Results
The mean age of participants was 44 years old, with 53.1% (26 women)
between 40 and 45, 31(63.3%) multiparous, 38(77.6%) euthyroid, 1(2%) hyperthyroid,
and 10(20.4%) subclinical hypothyroid. There was a significant relationship between
thyroid function and irregular bleeding ( P<0.05). Among women, 19(38.8%) had
menorrhagia, 16(32.7%) poly menorrhoea , 10(20.5%) intermittent bleeding, and
4(8.1%) oligo menorrhoea. AUB was caused by dysfunctional uterine bleeding in
24(49%), endometrial hyperplasia (with or without atypia) in 9(18.4%), adenomyosis
in 6(12.2%), fibroid in 5(10.2%), and ovarian cyst in 1(2%). Thyroid function did not
alter abnormal uterine haemorrhage causes.
Keywords
Perimenopause, Bleeding, Thyroid, Dysfunction
Received: 2025/07/11
Accepted: 2025/09/07
Published Online: 07 Apr. 2026
Corresponding Information:
Milal Muhammad Al-Jeborry,
College of Medicine, University of Babylon,
Babylon, Iraq
Email:
[email protected]
Copyright © 2025, This is an original open -access article distributed under the terms of the Creative Commons Attribution-noncommercial
4.0 International License which permits copy and redistribution of the material just in noncommercial usages with proper citation .
1. Introduction
Perimenopause is a transitional phase that typically
spans 2 to 8 years before the final menstrual period and
extends to one year after it. During this period, women
often experience Abnormal Uterine Bleeding (AUB),
which may be either physiological or pathological in
origin. Such bleeding can significantly impact a
woman’s quality of life and provoke considerable
anxiety. In certain cases, these abnormalities may
indicate serious conditions such as endometrial
hyperplasia or even endometrial cancer (1,2). AUB is
defined as any change in the regularity, duration,
frequency, or volume of menstrual bleeding, affecting
approximately 50% of perimenopause women (3). A
normal menstrual cycle is characterized by a frequency
of 24 to 38 days, a duration of 4 to 8 days, and a total
blood loss ranging from 5 to 80 ml per cycle. When
these parameters are disrupted, various underlying
causes must be considered. The most frequent cause is
bleeding of endometrial origin due to hormonal
fluctuations without any identifiable organic
pathology. However, organic causes may include
benign pelvic conditions such as fibroids,
adenomyosis, cervic al or endometrial polyps, as well
as infections, trauma, iatrogenic factors (e.g., hormone
replacement therapy, contraceptive use, or
anticoagulants), malignancies of the cervix,
endometrium, or ovaries, and systemic illnesses like
hypertension, diabetes mellitus, and thyroid disorders
(4). Among systemic disorders, thyroid dysfunction -
both hypothyroidism and hyperthyroidism -accounts
for approximately 30% to 40% of AUB cases (5).
Thyroid hormones play a critical role in regulating the
menstrual cycle. Thyroid-Stimulating Hormone (TSH)
shares a common beta subunit with both Follicle-
Banan Natiq Turkey, et al. 436
Volume 11, May 2026 Journal of Obstetrics, Gynecology and Cancer Research
Stimulating Hormone (FSH) and Luteinizing Hormone
(LH), and thyroid hormone receptors are also found in
the ovaries (6). The mechanisms through which thyroid
disorders lead to AUB include altered TSH response,
increased prolactin levels, changes in LH response,
effects on the peripheral conversion of androgens to
estrogens, alterations in Sex Hormone -Binding
Globulin (SHBG) levels, and disruptions in the
coagulation cascade -specifically reductions in factors
VII, VIII, IX, and XI. Hypothyroidism, in particu lar,
reduces SHBG production and alters estrogen
metabolism, thereby disrupting pituitary feedback
mechanisms (7,3). Hyperthyroidism is associated with
an increased gonadotropin response to Gonadotropin-
Releasing Hormone (GnRH) and elevated baseline
gonadotropin levels. Although hypomenorrhea in
hyperthyroid women may be attributed to changes in
coagulation factor VII, ovulation often still occurs, as
confirmed by endometrial biopsy findings (8).
