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                <title><![CDATA[Spectrum
of thyroid disorders among patients with type 2 diabetes mellitus]]></title>

                                    <author><![CDATA[Md Rakibul Hasan*]]></author>
                                    <author><![CDATA[Raisa Siddika]]></author>
                                    <author><![CDATA[Sayma Akther Mou]]></author>
                                    <author><![CDATA[Md Shahed Morshed]]></author>
                
                <link data-url="https://imcjms.com/registration/journal_full_text/556">
    https://imcjms.com/registration/journal_full_text/556
</link>
                <pubDate>Mon, 13 Jan 2025 12:14:46 +0000</pubDate>
                <category><![CDATA[Original Article]]></category>
                <comments><![CDATA[January 2025; Vol. 19(1):008]]></comments>
                <description>Abstract 
Background and objectives: Thyroid disorders (TD) are common
among patients with type 2 diabetes mellitus (T2DM). Information on types of
functional and structural TDs among Bangladeshi patients with T2DM is scarce in
the literature. The present study aimed to determine the magnitude and
characteristics of different TDs among Bangladeshi diabetic patients attending
an urban healthcare center in Dhaka.
Material and methods: The study included patients with T2DM
who attended an urban Endocrinology Outpatient consultation center in Dhaka over
a period of two years. Diagnosis of TDs was based either on previous medical
records or on investigational results of thyroid functions/gland during the
first visit. Standard criteria were used to diagnose TDs.
Results:
Total 1424 patients with T2DM were
enrolled in the study. The mean age of the study population was 48.8 ±
12.9&amp;nbsp;years and 45.2% and 54.8% were male
and female respectively. Among
1424 participants 217 (15.2%) had functional and/or structural abnormalities of
thyroid gland. For those with abnormal thyroid function (14.3%), the most
common was clinical hypothyroidism (10.5%), followed by subclinical
hypothyroidism (2.6%), and clinical thyrotoxicosis (1.3%). Except for one, all
patients with overt hypothyroidism had primary hypothyroidism. Among patients
with overt thyrotoxicosis, Graves’ disease was the most common entity (50%).
Multinodular goiter was the most frequent diagnosis among structural
abnormalities (7 out of 13). Female sex (OR: 3.0, 95%CI: 1.5, 6.1, p=0.003) and
obesity (OR: 2.3, 95%CI: 1.1, 5.0, p=0.039) had higher odds of having a
diagnosis of overt hypothyroidism among patients with T2DM. Hypertension,
dyslipidemia and obesity were significantly (p &amp;lt; 0.05) higher in diabetic
patients with overt hypothyroidism. 
Conclusion:
TDs especially hypothyroidism are common among female Bangladeshi patients with
T2DM. Dyslipidemia and obesity are significantly more in overt hypothyroidism
among patients with T2DM.
January 2025; Vol. 19(1):008.&amp;nbsp; DOI: https://doi.org/10.55010/imcjms.19.008
*Correspondence: Md Rakibul Hasan, Department of Endocrinology, Medical College for
Women and Hospital, Uttara, Dhaka 1230, Bangladesh. Email: dr.mrh46@gmail.com;
© 2025 The Author(s). This is an open access article
distributed under the terms of the Creative Commons Attribution
License(CC
BY 4.0).
&amp;nbsp;
Introduction 
Diabetes mellitus (DM) and thyroid disorders (TDs) are
the&amp;nbsp;two most commonly encountered endocrine disorders in day-to-day
endocrinology practice [1]. Worldwide 1 in 10 adults (20-79 years) are living
with DM with an estimated number of&amp;nbsp;537 million, and approximately 200
million people have been suffering from TD [2-3]. The prevalence of TDs varies
in different age groups and geographical regions based on their iodine
nutrition and autoimmune status [4-7]. Thyroid dysfunction affects blood
glucose control by altering insulin sensitivity, secretion, and peripheral
glucose utilization [8]. Very high blood glucose may also affect the thyroid
hormone concentration [9]. Moreover, anti-diabetic drugs have also been
reported to affect the thyroid function status [8]. TDs are very common in
the&amp;nbsp;general population with a prevalence ranging from 6.6% to 13.4%
[10-11]. Many observational studies reported a&amp;nbsp;relatively higher
prevalence of TDs ranging from 10% to 24% in type 2 diabetes mellitus (T2DM)
patients compared to non-diabetic counterparts [11,12]. Studies from Bangladesh
have also very similar findings [13,14]. However, studies from Bangladesh had
small sample sizes and&amp;nbsp;inappropriately defined the clinical hypothyroidism
and subclinical hypothyroidism affecting the overall prevalence [13]. All
studies in diabetic patients reported only the&amp;nbsp;functional status of
the&amp;nbsp;thyroid gland, omitting equally important structural disorders namely
thyroid nodule, thyroid malignancy and multinodular goiter. Also, no published
article from Bangladesh categorized types of hyperthyroidism based on the
etiology. In view of the above, the present study aimed to determine the prevalence
and associated clinical features of different TDs among Bangladeshi patients
with T2DM.
