Association of Inhaled Corticosteroid Use With Cataract Extraction in Elderly Patients

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1 Association of Inhaled Corticosteroid Use With Cataract Extraction in Elderly Patients Edeltraut Garbe, MD, MSc; Samy Suissa, PhD; Jacques LeLorier, MD, PhD, FRCPC Context. The use of systemic corticosteroids is a known risk factor for the development of cataracts. Objective. To determine whether treatment with inhaled corticosteroids is associated with cataract extraction in the elderly. Design. Case-control study. Setting. Quebec universal health insurance program for all elderly (provincial health insurance plan database [RAMQ database]). Patients. RAMQ enrollees 70 years and older. The 3677 cases were patients with a cataract extraction between 1992 and The controls were randomly selected from patients who did not have a diagnosis of cataract and matched to cases on the index date of the case. Main Outcome Measures. Odds ratio of cataract extraction in patients with prolonged cumulative exposure to inhaled corticosteroids compared with nonusers. Results. Excluding patients with systemic steroid treatment and after adjusting for age, sex, diabetes, systemic hypertension, glaucoma, ophthalmic steroids, and the number of physician claims for services, use of inhaled corticosteroids for more than 3 years was associated with undergoing cataract extraction (odds ratio [OR], 3.06; 95% confidence interval [CI], ). For high average daily doses of beclomethasone or budesonide ( 1 mg), the OR was elevated after more than 2 years of treatment (OR, 3.40; 95% CI, ), whereas for low to medium doses ( 1 mg) of these drugs, the OR was 1.63 (95% CI, ) after 2 years. Conclusion. Prolonged administration of high doses of inhaled corticosteroids increases the likelihood of undergoing cataract extraction in elderly patients. Further studies are needed to investigate the risk of developing cataracts for low to medium doses over longer periods. JAMA. 1998;280: INHALED corticosteroids have provided a significant advance in the management of asthma. Their use is now recommended at a much earlier stage of the From the Potsdam Institute of Pharmacoepidemiology and Technology Assessment, Potsdam, Germany (Dr Garbe); the Division of Clinical Epidemiology, Royal Victoria Hospital and the Department of Epidemiology and Biostatistics, McGill University (Dr Suissa) and the Centre de Recherche, Hôtel-Dieu de Montreal, Université de Montreal (Dr LeLorier), Montreal, Quebec. Reprints: Edeltraut Garbe, MD, MSc, Director, Potsdam Institute of Pharmacoepidemiology, and Technology Assessment, Otto-Erich-Str 7, Potsdam, Germany ( @compuserve.com). disease, coupled with a trend to prescribehigherdoses. 1-3 Theincreasinguse of inhaled corticosteroids over extended periods raises important questions relating to their safety and the possibility of adverse systemic effects. 4,5 For systemic corticosteroids, an increased risk for the development of posterior subcapsular cataract has been well established. 6-8 A number of case reports also suggested an increased risk of cataract for inhaled corticosteroids Several clinical studies initiated to investigate this association failed to find an elevated risk These studies were, however, of limited sample size and mostly conducted in children, in whom cataract is very rare. Recently, a cross-sectional study in the elderly reported an increased risk of cataracts associated with inhaled corticosteroid use. 18 Among limitations of their study, the authors discuss the large amount of missing data regarding both exposure-related variables and confounders. 18 The sample size of the study, although large in comparison with previous studies, was insufficient to investigate the influence of the daily dose and duration of inhaled steroid use. 19 Consideration of the daily dose is crucial, 20 since several studies suggest an increased risk of systemic effects only for high doses of inhaled corticosteroids. 4,5 In this study, we investigate whether the risk of cataract extraction is associated with the dose and duration of inhaled corticosteroid use and how the risk compares with that for systemic corticosteroids. METHODS Source of Data We conducted a case-control study among the elderly population of Quebec fortheyears1987to1994, usingdatafrom the provincial health insurance plan database (RAMQ database). This database includes all prescription drugs and medical services for all individuals 65 years or older. Of the estimated elderly in Quebec, more than were registered with the RAMQ in A high level of reliability and validity of the prescription data has been demonstrated. 21 Data in the records include information on the patient s age and sex, diagnoses, and all filled prescriptions and medical JAMA, August 12, 1998 Vol 280, No. 6 Cataracts and Exposure to Inhaled Corticosteroids Garbe et al 539