Hyperprolactinemia, another endocrine disturbance,
interferes with follicular maturation and corpus luteum
function. It inhibits the hypothalamic -pituitary axis by
suppressing the pulsatile release of GnRH, resulting in
inadequate LH and FSH secretion, and ultimately
leading to anovulation (7). The present study was
conducted with aim to investigate the relationship
between thyroid dysfunction and abnormal uterine
bleeding in perimenopausal women.
2. Materials and Methods
This cross-sectional study was conducted in Iraq/
Babylon province from September 2023 to April 2025.
The study population were 49 women between 40 -51
years old who complain from abnormal uterine
bleeding. The exclusion criteria were bleeding
disorder, pregnancy, Diabetes Mellitus ( DM),
hypertension, IUCD insertion, use hormonal
replacement therapy, cervical pathology. In patients
with thyroidectomy, the detailed history including age,
parity, bleeding pattern, past medical & surgical
history, and drug used was obtained. BMI w as
calculated as weight in kg divided on the height in
square meters. Abdominal and pelvic examination was
done. TFT and CBC were measured; then transvaginal
ultrasound and endometrial biopsy was performed.
FIGO (9) defines heavy menstrual bleeding as more
than 80 ml; however, our definition includes bleeding
that disrupts a woman's physical, emotional, and social
well-being, either independently or in conjunction with
other symptoms, as per the NICE guideline (10).
Abnormal uterine bleeding is defined as a ny bleeding
that is heavier, more frequent, or lasts longer than what
is considered normal for the individual.
Reference
Value Serum
T4: 60-120 ng/mL
Serum T3-0.8-16 ng/ml
Serum TSH-0.5-5 mU/ml
Then, a transvaginal ultrasound was done to
determine the uterine and ovarian pathology. The
patient, whose endometrial thickness exceeded 10.5
mm, underwent an endometrial biopsy for
histopathological study (11).
Data were analyzed using the Statistical Package for
the Social Sciences (SPSS) (version 26). Descriptive
statistics were expressed as frequencies and
percentages. Chi-square tests and t -tests were used to
show the association between the variables. P≤0.05
was considered as statistically significant.
3. Results
A total of 49 priemenopausal women with complaint
from abnormal uterine bleeding were included in this
study. The mean age of participants was 44 years old
(minimum 40 years and maximum 50 years).
Moreover, 26 women (53.1%) aged between 40 -45
years and 46. 9% between 46 -52 years old. Among
these women, 5(10.2%) were nulliparous, 4 had one
child (8.2%), 9(18.4%) had 2 children, and 31(63.3%)
were multiparous (Table 1). Regarding the endometrial
thickness, in 16 women (32.7%) was more than 10.5
mm and endometrial biopsy was done, and in
33(67.3%) was less than 10.5 mm.
Table 2 shows that thyroid status of women. There
was 38 women (77.6%) with euthyroidism, 1(2%)
hyperthyroidism, and 10(20.4%) subclinical
hypothyroidisms.
Table 3 shows the most common symptoms of
women was menorrhagia in 19(38.8%), poly
menorrhea in 16(32.7%), intermittent bleeding in
10(20.5%) and the least presentation was oligo
menorrhea in 4(8.1%).
The duration of AUB in most patients (40.8%) was
less than 6, months and between 6 -12 months in 16
(32.7%), and more than 12 months in 13(26.5%) (Table
4).
Table 5 shows that there was statistically significant
correlation between the thyroid status and pattern of
abnormal bleeding (P=0.006).
Table 6 shows that there was no significant
correlation between bleeding pattern and endometrial
thickness (P=0.514).
Table 7 shows that the most common cause of AUB
was dysfunctional uterine bleeding in 24 (49%), then
endometrial hyperplasia (with or without atypia) in 9
(18.4%), and adenomyosis in 6 (12.2%).
Table 8 shows that there was no significant
correlation between the causes of abnormal uterine
bleeding and thyroid status (P=0.532).
