• Users Online: 232
  • Print this page
  • Email this page

 Table of Contents  
REVIEW ARTICLE
Year : 2023  |  Volume : 2  |  Issue : 1  |  Page : 20-28

Prevalence and characteristics of women with polycystic ovary syndrome in Bangladesh – A narrative review


1 Department of Endocrinology, Mymensingh Medical College, Mymensingh, Bangladesh
2 Department of Gyne and Obs, Mymensingh Medical College Hospital, Mymensingh, Bangladesh
3 Department of Endocrinology, Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh

Date of Submission08-Oct-2022
Date of Acceptance11-Dec-2022
Date of Web Publication05-Jan-2023

Correspondence Address:
A B. M. Kamrul-Hasan
Department of Endocrinology, Mymensingh Medical College, Charpara, Mymensingh 2206
Bangladesh
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/bjem.bjem_14_22

Rights and Permissions
  Abstract 


Polycystic ovary syndrome (PCOS) is the most common endocrinopathy affecting reproductive-aged women. PCOS is not a homogeneous disease and can manifest as a range of multifaceted problems, including various reproductive, cosmetic, cardiometabolic, and psychiatric conditions. In Bangladesh, research defining the prevalence and characteristics of PCOS is not ample. This review summarizes the findings from published studies that provide consistent evidence on the prevalence and characteristics of women with PCOS in the country. The small-scale studies conducted among different subgroups of women indicate a high prevalence of the condition. Clinical presentations of PCOS in Bangladeshi women are also highly variable. A substantial portion has obesity, insulin resistance, abnormal glucose tolerance, dyslipidemia, and metabolic syndrome, which significantly threaten their cardiovascular health. Many of them have co-existent other endocrinopathies, including thyroid abnormalities. Moreover, highly prevalent psychiatric comorbidities among these women warrant routine screening for these conditions.

Keywords: Polycystic ovary syndrome, prevalence, glucose intolerance, metabolic syndrome, thyroid dysfunction, depression


How to cite this article:
Kamrul-Hasan A B, Aalpona FT, Mustari M, Selim S. Prevalence and characteristics of women with polycystic ovary syndrome in Bangladesh – A narrative review. Bangladesh J Endocrinol Metab 2023;2:20-8

How to cite this URL:
Kamrul-Hasan A B, Aalpona FT, Mustari M, Selim S. Prevalence and characteristics of women with polycystic ovary syndrome in Bangladesh – A narrative review. Bangladesh J Endocrinol Metab [serial online] 2023 [cited 2023 Mar 29];2:20-8. Available from: https://www.bjem.org/text.asp?2023/2/1/20/367277




  Introduction Top


Worldwide, polycystic ovary syndrome (PCOS) is a common condition in reproductive-aged women and probably the most common endocrinopathy in the age group.[1] The reported overall prevalence of PCOS according to diagnostic criteria of the National Institutes of Health (NIH), Rotterdam, and the Androgen Excess and PCOS Society is 6%, 10%, and 10%, respectively.[2] Moreover, a vast majority of affected women (up to 70%) remain undiagnosed.[3] The Rotterdam criteria are most widely used to define PCOS and include the presence of two of three of the following: oligo/anovulation, polycystic ovaries, and clinical or biochemical hyperandrogenism.[4] Women with PCOS present with diverse clinical features, including reproductive (irregular menstrual cycles, infertility, and pregnancy complications), cosmetic (hirsutism, acne, baldness), metabolic (obesity, insulin resistance [IR], metabolic syndrome, prediabetes, type 2 diabetes mellitus, and cardiovascular risk factors), and psychological (anxiety, depression, body image, psychosexual disorders) features.[1],[5] Presentation greatly varies by ethnicity, and in high-risk populations such as South Asian and Indigenous women, prevalence and complications are higher. PCOS is a lifelong disease that begins with menstrual irregularities with or without hirsutism in adolescents and ends as cardiovascular disease in later life.[6]

Given the substantial number of women who suffer from PCOS and its significant impact on the patients and their families, a better understanding of the current burden and clinical characteristics are essential. However, most epidemiological studies on PCOS have been conducted in developed countries, with only limited information available on the burden in other parts of the world.[7],[8] Meanwhile, few data on the epidemiology and clinical, metabolic, and endocrine aspects of PCOS in Bangladeshi women are available. This article aimed to review the literature on the epidemiology and characteristics of Bangladeshi women with PCOS.