&amp;nbsp;
Materials and methods
The study was conducted at an Endocrinology Outpatient
consultation center in Dhaka, Bangladesh. The study was approved by the Institutional Ethical
committee of the Medical College for Women and Hospital, Uttara, Dhaka. Study
participants’ identities were kept confidential and anonymous at all times.
Study population:
All consecutive non-pregnant T2DM patients, attending
Endocrinology Outpatient consultation center from August 2022 to September 2024
were primarily selected for the study. T2DM patients with pregnancy/gestational
diabetes, secondary, and other types of diabetic patients were excluded from
the study. Patients’ clinical and demographic information were maintained in a
prescription writing software database (Zilsoft Pro, Version 7.0). Clinical and
demographic information of the study population were converted to an Excel
document from the software database and imported to SPSS version 25.0 for statistical
analysis. 
Diagnosis of TDs
and other conditions: Diagnosis
of TDs was based either on previous medical records or on investigational
results of thyroid functions/gland during the first visit. The majority of the
patients with TDs was previously diagnosed and came for routine follow-up for
dose adjustment of existing medication. Functional TDs were diagnosed by
symptoms suggestive of TDs, thyroid function tests namely serum thyroid
stimulating hormone (TSH) and free thyroxine (FT4) tests. Estimation of TSH and
FT4 was carried out by an indirect chemiluminescence method. Thyroid
ultrasonogram findings were used to diagnose structural thyroid disease in
suspected cases. In hyperthyroid patients, TSH receptor antibody (TRAb), thyroid
scan, and radioactive iodine uptake tests were carried out to differentiate
Graves’ disease from other causes of thyrotoxicosis. Following criteria were
used to diagnose different types of TDs:
a. For non-pregnant adults, a TSH range between 0.35 &amp;amp;
5.5µIU/mL and an FT4 range between 0.78 &amp;amp; 2.19 ng/dL, were considered
normal based on laboratory cut-offs.
b. Subclinical hypothyroidism (SCH): FT4= 0.78 – 2.19 ng/dL and
TSH=5.5 to &amp;lt;20.0 µIU/m.
c. Primary hypothyroidism: FT4&amp;lt; 0.78 ng/dL and TSH ≥20.0 µIU/mL
d. Secondary hypothyroidism: FT4&amp;lt; 0.78 ng/dL and TSH=
undetectable to &amp;lt;20.0 µIU/mL
e. Subclinical thyrotoxicosis: FT4= 0.78 - 2.19 ng/dL and TSH
&amp;lt;0.35 µIU/mL
f. Primary thyrotoxicosis: FT4&amp;gt; 2.19 ng/dL and TSH &amp;lt;0.35
µIU/m. 
Solitary thyroid nodule and multinodular goiter were diagnosed based
on ultrasonogram and thyroid scan findings while thyroid malignancy was diagnosed
by histopathology. Clinical hypothyroid includes both primary and secondary
hypothyroidism.
Diabetes mellitus was diagnosed based on HbA1C and plasma glucose
levels and classic symptoms of hyperglycemia or hyperglycemic crisis [15]. Hypertension
was defined as systolic and diastolic blood pressure ≥140 and ≥90 mmHg
respectively. A body mass index (BMI) over 30 kg/m2 was considered
as obese (WHO, 2004).
Statistical analysis: Continuous variables are expressed as the
mean&amp;nbsp;±&amp;nbsp;standard deviation (SD), or median with interquartile range
(IQR) depending on their distribution. Categorical variables are presented as
frequency (number) and the percent. The association of baseline characteristics
with different thyroid dysfunctions was analyzed by Chi-square tests and post
hoc from adjusted residuals. Multivariable binary logistic regression was used
to see the predictive association of baseline characteristics for overt
hypothyroidism. Any value of &amp;lt;0.05 was used for statistical significance.