2 Table 1. Characteristics of Cases and Controls Characteristic Cases, No. (%) (n = 3677) procedures. The prescription data include the drug name, dispensation date, dose, dosage form, treatment duration, and quantity of drug dispensed. Drugs dispensed to patients during stays in hospitals or nursing homes are not included in the database. Diagnoses are coded according to the International Classification of Diseases, Ninth Revision (ICD-9). 22 The study was conducted using a 10% random sample of the database covering the years 1987 to Case and Control Selection Cases were subjects with a cataract extraction between 1992 and All had at least 5 years of prior follow-up logged in the database. The date of the cataract extraction was set as the index date for the case. If a patient had surgery for cataract on more than one occasion, the date of the first cataract extraction was set as the index date. Controls were randomly selected among all patientsinthedatabasewhodidnothave a diagnosis of cataract or had a cataract extraction. Like the cases, to be eligible controls were required to have been enrolled in the database for at least 5 years before a randomly assigned index date. Potential controls were matched to each case on the index date of the case to account for seasonal and secular trends in medication use. Up to 6 controls per case were then randomly selected from these matched sets. Controls, No. (%) (n = ) Odds Ratio* (95% CI) Age, y (21.0) 8013 (36.6) (41.3) 8187 (37.4) 1.8 ( ) (37.8) 5668 (25.9) 2.2 ( ) Sex Female 2479 (67.4) (57.1) 1.5 ( ) Diabetes mellitus treated with Oral antidiabetics 415 (11.3) 1908 (8.7) 1.1 ( ) Insulin 105 (2.9) 357 (1.6) 1.4 ( ) Systemic hypertension 1730 (47.1) 8288 (37.9) 1.1 ( ) Previous use of ocular steroids 383 (10.4) 1099 (5.0) 1.3 ( ) Previous use of oral steroids 112 (3.1) 245 (1.1) 2.1 ( ) Glaucoma 800 (21.8) 1574 (7.2) 2.7 ( ) 10 Physician claims 2727 (74.2) 8561 (39.2) 4.0 ( ) * for all other variables in the table. CI indicates confidence interval. In year before the index date. Corticosteroid Exposure We identified all dispensed prescriptions for inhaled and oral corticosteroids for cases and controls before the index date. The following inhaled corticosteroids are listed on the Quebec provincial drug formulary and were included in the exposure definition (ie, beclomethasone, budesonide, flunisolide, and triamcinolone). Oral corticosteroids on the drug formulary included cortisone, hydrocortisone, prednisone, prednisolone, triamcinolone, methylprednisolone, dexamethasone, and betamethasone. We defined recent exposure to inhaled corticosteroids as a drug dispensation that lasted into the 14-day period before the index date. We determined the influence of prolonged treatment with inhaled or oral corticosteroids by calculating the cumulative treatment duration with these drugs for each patient since entry into the database. For this calculation, we added the treatment durations of all dispensations of either inhaled or oral corticosteroids that were filled before the index date. For both groups of drugs, we defined the following categories of exposure duration: no exposure, exposure of 1 year or less, between 1 to 3 years, and more than 3 years. To eliminate confounding by concurrent oral corticosteroid use, we identified all patients who had not had systemic steroids dispensed before the index date. To reduce contamination by oral or inhaled corticosteroid use that could have taken place before the patient entered the database, we identified all patients who had not used inhaled or systemic steroids during their first year in the database. To investigate the influence of the daily dose of beclomethasone and/or budesonide, we determined for all patients the cumulative dose and cumulative duration of treatment with these drugs from the patients entry into the database until the index date. We calculated the average daily dose for each patient by dividing the cumulative dose of beclomethasone and/or budesonide by the cumulative treatment duration with these substances. We categorized this measure of the average daily dose into 1 mg or less or more than 1 mg of beclomethasone and/or budesonide per day, since doses of beclomethasone and budesonide below 1 mg/d have been suggested to be free of systemic adverse Table 2. Exposure to Different Substances of Inhaled Corticosteroids by Cases and Controls* Agent Cases Controls Triamcinolone 0 4 Flunisolide 7 34 Budesonide Beclomethasone Exposure to any inhaled steroids *Subjects may have been exposed to more than 1 corticosteroid preparation. effects in adults. 