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Overview of Endocrine Disorders

By

William F. Young, Jr

, MD, MSc, Mayo Clinic College of Medicine

Last full review/revision Apr 2022| Content last modified Apr 2022
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Endocrine disorders can result from

  • Dysfunction originating in the peripheral endocrine gland itself (primary disorders)

  • Understimulation by the pituitary (secondary disorders) whether due to intrinsic pituitary dysfunction or understimulation of the pituitary by the hypothalamus

  • Overstimulation by the pituitary (secondary disorders) whether due to intrinsic pituitary dysfunction or overstimulation of the pituitary by the hypothalamus

  • Rarely, because of abnormal tissue response to hormones (usually hypofunction).

The disorders can result in hormone overproduction (hyperfunction) or underproduction (hypofunction).

Endocrine hyperfunction

Hyperfunction of endocrine glands may result from overstimulation by the pituitary whether due to intrinsic pituitary dysfunction or overstimulation of the pituitary by the hypothalamus. However, hyperfunction of endocrine glands is most commonly due to hyperplasia or neoplasia of the gland itself. In some cases, cancers from other tissues can produce hormones (ectopic hormone production).

Hormone excess also can result from exogenous hormone administration. In some cases, patients take nonprescription products that contain hormones and may not know or tell the physician.

Enzyme defects in the synthesis of a peripheral endocrine hormone can result in overproduction of hormones proximal to the block. Finally, overproduction of a hormone can occur as an appropriate response to a disease state.

Endocrine hypofunction

Hypofunction of an endocrine gland can result from understimulation by the pituitary whether due to intrinsic pituitary dysfunction or understimulation of the pituitary by the hypothalamus.

Hypofunction originating within the peripheral gland itself can result from congenital or acquired disorders (including autoimmune disorders, tumors, infections, vascular disorders, and toxins).

Genetic disorders causing hypofunction can result from deletion of a gene or by production of an abnormal hormone. A decrease in hormone production by the peripheral endocrine gland with a resulting increase in production of pituitary regulating hormone can lead to peripheral endocrine gland hyperplasia. For example, if synthesis of thyroid hormone is defective, thyroid-stimulating hormone (TSH) is produced in excessive amounts, causing goiter Simple Nontoxic Goiter Simple nontoxic goiter, which may be diffuse or nodular, is noncancerous hypertrophy of the thyroid without hyperthyroidism, hypothyroidism, or inflammation. Except in severe iodine deficiency... read more .

Several hormones require conversion to an active form after secretion from the peripheral endocrine gland. Certain disorders can block this step (eg, renal disease can inhibit production of the active form of vitamin D). Antibodies to the circulating hormone or its receptor can block the ability of the hormone to bind to its receptor.

Disease or drugs can cause increased rate of clearance of hormones. Circulating substances may also block the function of hormones. Abnormalities of the receptor or elsewhere in the peripheral endocrine tissue can also cause hypofunction.

Laboratory Testing for Endocrine Disorders

Because symptoms of endocrine disorders can begin insidiously and may be nonspecific, clinical recognition is often delayed for months or years. For this reason, biochemical diagnosis is usually essential; it typically requires measuring blood levels of the peripheral endocrine hormone, the pituitary hormone, or both.

Because most hormones have circadian rhythms, measurements need to be made at a prescribed time of day. Hormones that vary over short periods (eg, luteinizing hormone) necessitate obtaining 3 or 4 values over 1 or 2 hours or using a pooled blood sample. Hormones with week-to-week variation (eg, estrogen) necessitate obtaining separate values a week apart.

Blood hormone measurements

Free or bioavailable hormone (ie, hormone not bound to a specific binding hormone) is generally believed to be the active form. Free or bioavailable hormones are measured using equilibrium dialysis, ultrafiltration, or a solvent-extraction method to separate the free and albumin-bound hormone from the binding globulin. These methods can be expensive and time-consuming. Analog and competitive free hormone assays, although often used commercially, are not always accurate and should not be used.

Blood hormone estimates

Free hormone levels can be estimated indirectly by assessing levels of the binding protein and using them to adjust levels of the total serum hormone. However, indirect methods are inaccurate if the binding capacity of the hormone-binding protein has been altered (eg, by a disorder).

In some cases, other indirect estimates are used. For example, because growth hormone (GH) secretion is pulsatile and GH has a short serum half-life, serum insulin-like growth factor 1 (IGF-1), which is produced in response to GH, is often measured as an index of GH activity. Whether measurement of circulating hormone metabolites indicates the amount of bioavailable hormone is under investigation.