&amp;nbsp;
&amp;nbsp;Results
Total 1424 patients with T2DM were
enrolled in the study. The mean age of the study population was 48.8 ±
12.9 years. Majority (77.5%) was above
40 years of age and 45.2% and 54.8% were male and female respectively. Mean
BMI of the participants was 29.2 ± 4.3
kg/ m2 while 24.9% was
obese. Detail profile of the study participants is shown in Table-1. Overall
prevalence of thyroid disorders was present
in 217 (15.2%) T2DM cases. Of the total study population, 1220 DM patients were
euthyroid (Table-1). Types of thyroid disorders in patients with DM
are shown in Table-2. Out of 217 patients with TDs, 204 (14.3%) and 13 (0.9%)
had functional and other structural
diseases respectively. The most common functional abnormality was overt
hypothyroidism (10.5%), followed by subclinical hypothyroidism (2.6%), and overt
thyrotoxicosis (1.3%). All except one
had primary hypothyroidism. There were no cases of subclinical thyrotoxicosis.
Graves’ disease was the most common (9/18) cause of thyrotoxicosis. Of
the total study population, 13 (0.9%) euthyroid
cases had morphological
abnormalities which included papillary thyroid carcinoma and goiters (Table-2).
&amp;nbsp;
Table-1: Distribution of age, gender and
clinical status of thyroid gland of the study population (N=1424)
&amp;nbsp;
&amp;nbsp;
Table-2: Types of thyroid disorders
in patients with T2DM (n= 1424)
&amp;nbsp;
&amp;nbsp;
Significant (p &amp;lt; 0.05) differences in
the frequency of sex distribution were observed in overt hypothyroidism and euthyroidism
cases (Table-3). There was an overall significant (p &amp;lt; 0.05) association of
different thyroid disorders with both dyslipidemia and hypertension. Significantly
(p &amp;lt; 0.05) more cases of overt hypothyroidism had hypertension, dyslipidemia
and obesity while it was opposite for diabetic patients with subclinical
hypothyroidism and overt thyrotoxicosis. BMI was significantly (p=0.001) higher
among those with overt hypothyroidism than euthyroidism (p=0.001).
&amp;nbsp;
Table-3: Characteristics of diabetic
patients with thyroid functional disorders (n= 1424)
&amp;nbsp;
&amp;nbsp;
A multivariable binary logistic
regression model showed higher odds for female and obese individuals to have a
diagnosis of clinical hypothyroidism than euthyroidism among people with DM
(Table-4). 
&amp;nbsp;
Table-4:
Predictors of overt hypothyroidism (vs. euthyroidism)
among people with DM (n=338)
&amp;nbsp;
&amp;nbsp;
Discussion
In the present study, the overall TDs among T2DM patients were 15.2%.The
most common form of thyroid dysfunction was overt hypothyroidism (10.5%),
followed by subclinical hypothyroidism (2.6%), and overt thyrotoxicosis (1.3%).
Female diabetics were more commonly affected compared to males in all types of
thyroid dysfunctions. Female sex and obesity were found to be&amp;nbsp;independent
predictors of overt hypothyroidism in diabetes. Overt hypothyroidism was seen
more commonly in the&amp;nbsp;elderly population aged above 40 years though it was
not statistically significant. Among the structural thyroid disorders,
euthyroid multinodular goiter was most prevalent among the study group. Thyroid
dysfunctions among DM patients were&amp;nbsp;observed with&amp;nbsp;almost similar
frequency in studies from Oman (12.6%), India (13.7%), and from Brazil (14%) [16-18].
However, many studies reported a&amp;nbsp;relatively higher prevalence of thyroid
dysfunctions among T2DM patients from Bangladesh (23.5%), India (23.6%), Jordan
(26.7%), and&amp;nbsp;Saudi Arabia (28.5%) [14,19-21]. A recent systematic review
and meta-analysis also reported a&amp;nbsp;higher prevalence (20.24%) of TDs among T2DM
patients [22].
The variation in the prevalence of thyroid dysfunction among diabetics
may be related to the study design and sampling technique. Most of the patients
in our study were previously diagnosed cases of thyroid dysfunction, and further
thyroid function tests were only done in the presence of suggestive symptoms
and risk factors of thyroid disease. This could contribute to a relatively low
frequency of subclinical hypothyroidism in our study (2.6%). Structural thyroid
disorders were not routinely screened among our patients. Diagnosis of
structural thyroid disorders was only attempted if the patient presented with suggestive
problems. Therefore, routine screening of structural thyroid disease could
yield higher frequency in our study as had been seen in a large-scale retrospective
study from China. They found the overall prevalence rate of thyroid nodule was
38.3% on thyroid ultrasonogram. Increasing age of the study participants and
the presence of diabetes had significant and positive co-relation with the
thyroid nodule and goiter [23].