437 Perimenopause Bleeding and Association
Volume 11, May 2026 Journal of Obstetrics, Gynecology and Cancer Research
Table 1. Parity of women with AUB
Parity No. Percentage (%)
Nulliparous 5 10.2
Para 1 4 8.2
Para 2 9 18.4
Para 3 and more 31 63.3
Total 49 100.0
Table 2. Thyroid status among perimenopousal women
Thyroid status No. Percent (%)
Euthyroidism 38 77.6
Hyperthyroidism 1 2.0
Subclinical hypothyroidism 10 20.4
Total 49 100.0
Table 3. Distribution of symptoms among women
Bleeding pattern NO. Percent (%)
Poly menorrhea 16 32.7
Menorrhagia 19 38.8
Oligo menorrhea 4 8.1
Intermittent bleeding 10 20.4
Total 44 100.0
Table 4. Duration of symptoms of patients with AUB
Duration No. of cases Percentage %
1-6 months 20 40.8
6-12 months 16 32.7
More than 12 months 13 26.5
Total 44 100.0
Table 5. Association between thyroid status and different forms of abnormal uterine bleeding
Bleeding pattern
Thyroid status
Total
Euthyroidisim Hyperthyroidism Subclinical
hypothyroidism
Intermittent bleeding 8(16.3%) 1(2%) 1(2%) 10(20.4%)
Menorrhagia 10(20.4%) 0 9(18.4) 19(38.8)
Oligo menorrhea 4(8.2%) 0 0 4(8.2%)
Polymenorrhea 16(32.7%) 0 0 16(32.7%)
Total 38(77.6%) 1(2%) 10(20.4%) 49(100%)
P-value 0.006
Banan Natiq Turkey, et al. 438
Volume 11, May 2026 Journal of Obstetrics, Gynecology and Cancer Research
Table 6. Association between bleeding pattern and endometrial thickness
Endometrial thickness
Bleeding pattern
Total Intermittent
bleeding
Menorrhagi
a
Oligo menorrhea
Polymenorrh
ea
=10.5mm 3(6-1%) 7(14.3%) 0 6(12.2%) 16
Total 10(20.4%) 19(38.8%) 4(8.2%) 16(32.7%) 49(100%)
P-value 0.5
Table 7. Distribution of causes of AUB among women
Cause of bleeding No. Percent (%)
Adenomyosis 6 12.2
Adenomyosis + fibroid 1 2.0
Endometrial hyperplasia (with and without atypia ) 9 18.4
Endometrial hyperplasia + ovarian cyst 1 2.0
Fibroid 5 10.2
Dysfunctional uterine bleeding 24 49
Ovarian cyst 1 2.0
Polyp 2 4.1
Total 49 100.0
Table 8. Association between causes of AUB and thyroid status
Causes of AUB
Thyroid status Total
Euthyroidisim Hyperthyroidism
Subclinical
hypothyroidism
Adenomyosis No.(%) 5(10.2%) 0(0.0%) 1(2.0%) 6(12.2%)
Adenomyosis + fibroid
No.(%) 1(2.0%) 0(0.0%) 0(0.0%) 1(2.0%)
Endometrial hyperplasia + ovarian
cyst No.(%) 1(2.0%) 0(0.0%) 0(0.0%) 1(2.0%)
Endometrial hyperplasia
No.(%) 8(16.3%) 0(0.0%) 1(2.0%) 9(18.4%)
Fibroid
No.(%) 2(4.1%) 1(2.0%) 2(4.1%) 5(10.2%)
Dysfunctional uterine bleeding
No.(%) 18(36.7%) 0(0.0%) 6(12.2%) 24(49.0%)
Ovarian cyst No.(%) 1(2.0%) 0(0.0%) 0(0.0%) 1(2.0%)
Polyp
No.(%) 2(4.1%) 0(0.0%) 0(0.0%) 2(4.1%)
Total
No.(%) 38(77.6%) 1(2.0%) 10(20.4%) 49(100.0%)
P-value 0.5
439 Perimenopause Bleeding and Association
Volume 11, May 2026 Journal of Obstetrics, Gynecology and Cancer Research
4. Discussion
Abnormal Uterine Bleeding (AUB) is a common
complaint among women in the perimenopausal
period, particularly those aged between 40 and 45
years. This result aligns with the findings of Meena et
al., (4) and Sahu HD et al. , (12), who reported similar
age distributions, with a mean age of 44 years. In our
study, most patients (63.3%) were Para 3 or more, a
finding consistent with Sahu HD et al. , (12), though
higher than that reported by Byna et al. , (13).
