasia: A Systematic Review. Epidemiol 6: 229. doi:10.4172/2161-1165.1000229

Table 5: Characteristics of studies included in the systematic review of Endometrial Hyperplasia and risk factor: medical history (diabetes, hypertension).

Volume 6 Issue 2 1000229

Page 8 of 15
Citation: Sanni OB, Kunzmann AT, Murray LJ, McCluggage WG, Coleman HG (2016) Risk Factors (Excluding Hormone Replacement Therapy) for
 No. Age, years
Author, Method of Quality scale
Controls/ Menopausal (range) Case definition Method of
Year, Study design No. Cases Control definition measuring medical Adjusted confounders score (max.
cohort status Cases/ including EH type diagnosis
Location history 9)

Epidemiol
size Controls
Reproductive factors

Age, race, ZIP code,

Epplein et al. Population- Histologically Randomly selected
Pre- and post- Complex EH or EH Dispensed years enrolled in Group
(2009) [39], based case- 45 462 18 confirmed by from the same health 7
menopausal with atypia prescription record Health, BMI, diabetes,
USA control 3 pathologists plan as cases
hypertension, smoking

Farquhar
Histologically
et al. Retrospective Simple/complex EH
46 1033 Pre-menopausal 17-50 confirmed by Not reported Patients' records Not reported 4

ISSN: 2161-1165 Epidemiol, an open access journal

(1999) [34], cohort with/without atypia
pathologist
New Zealand
Age 70,prior use of
Women who
oestrogen,hypertension,
Feldman et Hospital- received benign Structured
Pre- and Pathologic diabetes,menopause,
al. (1995) based case- 16 151 61.4/56.0[2] Complex EH diagnosis following questionnaire, 5
postmenopausal diagnosis nulliparity,history of non-
[40], USA control biopsy for abnormal interview
breast cancer,quetelet
vaginal bleeding
index
Non hysterectomized
Ricci et Hospital- women selected
Pre- and post- Histologically Self-reported,
al.(2002), based case- 129 258 35-74 Complex EH from hospitals Age, education 5
menopausal confirmed Questionnaire
[12] Italy control covering the same
area as cases
Menstrual history

Age, endometrial
Consecutive women
Cheung et al. Simple or complex Histologically thickness, average
with PCOS and
(2001) [30], Case-control 45 36 Pre-menopausal 23-41/ 21-39 EH with or without confirmed by Not reported inter-menstrual interval, 5
infertility due to
Canada atypia pathologist menses biopsy interval,
anovulation
last OC use.

Non hysterectomized
Ricci et Hospital- women selected
Pre- and post- Histologically Self-reported,
Endometrial Hyperplasia: A Systematic Review. Epidemiol 6: 229. doi:10.4172/2161-1165.1000229

al.(2002) based case- 129 258 35-74 Complex EH form hospitals Age, education 5
menopausal confirmed Questionnaire
[12], Italy control covering the same
area as cases
Pregnancy, severe
Histologically infection, CVD, history
Shan et Simple or complex Height and weight
Cross- confirmed of breast cancer,
al.(2014), 194 39 Pre-menopausal 18-35 EH with or without Not reported measured to 7
sectional by at least 2 malignancies in the
[28] China atypia calculate BMI
pathologists reproductive system,
HRT use, age, BMI
Table 6: Characteristics of studies included in the systematic review of Endometrial Hyperplasia and risk factor: reproductive factors (oral contraceptive use and parity) and menstrual history (menopausal status
and age at menopause).
1
Investigated oral contraceptive use and parity
2
Mean
3
Investigated menopausal status and age at menopause
4
Investigated menopausal status

Volume 6 Issue 2 1000229

Page 9 of 15
Citation: Sanni OB, Kunzmann AT, Murray LJ, McCluggage WG, Coleman HG (2016) Risk Factors (Excluding Hormone Replacement Therapy) for
Citation: Sanni OB, Kunzmann AT, Murray LJ, McCluggage WG, Coleman HG (2016) Risk Factors (Excluding Hormone Replacement Therapy) for
Endometrial Hyperplasia: A Systematic Review. Epidemiol 6: 229. doi:10.4172/2161-1165.1000229

Page 10 of 15

Study OR (95% CI) Weight

Balbi et al, 2012 3.19 (1.20, 8.48) 20.61

Epplein et al, 2008 0.66 (0.40, 1.10) 27.97

Ricci et al, 2002 1.20 (0.60, 2.40) 25.13

Vorgias et al, 2005 2.51 (1.35, 4.66) 26.29

Overall (I-squared = 79.1%, p = 0.002) 1.51 (0.72, 3.15) 100.00

.5 1 2 4 8

Figure 4: Adjusted meta-analysis comparing women with hypertension with normotensive women in relation to EH risk.

