|
|
ORIGINAL ARTICLE |
|
Year : 2020 | Volume
: 33
| Issue : 1 | Page : 20-24 |
|
Prevalence of overt and subclinical thyroid dysfunction among Iraqi population in Baghdad city
Noor Thair Tahir1, Hadeel Delman Najim2, Aufaira Shaker Nsaif1
1 National Diabetes Center, Al-Mustansiriyah University, Baghdad, Iraq 2 Department of Clinical Pharmacy, College of Pharmacy, University of Al-Mustansiriyah, Baghdad, Iraq
Date of Submission | 08-Jan-2019 |
Date of Decision | 20-Feb-2020 |
Date of Acceptance | 21-Apr-2020 |
Date of Web Publication | 29-Jun-2021 |
Correspondence Address: Noor Thair Tahir National Diabetes Center, Al-Mustansiriyah University, Baghdad Iraq
 Source of Support: None, Conflict of Interest: None
DOI: 10.4103/IRJCM.IRJCM_3_20
Background: Thyroid hormones control most of the body's metabolic processes; T3 and T4 from the thyroid gland and thyroid-stimulating hormone (TSH) from the pituitary gland. Any defect in these hormones may have a serious clinical impact on different body organs. Objective: This study focus on the prevalence of thyroid diseases (subclinical and overt) in the Iraqi population and the possibility of linking their incidence and progression to specific factors. Patients and Methods: Cross-sectional study was conducted in the National Diabetes Center for Treatment and Research/Mustansiriyah University in Al-Karkh side from Baghdad/Iraq. Thousand and eight hundred patients, both gender (males and females) from different age groups (12–62 years), have been involved for 6 months. This study was measured serum TSH, thyroxin hormone (T4), and triiodothyroxin hormone (T3). Patients were categorized according to their thyroid status at the time of testing based on both the traditional definitions of thyroid dysfunction and using TSH and T4 levels of subclinical hyper- and hypothyroidism, overt hyper- and hypothyroidism. Results: Of 1800 cases collected over 6 months, 3.2% were overt hypothyroid (22.4% males and 77.6% females) (P < 0.0001). Moreover, 14.1% were subclinical hypothyroid cases (19.7% males and 80.3% females) (P < 0.0001). Overt hyperthyroid cases represent 3% (27.8% in male and 72.2% in females) (P < 0.0001). Subclinical hyperthyroid cases were 4% (18.3% in male and 81.7% in females) (P < 0.0001). Distribution of thyroid status (euthyroid, subclinical, and overt thyroid) in females significantly higher than in males (75.7%, 6.2%, and 18.1% respectively, P < 0.0001). Subclinical hypo- and hyperthyroid appeared in the age group (32–51 years) was significantly higher than other studied ages (P < 0.05), and overt hyperthyroid appeared in the age group (42–51 years) higher than other age of studied groups (P < 0.05), while overt hypothyroid was distributed equally in all age groups (P > 0.05). Less than ten percent of total patients were taking thyroid medication for hypo- and hyperthyroidism. Subclinical and overt thyroid cases received treatments were (47.4% and 42.9%, respectively). Treated old subjects >52 years represent about (17.6%) from the total patients. Conclusion: The majority of thyroid problems occur in adult age (32–50) and in females. Understanding the prevalence and risk factors of subclinical thyroid disease could be a help to identify the patients for screening and follow-up. Treatment recommendations must base on measuring thyroid-stimulating hormone concentrations and underlying comorbidities.