  Methodology Top


A detailed literature search was conducted utilizing PubMed and Google search engines using the keywords “polycystic ovary syndrome,” “polycystic ovarian syndrome,” “polycystic ovarian disease,” “PCOS,” “PCOD,” and “Bangladesh.” All review articles and original studies describing the epidemiology and characteristics of subjects with PCOS were appraised in synthesizing this review.


  Prevalence of Polycystic Ovary Syndrome in Bangladesh Top


Eight studies searched for the prevalence of PCOS in the country; all but one study was single centered [Table 1].[9],[10],[11],[12],[13],[14],[15],[16] Most of these studies were conducted among infertile women; one was conducted among hirsute women, and another among those presented with acne. Three studies used revised Rotterdam criteria for PCOS diagnosis, while the other five did not mention the diagnostic criteria used. The prevalence of PCOS ranged from 6.11% (among the subjects visiting the gynecology outpatient department) to 92.16% (in subjects consulted for hirsutism). The prevalence was 29.9%–46.15% among infertile women.[9],[11],[13],[15],[16] A single study conducted among medical students reported a 37% prevalence.[14] No population-based study for PCOS prevalence was available in the existing literature.
Table 1: Prevalence of polycystic ovary syndrome in Bangladesh

Click here to view



  Presentations of Polycystic Ovary Syndrome Top


Most of the studies conducted among Bangladeshi subjects with PCOS described the clinical presentations of the syndrome [Table 2].[13],[14],[16],[17],[18],[19],[20],[21],[22],[23],[24],[25],[26],[27] Menstrual irregularities, hirsutism, acne, subfertility, and polycystic ovarian morphology (PCOM) were the most frequently described presentations of PCOS though reported frequencies varied highly among the studies. The frequencies of menstrual irregularity ranged from 60% to 100%; oligomenorrhea was the most common type of menstrual abnormality reported by these studies.[13],[14],[16],[18],[19],[20],[21],[22],[23],[24],[25],[26],[27] The frequency of hirsutism was 44%–97%; the cutoff values of modified Ferriman–Gallwey for defining hirsutism were not the same for the studies.[13],[14],[16],[17],[18],[19],[20],[21],[22],[23],[24],[25],[26],[27] Similarly, the reported frequencies of acne were as low as 7.4% to as high as 55.6%.[14],[16],[21],[22] The study reported 14%–72% frequencies of subfertility.[13],[19],[21],[22],[24],[26],[27] The reported frequencies of PCOM also varied greatly, ranging from 40.7%–95%.[13],[14],[16],[17],[19],[20],[21],[22],[24],[25],[26],[27]
Table 2: Presentations of patients with polycystic ovary syndrome

Click here to view



  Phenotypic Characteristics of Polycystic Ovary Syndrome Top


Four studies categorized subjects with PCOS according to phenotypes [Table 3].[14],[21],[22],[28] Two studies identified phenotype A as the most prevalent phenotype of PCOS;[22],[28] phenotype B was most prevalent in the other two studies.[14],[21]
Table 3: Phenotypic characteristics of patients with polycystic ovary syndrome

Click here to view



  Metabolic Characteristics of Polycystic Ovary Syndrome Top


The studies describing the metabolic characteristics of Bangladeshi women with PCOS are given in [Table 4].
Table 4: Metabolic characteristics of patients with polycystic ovary syndrome

Click here to view


Obesity and central obesity

Twelve studies reported the prevalence of overweight/obesity, ranging from 38% to 87.3%.[13],[14],[16],[19],[21],[22],[23],[24],[25],[26],[27],[30] The body mass index (BMI) cutoff to define obesity was not similar in the studies; some studies used BMI ≥23 kg/m2 while others used BMI ≥25 kg/m2 for categorizing the study subjects as overweight/obese. The prevalence of central obesity ranged from 35% to 84.6%, as reported by seven studies; again, some used waist circumference ≥80 cm while others used ≥88 cm to define central obesity.[16],[17],[22],[23],[25],[26],[27] The reported prevalence of acanthosis nigricans by eight studies was 15%–82.2%.[14],[16],[17],[20],[21],[22],[25],[27]

Hypertension

Nine studies reported the prevalence of elevated blood pressure (BP) [pre-hypertension or hypertension (HTN)] ranging from 3% to 37.1%.[16],[17],[19],[21],[22],[24],[25],[26],[27] Among these, the prevalence of HTN (BP ≥140/90 mmHg) was 3%–9.3%;[24],[25],[26],[27] that of pre-HTN (Systolic BP 120-139 or diastolic BP 80-89 mmHg) was 19.3%–34.6%.[22],[25] One study reported 19% of subjects with BP ≥130/85 mmHg.[16] The cutoff defining HTN was not defined in three studies reporting the prevalence.[17],[19],[21]