5 To investigate the influence of the dose according to the duration of use, we categorized the cumulative duration of use of beclomethasone and/or budesonide into 1 year or less of treatment, 1 to 2 years of treatment, and more than 2 years of treatment. Covariates Covariates included age, sex, systemic hypertension, diabetes mellitus, glaucoma, the number of physician claims for services in the year before the index date, and previous use of oral or ophthalmic corticosteroids. Systemic hypertension was defined by a diagnosis of hypertension before the index date. Diabetes mellitus was defined by an oral hypoglycemic drug or insulin being dispensed before the index date. We defined glaucoma by either a diagnosis of or medical treatment for glaucoma, including therapy with ocular -blockers, ocular parasympathomimetics, ocular -agonists, and carboanhydrase inhibitors. Because of codinginthedatabase, thisdefinitionalso includes patients with ocular hypertension without manifest glaucoma. We classified patients according to ophthalmic steroid use (any previous use vs no use) and oral steroid use (use of oral steroids for more than 365 days vs 365 days or less). We categorized the number of physician claims for services into 10 claims or less vs more than 10 claims in the year before the index date. Statistical Analysis The rate ratio of cataract extraction for each exposure group was estimated from odds ratios(ors) calculated by conditional logistic regression using the SAS PHREG program (SAS Institute Inc, Cary, NC). 23 We constructed individual models characterizing patients according to recent exposure to inhaled corticosteroids, the cumulative duration of inhaled corticosteroid treatment, and the dose and duration of beclomethasone and/or budesonide treatment. These analyses were either adjusted for oral corticosteroid use or restricted to patients who had not used oral corticosteroids before the index date. In some analyses, we also excluded patients who had used inhaled corticosteroids during their first year after entry into the da- 540 JAMA, August 12, 1998 Vol 280, No. 6 Cataracts and Exposure to Inhaled Corticosteroids Garbe et al

3 tabase. We alsoanalyzed the risk for systemic corticosteroids, using the same cumulative exposure periods as for inhaled corticosteroids, while in one analysis, we excluded patients treated with systemic corticosteroids during their first year in the database. For all these analyses, the reference category was the absence of exposure to the respective form of corticosteroid after entry into the database. All models simultaneously controlled for all covariates listed above. Two-tailed P values less than.05 were considered significant and 95% confidence intervals (CIs) were calculated for all relative risks. We further calculated the excess risk (ER) of cataract extraction by determiningthebaselineincidencerate(i 0 ) in our study sample and applying the OR as an estimator of the risk ratio (RR) to this rate by using the following formula 24 : ER = (RR-1)I 0. RESULTS We identified patients with cataract extractions, of whom 6537 patients did not meet the eligibility criterion of being in the database for at least 5 years before the index event, leaving a group of 3677 cases. We selected controls who fulfilled the matching and eligibility criteria, that is an average of 5.9 controls per case. The mean (SD) follow-up period in the database was similar for cases and controls, with 2354 days (SD, 309) for cases and 2308 days (SD, 305) for controls. Characteristics of cases and controls are summarized in Table 1. The risk of cataract extraction increased with age and was elevated in women, in patients with diabetes, in patients with glaucoma, and in patients who had been dispensed ophthalmic or oral steroids before the index date. For patients who had more than 10 physician claims for services in the year before the index date, the risk was increased 4-fold compared with patients who had 10 or fewer physician claims. Table 2 shows that, anytime during the observation period, 428 cases and 1946 controls were exposed to inhaled corticosteroids. Beclomethasone and budesonide accounted for the majority of prescriptions. Seventy-six cases and 278 controls had used more than 1 type of inhaled corticosteroid. A total of 163 cases and 581 controls had been exposed recently to inhaled glucocorticoids, yielding an adjusted OR of 1.28 (95% CI, ). Table 3 displays the risk estimates for inhaled corticosteroids associated with different cumulative periods of use. Excluding patients with systemic corticosteroid use, there was no increase in risk observed in patients who had used inhaled glucocorticoids for 1 year or less Table 3. Odds Ratios of Cataract Extraction According to Cumulative Treatment Duration With Inhaled Corticosteroids Cumulative Treatment Duration Cases/Controls Crude Odds Ratio Odds Ratio* (95% CI) Adjusting for Oral Steroid Use No treatment 3249/ Up to 1 y 296/ ( ) 1-3 y 86/ ( ) 3 y 46/ ( ) Excluding Patients With Oral Steroid Use No treatment 3032/ Up to 1 y 187/ ( ) 1-3 y 27/ ( ) 3 y 15/ ( ) Also Excluding Patients With Inhaled Steroid Use During Their First Year in the Database No treatment 3032/ Up to 1 y 173/ ( ) 1-3 y 18/ ( ) 3 y 6/ ( ) *Odds ratio