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Osteoporosis: Progress and Promise
Publication Date: August 2000

About Osteoporosis

Osteoporosis is a skeletal disorder characterized by compromised bone strength predisposing to an increased risk of fracture. Bone strength reflects the integration of two main features: bone density and bone quality. Osteoporosis is the most common of the bone diseases that affect Americans. Although it is the underlying cause of most fractures in older people, the condition is silent and undetected in many cases until a fracture occurs.

Osteoporosis is a major health risk for 28 million Americans. In the United States today, 10 million individuals already have osteoporosis and 18 million more have low bone mass, placing them at increased risk for this disease. American women are four times more likely to develop osteoporosis than men. One out of every two women and one in eight men over 50 will have an osteoporosis-related fracture in her or his lifetime. Osteoporosis may be attributed to three factors: (1) accelerated bone loss at menopause in women or as men and women age; (2) suboptimal bone growth during childhood and adolescence resulting in failure to reach peak bone mass; and (3) bone loss secondary to disease conditions, eating disorders, or certain medications and medical treatments.

Osteoporosis is responsible for more than 1.5 million fractures annually, including 300,000 hip fractures, approximately 700,000 vertebral (spinal) fractures, 250,000 wrist fractures, and more than 300,000 fractures at other sites. In the presence of osteoporosis, fractures can occur from normal lifting and bending, as well as from falls. Furthermore, osteoporotic fractures, particularly vertebral fractures, can be associated with disabling pain.

Of all the fractures, hip fractures have the greatest morbidity and socioeconomic impact. One in five patients is no longer alive 1 year following an osteoporotic hip fracture. This means people can and do die as a result of hip fractures. Fifty percent of those people experiencing a hip fracture will be unable to walk without assistance, and 28 percent will require long-term care. The burden of health care costs due to osteoporotic fractures is estimated to be $10 to $15 billion per year.

Research has enhanced our knowledge about how to maintain a healthy skeleton throughout life. This has led to progress in understanding the causes, prevention, diagnosis, and treatment of osteoporosis. Every research advance brings us closer to eliminating the pain and suffering caused by this disease.

Addressing Osteoporosis: A Collaborative Approach

Substantial efforts are underway at the Federal level to address this serious public health problem. Recognizing that significant advances have been made since the National Institutes of Health (NIH) hosted an osteoporosis consensus development conference in 1984, the Office of Medical Applications of Research (OMAR) and the National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) were primary sponsors of the Consensus Development Conference on Osteoporosis Prevention, Diagnosis, and Therapy that was held in March 2000. The consensus panel issued a statement based upon information that addressed five questions: (1) What is osteoporosis and what are its components? (2) How do risks vary among different segments of the population? (3) What factors are involved in building and maintaining skeletal health throughout life? (4) What are the optimal evaluation and treatment of osteoporosis and fractures? and (5) What are the directions for future research?

Several components of the NIH are currently supporting basic and/or clinical research on osteoporosis and related bone diseases. NIAMS has taken the lead in initiating the Federal Working Group on Bone Diseases. This group provides a forum for sharing information among NIH institutes and other Federal agencies to enhance communication and to coordinate research efforts.

The Study of Osteoporotic Fractures (SOF), supported by NIAMS and the National Institute on Aging (NIA) and involving more than 9,000 Caucasian women 65 years or older, described risk factors for hip, wrist, and spine fractures. The study demonstrated that bone mineral density predicts hip and other types of fractures, and also provided evidence that women with low bone density have an increased risk of stroke, as well as evidence of a relationship between bone mineral density and breast cancer incidence. The NIH Women's Health Initiative currently supports the largest study of osteoporosis and fractures ever conducted. This study will determine the usefulness of calcium and vitamin D supplements, and may lead to new public health initiatives to optimize the intake of these nutrients in the U.S. population.

While osteoporosis in women has received substantial attention, less scrutiny has been devoted to osteoporosis in men. Perhaps this is because men tend to have a higher peak bone mass at maturity and a more gradual reduction in sex hormones, resulting in a later development of osteoporosis. Yet, an estimated one-third of hip fractures worldwide occur in men. The cause and pathology of osteoporosis in men is now receiving research attention under a seven-center grant supported by NIAMS, NIA, and the National Cancer Institute (NCI).

Addressing Osteoporosis: The NIAMS Research Agenda

NIAMS leads the Federal research effort on osteoporosis and related bone diseases and, NIH-wide, is responsible for about one-third of the funding for research in this area. This funding exceeded $136 million in FY 1999. NIAMS-supported research ranges from basic studies to clinical and translational research, as well as early intervention and prevention projects such as "Camp Calcium," a novel program for adolescent girls. The goal of the Camp Calcium program is to determine how much calcium growing girls need in their diets so that they can develop the strongest possible bones, which will help reduce their chance of getting osteoporosis later in life.