Menorrhagia emerged as the most frequent clinical
presentation among perimenopausal women,
accounting for 38.8% of cases in the present study,
which corresponds with the findings of Some studies
(4,6,12,14). Polymenorrhagia was the next most
common presentation (32.7%) of our study, which
agrees with the results of Begum et al., (15). Regarding
thyroid function, most women in our study were
euthyroid (77.6%), followed by subclinical
hypothyroid cases (20.4%). This distribution is
comparable to the findings by Byna et al. , (13), who
reported 64.5% euthyroid, 21.8% hypothyroid, and
12.72% hyperthyroid patients, as well as Sharma et al.,
(16), who reported 64% with euthyroid and 22%
hypothyroid. Our study identified only 2% of patients
with hyperthyroidism, slightly lower than that (4%)
reported by Sahu et al. , (12), which may be attributed
to the smaller sample size and regional variation in our
study population. In terms of healthcare -seeking
behavior, 40.8% of women in our study presented for
medical evaluation within six months of symptom
onset, like the findings of Meena et al. , (4).
Importantly, our study demonstrated a significant
correlation between thyroid dysfunction and AUB.
Among those with subclinical hypothyroidism, 20.4%
presented with menorrhagia and polymenorrhagia.
This pattern is consistent with that reported by Meena
et al., (4), who found that 20% of patients with AUB
had subclinical hypothyroidism. Meanwhile, 77.6% of
euthyroid women in our study experienced AUB, most
commonly in the form of polymenorrhea, a slightly
higher proportion than that (64.5%) reported by Byna
et al., (13). Dysfunctional Uterine Bleeding (DUB) was
identified as the most prevalent underlying cause of
AUB in our cohort, affecting 49% of patients.
Endometrial hyperplasia (with or without atypia) was
present at 18%, and adenomyosis in 12.2%. These
findings differ from those of Sahu et al. , (12), who
reported DUB in only 12% of cases and a higher
incidence of adenomyosis (33.6%). This variation may
stem from differences in the age range and
demographics of the populations studied. While Subedi
et al. , (17) found hypothyroidism as the commonly
associated with DUB, our results showed that 36.7% of
women with DUB were euthyroid, and no significant
association was found between specific causes of AUB
and thyroid status.
A key limitation of our study is that it was conducted
in a single center with a relatively small sample size,
despite covering an extended study period. This may
limit the generalizability of the findings and
underscores the need for larger, multicenter s tudies to
further clarify the relationship between thyroid
dysfunction and abnormal uterine bleeding.
5. Conclusion
Most common presentation of AUB was
menorrhagia and polymenorrhea in women during
perimenopause period commonly aged between 40 -45
years old with dysfunctional uterine bleeding being
most common cause fallowed by endometrial
hyperplasia (with or without at ypia). Thyroid status
was correlated with AUB and subclinical
hypothyroidism being the most common form of
thyroid dysfunction.
6. Declarations
Acknowledgments
The authors would like to thank Babylon college of
medicine/university of Baghdad for supporting this
research.
Ethical Considerations
This research has received ethical approval from Al-
kindy College of medicine/university of Baghdad with
the number 322 in 25-2-2025.
Authors' Contributions
BT designed the idea of the study, planned the
experiments, collected and analyzed the data, and
wrote the first draft of the manuscript. MM finished
analyzing the data, reading the manuscript, and helped
plan the study. HH read and made changes to the
manuscript. All authors read and approved the final
version of the article.
Conflict of Interest
The authors declared no conflict of interest.
Fund or Financial Support
The authors declared no fund.
Banan Natiq Turkey, et al. 440
Volume 11, May 2026 Journal of Obstetrics, Gynecology and Cancer Research
1. Dreisler E, Frandsen CS, Ulrich L.
Perimenopausal abnormal uterine bleeding.
Maturitas. 2024 ;184:107944.
[doi:10.1016/j.maturitas.2024.107944]
2. Hameed Z, Abdulrazzaq M, Mahood A, Salem
K, Hassooni Z, Abbas H. Histological and
molecular study of HOXA11 gene in
endometrial carcinoma. J Obstet Gynecol
Cancer Res. 2024;9(5):562 -77.
[doi:10.30699/jogcr.9.5.562]
3. Shahbazian N, Zargar M, Barati M, Saadati N,
Direkvand E. Comparison of pregnancy
outcomes in pregnant women with positive and
negative anti -thyroid peroxidase antibody. J
Obstet Gynecol Cancer Res. 2024;9(3):249 -56.
[doi:10.30699/jogcr.9.3.249]
4. Meena N, Mittal S. Evaluating the causes of
abnormal uterine bleeding in perimenopausal
women: a cross -sectional study. Hypertension.