Insulin resistance, diabetes, and prediabetes

We found ten studies reporting the prevalence of abnormal glucose tolerance (AGT, including diabetes, impaired fasting glucose, and impaired glucose tolerance), which ranged from 21.8% to 56%.[16],[17],[19],[20],[21],[22],[25],[27],[28],[30] The reported prevalence of diabetes was 4.9%–10%.[16],[20],[25],[27],[28],[30] 16%–77% of the study subjects had insulin resistance (IR), as reported by seven studies.[19],[20],[23],[26],[27],[28],[29] IR was not clearly defined in two of these studies;[19],[29] one study diagnosed IR by the presence of one or more of the following: fasting insulin >20 μU/ml, fasting glucose/insulin ratio <4.5, homeostatic model of the assessment of insulin resistance (HOMA-IR)>3.8 in this study;[28] HOMA-IR cutoff >2 defined IR in another study;[23] while others used HOMA-IR ≥2.6.[20],[26],[27]

Dyslipidemia and metabolic syndrome

Dyslipidemia prevalence was 45.7% to 93.7%, as reported by four studies.[17],[22],[23],[25] Having one or more of total cholesterol (TC) ≥200 mg/dL, low-density lipoprotein (LDL) cholesterol ≥100 mg/dL, high-density lipoprotein (HDL) cholesterol <40 mg/dL, and triglyceride (TG) ≥150 mg/dL defined dyslipidemia in two studies (93% and 90.4% prevalence);[22],[25] while the presence of one or more of the same cutoffs for TC, HDL, TG, and LDL ≥130 mg/dL was used by another (93.7% prevalence);[23] the criteria were not defined in the other study reporting 45.7% prevalence).[17] One study reported the frequencies of subjects with TC ≥200 mg/dL, HDL cholesterol <50 mg/dL, and TG >150 mg/dL as 16%, 12%, and 12%, respectively.[16] The prevalence of metabolic syndrome was reported by nine studies, which ranged from 15% to 57%.[16],[17],[20],[21],[22],[23],[25],[27],[28] The prevalence of metabolic syndrome using international diabetes federation criteria in three studies ranged from 42.9% to 57%;[22],[23],[27] the range was 15% to 50.5% in the four studies using the National Cholesterol Education Program Adult Treatment Panel III criteria.[16],[20],[25],[28] Other studies did not mention the diagnostic criteria of metabolic syndrome.[17],[21]

One study assessed the use of neck circumference (NC) as a tool to define obesity, central obesity, and metabolic syndrome in subjects with PCOS.[31] NC positively correlated with some other metabolic parameters and testosterone levels. NC cutoff 32.75 cm showed 87.3% sensitivity and 74.4% specificity in detecting abdominal obesity and 88% sensitivity and 68.0% specificity for diagnosing overweight/obesity, while NC 34.25 cm showed 63.0% sensitivity and 64.0% specificity for the diagnosis of metabolic syndrome.[31] In another study, Banu et al. identified that lipid accumulation product had more associations with cardiometabolic risks (age, systolic and diastolic blood pressure, and total and low-density lipoprotein cholesterol) than visceral adiposity index and was a moderate discriminator of IR in lean PCOS.[32] Albuminuria (albumin-creatine ratio ≥30 mg/g) as a cardiovascular risk marker in PCOS was investigated in one study; the frequency was 21.1%. Albuminuric subjects had higher plasma glucose values at 2 h of oral glucose tolerance test and a higher frequency of metabolic syndrome than nonalbuminuric ones.[33]


  Vitamin D in Polycystic Ovary Syndrome Top


Two studies reported Vitamin D status in PCOS.[34],[35] One study said none of the women with PCOS and healthy volunteers were sufficient (≥30 ng/mL) of Vitamin D; Vitamin D insufficiency, deficiency, and severe deficiency were 25%, 68.33%, 6.67% of women in the PCOS group; in the control group, the frequency was 12%, 50%, and 38%, respectively.[34] In the other study, the frequency of Vitamin D deficiency was 65.5%; the frequency was higher in subjects with metabolic syndrome who also had lower Vitamin D levels than those without metabolic syndrome. The study also found positive correlations between vitamin D levels with plasma glucose after 2 h of oral glucose tolerance test, TG, total, and LDL-cholesterol.[35]


  Hormonal Parameters in Polycystic Ovary Syndrome Top


Fourteen studies describing the hormonal characteristics of PCOS are summarized in [Table 5].[13],[14],[16],[17],[18],[19],[21],[24],[25],[26],[27],[36],[37],[38]
Table 5: Hormonal characteristics of patients with polycystic ovary syndrome

Click here to view


Biochemical hyperandrogenism in polycystic ovary syndrome

The prevalence of biochemical hyperandrogenism in PCOS reported by eight studies was 19.6%–52.5%.[13],[14],[16],[24],[25],[26],[27],[38] All these studies measured serum total testosterone (TT), although the assay method and cutoff values of TT to detect biochemical hyperandrogenism were not unique.