Overall, significant advances in preventing and treating osteoporosis are available today, as the direct result of research focused on (1) determining the causes and consequences of bone loss at cellular and tissue levels; (2) assessing risk factors; (3) developing strategies to maintain and even enhance bone density; and (4) exploring the roles of such factors as hormones, calcium, vitamin D, drugs, and exercise on bone mass.

Selected Scientific Advances

  • Identification of a gene essential for the formation of bone. Through a convergence of efforts by investigators around the world, research has shown that normal skeletal development--in both mice and humans--requires two active copies of the gene Cbfa1. This discovery is expected to open a number of exciting new research areas.
  • Finding that estrogen causes "programmed cell death" in cells that are responsible for degradation of bone (osteoclasts). By paving the way for future assessment of whether drugs can also affect the programmed cell death of osteoclasts (thereby making them potentially useful as bone-protecting treatments), this discovery represents an exciting link between basic research and tangible patient benefit.
  • Finding that one of a collection of molecules created by researchers (called peptidomimetics) successfully blocks part of the bone resorption process. This is the first clear indication that a particular synthetic antagonist may be effective in the prevention of osteoporosis. The finding may hold promise for combating bone loss in women who cannot tolerate estrogen.
  • Patient-based research showing that elderly women who already had several spine fractures at the start of a study experienced the greatest health benefit from calcium supplementation (both in terms of reducing the rate of new spine fractures and stopping bone loss). This finding has clear implications for developing and targeting new preventive strategies.
  • Low-dose estrogen study. A recent study supported by NIAMS tested the usefulness of daily low-dose estrogen plus progesterone in women over age 65 and found that these women showed significant increases in spine, forearm, and total body bone mineral density. This study provides proof that low-dose estrogen can be an effective preventive and therapeutic option.
  • Study of osteoporotic fractures (SOF). The development of risk-prediction models for osteoporotic fractures that incorporate clinical risk factors along with bone mineral density measurements is an important advance in identifying persons at greatest risk for fractures and for whom intervention measures may be suitable. The SOF, a study of postmenopausal Caucasian women, led to the identification of 14 clinical risk factors. Possession of five or more of these factors greatly increased the risk of fracture in the women in the study.
  • Secondary osteoporosis. Information regarding the diseases, physical states, medical treatments, and drugs that can lead to the development of secondary osteoporosis is now available to physicians. The information alerts physicians to the appropriate use of treatment, the monitoring of patients at risk, and, where possible, the use of intervention measures to prevent the development of osteoporosis. For example, it is generally agreed that patients on glucocorticoid therapy for 2 months or longer and patients whose conditions place them at high risk for osteoporotic fractures should be considered for bone density measurement.
  • Screening in the general population. Because there is a lack of sufficient evidence regarding the cost-effectiveness of routine screening or the efficacy of early initiation of preventive drugs, an individualized approach is recommended for testing for bone loss.
  • Testosterone study. Circulating levels of testosterone are known to decline in men as they age, leading to bone loss. A recent clinical trial of testosterone supplementation in a group of older men with low hormone levels revealed little difference in bone mineral density between the placebo- and testosterone-treated men, indicating that hormone therapy to replace bone mass is not necessary for most older men.
  • Gene for osteoporotic fractures. A recent study showed that women 65 and older with the apolipoprotein E (APOE*4) gene on chromosome 19 were nearly twice as likely as those without the gene to suffer hip and wrist fractures. Women with this gene experience weight loss that contributes to bone loss and may have reduced levels of vitamin K, which stimulates bone formation and reduces bone-cell loss.
  • Body mass index. Suboptimal bone growth in childhood and adolescence is as important as bone loss to the development of osteoporosis. Growth hormone and insulin-like growth factor-I, which are secreted the most during puberty, play a role in acquiring and maintaining bone mass and in determining body composition into adulthood. Children and youth with low body mass index (BMI) are likely to have a lower-than-average peak bone mass. There is a direct association between BMI and bone mass throughout the adult years, and several studies of fractures in older persons have shown an inverse relationship between fracture rates and BMI.
  • Nutritional studies. It is known that calcium is essential for building strong bones and reducing fracture risk. Vitamin D is required for optimal calcium absorption by the body. Both substances should be part of any osteoporosis treatment. Recent studies have shown that while some substances, such as high dietary protein, caffeine, phosphorus, and sodium, can adversely affect calcium balance, their effects appear not to be important in individuals who have an adequate calcium intake.
  • Gender/ethnicity. Caucasian postmenopausal women experience almost three-quarters of hip fractures. However, women of other age, racial, and ethnic groups, as well as men and children, are also affected by osteoporosis. Much of the difference in fracture rates among these groups appears to be explained by differences in peak bone mass and rate of bone loss. Differences in bone geometry, frequency of falls, and presence of other risk factors also appear to play a role.
  • New drugs. Bisphosphonates and selective estrogen receptor modulators (SERMs) are fairly recent prevention and treatment options for osteoporosis. Randomized placebo-controlled trials and meta-analysis of bisphosphonates (etidronate, alendronate, and risedronate) show that all increase bone mineral density at the spine and hip in a dose-dependent manner and reduce the risk of vertebral fractures by 30 to 50 percent. In large clinical trials, raloxifene, a SERM recently approved by the Food and Drug Administration, reduced the risk of vertebral fracture by 36 percent.
  • Exercise and falls. There is some evidence that childhood exercise, particularly resistance and high-impact exercise (such as weight training), contributes to higher peak bone mass. While there are health benefits to low-impact exercise, such as walking, it has minimal benefit for bone mineral density. Acknowledging that falls are a major risk factor for osteoporotic fractures, researchers conducted randomized clinical studies of exercise during adulthood and later in life that showed that the conditioning, balance-enhancing, and muscle-building effects of exercise reduce falls by approximately 25 percent.
  • Ultrasound. Clinical trials of drug therapy for osteoporosis have most often used dual energy x-ray absorptiometry (DXA) to measure bone mineral density. Studies of the less cumbersome and less expensive quantitative ultrasound (QUS) of the heel show that QUS predicts hip fracture and other nonvertebral fractures nearly as well as DXA at the femoral neck.
  • Biomarkers. Biomarkers of bone remodeling (formation and breakdown), such as alkaline phosphatase and osteocalcin (serum markers) and pyridinolines and deoxypyridinolines (urinary markers), are of limited utility in evaluating individual patients because they do not predict bone mass or fracture risk. However, research studies show that biomarkers correlate with changes in indices of bone remodeling and may provide insights into the mechanisms of bone loss.

