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Hypothyroidism !

Hypothyroidism means the thyroid gland makes too little hormone, slowing the body: tiredness, feeling cold, weight gain and dry skin.

Updated 2026-10-29

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Why it happens

What it is

Deficiency of thyroid hormone that slows the body's metabolism. It is usually primary, from failure of the thyroid gland itself, and most often due to autoimmune (Hashimoto) thyroiditis.

Who gets it

Common, and much more frequent in women and older adults. Iodine deficiency once caused endemic goitre and cretinism in Andean regions of Latin America; salt iodisation has largely controlled it. Congenital hypothyroidism is sought by newborn screening.

Causes

  • Chronic autoimmune (Hashimoto) thyroiditis: commonest where iodine intake is adequate
  • Iodine deficiency: the commonest cause worldwide
  • After radioactive iodine, thyroid surgery or neck radiotherapy
  • Drugs: lithium, amiodarone, immune checkpoint inhibitors
  • Thyroiditis (postpartum, subacute) with a transient phase
  • Central: pituitary or hypothalamic disease; congenital: thyroid dysgenesis or dyshormonogenesis

Risk factors

  • Female sex and older age
  • Family history of thyroid disease
  • Other autoimmune diseases (type 1 diabetes, vitiligo, celiac disease)
  • Down and Turner syndromes
  • Pregnancy and the year after delivery
  • Previous thyroid surgery, radioiodine or neck irradiation

Pathophysiology

Low thyroid hormone slows metabolism in almost every tissue, reducing heat production, heart rate and gut motility. In primary disease, loss of negative feedback raises TSH, which may enlarge the gland. Glycosaminoglycans build up in the skin and tissues (myxoedema). In the fetus and infant, lack of hormone harms brain development.

Classification

  • Primary (thyroid), central (pituitary or hypothalamic)
  • Overt: high TSH, low free T4
  • Subclinical: high TSH, normal free T4
  • Congenital or acquired

Symptoms and signs

  • Tiredness, slowness, cold intolerance
  • Weight gain despite poor appetite
  • Constipation
  • Dry skin, hair loss, puffy face and eyelids, hoarse voice
  • Menstrual changes, low mood, poor memory
  • Bradycardia, slow-relaxing tendon reflexes, goitre in some
  • Newborn: prolonged jaundice, poor feeding, large tongue, umbilical hernia (often no signs at birth)

Diagnosis

Clinical
Symptoms are nonspecific and develop slowly, so diagnosis rests on blood tests. A goitre, bradycardia and delayed reflex relaxation support it.
Tests
TSH is the screening test; free T4 confirms and grades it. Thyroid peroxidase (TPO) antibodies support Hashimoto. Low or normal TSH with low free T4 points to central disease. Raised cholesterol, CK and hyponatraemia may be found. Newborn TSH screening.
Imaging
Not routine. Thyroid ultrasound if there is a nodule or asymmetric goitre; pituitary MRI in central hypothyroidism.

Differential diagnosis

  • Depression
  • Non-thyroidal illness (sick euthyroid syndrome)
  • Anaemia
  • Chronic kidney disease
  • Adrenal insufficiency
  • Obstructive sleep apnoea

Goal of treatment

Replace thyroid hormone to restore normal metabolism and, in primary disease, bring TSH into the reference range; in newborns, protect brain development by starting treatment early.

Treatment

Medical
Lifelong oral replacement with synthetic thyroxine (T4), taken on an empty stomach; the dose is adjusted to the TSH and to age and heart disease.
Follow-up
TSH rechecked some weeks after each dose change, then periodically; free T4 is used instead in central disease. Requirements rise in pregnancy.
Acute
Myxoedema coma: intensive care, intravenous thyroid hormone, corticosteroids until adrenal insufficiency is excluded, warming and support of breathing and circulation.
Medical
Congenital hypothyroidism: replacement started as soon as screening is confirmed, with close follow-up of growth and development.

Drugs for this condition

Complications

  • Myxoedema coma
  • Dyslipidaemia and atherosclerotic heart disease
  • Heart failure, pericardial effusion
  • Infertility and pregnancy complications
  • Intellectual disability if congenital disease goes untreated
  • Over-replacement: atrial fibrillation and bone loss

Prognosis

With correct replacement most people return to normal health and life expectancy. Congenital hypothyroidism treated early allows normal development. Myxoedema coma still carries a high mortality.

Prevention

  • Adequate dietary iodine (iodised salt)
  • Universal newborn screening
  • Periodic thyroid tests after radioiodine, thyroid surgery or neck radiotherapy, and in people on lithium or amiodarone

Test yourself

Think of the answer, then tap the question to see it.

What is the most common cause of hypothyroidism where iodine intake is adequate?

Chronic autoimmune (Hashimoto) thyroiditis.

Which laboratory pattern defines overt primary hypothyroidism?

High TSH with low free T4.

Which pattern suggests central (secondary) hypothyroidism?

Low free T4 with a low or inappropriately normal TSH.

Why are newborns screened for congenital hypothyroidism?

Most have no signs at birth, and early treatment prevents intellectual disability.

In myxoedema coma, why are corticosteroids given before or with thyroid hormone?

Coexisting adrenal insufficiency may be present, and thyroid hormone can precipitate an adrenal crisis.

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Educational information, not medical advice. For any symptom, see a health professional.

Sources: Hypothyroidism (StatPearls (NCBI Bookshelf), 2024).

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Representative model, for educational purposes only.

Thyroid gland highlighted on the Durgical 3D model