In our study, the majority of thyroid dysfunctions were previously
diagnosed. During the study period, only patients with suggestive symptoms of TDs
were screened for possible thyroid dysfunction. So, overt hypothyroid cases
constituted a large proportion in our study group. Subclinical thyroid
disorders were seen as less prevalent as routine screening for thyroid
dysfunction was not advised in asymptomatic patients. Many cross-sectional
studies reported a high prevalence of subclinical hypothyroid cases in diabetics,
which was not seen in our study. This could be attributed to the study design. Antibody
status was not tested and therefore, type 1 DM could not be identified and excluded.
Besides, this was a single-center study and hence not a true representative of entire
country. Despite having these limitations, a large sample size provided the
true representation of TDs in T2DM patients. Inclusion of structural TDs and biochemical
indices in TDs in diabetic patients provided further valuable clinical
information to the existing evidence. 
The observed frequency of thyroid dysfunction among T2DM patients
was very high in our study, and females were more prone to develop thyroid
dysfunctions. Females with obesity in the presence of T2DM should be routinely
screened for clinical and subclinical hypothyroidism. 
&amp;nbsp;
Conflict of Interest
The authors have no conflicts of interest to declare. 
&amp;nbsp;
Fund
None.
&amp;nbsp;
References
1.&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; Ale AO, Odusan O. Spectrum of endocrine
disorders as seen in a tertiary health facility in Sagamu, Southwest Nigeria. Niger Med J. 2019; 60(5): 252-256. DOI: 10.4103/nmj.NMJ_41_19.
2.&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; International Diabetes Federation. IDF
Diabetes Atlas, 10th ed. Brussels, Belgium: 2021. Available at:
https://www.diabetesatlas.org.
3.&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; Thyroid disease - more research needed. Lancet. 2012; 379(9821): 1076. DOI: 10.1016/S0140-6736(12)60445-0.
4.&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; Zhang X, Wang X, Hu H, Qu H, Xu Y, Li Q. Prevalence
and trends of thyroid disease among adults, 1999-2018. Endocr Pract. 2023; 29(11):
875-880. DOI: 10.1016/j.eprac.2023.08.006.
5.&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; Fan X, Zhao L, Wang S, Song K, Wang B, Xie
Y, et al. Relation between iodine nutrition and thyroid diseases in Qinghai,
China. Front Endocrinol (Lausanne).
2023; 14: 1234482. DOI:
10.3389/fendo.2023.1234482.
6.&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; Unnikrishnan AG, Kalra S, Sahay RK, Bantwal
G, John M, Tewari N. Prevalence of hypothyroidism in adults: An epidemiological
study in eight cities of India. Indian J
Endocrinol Metab. 2013; 17(4): 647-52.
DOI: 10.4103/2230-8210.113755.
7.&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; Yan Y, You L, Wang X, Zhang Z, Li F, Wu H, et
al. Iodine nutritional status, the prevalence of thyroid goiter and nodules in
rural and urban residents: A cross-sectional study from Guangzhou, China. Endocr Connect. 2021; 10(12): 1550-1559. DOI:
10.1530/EC-21-0418. 
8.&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; Eom YS, Wilson JR, Bernet VJ. Links between
thyroid disorders and glucose homeostasis. Diabetes
Metab J. 2022; 46(2): 239-256. DOI:
10.4093/dmj.2022.0013.
9.&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; Iwamoto Y, Kimura T, Tatsumi F, Sugisaki T,
Kubo M, Nakao E, et al. Effect of hyperglycemia-related acute metabolic
disturbance on thyroid function parameters in adults. Front Endocrinol (Lausanne). 2022; 13: 869869. DOI: 10.3389/fendo.2022.869869.
10.&amp;nbsp; Palma CC, Pavesi M, Nogueira VG, Clemente EL,
Vasconcellos Mde F, Pereira LC Júnior, et al. Prevalence of thyroid dysfunction
in patients with diabetes mellitus. Diabetol
Metab Syndr. 2013; 5(1): 58. DOI:
10.1186/1758-5996-5-58. 
11.&amp;nbsp; Umpierrez GE, Latif KA, Murphy MB, Lambeth HC,
Stentz F, Bush A, et al. Thyroid dysfunction in patients with type 1 diabetes: A
longitudinal study. Diabetes Care.