Hyperprolactinemia in polycystic ovary syndrome

Six studies reported prolactin status in PCOS, and the prevalence was 6%–60%.[16],[17],[18],[21],[36],[38] The studies were conducted among divergent groups of subjects with PCOS; subfertile women with PCOS had the highest frequency of hyperprolactinemia.[36] All these studies used serum prolactin >25 ng/mL to define hyperprolactinemia. None of these studies revealed follow-up data for such high prolactin levels.

Thyroid dysfunction in polycystic ovary syndrome

We found eight studies reporting thyroid hormone status in PCOS; the prevalence ranged from 11.4% to 74%.[14],[16],[17],[18],[21],[36],[37],[38] Most studies defined thyroid dysfunction as elevated levels of thyroid-stimulating hormone (TSH), including those with mildly elevated TSH, though the cutoff values were not similar. The study reporting the highest prevalence of 74% was a single-centered study with only 50 samples of subfertile women.[36] Only one multicenter study described thyroid dysfunction categories; the prevalence of thyroid dysfunction was 17% (subclinical hypothyroidism 11%, overt hypothyroidism 5.2%, subclinical hyperthyroidism 0.4%, and overt hyperthyroidism 0.4%). This study also reported the prevalence of anti-thyroid peroxidase (anti-TPO) in subjects with PCOS, which was 20.6%.[38] One study searching the impact of subclinical hypothyroidism on clinical and metabolic parameters in PCOS found that subclinical hypothyroid women with PCOS had similar frequencies of dysglycemia, dyslipidemia, and metabolic syndrome.[39] Another study conducted to explore the relationship of IR with TSH found no association between them.[37]

Luteinizing hormone to follicle-stimulating hormone ratio in polycystic ovary syndrome

Seven studies reported luteinizing hormone/follicle-stimulating hormone (LH/FSH) ratio in PCOS; the prevalence of altered LH/FSH ratio with cutoff >2 used in five of these studies ranged from 22.3% to 60%.[13],[16],[19],[21],[26] Other two studies defined altered LH/FSH as >1 and found a higher prevalence of 70.7% and 75.5%.[24],[27] One study found a predictive association of LH/FSH ratio with hyperandrogenemia in women with PCOS.[24]


  Anti-MÜLlerian Hormone in Polycystic Ovary Syndrome Top


Two studies evaluated serum anti-müLlerian hormone (AMH) levels as a diagnostic tool for PCOS; AMH levels were higher in the PCOS group than in the control group.[40],[41] Sadiqa-Tuqan et al. (2016) identified 67% sensitivity and 78.33% specificity of AMH with the cutoff value at 3.5 ng/mL.[40] The optimal sensitivity and specificity were achieved at a cutoff level of 4.85 ng/mL, as reported by Afreen et al. (2020).[41]


  Other Metabolic and Endocrine Parameters in Polycystic Ovary Syndrome Top


One study found higher serum prostate-specific antigen levels in PCOS than in healthy controls and a positive correlation of prostate-specific antigen levels with polycystic ovarian morphology in the PCOS group.[42] In another study, Mohana et al. (2022) found higher leptin levels and leptin/adiponectin ratio in PCOS than in controls. They observed negative correlations between leptin levels and waist circumference, waist/hip ratio, and waist/height ratio. PCOS group had significantly higher cardiovascular risks than the healthy control when they were categorized according to the adiponectin/leptin ratio in the study.[43]


  Characteristics of Adolescents with Polycystic Ovary Syndrome Top


Only one study conducted by Kamrul-Hasan et al. (2021), evaluated adolescents diagnosed with PCOS.[44] In the study, 27.4% of participants had a first-degree relative with PCOS, and 12% had a first-degree relative with type 2 diabetes. Oligomenorrhea was the most common (88%) menstrual problem; 77.7% had acanthosis nigricans, 69.1% were overweight or obese, 6.3% were underweight, 65.7% had central obesity, 23.4% had elevated BP, 24% had abnormal glucose tolerance (prediabetes 21.1%, diabetes 2.9%), 90.9% had dyslipidemia, and 42.3% had metabolic syndrome.[44]