Dynamic tests

Treatment of Endocrine Disorders

  • Replacing deficient hormone

  • Suppressing excessive hormone production

Hypofunction disorders are usually treated by replacement of the peripheral endocrine hormone regardless of whether the defect is primary or secondary (an exception is growth hormone, a pituitary hormone replacement used for growth hormone deficiency). If resistance to the hormone exists, drugs that reduce resistance can be used (eg, metformin or thiazolidinediones for type 2 diabetes mellitus Diabetes Mellitus (DM) Diabetes mellitus is impaired insulin secretion and variable degrees of peripheral insulin resistance leading to hyperglycemia. Early symptoms are related to hyperglycemia and include polydipsia... read more ). Occasionally, a hormone-stimulating drug is used (eg, a sulfonylurea to stimulate insulin secretion).

Radiation therapy, surgery, and drugs that suppress hormone production are used to treat hyperfunction disorders. In some cases, a receptor antagonist is used (eg, pegvisomant is a growth hormone receptor antagonist used in patients with growth hormone secreting pituitary adenomas).

Aging and Endocrinology

Hormones undergo many changes as a person ages.

  • Most hormone levels decrease.

  • Some hormone levels remain stable.

  • Some hormone levels increase.

Many aging-related changes are similar to those in patients with hormone deficiency. Replacing certain hormones in older adults can improve functional outcomes (eg, muscle strength, bone mineral density), but little evidence exists regarding effects on mortality. In some cases, replacing hormones may be harmful, as in an increase in risk of breast cancer with menopausal estrogen and progesterone therapy.

A competing theory is that the age-related decline in hormone levels represents a protective slowing down of cellular metabolism. This concept is based on the rate of living theory of aging (ie, the faster the metabolic rate of an organism, the quicker it dies). This concept is seemingly supported by studies on the effects of dietary restriction. Restriction decreases levels of hormones that stimulate metabolism, thereby slowing metabolic rate; restriction also prolongs life in rodents.

Specific age-related hormone decreases

Hormone levels that decrease with aging include

  • Dehydroepiandrosterone (DHEA) and DHEA sulfate

  • Estrogen

  • Growth hormone and insulin-like growth factor 1

  • Melatonin

  • Pregnenolone

  • Testosterone

Dehydroepiandrosterone (DHEA) and DHEA sulfate levels decline dramatically with age. Despite optimism for the role of DHEA supplementation in older people, most controlled trials failed to show any major benefits.

Pregnenolone is the precursor of all known steroid hormones. As with DHEA, its levels decline with age. Studies in the 1940s showed its safety and benefits in people with arthritis, but additional studies failed to show any beneficial effects on memory and muscle strength.

Levels of growth hormone (GH) and its peripheral endocrine hormone (insulin-like growth factor 1 [IGF-1]) decline with age. GH replacement in older people sometimes increases muscle mass but does not increase muscle strength (although it may in malnourished people). Adverse effects (eg, carpal tunnel syndrome, arthralgias, water retention) are very common. GH may have a role in the short-term treatment of some undernourished older patients, but in critically ill undernourished patients, GH increases mortality. Secretagogues that stimulate GH production in a more physiologic pattern may improve benefit and decrease risk.

Levels of melatonin, a hormone produced by the pineal gland, also decline with aging. This decline may play an important role in the loss of circadian rhythms with aging.

Specific hormones that remain unchanged during aging

Hormone levels that remain stable as a person ages include

  • Adrenocorticotropic hormone (basal)

  • Cortisol (basal)

  • 1,25-Dihydroxycholecalciferol

  • Estradiol (in men)

  • Insulin (sometimes increases)

  • Thyroid-stimulating hormone (TSH)

  • Thyroxine

Specific age-related hormone increases

Hormones that increase in relation to aging are associated with either receptor defects or postreceptor defects, resulting in hypofunction. These hormones include

  • Adrenocorticotropic hormone (ACTH—increased response to corticotropin-releasing hormone)

  • Activin (in men)

  • Atrial natriuretic factor

  • Cholecystokinin

  • Follicle-stimulating hormone

  • Gonadotropins (in women)

  • Norepinephrine

  • Parathyroid hormone

  • Sex-hormone binding globulin

  • Vasoactive intestinal peptide

  • Vasopressin (also loss of circadian rhythm)

Drugs Mentioned In This Article

Drug Name Select Trade
OZURDEX
GLUCOPHAGE
SOMAVERT
DELATESTRYL
NATPARA
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