2024;7(1):7-9.
[doi:10.33545/26649861.2025.v7.i1a.31]
5. Tamilarasi S, Minnalkodi SN, Prasad G.
Thyroid disorders in patients with abnormal
uterine bleeding in tertiary care hospital in
Chengalpattu district. Int J Reprod Contracept
Obstet Gynecol. 2020;9(9):3847 -52.
[doi:10.18203/2320-1770.ijrcog20203515]
6. Joshi BR, Rizal S, Subedi S. Thyroid
dysfunction in patient with abnormal uterine
bleeding in a tertiary hospital of eastern Nepal:
a descriptive cross -sectional study. JNMA J
Nepal Med Assoc. 2021;5 8(225):333-7.
[doi:10.31729/jnma.5033]
7. Ali AE, Ibrahim SA, Mostafa Mohamed AA,
Zaitoun MM. The relationship between thyroid
disorders and prolactin level in the blood of
perimenopausal women with abnormal uterine
bleeding. Zagazig Univ Med J.
2024;30(6):2678-86.
[doi:10.21608/zumj.2023.242418.2958]
8. Gowri M, Radhika BH, Harshini V, Ramaiaha
R. Role of thyroid function tests in women with
abnormal uterine bleeding. Int J Reprod
Contracept Obstet Gynecol. 2014;3(1):54 -7.
[doi:10.5455/2320-1770.ijrcog20140310]
9. Fraser IS, Critchley HO, Munro MG, Broder M.
A process designed to lead to international
agreement on terminologies and definitions used
to describe abnormalities of menstrual bleeding.
Fertil Steril. 2007;87(3):466 -76.
[doi:10.1016/j.fertnstert.2007.01.023]
10. National Institute for Health and Care
Excellence. Heavy menstrual bleeding:
assessment and management. NICE guideline
[NG88]. 2018. (Accessed in 2026, January 12,
at https://www.nice.org.uk/guidance/ng88)
11. Kumari P, Gaikwad HS, Nath B. Endometrial
cut-off thickness as predictor of endometrial
pathology in perimenopausal women with
abnormal uterine bleeding: a cross -sectional
study. Obstet Gynecol Int. 2022;2022:5073944.
[doi:10.1155/2022/5073944]
12. Sahu HD, Varma AV, Karmarkar S, Malukani
K, Khanuja A, Kesharwani P, et al. Endometrial
histopathology in abnormal uterine bleeding and
its relation with thyroid profile and endometrial
thickness. Cureus. 2023;15(4):e37859.
[doi:10.7759/cureus.37931]
13. Byna P, Siddula S, Kolli S, Shaik MV. Thyroid
abnormality in perimenopausal women with
abnormal uterine bleeding. Int J Res Med Sci.
2015;3(11):3250-3. [ doi:10.18203/2320-
6012.ijrms20151171]
14. Jetley S, Rana S, Jairajpuri ZS. Morphological
spectrum of endometrial pathology in middle -
aged women with atypical uterine bleeding: a
study of 219 cases. J Midlife Health.
2013;4(4):216-20. [ doi:10.4103/0976-
7800.122242]
15. Begum M. Association between thyroid
disorders and abnormal uterine bleeding in
reproductive ages in a private medical college
hospital, Dhaka, Bangladesh. Sch Int J Obstet
Gynec. 2021;4(11):476 -80. [doi:10.5455/2320-
1770.ijrcog20140310]
16. Sharma N, Sharma A. Thyroid profile in
menstrual disorders. JK Sci. 2012;14(1):14-7.
17. Subedi S, Banerjee B, Manisha C. Thyroid
disorders in women with dysfunctional uterine
bleeding. J Pathol Nepal. 2016;6(12):1018 -20.
[doi:10.3126/jpn.v6i12.16253]
References
441 Perimenopause Bleeding and Association
Volume 11, May 2026 Journal of Obstetrics, Gynecology and Cancer Research
How to Cite This Article:
Natiq Turkey B, Al-Jeborry M.M, Khudheir Hussein H. Causes of Perimenopause Bleeding and Association with
Thyroid Dysfunction: A Cross-Sectional Study. J Obstet Gynecol Cancer Res. 2026;11(5):435-441.
Download citation: RIS | EndNote | Mendeley |BibTeX |