Current and Planned Initiatives

In the past decade, there has been an explosion of basic and clinical research in osteoporosis. However, many fundamental advances in molecular and cellular biology, immunology, genetics, and bioengineering have not yet been applied to skeletal biology. In addition, research on SERMs holds promise for reducing bone loss in postmenopausal women without adverse effects on other organs. Vast opportunities exist to expand the current knowledge base, continuing in a diverse approach to osteoporosis. Initiatives that may serve as springboards for further research include:

  • Multicenter clinical intervention studies on combination therapies for osteoporosis. Because pharmaceutical companies tend to focus resources on bringing individual drugs to market, Federal support is needed to test combinations of drugs, as well as possible exercise and nutritional modifications to various drug combinations. Lower doses and combinations of effective agents may reduce the side effects and risks associated with current individual drug treatments, and may improve overall responsiveness. These studies will also generate information on osteoporosis in men, children, adolescents, and those who have diseases and conditions that put them at high risk for osteoporosis, moving beyond postmenopausal women, the group on whom most private sector research has been concentrated.
  • The bone density, biomarkers, and physical activity component of the National Health and Nutrition Examination Survey (NHANES) IV. National Health and Nutrition Examination Surveys have been conducted periodically since the 1960s, through household interviews and physical examinations provided in specially designed mobile examination centers, and with data collection periods ranging from 3 to 6 years. NHANES IV is planned as a continuous survey, and new data collection began in 1999. NIAMS is specifically interested in information from three tests to be included in the exam: dual energy x-ray absorptiometry (DXA), measurements of markers of bone resorption in urine and blood samples, and assessment of musculoskeletal strength in participants aged 50 and over.
  • Understanding the effects of therapeutic agents. While estrogen continues to be an important hormone for the treatment of osteoporosis, particularly in postmenopausal women, new treatment drugs have recently been introduced into the marketplace that may prove helpful to a broader population. These include alendronate, a bisphosphonate, and raloxifene, a selective estrogen receptor modulator. Recent knowledge about the link between bone and the cardiovascular system suggests that drugs commonly used to reduce cholesterol may also have beneficial effects on the skeleton. NIAMS is supporting research that examines the molecular and cellular mechanisms by which currently used agents work in the hope of advancing knowledge about their application to bone.
  • Animal models to study the bone matrix. There is growing evidence suggesting that the bone matrix is a source of important biochemical signals that influence the activity of bone cells, telling them where to break down or form new bone. The identification of matrix components that influence cell function could lead to new drugs that mimic these signals. NIAMS supports research that uses new, genetically modified mice as a model to examine the interaction between bone cells and the bone matrix.
  • Control of osteoblast differentiation. Osteoblasts (bone-forming cells) arise from precursor cells that differentiate to form different tissues. Some osteoblasts differentiate further to become osteocytes, the cells that are thought to be important for the response of bone to mechanical loading. The complex balance between the generation of precursor cells, their differentiation into osteoblasts and osteocytes, and ultimately their death, determines the rate of new bone formation. NIAMS is encouraging research that addresses the control of osteoblast differentiation and the generation of genetic resources to advance this research.
  • Effect of loading on bone development early in life. Bone mass during adult life reflects the amount acquired during growth minus that which is subsequently lost. Thus, maximizing peak bone mass may provide an effective strategy to prevent osteoporosis. Two hundred prepubescent children are participating in a study to determine the impact of jumping, a high weight-bearing exercise, on the development of bone mass. The study may show that implementing a specific bone-loading program during childhood will enhance the development of both bone mass and mineralization at an earlier age. This would provide a larger foundation for mineralization and growth through adolescence, thereby reducing the risk of future osteoporotic fractures.
  • Genetic analysis of bone mass. Although lifestyle and environmental factors play a role, up to 75 percent of bone mineral density is genetically determined. Researchers are employing a new method of mapping genes that influence continuously varying traits, such as bone mass. In mouse experiments, researchers have identified 17 candidate genes that may influence the development of peak bone mass during skeletal growth. The mapping of risk and protective genes in mice and the development of unique animal models for isolating the effects of those genes offer an important route to the possible identification of risk and protective genes in humans. This would allow prediction of individual--rather than general--risk, which in turn could lead to effective targeting of prevention-based treatment.
  • Understanding the molecular pathways that mediate PTH. Intermittently administered parathyroid hormone (PTH) can stimulate increases in bone mass. Although practical problems may limit the use of PTH in this way, current research on the molecular pathways that mediate PTH action may make it possible to derive a similar beneficial effect in other ways.

