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Paget Disease of Bone

(Osteitis Deformans; Paget's Disease of Bone)


Julia F. Charles

, MD, PhD, Brigham and Women's Hospital

Reviewed/Revised May 2023
Topic Resources

Paget disease of bone is a chronic disorder of the skeleton in which areas of bone undergo abnormal turnover, resulting in areas of enlarged and softened bone.

  • The breakdown and formation of bone increase, resulting in bones that are thicker, but weaker, than normal.

  • Symptoms may be absent or may include bone pain, bone deformity, arthritis, and painful nerve compression.

  • X-rays show the bone abnormalities.

  • Pain and complications are treated, and bisphosphonates may be given.

Paget disease can affect any bone, but the most commonly affected bones are the pelvis, thighbone (femur), and skull. The shin (tibia), spine (vertebrae), collarbone (clavicle), and upper arm bone (humerus) are affected less commonly.

In the United States, about 2 to 3% of people older than 55 have the disorder, and the prevalence increases with age. However, the overall prevalence of the disease seems to be decreasing. Men are more likely than women to develop Paget disease. The disease is most common in the United Kingdom and European countries including Spain, France, and Italy, as well as in countries settled by European immigrants (for example,, Australia, New Zealand, the United States, and Canada). Paget disease is rare in Scandinavian countries and Asia.

Causes of Paget Disease of Bone

Normally, cells that break down old bone (osteoclasts) and cells that form new bone (osteoblasts) work in balance to maintain bone structure and integrity. In Paget disease, both osteoclasts and osteoblasts become overactive in some areas of bone, and the rate at which bone is broken down and rebuilt (called bone remodeling Bones Bones ) in these areas increases tremendously. The overactive areas enlarge but, despite being large, are structurally abnormal and weak.

The cause of Paget disease is unknown in most people. The disorder tends to run in families. Specific, identified gene abnormalities contribute in about 10% of people who have Paget disease, and other genetic abnormalities probably contribute in others. Also, some evidence suggests that a virus may be involved. However, there is no evidence that the disorder is contagious.

Symptoms of Paget Disease of Bone

Paget disease usually causes no symptoms. However, bone pain, bone enlargement, or bone deformity may occur. Bone pain may be deep, aching, and occasionally severe and may worsen at night. The enlarging bones may compress nerves, causing more pain. If osteoarthritis occurs, joints become painful and stiff.

Other symptoms vary depending on which bones are affected.

The skull may enlarge, and the brow and forehead may look more prominent (called frontal bossing). A person may notice this enlargement when a larger hat is needed. Enlarged skull bones may damage the inner ear (cochlea), which can cause hearing loss, and dizziness. The enlarged skull bones can compress nerves, which causes headaches. The veins on the scalp may bulge, possibly because of the increased blood flow through the skull bones.

Bones the upper arm, thigh, or calf may appear bowed and are more likely to break because the bone is weakened by Paget disease. The vertebrae may enlarge, collapse, or both because bones affected by Paget disease are weak. Weakened vertebrae could result in a loss of height, a hunched posture, or pinching of the nerves of the spinal cord, causing pain, numbness, or weakness.


The most common complication of Paget disease of bone is

Osteoarthritis develops in up to 50% of people and develops in joints next to the involved bone.

Fractures tend to occur more easily than normal at involved bones because these bones are weakened by Paget disease. Such fractures are called pathologic fractures.

Rarely, heart failure Heart Failure (HF) Heart failure is a disorder in which the heart is unable to keep up with the demands of the body, leading to reduced blood flow, back-up (congestion) of blood in the veins and lungs, and/or... read more Heart Failure (HF) develops because the increased blood flow through the affected bone puts extra stress on the heart. Because blood flow through affected bones is unusually high, those bones may bleed excessively during surgery. The affected bone becomes cancerous in less than 1% of people who have Paget disease. People whose disease progresses to bone cancer usually develop an osteosarcoma Osteosarcomas (osteogenic sarcoma) Tumors that originally start in the bone are called primary bone tumors. Primary bone tumors may be noncancerous (benign) or cancerous (malignant). After cancer is diagnosed, it is staged. Staging... read more Osteosarcomas (osteogenic sarcoma) (a cancerous bone tumor).

Diagnosis of Paget Disease of Bone

  • X-rays

  • Blood tests

  • Bone scan

Paget disease is often discovered accidentally when x-rays or laboratory tests are done for other reasons. Otherwise, the diagnosis of Paget disease may be suspected based on the symptoms and a physical examination.

The diagnosis of Paget disease of bone can be confirmed by x-rays showing abnormalities characteristic of Paget disease and by a laboratory test to determine blood levels of alkaline phosphatase (an enzyme involved in bone formation), calcium, and phosphate.

Treatment of Paget Disease of Bone

  • Treatment of pain and complications

  • Bisphosphonates

A person who has Paget disease needs treatment if the symptoms cause discomfort or if there is a significant risk or suggestion of complications, such as hearing loss, osteoarthritis, and deformity. People who do not have symptoms may not need any treatment.

Commonly used pain relievers (analgesics) such as acetaminophen and nonsteroidal anti-inflammatory drugs (NSAIDs) help reduce bone pain. If one leg becomes bowed and shortened, heel lifts can help make walking easier. Sometimes surgery is needed to relieve pinched nerves or to replace a joint that has become arthritic from Paget disease.

Bisphosphonates are medications that inhibit bone turnover and can be used to slow the progression of Paget disease. Zoledronic acid is the bisphosphonate of choice. Other bisphosphonates such as alendronate, risedronate, pamidronate, tiludronate, and etidronate are sometimes used as an alternative. Except for pamidronate and zoledronic acid, which are usually given by vein (intravenously), these medications are given by mouth. These medications are given to treat pain caused by Paget disease and not by another source, such as osteoarthritis. Bisphosphonates are also sometimes indicated for the following clinical scenarios:

  • Before orthopedic surgery to prevent or reduce bleeding during surgery

  • To prevent or slow the progression of complications (such as hearing loss, bone deformity, arthritis, weakness, or paralysis), especially in people who cannot have surgery

  • For people with a blood level of alkaline phosphatase twice the normal level or higher

Calcitonin is occasionally used as an alternative to bisphosphonates in people who cannot take bisphosphonates or do not tolerate them. Calcitonin is injected under the skin or into muscle.

Doctors encourage weight bearing (such as standing and walking) and discourage excessive bed rest (except for sleeping at night).

Because bone is being remodeled rapidly, people should consume adequate amounts of calcium and vitamin D in their diet. Vitamin D helps the body absorb calcium and add it to bone (a process called bone mineralization). Vitamin D and calcium supplements are often needed. Otherwise, poor bone mineralization and bone weakening (osteomalacia) may occur.

Prognosis for Paget Disease of Bone

The prognosis for people with Paget disease is most often very good. However, the few people who develop bone cancer have a poor prognosis. People who develop other rare complications, such as heart failure or compression of the spinal cord, may also have a poor prognosis, unless treatment of these complications is timely and successful.

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