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Thyroid Disorders in Malaysia: A Nationwide Multicentre Study

Thyroid Disorders in Malaysian: A Nationwide Multicentre Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02190214
Acronym
MyEndo-Thyroid
Enrollment
2498
Registered
2014-07-15
Start date
2014-08-31
Completion date
2016-09-30
Last updated
2016-10-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Genetic Susceptibility, Graves Disease, Hashimoto's Thyroiditis, Hyperthyroidism, Hypothyroidism, Iodine Deficiency, Subclinical Hyperthyroidism, Subclinical Hypothyroidism

Keywords

Hyperthyroidism, Hypothyroidism, Autoimmune thyroid disorders, Iodine deficiency, Genetic susceptibility

Brief summary

This will be a population based study looking at the prevalence of thyroid disorders in Malaysia (including hypo- and hyperthyroidism, subclinical hypo- or hyperthyroidism) and its association with different ethnicity and iodine status. The study will also look at genetic susceptibility for autoimmune thyroid disorders in the Malaysian population General hypotheses: The prevalence of thyroid disorders in Malaysia is 10% for hypothyroidism and 2% for hyperthyroidism Hypo- and hyperthyroidism is associated with iodine status in our population There are different susceptibility gene for autoimmune thyroid disorder in different ethnicity in our population

Detailed description

This will be a cross-sectional population based study involving Malaysian adults (aged 18 year old and above). Cluster sampling will be used to select respondents that will be representative of the Malaysian population. Selected respondent will be interviewed, anthropometric measurement taken, blood and urine sample taken. Blood will be analyzed for thyroid function (thyroxine, triiodothyronine and thyroid stimulating hormone), autoantibodies (anti-thyroperoxidase and anti-thyroglobulin). Urine will be analyzed for urinary iodine. Those diagnosed with autoimmune thyroid disorders with strong family history of thyroid disorders (multiplex multi-generation family involvement) will have their blood sent for whole exome sequencing and linkage analysis done to identify possible susceptible gene for autoimmune thyroid disorders Respondents detected to have hypo- or hyper- and subclinical hypo- or hyperthyroidism will be referred to their nearest health centre for further evaluation and treatment appropriate for their condition.

Interventions

None listed

Sponsors

Malaysian Endocrine and Metabolic Society
CollaboratorOTHER
National University of Malaysia
CollaboratorOTHER
University of Malaya
CollaboratorOTHER
IMU University, Malaysia
CollaboratorOTHER
International Islamic University Malaysia
Lead SponsorOTHER

Study design

Observational model
ECOLOGIC_OR_COMMUNITY
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Aged equal or more than 18 years old at the time of sampling * Malaysian citizen

Exclusion criteria

* Respondents who did not give consent

Design outcomes

Primary

MeasureTime frameDescription
Number of participants with abnormal thyroid functionDay 0Overt or subclinical hypothyroidism Overt or subclinical hyperthyroidism

Secondary

MeasureTime frameDescription
Number of participants with positive thyroid autoantibodiesDay 0Anti-thyroglobulin Anti-thyroperoxidase
Number of participants with Iodine deficiency statusDay 0Urinary iodine level

Other

MeasureTime frameDescription
Number of participants with genetic susceptibility to autoimmune thyroid disordersDay 0whole exome sequencing and linkage analysis in families with autoimmune thyroid disorders (multiplex multi-generation involvement)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026