Keywords: Baghdad, prevalence, thyroid dysfunction
How to cite this article: Tahir NT, Najim HD, Nsaif AS. Prevalence of overt and subclinical thyroid dysfunction among Iraqi population in Baghdad city. IRAQI J COMMUNITY MED 2020;33:20-4 |
How to cite this URL: Tahir NT, Najim HD, Nsaif AS. Prevalence of overt and subclinical thyroid dysfunction among Iraqi population in Baghdad city. IRAQI J COMMUNITY MED [serial online] 2020 [cited 2023 Dec 4];33:20-4. Available from: http://www.journalijcm.org/text.asp?2020/33/1/20/319641 |
Introduction | |  |
Thyroid hormones play an important role in different metabolism processes and energy homeostasis as well as regulation of many organs performance. The main thyroid hormones; thyroxine (T4), and triiodothyronine (T3); are synthesized according to thyrotrophin (TSH) stimulation secreted from the anterior pituitary gland. Subclinical thyroid disease, either subclinical hypothyroid or subclinical hyperthyroid, present as a condition of normal thyroid hormones (T3, T4) with the change in TSH hormone without apparent symptoms.[1]
Elevated or depressed TSH is associated with indefinite and not serious symptoms in most cases.[2] However, some studies have shown that the risk of cardiovascular disease, cognitive impairment, polycystic ovarian syndrome, bone turnover, and some metabolic syndrome increases in patients with abnormal TSH.[3],[4],[5],[6],[7] Baseline TSH level, old age (over 60 years), female sex, and the presence of thyroid autoantibodies are the major risk factors possibly related to subclinical thyroid diseases as well as the progression to overt thyroid disease.[8],[9],[10]
The management of subclinical conditions is even debatable. Usually, treatment of subclinical hypothyroidism is considered only in patients with special conditions as in pregnant, infertile, or patients with high risk of progression to overt hypothyroidism.[11] In subclinical hyperthyroidism, treatment tends to be considered when the patient is old or when there is high risk of cardiovascular diseases or osteoporosis or a high risk of progression to overt hyperthyroidism.[8],[12]
High prevalence of subclinical thyroid diseases in different populations was recorded according to many studies, they stated that >50% of subclinical thyroid disease eventually progressed to overt thyroid disease over 20 years. Therefore, screening and follow-up on the subclinical conditions of thyroid problems and prediction of progression to overt thyroid diseases is very important to reduce the clinical impact of these conditions that expected in future.[13],[14],[15],[16],[17]
Aim of the study
The aim of this study was to assess the prevalence of thyroid dysfunction (subclinical and overt) in the Iraqi population and the possibility of linking their incidence and progression to age and gender factors.
Patients and Methods | |  |
This cross-sectional study was conducted on the daily attendance of patients to the National Diabetes Center for Treatment and Research/Mustansiriyah University in Al-Karkh side from Baghdad/Iraq. A total of 1800 patients have been involved over a period of 6 months (from July to December 2018) after approval from the scientific committee in the center. This study involved both males and females from different age groups. After the physical examination and according to the specialist decision, all patients were subjected to laboratory tests (thyroid function test) to check thyroid hormones. For each individual, blood samples were collected and the following hormones were measured: serum thyroid-stimulating hormone (TSH), thyroxin hormone (total T4), and triiodothyroxin hormone (total T3) and recorded if the patient has received thyroid medication or not. Thyroid hormone measurements were done in the laboratory of the center by Enzyme-Linked Fluorescent Assay using a compact automated immunoassay system, MINI VIDAS® commercial kit (Biomerieux, France). The normal ranges of the MINI VIDAS® T3, T4, and TSHare (0.95–25 nmol/L), (60–160 nmol/L) and (0.25–5 μmol/L), respectively.[18]
Patients were categorized according to their thyroid status at the time of testing based on both the traditional definitions of thyroid dysfunction and using TSH and T4 levels of subclinical (hyper and hypothyroidism) overt (hyper and hypothyroidism as shown in [Table 1].[19]
Statistical analysis
Results were expressed as mean and percentages using Microsoft Excel 2010 for the statistical analyses. Chi-square was used to compare percentages. Value of P < 0.05 was considered significant.
