D. Ledford et al., OSTEOPOROSIS IN THE CORTICOSTEROID-TREATED PATIENT WITH ASTHMA, Journal of allergy and clinical immunology, 102(3), 1998, pp. 353-362
Osteoporosis affects 40% of white women older than 45 years of age and
15% of white men older than 50 years of age, resulting in approximate
ly 1.5 million annual fractures in the United States. Systemic cortico
steroid therapy increases the probability of osteoporosis, even with a
lternate-day dosing and with dosages sufficiently low so as not to aff
ect the hypothalamic-pituitary-adrenal axis. Inhaled corticosteroid th
erapy may affect bone density if high-dose therapy is given to select
individuals. The potential of increasing osteoporosis with inhaled cor
ticosteroid asthma therapy is a concern because of the availability of
more potent inhaled corticosteroid agents and recommendations that in
haled corticosteroid therapy be initiated earlier in the course of ast
hma, This article provides suggestions, on the basis of the medical li
terature and consensus of the authors when specific information was no
t available, for assessing and treating osteoporosis in subjects with
asthma, Suggested risk categories are ''low risk'' (inhaled corticoste
roid dosage of less than or equal to 800 mu g of beclomethasone diprop
ionate [BDP]/day in adults or less than or equal to 400 mu g BDP or eq
uivalent in children), ''moderate risk'' (inhaled BDP >800 mu g/day in
adults or >400 mu g/day in children), and ''high risk'' (systemic cor
ticosteroid therapy 4 times a year or daily or alternate-day systemic
corticosteroid therapy). Dosage of nasal corticosteroid probably shoul
d be added to the orally inhaled corticosteroid for total burden of in
haled corticosteroid. Potential treatment strategies based on risk fac
tors and bone density if indicated are offered to assist physicians tr
eating patients with asthma.