  Characteristics of Lean Polycystic Ovary Syndrome Top


One study evaluated women with PCOS (BMI <23 kg/m2); the frequency was 23.3% of 523 women with PCOS.[25] Although metabolic abnormalities are more frequently observed when obesity is associated with PCOS, lean women with PCOS also have adverse metabolic consequences (acanthosis nigricans in 45.9%, prediabetes in 13.1%, diabetes in 1.6%, prehypertension in 9.8%, hypertension in 0.8%, and metabolic syndrome in 14.8%).[25]


  Oxidative Stress in Polycystic Ovary Syndrome Top


One study reported that the levels of antioxidant Vitamins A and C were lower in PCOS cases compared to the healthy pregnancy group.[45] This study and the other two studies found higher plasma malondialdehyde levels in PCOS than in the control group, indicating higher oxidative stress in PCOS.[45],[46],[47] Lower plasma catalase (a marker for antioxidant) levels in PCOS than in controls described by the latter two studies demonstrate poor antioxidant status in PCOS.[46],[47] Furthermore, measures of sympathetic reactivity and reduced parasympathetic activity were related to oxidative stress in PCOS.[46],[47]


  Psychiatric Comorbidities in Polycystic Ovary Syndrome Top


Two studies searched for psychiatric comorbidities in PCOS.[48],[49] PCOS was associated with a 5.12-fold higher risk of major depression, according to Kamrul-Hasan et al. (2020).[48] The frequency of depression assessed by administering the PRIME-MD Patient Health Questionnaire was 80% in PCOS (mild 29%, moderate 29%, moderately severe 14.5%, and severe 7.5%), and prediabetes/diabetes was identified as the risk factor of major depression in this study.[48] Another internet-based survey revealed that 71%, 88%, and 60% of women with PCOS suffered from loneliness, generalized anxiety disorder, and depressive illness, respectively.[49] According to the study, financial condition, physical exercise, mealtime, food habit, daily water consumption, birth control method, and long-term oral contraceptive pills contribute to the development of mental health disorders among females with PCOS in Bangladesh.[49]


  Conclusion Top


To date, no large-scale community-based data are available describing the prevalence and characteristics of women with PCOS in Bangladesh. Nevertheless, available data warn of the high prevalence of PCOS in the country. The data also remind of emphasizing the routine screening of comorbidities of PCOS, especially the cardiovascular and psychiatric ones. Large-scale, multicenter, community-based studies are of utmost importance to clearly describe the disease in the country.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.



 
  References Top

1.
Joham AE, Norman RJ, Stener-Victorin E, Legro RS, Franks S, Moran LJ, et al. Polycystic ovary syndrome. Lancet Diabetes Endocrinol 2022;10:668-80.  Back to cited text no. 1
    
2.
Bozdag G, Mumusoglu S, Zengin D, Karabulut E, Yildiz BO. The prevalence and phenotypic features of polycystic ovary syndrome: A systematic review and meta-analysis. Hum Reprod 2016;31:2841-55.  Back to cited text no. 2
    
3.
March WA, Moore VM, Willson KJ, Phillips DI, Norman RJ, Davies MJ. The prevalence of polycystic ovary syndrome in a community sample assessed under contrasting diagnostic criteria. Hum Reprod 2010;25:544-51.  Back to cited text no. 3
    
4.
Rotterdam ESHRE/ASRM-Sponsored PCOS consensus Workshop Group. Revised 2003 consensus on diagnostic criteria and long-term health risks related to polycystic ovary syndrome (PCOS). Hum Reprod 2004;19:41-7.  Back to cited text no. 4
    
5.
Islam H, Masud J, Islam YN, Haque FK. An update on polycystic ovary syndrome: A review of the current state of knowledge in diagnosis, genetic etiology, and emerging treatment options. Womens Health (Lond) 2022;18:1-23.  Back to cited text no. 5
    
6.
Wolf WM, Wattick RA, Kinkade ON, Olfert MD. Geographical prevalence of polycystic ovary syndrome as determined by region and race/ethnicity. Int J Environ Res Public Health 2018;15:2589.  Back to cited text no. 6
    