Results | |  |
The characteristics of this study sample are demonstrated in [Table 2]. The mean age for male was 33.9 years and for female was 38.7 years, percentage of the age distribution of the studied sample was as follows: <12 years was 8.1%, from 12 to 21 years was 12.8%, from 22 to 31 years was 15.8%, from 32 to 41 years was 19.9%, from (42 to 51) years was 21.7%, from 52 to 61 years was 14.6% and >62 years was 7.3%. Males represent 21.6%, while females represent (78.4%) from the study sample. Of 1800 subjects, euthyroid cases were 1363 (75.7%), overt thyroid and subclinical thyroid cases were 112 (6.2%), and 325 (18.1%) respectively.
Patients taking thyroid medication for hypo- and hyperthyroidism (170 patients) were as follows: the percentage of treated males was 9.8% and the percentage of treated females was 9.3% from the total. Subclinical and overt thyroid cases received treatments were 16.6% and 25.9%, respectively.
[Table 3] shows the prevalence of thyroid abnormalities between males and females among the study sample. Overt hypothyroid cases represent 58 (3.2%), 13 (22.4%) males and 45 (77.6%) females (P < 0.0001). Subclinical hypothyroid cases were 254 (14.1%), 50 (19.7%) males and 204 (80.3%) females (P < 0.0001). Overt hyperthyroid cases represent 54 (3%), 15 (27.8%) in males and 39 (72.2%) in females (P < 0.0001). Subclinical hyperthyroid cases were 71 (4%), 13 (18.3%) in males and 58 (81.7%) in females (P < 0.0001).
[Figure 1] shows the distribution of thyroid status (euthyroid, subclinical, and overt thyroid) between males and females, as percentages of females significantly higher than males in the mentioned conditions (75.7%, 18.1%, and 6.2%, respectively), P < 0.0001. | Figure 1: Distribution of thyroid status among study sample between males and females * represent significant difference (P < 0.0001)
Click here to view |
[Figure 2] shows the distribution of thyroid status among different age groups in the study sample, subclinical hypo-and hyperthyroid appeared in the age group (32–41) year which was significantly higher than other age groups (P < 0.05), and overt hyperthyroid appeared in the age group (42–51) higher than other age groups (P < 0.05), while overt hypothyroid was distributed equally in all age groups (P > 0.05). | Figure 2: Distribution of thyroid status among different age groups in study sample; * represent significant difference (P < 0.05)
Click here to view |
Discussion | |  |
Prevalence of thyroid disease in Iraq was not clearly stated, this study has benefited from previous reports studied thyroid disease in different regions in Iraq. The present study focused on the prevalence of thyroid disease in Al-Kark hside from Baghdad city depend on data recorded in the diabetes center in this area.
The present study concerning the distribution of thyroid disease compatible with a previous study done in Baquba city by Athab et al. in 2014,[20] euthyroid status represent the greater percent of thyroid cases pointing to the fact that most patients suffer from thyroid symptoms (goiter) were with normal thyroid function test (normal T3, T4, TSH).