Study OR (95% CI) Weight

Balbi et al, 2012 3.19 (1.20, 8.48) 20.61

Epplein et al, 2008 0.66 (0.40, 1.10) 27.97

Ricci et al, 2002 1.20 (0.60, 2.40) 25.13

Vorgias et al, 2005 2.51 (1.35, 4.66) 26.29

Overall (I-squared = 79.1%, p = 0.002) 1.51 (0.72, 3.15) 100.00

.5 1 2 4 8

Figure 5: Adjusted meta-analysis comparing women with hypertension with normotensive women in relation to EH risk.

to differences in the reference groups analysed. While two studies likely to develop EH without atypia (OR 0.65, 95%CI 0.172.50) but
Farquhar et al and Feldman et al used multiparous women as reference they were more likely to develop EH with atypia (OR 2.40, 95%CI
group, Epplein et al and Ricci et al. [12] used nulliparous women as 0.4313.27) when compared with premenopausal women, although
reference group. these estimates did not achieve statistical significance. Similarly,
another study 12 also reported a significant reduced risk of complex
Menstrual history
EH among postmenopausal women in comparison with pre- and peri-
Menopausal status menopausal women (OR 0.2, 95%CI 0.10.5). The authors also found
a non-significant 20% increased risk of complex EH among women
Two hospital-based case-control studies [12,29] evaluated
who reported menopause at 53 years versus <50 years at menopause
menopausal status in relation to EH risk (Table 6). One study among
[12] (Table 1). One of the studies reported adjusting for BMI and HRT
Chinese women 29 found that postmenopausal women were less
use as shown in Table 6. One further study suggested that polycystic

Epidemiol
ISSN: 2161-1165 Epidemiol, an open access journal Volume 6 Issue 2 1000229
 No. Case
Author, Age, years Method of Quality scale
Study Controls/ Menopausal definition Method of
Year, No. Cases (range) Cases/ Control definition measuring Adjusted confounders score (max.
design cohort status including EH diagnosis
Location Controls medical history 9)

Epidemiol
size type
Age
Women who
received benign Prior use of oestrogen,
Feldman et Hospital- Structured
Pre- and post- Pathologic diagnosis hypertension, diabetes,
al.(1995) based case- 16 151 61.4/56.0[1] Complex EH questionnaire, 6
menopausal diagnosis following biopsy for menopause, nulliparity, history of
[40], USA control interview
abnormal vaginal non-breast cancer, quetelet index
bleeding

Non
hysterectomized
Ricci et Hospital-

ISSN: 2161-1165 Epidemiol, an open access journal

Pre- and post- Histologically women selected Self-reported,
al.(2002) based case- 129 258 35-74 Complex EH Education 5
menopausal confirmed form hospitals Questionnaire
[12], Italy control
covering the same
area as cases

Socio-economic status
Kreiger et Randomly selected
Population-
al.(1986) Pre- and post- Adenomatous Confirmed by 3 from same
based 149 248 40-74 Self-reported Menopausal status 6
[35], menopausal hyperplasia pathologists neighbourhood as
case-control
Canada cases
Non
hysterectomized
Ricci et Hospital-
Pre- and post- Histologically women selected Self-reported,
al.(2002) based case- 129 258 35-74 Complex EH Age 5
menopausal confirmed form hospitals Questionnaire
[12], Italy control
covering the same
area as cases

Table 7: Characteristics of studies included in the systematic review of Endometrial Hyperplasia and risk factor: Age and Socio-economic status (income and education).
Endometrial Hyperplasia: A Systematic Review. Epidemiol 6: 229. doi:10.4172/2161-1165.1000229

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Page 11 of 15
Citation: Sanni OB, Kunzmann AT, Murray LJ, McCluggage WG, Coleman HG (2016) Risk Factors (Excluding Hormone Replacement Therapy) for
Citation: Sanni OB, Kunzmann AT, Murray LJ, McCluggage WG, Coleman HG (2016) Risk Factors (Excluding Hormone Replacement Therapy) for
Endometrial Hyperplasia: A Systematic Review. Epidemiol 6: 229. doi:10.4172/2161-1165.1000229