adjusted for age, sex, diabetes mellitus, systemic hypertension, glaucoma, previous ocular steroid use, and number of physician claims for services. CI indicates confidence interval. Dispensations of oral corticosteroids for more than 1 year. Also excluding patients who had any dispensation of oral corticosteroids since entry into the database. Table 4. Odds Ratios of Cataract Extraction According to Average Daily Dose of Inhaled Corticosteroid, Stratified by Cumulative Duration of Inhaled Corticosteroid Use* Dose of Inhaled Corticosteroid Cases/Controls Crude Odds Ratio Odds Ratio (95% CI) No treatment 3032/ Cumulative Treatment Duration With Inhaled Steroids for 1 Year Low to medium dose 114/ ( ) High dose 72/ ( ) Cumulative Treatment Duration With Inhaled Steroids for 1-2 Years Low to medium dose 11/ ( ) High dose 6/ ( ) Cumulative Treatment Duration With Inhaled Steroids for 2 Years Low to medium dose 14/ ( ) High dose 10/ ( ) *Excluding patients with dispensations of oral corticosteroids, flunisolide, or triamcinolone. odds ratio for age, sex, diabetes mellitus, hypertension, glaucoma, previous ocular steroid use, and number of physician claims for services. CI indicates confidence interval. Low to medium dose, average daily dose of up to 1 mg of beclomethasone or budesonide. High dose, average daily dose of more than 1 mg of beclomethasone or budesonide. Table 5. Odds Ratios of Cataract Extraction According to Cumulative Treatment Duration With Oral Corticosteroids Cumulative Treatment Duration Cases/Controls Crude Odds Ratio Odds Ratio* (95% CI) Patients Exposed to Oral Corticosteroids No treatment 3261/ Up to 1 y 304/ ( ) 1-3 y 64/ ( ) 3 y 48/ ( ) Excluding Patients With Oral Steroid Use During Their First Year in the Database No treatment 3261/ Up to 1 y 271/ ( ) 1-3 y 46/ ( ) 3 y 13/ ( ) *Odds ratio adjusted for age, sex, diabetes mellitus, hypertension, previous ocular steroid use, and number of physician claims for services. CI indicates confidence interval. and in patients whose cumulative treatment duration ranged from 1 to 3 years. Patients who had used inhaled steroids for more than 3 years had an elevated risk with an adjusted OR of 3.06 (95% CI, ). A further slight increase in risk was observed when the analysis excluded patients who had used inhaled steroids during their first year after entry into the database. Afterexcludingpatientswithsystemic steroid use, we identified 227 cases and 1202 controls who had beclomethasone and/or budesonide dispensed (Table 4). JAMA, August 12, 1998 Vol 280, No. 6 Cataracts and Exposure to Inhaled Corticosteroids Garbe et al 541

4 After patients were stratified by the cumulative treatment duration, cataract extraction was more frequent among patients who had received high doses of beclomethasone or budesonide for more than 2 years (adjusted OR, 3.40; 95% CI, ). The OR for low to medium doses of beclomethasone or budesonide given for more than 2 years was 1.63 (95% CI, ). For less than 2 years of treatment, there was no increase in risk seen for either low or high doses. A total of 416 cases and 1724 controls were exposed to oral glucocorticoids before the index date. Table 5 shows the risk estimates for oral corticosteroids associated with different cumulative treatment durations. In comparison with inhaled corticosteroids, the risk of cataract extraction was already increased after more than 1 year of oral steroid use. A further increase in risk was observed for a cumulative exposure of more than 3 years. Excluding patients from the analysis who had used oral corticosteroids during their first year after entry into the database, as we did in the analysis for inhaled corticosteroids, did not result in important changes of these risk estimates. In our study sample, the baseline incidence of cataract extraction was 1.75% per year. Applying our estimate of the rate ratio 3.06 for more than 3 years of inhaled steroid use to this baseline incidence, we calculated an ER of 3.61% per year, or 361 additional cases per elderly persons per year. COMMENT The results of our study suggest that prolonged use of inhaled corticosteroids increases the risk of cataract extraction in the elderly. Patients who had no use of oral corticosteroids recorded for at least 5 years, but had been treated with inhaled corticosteroids for more than 3 years, had a 3-fold increased risk of cataract extraction compared with patients not treated with inhaled steroids. Based on this risk estimate, we calculated that such extended use of inhaled corticosteroids would give rise to 361 additional cases of cataract extraction per elderly patients per year. Our findings are consistent with the known relation between use of systemic steroids and cataract formation 6,25 and confirm the results of a recent study from Australia. 