7.
Ganie MA, Vasudevan V, Wani IA, Baba MS, Arif T, Rashid A. Epidemiology, pathogenesis, genetics & management of polycystic ovary syndrome in India. Indian J Med Res 2019;150:333-44.  Back to cited text no. 7
[PUBMED]  [Full text]  
8.
Miazgowski T, Martopullo I, Widecka J, Miazgowski B, Brodowska A. National and regional trends in the prevalence of polycystic ovary syndrome since 1990 within Europe: The modeled estimates from the Global Burden of Disease Study 2016. Arch Med Sci 2021;17:343-51.  Back to cited text no. 8
    
9.
Akhter S, Alam H, Khanam NN, Zabin F. Characteristics of infertile couples. Mymensingh Med J 2011;20:121-7.  Back to cited text no. 9
    
10.
Begum S, Hossain MZ, Rahman MF, Banu LA. Polycystic ovarian syndrome in women with acne. J Pak Assoc Dermatol 2012;22:24-9.  Back to cited text no. 10
    
11.
Fatima P, Ishrat S, Rahman D, Banu J, Deeba F, Begum N, et al. Quality and quantity of infertility care in Bangladesh. Mymensingh Med J 2015;24:70-3.  Back to cited text no. 11
    
12.
Walid KM, Khan MM, Tasnim M, Haque KM, Haque MS, Islam MN, et al. Clinico-pathologycal study in women with Hirsutism in a rural tertiary hospital of Bangladesh. J Diabet Assoc Med Coll 2018;2:11-4.  Back to cited text no. 12
    
13.
Mahjabeen N, Nasreen SZ, Mustary F. Clinical profile of 500 cases of polycystic ovary syndrome in a tertiary hospital. Bangladesh J Obstet Gynaecol 2018;33:45-8.  Back to cited text no. 13
    
14.
Quadir F, Barua M, Pathan F, Kuryshi SA, Chakma PJ, Barua B, et al. Frequency of polycystic ovary syndrome among the students of a medical college in Dhaka City. IOSR J Dent Med Sci 2020;19:48-55.  Back to cited text no. 14
    
15.
Afreen S, Afreen T, Afreen N, Rumanaz A, Jahan L, Sigma S, et al. Etiological factors and clinical patterns of subfertility among the couples attending in a tertiary care hospital in Bangladesh. Sir Salimullah Med Coll J 2021;29:136-40.  Back to cited text no. 15
    
16.
Fatema K, Das T, Kazal R, Mahamood S, Pervin H, Noor F, et al. Prevalence and characteristics of polycystic ovarian syndrome in women attending in outpatient department of obstetrics and gynecology of Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh. Int J Reprod Contracept Obstet Gynecol 2021;10:830-5.  Back to cited text no. 16
    
17.
Islam S, Pathan F, Ahmed T. Clinical and biochemical characteristics of polycystic ovarian syndrome among women in Bangladesh. Mymensingh Med J 2015;24:310-8.  Back to cited text no. 17
    
18.
Mustari M, Hasanat M, Hasan Q, Tuqan S, Emran MS, Aktar N, et al. Association of altered thyroid function and prolactin level in polycystic ovarian syndrome. Bangladesh Med J 2016;45:1-5.  Back to cited text no. 18
    
19.
Begum N, Yousuf NA, Farooq MS, Chowdhury MA, Ferdous M. Association of impaired glucose tolerance and insulin resistance in women with polycystic ovary syndrome. Bangladesh J Obstet Gynaecol 2019;34:93-8.  Back to cited text no. 19
    
20.
Shah S, Banu H, Sultana T, Akhtar N, Begum A, Moriom Zamila B, et al. Increased ratio of total testosterone to dihydrotestosterone may predict an adverse metabolic outcome in polycystic ovary syndrome. J Endocrinol Metab 2019;9:186-92.  Back to cited text no. 20
    
21.
Jesmin ZF, Saha E, Yasmin F, Ara A, Khaliduzmnan S. Diagonostic parameters of polycystic ovarian syndrome in outpatient setting. Bangladesh Med J Khulna 2020;53:17-22.  Back to cited text no. 21
    
22.
Kamrul-Hasan AB, Aalpona FT, Mustari M, Akter F, Rahman MM, Selim S. Divergences in clinical, anthropometric, metabolic, and hormonal parameters among different phenotypes of polycystic ovary syndrome presenting at endocrinology outpatient departments: A multicenter study from Bangladesh. J Hum Reprod Sci 2020;13:277-84.  Back to cited text no. 22
  [Full text]  
23.
Ishrat S, Hussain M. Prevalence of insulin resistance, dyslipidemia and metabolic syndrome in infertile women with polycystic ovary syndrome. J Bangladesh Coll Physicians Surg 2021;39:225-32.  Back to cited text no. 23
    