Page 12 of 15

ovarian syndrome patients with longer intermenstrual intervals have non-significant positive association between hypertension and EH risk.
a significant increased risk of developing EH (OR 1.43, 95%CI 1.78- Some authors have reported that hypertension is positively associated
1.15) after adjusting for confounders including last oral contraceptive with EH 40 or endometrial cancer [42]. However, this association
use [31]. was found among overweight or obese women compared with lean
women [42], this observation should therefore be viewed with caution
Other factors
as it is likely to be confounded, considering the association between
Age obesity and hypertension. Hypertension has previously been linked
to insulin-like growth factor 1 (IGF-1), and measures of body fatness
Two hospital-based case-control studies reported risk estimates for
such as waist-hip ratio and obesity were reported to be higher among
age with regards to EH [12,41]. Characteristics and results from these
hypertensive patients than controls [43,44]. IGF-1 is known to be
studies are shown in Tables 1 and 7 . One study reported a significant
related to cell growth and cancer progression [45].
increased risk of EH or EC amongst women 70 years old versus women
49-59 years old after adjusting for confounders including prior use of We found a non-significant increased EH risk among diabetic
oestrogen, and another study reported a non-significant decreased versus non-diabetic women. Although the mechanism for a potential
risk of EH amongst women 65 years old versus <45 years old. Meta association between diabetes and EH is not very clear, diabetes has been
analyses were not conducted because only two studies [12,41] provided linked to IGF-1 [46]. Low levels of IGF-1were found to be positively
risk estimates for age in relation to development of EH, reports from the associated with diabetes after adjusting for confounders including BMI
studies were mixed (Table 1). One of the studies adjusted for quetelet [46]. In a rat model, Type 1 diabetes was also been shown to induce EH
index, a measure of body fatness as shown in . development, potentially mediated by oestrogen receptor alpha and p16
expression [47]. Several authors have reported overweight/obesity as
Socio-economic status
one of the most important modifiable risk factors for diabetes [48,49].
Two studies [12,36] examined education and income in relation Despite the well-known relationship between obesity and diabetes, few
to EH risk (Table 7). In one study, a positive association was observed of the studies included in our meta-analysis adequately adjusted for this
among women who had 12 compared with <7 years of education (OR confounder.
2.8 95% CI 1.704.80).
Meta-analysis of three studies showed no association between
Similarly, women who earned $30,000 were found to have higher tobacco smoking and risk of EH. An earlier literature review suggested
chances of developing EH when they were compared with women who that smoking has an anti-oestrogenic effect, which can reduce the rate
earned less than $30,000 in a Canadian study (Table 1). The observed of androgen-oestrogen conversion [50]. Smoking has also been linked
association was significant for premenopausal women (OR 1.85, 95%CI to early menopause [51-53]. Women who undergo menopause early are
1.16 2.96) but not for postmenopausal women (OR 1.15, 95%CI 0.78 less exposed to oestrogen than women who are older at menopause.
1.69) [36]. Neither of the studies reported adjusting for HRT use or However, smoking has been consistently linked to the development of
BMI as shown in Table 7. many neoplastic conditions and is certainly not advised [54,55]. It is
plausible that known carcinogenic effects of smoking may be countered
Comment by the aforementioned anti-oestrogenic effect, explaining the observed
Main findings null association for tobacco smoking and EH risk.