18 Previous studies investigating this association did not find an increased risk, which may have resulted from insufficient power of these studies. In the Australian study, Cumming et al 18 suggested an increased risk of posterior subcapsular cataract with increasing lifetime doses of inhaled corticosteroids. Due to the limited sample size in their study, they could not investigate the risk according to the daily dose of inhaled steroid and its duration of use. 19 In a review of clinical pharmacological studies, it has been suggested that both beclomethasone and budesonide in doses less than 1 mg/d were free of systemic adverse effects in adults, while in doses more than 1 mg/d, there was a potential for systemic effects. 5 Classifying the average daily dose of beclomethasone and budesonide in study patients according to this cut point into low to medium or high doses, we did not observe an increased risk of cataract for either dose category for a treatment duration of up to 2 years. After more than 2 years of treatment, the risk was elevated more than 3-fold for high doses, whereas a much smaller and statistically not significant increase in risk was seen for low to medium doses. Our study also confirmed an increased risk for various previously described risk factors for cataract, among them old age, female sex, diabetes mellitus, glaucoma, and systemic and ophthalmic steroid use For systemic corticosteroids, we observed an increasing risk with increasing cumulative duration of treatment that already became apparent after treatment exceeded 1 year. The risk was also considerably elevated for patients with a higher number of physician encounters, which may reflect an increased risk of cataract extraction in patients with higher comorbidity. Also, cataract extraction is an elective procedure, and its timing will also depend on the physician s advice. Some limitations of the study design need to be considered. We defined cases by cataract extraction, an end point that has often been used in the investigation of risk factors for cataract. 15,32-39 Cataracts requiring extraction are those sufficiently severe to affect vision and, therefore, are of greatest clinical and public health impact. It would have been desirable to investigate the risk also according to the subtype of cataract leading to the surgical procedure, but this information was not available to us. Lack of classification by subtype, however, cannot explain any of the positive associations we observed. If an association is not common to all cataract subtypes, then an examination of the subtype-specific risk will yield even a higher point estimate of the risk than the one presented in our study. Although we had for each patient at least 5 years of detailed drug exposure information preceding the index date, we did not have information on the patients drug use before the age of 65 years. The different exposure durations we calculated may therefore actually be longer when the patients used the medications also before they entered the database. We also cannot rule out that among the patients with no systemic corticosteroid use some had used oral glucocorticoids before the age of 65 years. To address this concern of confounding by previous oral corticosteroid use, we investigated the risk of cataract extraction in patients who had not used oral corticosteroids and, in addition, had not used inhaled corticosteroids during their first year in the database. Since the risk estimate did not substantially change in this group of patients, which more likely represents new users of inhaled corticosteroids, confounding by previous systemic corticosteroid use appears to be of less concern. Since the database does not contain information about drugs dispensed in hospitals, we cannot exclude that some patients may have received systemic corticosteroids while hospitalized. Short treatment courses with systemic steroids in the hospital will be of minor importance for the development of cataract, since longer treatment periods with systemic corticosteroids are usually needed to increase the risk. 7 In patients treated with systemic corticosteroids for an extended period, the corticosteroid is usually tapered and is likely to be continued after discharge from the hospital and will, therefore, also appear in the ambulatory records of drug dispensations. In our analysis, we controlled for several factors that have been discussed as risk factors for cataract; however, we did not have information on others, such as trauma, UV radiation, alcohol, and smoking. We have no reason to believe that trauma, UV radiation, or alcohol intake are related to exposure with inhaled corticosteroids and, therefore, do not expect confounding by these variables. Smoking, described as a risk factor for cataract in some studies, 25 but not in others, 40,41 is a known risk factor for respiratory diseases. Although it has been suggestedthatsmokerswhodeveloprespiratory symptoms for any reason tend to quit smoking, 42 this may not necessarily be the case. 43 However, since the risk of cataract in smokers is not high, 25 failing to adjust for smoking should not affect the risk estimates in an important way. In summary, the results of our study demonstrate an increased risk of cataract for prolonged use of high doses of inhaled corticosteroids. Further studies are needed to investigate the risk according to the dose over more extended treatment periods, since an increased risk also for lower doses of inhaled steroids cannot be ruled out by our study findings. In addition, in vitro studies 542 JAMA, August 12, 1998 Vol 280, No. 6 Cataracts and Exposure to Inhaled Corticosteroids Garbe et al