Concerning thyroid abnormalities between genders, the present study reported that thyroid diseases in females significantly higher than in males, these results were agreed with previous studies in the same (or other) region. Two studies in Baghdad and Baquba found the same results concerning hypo and hyperthyroid diseases between males and females.[20],[21] We also agree with Dashty in his work in Erbil who stated that females were four times higher than males in getting hyperthyroidism.[22] Pakistan and India studied results also revealed that female is the predominant gender.[22],[23],[24]
In UAE study, females are more likely to develop overt hypothyroidism as stated by Alameri et al.[25] The higher incidence of thyroid problems in females may be attributed to stress-related to the nature of their life, women (especially Asian) had more domestic responsibilities than men. Females also are more exposed to nutritional deficiencies that can cause health problems such as goiter, anemia, and other disorders.[26] Meng et al. reported that females with high TSH and high free T3 (FT3) had higher metabolic syndrome risks than males.[27]
Regarding the prevalence of thyroid diseases among different age groups, there were conflicting results among reported studies. In the present study, a high prevalence of thyroid disease was seen in adult age (32–51 years) followed by, almost constant, old age (≥52 years) and young age (≤30 years) and then in children (<12 years). Two studies from India and Malaysia found thyroid diseases was observed more in the patient's age (41–60 years).[28],[29]While a study from Ethiopia revealed the majority of thyroid diseases occurred in the age (30–39 years).[30]
It has been approved that the effect of both overt and subclinical hyperthyroid is similar and potential complications of untreated subclinical hyperthyroidism will be at high risk of incidence. The most profound consequences of subclinical overactive thyroid dysfunction are observed on the cardiovascular system and the skeleton.[31],[32] A prospective cohort study with a follow-up period of 10 years, showed that low serum TSH level is a risk factor for atrial fibrillation.[33] Small-scale uncontrolled studies have shown an improvement in cardiac parameters of patients after the reconquest of the euthyroid state.[34],[35] A risk of dementia also associated with long-term untreated subclinical hyperthyroidism.[5],[36]
On the other side, strong evidence associated untreated subclinical hypothyroidism with progression to overt hypothyroidism recorded in prospective cohort studies.[8],[37],[38] Females and those with higher baseline TSH are more likely to develop overt hypothyroidism as stated by Alameri et al.[25] The presence of thyroid antibody raises the risk of developing subclinical and then progressing to overt hypothyroidism. Smoking status, environmental temperature, and ethnicity are also risk factors for subclinical hypothyroidism. The role of iodine is somewhat controversial.[39],[40]
Because of the high progression rate of subclinical thyroid to overt thyroid, treatment is compulsory, especially in high-risk population such as older patients (>65 years) or in presence of comorbidities (such as osteoporosis and atrial fibrillation).[41],[42] In the present study, less than half subclinical thyroid patients (including old age patients) were received thyroid medication suggesting an increased likelihood of thyroid complications and increase progression to overt thyroid dysfunction in future. Biondi et al. recommend treating elderly patients with subclinical hyperthyroidism patients because of high cardiovascular and skeletal risks and the frequent progression of subclinical hyperthyroidism to overt hyperthyroidism.[42]
Conclusion | |  |
The majority of thyroid problems occur in adult age and in females. Understanding the prevalence and risk factors of subclinical thyroid disease could be a help to identify the patients for screening and follow-up. Treatment recommendations must base on thyroid-stimulating hormone concentrations and underlying comorbidities.