24.
Morshed M, Banu H, Akhtar N, Sultana T, Begum A, Zamilla M, et al. Luteinizing hormone to follicle-stimulating hormone ratio significantly correlates with androgen level and manifestations are more frequent with hyperandrogenemia in women with polycystic ovary syndrome. J Endocrinol Metab 2021;11:14-21.  Back to cited text no. 24
    
25.
Kamrul-Hasan AB, Aalpona FT. Comparison of clinical, metabolic, and hormonal parameters in lean vs. obese women with polycystic ovary syndrome: A single-center study from Bangladesh. Sri Lanka J Diabetes Endocrinol Metab 2021;11:15-25.  Back to cited text no. 25
    
26.
Hurjahan-Banu, Shahed-Morshed M, Nazma-Akhtar, Tania-Sultana, Afroza-Begum, Moriom-Zamilla, et al. Total testosterone significantly correlates with insulin resistance in polycystic ovary syndrome. Gynecol Reprod Endocrinol Metab 2021;2:106-11.  Back to cited text no. 26
    
27.
Zamila BM, Banu H, Morshed M, Shah S, Begum A, Sultana T, et al. Manifestations of polycystic ovary syndrome are similar regardless of the degree of menstrual cycle variation. Int J Hum Health Sci 2022;6:96-103.  Back to cited text no. 27
    
28.
Tania-Sultana, Hurjahan-Banu, Nazma-Akhtar, Sukanti-Shah, Moriom-Zamila B, Afroza-Begum, et al. Metabolic disorders among phenotypes of polycystic ovary syndrome. Int J Endocrinol Metab Disord 2018;4:1-6.  Back to cited text no. 28
    
29.
Banu J, Fatima P, Sultana P, Chowdhury MA, Begum N, Anwary SA, et al. Association of infertile patients having polycystic ovarian syndrome with recurrent miscarriage. Mymensingh Med J 2014;23:770-3.  Back to cited text no. 29
    
30.
Laila R, Mahmud N, Nargis M, Chowdhury T. Prevalence of glucose intolerance in women with polycystic ovary syndrome: Experience from a tertiary care hospital. BIRDEM Med J 2016;6:36-9.  Back to cited text no. 30
    
31.
Kamrul-Hasan AB, Aalpona FT. Neck circumference as a predictor of obesity and metabolic syndrome in Bangladeshi women with polycystic ovary syndrome. Indian J Endocrinol Metab 2021;25:226-31.  Back to cited text no. 31
    
32.
Banu H, Morshed MS, Sultana T, Shah S, Afrine S, Hasanat MA. Lipid accumulation product better predicts metabolic status in lean polycystic ovary syndrome than that by visceral adiposity index. J Hum Reprod Sci 2022;15:27-33.  Back to cited text no. 32
  [Full text]  
33.
Kamrul-Hasan AB, Aalpona FZ, Chanda PK, Ananya KF, Kobra T, Miah OF, et al. Frequency and correlates of albuminuria in adult Bangladeshi women with polycystic ovary syndrome. Mymensingh Med J 2020;29:234-40.  Back to cited text no. 33
    
34.
Kamrul-Hasan AB, Aalpona FZ, Chanda PK, Ariful-Islam M, Palash-Molla M, Rabaya-Akter M, et al. Vitamin D status in polycystic ovarian syndrome patients attending a tertiary hospital of Bangladesh. Mymensingh Med J 2018;27:730-6.  Back to cited text no. 34
    
35.
Kamrul-Hasan AB, Aalpona FZ. Association of vitamin D status with metabolic syndrome and its components in polycystic ovary syndrome. Mymensingh Med J 2019;28:547-52.  Back to cited text no. 35
    
36.
Anwary S, Chowdhury S, Fatima P, Alfazzaman M, Begum N, Banu J. A study on subfertile women suffering from polycystic ovarian syndrome with hyperprolactinaemia and hypothyroidism as associated factors. J Bangladesh Coll Physicians Surg 2013;31:140-3.  Back to cited text no. 36
    
37.
Naher S, Begum SR, Ali L, Hakim M. Association of thyroid stimulating hormone with insulin resistance in women with polycystic ovarian syndrome. J Armed Forces Med Coll Bangladesh 2015;11:69-73.  Back to cited text no. 37
    