In this novel systematic review of risk factors for EH (excluding One study reported a non-significant increased EH risk for women
hormone replacement therapies), meta-analyses suggested a significant with self-reported higher levels of physical activity compared to those
positive association between increased BMI and risk of EH; no who reported lower levels of physical activity. However, as with all self-
significant associations were detected between smoking, hypertension reported information of desirable lifestyle factors, this result should be
or diabetes and EH risk in pooled analyses of a limited number of interpreted with caution. Physical activity has previously been shown
studies. However, there was paucity of high quality, consistent evidence to be protective against endometrial carcinoma, given that physical
for the aforementioned and other factors in the review. There was also activity may modulate metabolism, and excretion of endogenous sex
inadequate adjustment for relevant confounders, namely HRT and hormones such as oestrogen which is also known to be responsible for
BMI, in some of the included studies. development of EH [56]. Interestingly the previously described EH
diabetic rat model did observe a significant reduction in oestrogen-
The importance of pooling risk estimates is demonstrated by the receptor alpha and p16 expression for those rats undertaking aerobic
expected finding that higher BMI is positively associated with EH exercise [48].
compared with lower BMI, considering that only three out of six
studies which reported a positive association between BMI and EH risk Contrasting results were reported for parity and EH risk by
showed statistical significance. EH is an oestrogen-driven disease. From individual studies included in this review, although the majority
a biologically plausible viewpoint, it is well known that oestrogen can reported protective effects of child-bearing for EH risk. Nulliparity is
be synthesized from adipose tissue, this increases the level of circulating known to be associated with an increased risk of endometrial cancer
oestrogen which in turn stimulates growth of the endometrium. [57] - a possible mechanism for this is that during pregnancy, a woman
Reduction in high heterogeneity which occurred when the study of is exposed to larger amounts of progesterone as opposed to oestrogen.
simple EH 30 was excluded during sensitivity analyses suggests that the Contrasting reports were also observed for the two studies investigating
relationship between BMI and EH may differ according to the presence OC use and EH risk. It should however be noted that OC usage has
of atypia. Due to the role of body fatness in the development of EH and consistently been found to reduce EC risk among users when compared
endometrial cancer, it is important for women to maintain a healthy with non-users [58,59]. Biologically, this is related to the low dose of
weight [15]. oestrogen in relation to progestin contained in OC, which inhibits
endometrial proliferation [60,61].
Pooled analysis of studies that investigated hypertension showed

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ISSN: 2161-1165 Epidemiol, an open access journal Volume 6 Issue 2 1000229
Citation: Sanni OB, Kunzmann AT, Murray LJ, McCluggage WG, Coleman HG (2016) Risk Factors (Excluding Hormone Replacement Therapy) for
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Page 13 of 15

A significant decreased risk of complex EH was reported among The relationship between a high BMI and EH cannot be
postmenopausal versus pre- and peri-menopausal in an Italian study. overemphasized as is shown in this review. Notably, no studies evaluated
Conversely, findings from a further study included in our review nutrition or dietary factors in relation to EH risk, even though several
suggesting an increased risk of atypical EH among postmenopausal aspects of diet, for example coffee and high glycaemic load intake, have
versus premenopausal women, which may indicate that HRT use, been associated with endometrial cancer risk [15]. We hope that this
a well-known risk factor for EH, has more of a propensity to invoke review stimulates further work in this area in an effort to identify more
atypical than non-atypical EH. We however did not assess use of HRT modifiable, preventative factors for EH.
in this review due to an earlier Cochrane review which assessed the
effects of different hormone therapy regimens on the postmenopausal Conclusions
endometrium. The reviewers found unopposed oestrogen to be In conclusion, body fatness was found to be associated with an
associated with increased risk of all types of EH at all doses, in line with increased risk of EH, therefore women should be encouraged to
the existing literature. Although the reviewers did not perform sub- maintain a normal body weight. No significant associations were
group analysis for the different types of EH, they found no difference in detected for other factors and EH risk. However, relatively few studies
the risk of EH in women who took low dose oestrogen combined with have been conducted and further aetiological studies which might help
progestogen compared with controls who took placebo [13]. identify other non-modifiable risk factors for EH are warranted.
It is notable that one study reported an increased risk of complex Funding
EH in women with higher versus lower level of education while
OS is being funded by a QUB International PhD studentship
another reported the same association amongst women with higher
versus lower income. Measures of social class have been implicated in References
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ISSN: 2161-1165 Epidemiol, an open access journal Volume 6 Issue 2 1000229
Citation: Sanni OB, Kunzmann AT, Murray LJ, McCluggage WG, Coleman HG (2016) Risk Factors (Excluding Hormone Replacement Therapy) for
Endometrial Hyperplasia: A Systematic Review. Epidemiol 6: 229. doi:10.4172/2161-1165.1000229

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Epidemiol
ISSN: 2161-1165 Epidemiol, an open access journal Volume 6 Issue 2 1000229
Citation: Sanni OB, Kunzmann AT, Murray LJ, McCluggage WG, Coleman HG (2016) Risk Factors (Excluding Hormone Replacement Therapy) for
Endometrial Hyperplasia: A Systematic Review. Epidemiol 6: 229. doi:10.4172/2161-1165.1000229

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ISSN: 2161-1165 Epidemiol, an open access journal Volume 6 Issue 2 1000229