Information Dissemination and Education Efforts

The NIH Osteoporosis and Related Bone Diseases-National Resource Center (NIH ORBD-NRC) was created by NIAMS in 1994 in response to a groundswell of interest by several voluntary and professional groups and key congressional leaders. In addition to NIAMS, other Federal partners now support the resource center. These include the National Institute on Aging, as well as the National Institute of Child Health and Human Development, the National Institute of Dental and Craniofacial Research, the National Institute of Environmental Health Sciences, the NIH Office of Research on Women's Health, and the Department of Health and Human Services' Office of Women's Health, in cooperation with the National Osteoporosis Foundation, the Paget Foundation, and the Osteogenesis Imperfecta Foundation. The ORBD-NRC provides an important link to resources and information on metabolic bone diseases. Its mission is to expand awareness and enhance knowledge and understanding of the prevention, early detection, and treatment of these diseases as well as developing strategies for coping with them.

Osteoporosis can occur in all populations, but only recently have efforts evolved to reach different ethnic populations. The NIH ORBD-NRC has developed a partnership with the National Alliance for Hispanic Health in a program to increase calcium consumption and physical activity among Hispanic girls between the ages of 9 and 12. The organizations are developing a culturally sensitive, age-appropriate health education model that will be implemented in the fall of 2000. The program is being designed for easy replication at the local level.

Through the resource center, collaborative efforts to enhance strategies to promote bone health for women are being initiated through the National Osteoporosis Education Campaign. The first step will be to encourage teenage women to develop positive health behaviors (for example, diet, exercise, calcium intake) that can have effects on bone strength that last a lifetime.

For information on osteoporosis and other bone diseases, contact:
NIH Osteoporosis and Related Bone Diseases--National Resource Center
1232 22nd Street, NW, Suite 500
Washington, DC 20037-1292
Phone: (202) 223-0344 or (800) 624-BONE (2663)
TTY: (202) 466-4315
Fax: (202) 293-2356
World Wide Web: www.osteo.org

For general information on NIAMS and its research programs, contact:
Office of Communications and Public Liaison
National Institute of Arthritis and Musculoskeletal and Skin Diseases
National Institutes of Health
Building 31, Room 4C02
31 Center Drive, MSC 2350
Bethesda, MD 20892-2350
Phone: (301) 496-8190
TTY: (301) 565-2966
Fax: (301) 480-2814
World Wide Web: http://www.niams.nih.gov/

Information provided by:

The mission of the National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS), a part of the National Institutes of Health (NIH), is to support research into the causes, treatment, and prevention of arthritis and musculoskeletal and skin diseases; the training of basic and clinical scientists to carry out this research; and the dissemination of information on research progress in these diseases. The National Institute of Arthritis and Musculoskeletal and Skin Diseases Information Clearinghouse is a public service sponsored by the NIAMS that provides health information and information sources. Additional information can be found on the NIAMS Web site at www.niams.nih.gov.

The National Institute of Arthritis and Musculoskeletal and Skin Diseases Information Clearinghouse
National Institutes of Health
1 AMS Circle
Bethesda, MD 20892-3675
Telephone: (301) 495-4484
Fax: (301) 718-6366
TTY: (301) 565-2966