Acknowledgment
The authors would like to thank Mustansiriyah University (www.uomustansiriyah.edu.iq) and National Diabetes Center/Baghdad-Iraq for their support in the present work.
Financial support and sponsorship
Nil.
Conflicts of interest
There are no conflicts of interest.
References | |  |
1. | McAninch EA, Bianco AC. Thyroid hormone signaling in energy homeostasis and energy metabolism. Ann N Y Acad Sci 2014;1311:77-87. |
2. | Bell RJ, Rivera-Woll L, Davison SL, Topliss DJ, Donath S, Davis SR. Well-being, health-related quality of life and cardiovascular disease risk profile in women with subclinical thyroid disease: A community-based study. Clin Endocrinol (Oxf) 2007;66:548-56. |
3. | Rodondi N, den Elzen WP, Bauer DC, Cappola AR, Razvi S, Walsh JP, et al. Subclinical hypothyroidism and the risk of coronary heart disease and mortality. JAMA 2010;304:1365-74. |
4. | Gencer B, Collet TH, Virgini V, Bauer DC, Gussekloo J, Cappola AR, et al. Subclinical thyroid dysfunction and the risk of heart failure events: An individual participant data analysis from 6 prospective cohorts. Circulation 2012;126:1040-9. |
5. | Vadiveloo T, Donnan PT, Cochrane L, Leese GP. The thyroid epidemiology, audit, and research study (TEARS): Morbidity in patients with endogenous subclinical hyperthyroidism. J Clin Endocrinol Metab 2011;96:1344-51. |
6. | Ceresini G, Lauretani F, Maggio M, Ceda GP, Morganti S, Usberti E, et al. Thyroid function abnormalities and cognitive impairment in elderly people: Results of the invecchiare in Chianti study. J Am Geriatr Soc 2009;57:89-93. |
7. | Benseñor IM, Lotufo PA, Menezes PR, Scazufca M. Subclinical hyperthyroidism and dementia: The Sao Paulo ageing & health study (SPAH). BMC Public Health 2010;10:298. |
8. | Imaizumi M, Sera N, Ueki I, Horie I, Ando T, Usa T, et al. Risk for progression to overt hypothyroidism in an elderly Japanese population with subclinical hypothyroidism. Thyroid 2011;21:1177-82. |
9. | Hollowell JG, Staehling NW, Flanders WD, Hannon WH, Gunter EW, Spencer CA, et al. Serum TSH, T(4), and thyroid antibodies in the United States population (1988 to 1994): National health and nutrition examination survey (NHANES III). J Clin Endocrinol Metab 2002;87:489-99. |
10. | Canaris GJ, Manowitz NR, Mayor G, Ridgway EC. The Colorado thyroid disease prevalence study. Arch Intern Med 2000;160:526-34. |
11. | Surks MI, Ortiz E, Daniels GH, Sawin CT, Col NF, Cobin RH, et al. Subclinical thyroid disease: Scientific review and guidelines for diagnosis and management. JAMA 2004;291:228-38. |
12. | Calsolaro V, Niccolai F, Pasqualetti G, Calabrese AM, Polini A, Okoye C, et al. Overt and Subclinical hypothyroidism in the elderly: When to treat? Front Endocrinol (Lausanne) 2019;10:177. |
13. | Iervasi G, Molinaro S, Landi P, Taddei MC, Galli E, Mariani F, et al. Association between increased mortality and mild thyroid dysfunction in cardiac patients. Arch Intern Med 2007;167:1526-32. |
14. | Boekholdt SM, Titan SM, Wiersinga WM, Chatterjee K, Basart DC, Luben R, et al. Initial thyroid status and cardiovascular risk factors: The EPIC-Norfolk prospective population study. Clin Endocrinol (Oxf) 2010;72:404-10. |
15. | Biondi B, Cooper DS. The clinical significance of subclinical thyroid dysfunction. Endocr Rev 2008;29:76-131. |
16. | Cooper DS, Biondi B. Subclinical thyroid disease. Lancet 2012;379:1142-54. |
17. | Biondi B. Natural history, diagnosis and management of subclinical thyroid dysfunction. Best Pract Res Clin Endocrinol Metab 2012;26:431-46. |
18. | Anderson R, Mueller R, Reese S, Wehner A. Evaluation of an automated enzyme-linked fluorescent assay for thyroxine measurement in cat and dog sera. J Vet Diagn Invest 2017;29:278-86. |
19. | Christian S, Jonas BO, Morten LH, Lene MK, Jesper CM, Peter RH, et al. Subclinical and Overt thyroid dysfunction and risk of all-cause mortality and cardiovascular events: A large population study. J Clin Endocrinol Metab 2014;99:2372-82. |