38.
Kamrul-Hasan AB, Aalpona FT, Mustari M, Akter F, Chanda PK, Rahman MM, et al. Prevalence of thyroid dysfunction and thyroid autoimmunity in polycystic ovary syndrome: A multicenter study from Bangladesh. Thyroid Res Pract 2020;17:76-81.  Back to cited text no. 38
  [Full text]  
39.
Kamrul-Hasan A, Aalpona FT, Selim S. Impact of subclinical hypothyroidism on reproductive and metabolic parameters in polycystic ovary syndrome – A cross-sectional study from Bangladesh. Eur Endocrinol 2020;16:156-60.  Back to cited text no. 39
    
40.
Sadiqa-Tuqan, Hasanat MA, Marufa-Mustari, Hurjahan-Banu, Nazma-Akhtar, Fariduddin M. Anti-müllerian hormone is found raised in polycystic ovarian syndrome. Am Res J Endocrinol 2019;1:1-8.  Back to cited text no. 40
    
41.
Afreen S, Yasmin N, Afreen N, Afreen T, Rahman S. Anti-Mullerian hormone as A diagnostic tool for PCOS patient: Study in a tertiary level hospital. J Shaheed Suhrawardy Med Coll 2020;11:142-6.  Back to cited text no. 41
    
42.
Hurjahan-Banu, Hasanat MA, Nazma-Akhtar, Sukanti-Shah, Tania-Sultana, Sadiqa-Tuqan, et al. Prostate specific antigen is raised in polycystic ovary syndrome. Endocrinol Metab Int J 2018;6:297-300.  Back to cited text no. 42
    
43.
Mohana CA, Hasanat MA, Rashid EU, Jahan IA, Morshed MS, Banu H, et al. Leptin and Leptin adiponectin ratio may be promising markers for polycystic ovary syndrome and cardiovascular risks. Bangladesh Med Res Counc Bull 2022;47:266-72.  Back to cited text no. 43
    
44.
Kamrul-Hasan A, Aalpona FT, Selim S. Clinical, metabolic and hormonal profiles of Bangladeshi adolescents with polycystic ovary syndrome. touchREV Endocrinol 2021;17:54-8.  Back to cited text no. 44
    
45.
Mahmud AA, Anu UH, Foysal KA, Hasan M, Szib SM, Ragib AA, et al. Elevated serum malondialdehyde (MDA), insulin, follicle-stimulating hormone (FSH), luteinizing hormone (LH), and thyroid-stimulating hormone (TSH), and reduced antioxidant vitamins in polycystic ovarian syndrome patients. Narra J 2021;2:E56.  Back to cited text no. 45
    
46.
Akhter A, Mostafa M, Sultana S, Ferdousi S. Inter relationship of sympathetic reflex response and oxidative stress in polycystic ovary syndrome. J Bangladesh Soc Physiologist 2022;16:61-9.  Back to cited text no. 46
    
47.
Mostafa M, Ferdousi S, Sultana S, Akhter A. Autonomic impairment and oxidative stress: Relationship in PCOS patients. J Bangladesh Soc Physiologist 2020;14:82-8.  Back to cited text no. 47
    
48.
Kamrul-Hasan AB, Aalpona FT, Selim S. Frequency and correlates of comorbid depression in polycystic ovary syndrome. Sri Lanka J Diabetes Endocrinol Metab 2020;10:11-7.  Back to cited text no. 48
    
49.
Hasan M, Sultana S, Sohan M, Parvin S, Rahman MA, Hossain MJ, et al. Prevalence and associated risk factors for mental health problems among patients with polycystic ovary syndrome in Bangladesh: A nationwide cross-Sectional study. PLoS One 2022;17:e0270102.  Back to cited text no. 49
    



 
 
    Tables

  [Table 1], [Table 2], [Table 3], [Table 4], [Table 5]



 

Top
 
 
  Search
 
Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
 Related articles
Access Statistics
Email Alert *
Add to My List *
* Registration required (free)

 
  In this article
Abstract
Introduction
Methodology
Prevalence of Po...
Presentations of...
Phenotypic Chara...
Metabolic Charac...
Vitamin D in Pol...
Hormonal Paramet...
Anti-MÜLler...
Other Metabolic ...
Characteristics ...
Characteristics ...
Oxidative Stress...
Psychiatric Como...
Conclusion
References
Article Tables

 Article Access Statistics
    Viewed520    
    Printed41    
    Emailed0    
    PDF Downloaded27    
    Comments [Add]    

Recommend this journal


[TAG2]
[TAG3]
[TAG4]