RISK FRACTURES ASSOCIATED WITH OSTEOPOROSIS
The most common risk factors for osteoporosis in women include genetic
predisposition, ethnicity, old age, low body mass index, estrogen deficiency and
use of steroid medications. Other or less common risk factors include excessive
alcohol use, smoking, low calcium intake, reduced physical activity, previous
fracture, poor balance, use of certain medications, and history of certain
diseases. Over a lifetime, women lose about 50% of bone density at the spine and
30% at the hip.
- Genetic Predisposition
Bone mass is thought to be largely determined by genetics. Genetic factors
account for approximately 60% of the variance in bone mass. Genetics also
play a role in body mass index. A history of maternal hip fracture and
greater height has also been associated with increased risk of fractures.
- Ethnicity
Caucasian and Asian ethnicity increases the risk of osteoporosis over
African Americans and Hispanics. Hispanics tend to have bone density similar
to Caucasians, but they have a lower fracture incidence.
- Old Age
The rate of bone loss increases with age. Studies suggest there is a fairly
linear decrease in cortical bone mass with increasing age.
- Low Body Mass Index (BMI)
Women with a thin body frame are at greater risk of osteoporosis that those
with a high BMI. It has been suggested that a high BMI may be protective
against osteoporosis.
- Estrogen Deficiency
Estrogen deficiency is a dominant pathogenic factor in bone loss. In young
women, anorexia nervosa, menstrual irregularities or amenorrhea are
associated with decreased bone density. Estrogen deficiencies in these
situations leads to an imbalance in bone remodeling, enhancing bone
resorption. Estrogen deficiency also reduces intestinal calcium absorption,
which decreases bone density.
- Rapid bone loss is associated with menopause. Menopause results in a 3%
reduction in bone mass per year for the first five years. The rate of bone
loss after the first five years following menopause ranges from 1% to 2% per
year. This results in dramatic changes in bone architecture, which increases
the risk of fracture. The accelerated loss of bone mass with menopause causes
increased osteoclastic activity, or increased bone resorption. In menopause, a
decreased level of estrogen diminishes the effects of growth factors and
calcitonin, and decreases vitamin D metabolism and calcium absorption. Vitamin
D is required for intestinal calcium absorption. With advancing age, the
kidney produces less active vitamin D and there is less efficiency in
intestinal absorption of vitamin D and calcium.
- Steroid Medications
The use of steroids results in increased renal excretion of calcium and
decreased intestinal absorption of calcium. Parathyroid hormone levels
increase with decreased levels of calcium, resulting in increased bone
resorption. Bone loss occurs in patients taking as little as 7.5mg of
prednisone a day, with the greatest loss occurring during the first three
months of steroid treatment. Postmenopausal women lose bone faster with even
less steroid dosages. It has been documented that patients taking 35mg to
50mg of prednisone every two days results in a 17% bone loss per year.
- Excessive Alcohol Consumption
Excessive use of alcohol has been associated with bone loss, but the exact
mechanism by which this occurs is unclear.
- Smoking
Smoking tobacco has been found to have negative effects on bone also.
- Low Calcium Intake
The adequate intake of calcium is critical to achieving optimal peak bone
mass and modifying the rate of bone loss associated with aging. Most
Americans fail to meet the recommended daily allowance for calcium after age
10. Ninety-nine percent of total body calcium is found in bone. Calcium
requirements vary throughout an individual's lifetime, with greater needs in
childhood and adolescence to build peak bone mass, and in later adult life
to prevent excessive loss of bone mass. Calcium insufficiency due to low
calcium intake and reduced absorption results in an accelerated rate of
age-related bone loss in the elderly population.
- Reduced Physical Activity
Immobilization and bed rest results in an increase rate of bone loss. A
decrease in physical activity can also lead to decreased balance, increasing
the risk of falls. Inactivity also leads to an increase in urinary calcium
excretion.
- Excess Thyroid Hormone
An excess of thyroid hormone is usually due to either over-replacement or
Grave's disease. Postmenopausal women who are not taking estrogen and have
hyperthyroidism have an increased risk of developing osteoporosis.
- Rheumatoid Arthritis
It has also been found that women with rheumatoid arthritis are twice as
likely as other women to have osteoporosis. Significant reductions in bone
mass density are found in the femoral neck, total hip area, and in the spine
at L2-4 in women with rheumatoid arthritis.
Although most research in osteoporosis has focused on women, several studies
have been performed focusing strictly on men. The studies have found that most
risk factors for women also apply to men.
- Age Related Changes in Bone Mass
Changes in bone mass with aging in men have been found to be similar as the
changes in postmenopausal women. Studies have found that age is associated
with a linear decrease in cortical bone mass in both men and women, and that
bone mineral density decreases in men after 50 years of age. The specific
bone remodeling imbalance that is responsible for the age related decline in
bone mass in men is unclear.
- Clinical Hypogonadism
Bone loss results from the appearance of hypogonadism in adults, and a
failure to achieve peak bone mass with the onset of hypogonadism before the
onset of puberty.
- Weight
Heavier men have greater bone density and weight loss has been associated
with greater rates of bone loss and higher rates of fracture in older men.
- Corticosteroid Use
Use of corticosteroids has been found to lead to a 2.6 fold increase in the
risk for osteoporosis in men.
- Tobacco Use
A 2.3 fold risk increase in osteoporosis has been found in men using
tobacco.
- Genetics
A major part of the determination of adult bone mass is under genetic
control; however, the nature of the relationship is not well established in
either sex.
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