20. | Athab AM, Salih AH, Mohammad NK. Evaluation of patients with thyroid diseases in Baquba City according to thyroid function tests. Diyala J Med 2014;7:76-9. |
21. | Hassen AF, Ahmed SA. Assessment contributing factors related to hypothyroidism/hyperthyroidism for adult patient at Bagdad teaching hospitals. Kufa J Nurs Sci 2015;5:1-9. |
22. | Khan A, Khan MM, Akhtar S. Thyroid disorders, etiology and prevalence. Pak J Med Sci 2002;2:89-94. |
23. | Usha Menon V, Sundaram KR, Unnikrishnan AG, Jayakumar RV, Nair V, Kumar H. High prevalence of undetected thyroid disorders in an iodine sufficient adult south Indian population. J Indian Med Assoc 2009;107:72-7. |
24. | Pradeepkumar NS, Singh R, Joseph NM. Emerging trends in thyroid diseases in tsunami hit coastal areas of Puducherry and Cuddalore, India. J Evol Med Dent Sci 2012;1:857-63. |
25. | Alameri M, Wafa W, Moriarty M, Lessan N, Barakat MT. Rate of progression of subclinical hypothyroidism to overt hypothyroidism: A 10-year retrospective study from UAE. Endocrine Abstracts 2018;59:202. |
26. | Khattak KN, Akhter S, Khan A, Siddiqui MM, Nawab G. Distribution of thyroid patients between age groups, sex and seasons in the thyroid patients referred to Irnum Peshawar. J Med Sci 2001;1:400-3. |
27. | Meng Z, Liu M, Zhang Q, Liu L, Song K, Tan J, et al. Gender and age impacts on the association between thyroid function and metabolic syndrome in Chinese. Medicine (Baltimore) 2015;94:e2193. |
28. | Htwe TT, Hamdi MM, Swethadri GK, Wong JO, Soe MM, Abdullah MS. Incidence of thyroid malignancy among goitrous thyroid lesion from Sarawak General Hospital 2000–2004. Singapore Med J 2009;50:724-8. |
29. | Guhamallick M, Sengupta S, Bhattacharya NK, Basu N, Roy S, Ghosh AK, et al. Cytodiagnosis of thyroid lesions – Usefulness and pitfalls: A study of 288 cases. J Cytol 2008;25:6-9. [Full text] |
30. | Tsegaye B, Ergete W. Histopathologic pattern of thyroid disease. East Afr Med J 2003;80:525-8. |
31. | Wartofsky L. Management of subclinical hyperthyroidism. J Clin Endocrinol Metab 2011;96:59-61. |
32. | Klein I, Danzi S. Thyroid disease and the heart. Circulation 2007;116:1725-35. |
33. | Sawin CT, Geller A, Wolf PA, Belanger AJ, Baker E, Bacharach P, et al. Low serum thyrotropin concentrations as a risk factor for atrial fibrillation in older persons. N Engl J Med 1994;331:1249-52. |
34. | Sgarbi JA, Villaça FG, Garbeline B, Villar HE, Romaldini JH. The effects of early antithyroid therapy for endogenous subclinical hyperthyroidism in clinical and heart abnormalities. J Clin Endocrinol Metab 2003;88:1672-7. |
35. | Faber J, Wiinberg N, Schifter S, Mehlsen J. Haemodynamic changes following treatment of subclinical and overt hyperthyroidism. Eur J Endocrinol 2001;145:391-6. |
36. | Aubert CE, Bauer DC, da Costa BR, Feller M, Rieben C, Simonsick EM, et al. The association between subclinical thyroid dysfunction and dementia: The health, aging and body composition (Health ABC) study. Clin Endocrinol (Oxf) 2017;87:617-26. |
37. | AlJadir S. Subclinical thyroid disease: Consensus or conundrum? Endocrinol MetabInt J 2017;4:00093. |
38. | Heymann R, Brent GA. Rapid progression from subclinical to symptomatic overt hypothyroidism. Endocr Pract 2005;11:115-9. |
39. | Raza SA, Mahmood N. Subclinical hypothyroidism: Controversies to consensus. Indian J Endocrinol Metab 2013;17:S636-42. |
40. | Kim YA, Park YJ. Prevalence and risk factors of subclinical thyroid disease. Endocrinol Metab (Seoul) 2014;29:20-9. |
41. | Palacios SS, Corrales EP, Galofre JC. Management of subclinical hyperthyroidism. Int J Endocrinol Metab 2012;10:490-6. |
42. | Biondi B, Bartalena L, Cooper DS, Hegedüs L, Laurberg P, Kahaly GJ. The 2015 European thyroid association guidelines on diagnosis and treatment of endogenous subclinical hyperthyroidism. Eur Thyroid J 2015;4:149-63. |
[Figure 1], [Figure 2]
[Table 1], [Table 2], [Table 3]
|