2003; 26(4): 1181-1185. DOI:
10.2337/diacare.26.4.1181.
12.&amp;nbsp; Gharib H, Tuttle RM, Baskin HJ, Fish LH,
Singer PA, McDermott MT. Subclinical thyroid dysfunction: A joint statement on
management from the American Association of Clinical Endocrinologists, the
American Thyroid Association, and the Endocrine Society. J Clin Endocrinol Metab. 2005; 90(1): 581-585. DOI: 10.1210/jc.2004-1231.
13.&amp;nbsp; Moslem F, Bithi TS, Biswas A. Prevalence of thyroid
dysfunction among type-2 diabetes patients in an urban diabetes hospital,
Bangladesh. Open Sci J Clin Med. 2015;
3(3): 98-102.
14.&amp;nbsp; Khan NZ, Muttalib MA, Sultana GS. Association
of thyroid hormone levels among type 2 diabetic patients attending a tertiary
care hospital. Bangladesh Med Res Counc
Bull. 2017; 42(2): 90-94.
15.&amp;nbsp; American Diabetes Association. Classification
and diagnosis of diabetes mellitus. Diabetes Care. 2017; 34(1): 2-7.
16.&amp;nbsp; Al-Sumry&amp;nbsp;S,&amp;nbsp;Al-Ghelani&amp;nbsp;T,&amp;nbsp;Al-Badi&amp;nbsp;H,
Al-Azri M, Elshafie K. Thyroid diseases in Omani type 2 diabetics: A
retrospective cross-sectional study. Adv Endocrinol. 2015; 2015: 1-6.
DOI: 10.1155/2015/353121.
17.&amp;nbsp; Jain A, Patel RP. A study of thyroid disorder
in type 2 diabetes mellitus. Sch J App
Med Sci. 2016; 4(12B): 4318-4320.
DOI:&amp;nbsp;10.36347/sjams.2016.v04i12.027.
18.&amp;nbsp; Palma CC, Pavesi M, Nogueira VG, Clemente EL,
Vasconcellos Mde F, Pereira LC Júnior, et al. Prevalence of thyroid dysfunction
in patients with diabetes mellitus. Diabetol
Metab Syndr. 2013; 5(1): 58.
doi: 10.1186/1758-5996-5-58.
19.&amp;nbsp; Asuti S, Purad S, Hosamani P. Pattern of thyroid
dysfunction in Type II diabetes mellitus patients in a tertiary care center: A cross-sectional
study. J Med Sci Health. 2023; 9(2): 204-210. DOI: 10.46347/jmsh.v9i2.23.125.
20.&amp;nbsp; Khassawneh AH, Al-Mistarehi AH, Zein Alaabdin
AM, Khasawneh L, AlQuran TM, Kheirallah KA, et al. Prevalence and predictors of
thyroid dysfunction among type 2 diabetic patients: a case–control study. Int
J Gen Med. 2020; 13: 803-816. DOI://doi.org/10.2147/IJGM.S273900.
21.&amp;nbsp; Al-Geffari M, Ahmad NA, Al-Sharqawi AH,
Youssef AM, Alnaqeb D, Al-Rubeaan K. Risk factors for thyroid dysfunction among
type 2 diabetic patients in a highly diabetes mellitus prevalent society. Int J Endocrinol. 2013; 2013: 417920. doi: 10.1155/2013/417920.
22.&amp;nbsp; Hadgu R, Worede A, Ambachew S. Prevalence of
thyroid dysfunction and associated factors among adult type 2 diabetes mellitus
patients, 2000-2022: a systematic review and meta-analysis. Syst Rev. 2024; 13(1): 119. doi: 10.1186/s13643-024-02527-y.
23.&amp;nbsp; Xu J, Lau P, Ma Y, Zhao N, Yu X, Zhu H, Li Y. prevalence
and associated factors of thyroid nodules among 52,003 Chinese ‘Healthy’ individuals
in Beijing: A retrospective cross-sectional study.&amp;nbsp;Risk Manag Healthc
Policy. 2024; 17: 181-189.
doi.org/10.2147/RMHP.S442062
&amp;nbsp;
&amp;nbsp;
Cite
this article as:
Hasan MR, Siddika R,
Mou SA, Morshed MS. Spectrum of thyroid disorders among patients with type 2
diabetes mellitus. IMC J Med Sci.
2025; 19(1): 008. DOI:https://doi.org/10.55010/imcjms.19.008</description>

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