5 have demonstrated different ratios of topical to systemic activity for different inhaled steroids 4,44 ; therefore, studies are also needed that investigate the risk according to the steroid substance. The Pharmacoepidemiology Unit of the Centre Hospitalier de l Université de Montreal, Campus Hôtel-Dieu, and the McGill Pharmacoepidemiology Research Unit are funded by the Fonds de la Recherche en Santé du Québec. Dr Samy Suissa is the recipient of a Senior Scientist Award from the Medical Research Council of Canada, Ottawa. Cooperation on this project was supported by the Association of Clinical Pharmacology, Berlin/Brandenburg, Germany. The authors would like to thank Jacques Barry LSC, ADM, MBA, of the Régie de l assurance maladie du Québec for providing and facilitating access to the databases, Jean-Francois Boivin, MD, DSc, of McGill University for his critical reading of the manuscript, and Anne-Marie Castilloux, MSc, from the Pharmacoepidemiology Unit, Centre Hospitalier de l Université de Montreal, Campus Hôtel- Dieu, for her assistance in the data management. References 1. Reed CE. Aerosol glucocorticoid treatment of asthma. Am Rev Respir Dis. 1990;141(suppl):S82- S British Thoracic Society. Guidelines for management of asthma in adults, I: chronic persistent asthma. BMJ. 1990;301: British Thoracic Society. Guidelines for the management of asthma: a summary. BMJ. 1993;306: Barnes PJ. Inhaled glucocorticoids for asthma. N Engl J Med. 1995;332: Barnes NC. Safety of high-dose inhaled corticosteroids. Respir Med. 1993;87(suppl): Black RL, Oglesby RB, von Sallmann L, Bunim JJ. 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Absence of posterior subcapsular cataracts in young patients treated with inhaled glucocorticoids. Lancet. 1993;342: Tinkelman DG, Reed CE, Nelson HS, Offord KP. Aerosol beclomethasone dipropionate compared with theophylline as primary treatment of chronic, mild to moderately severe asthma in children. Pediatrics. 1993;92: Toogood JH, Markov AE, Baskerville J, Dyson C. Association of ocular cataracts with inhaled and oral steroid therapy during long-term treatment of asthma. J Allergy Clin Immunol. 1993;91: Nassif E, Weinberger M, Sherman B, Brown K. Extrapulmonary effects of maintenance corticosteroid therapy with alternate-day prednisone and inhaled beclomethasone in children with chronic asthma. J Allergy Clin Immunol. 1987;80: Cumming RG, Mitchell P, Leeder SR. Use of inhaled corticosteroids and the risk of cataracts. N Engl J Med. 1997;337: Cumming RG, Mitchell P, Leeder SR. Inhaled corticosteroids and the risk of cataract. N Engl J Med. 1997;337: Garbe E, Suissa S. 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Allopurinol and cataracts. Am J Ophthalmol. 1984;98: Walker AM, Jick H, Gorman MR, Wallach RW. Steroids, diabetes, analgesics, and the risk of cataract: lessons from the epidemiology of cataract extraction. J Clin Res Drug Dev. 1988;2: Harding JJ, van Heyningen R. Drugs, including alcohol, that act as risk factors for cataract, and possible protection against cataract by aspirin-like analgesics and cyclopenthiazide. Br J Ophthalmol. 1988;72: Dolezal JM, Perkins ES, Wallace RB. Sunlight, skin sensitivity, and senile cataract. Am J Epidemiol. 1989;129: Munoz B, Tajchman U, Bochow T, West S. Alcohol use and risk of posterior subcapsular opacities. Arch Ophthalmol. 1993;111: The Italian-American Cataract Study Group. Risk factors for age-related cortical, nuclear, and posterior subcapsular cataracts. Am J Epidemiol. 1991;133: Mohan M, Sperduto RD, Angra SK, et al. India- US case-control study of age-related cataracts. 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6 1. Carpenter CT, Kaiser AB. Purpura fulminans in pneumococcal sepsis: case report and review. Scand J Infect Dis. 1997;29: Pipe SW, Schmaier AH, Nichols WC, et al. Neonatal purpura fulminans in association with factor V R506Q mutation. J Pediatr. 1996;128: Sackesen C, Secmeer G, Gurgey A, et al. Homozygous factor V Leiden mutation in a child with meningococcal purpura fulminans. Pediatr Infect Dis J. 1998;17: Inbal A, Kenet G, Zivelin A, et al. Purpura fulminans induced by disseminated intravascular coagulation following infection in 2 unrelated children with double heterozygosity for factor V Leiden and protein S deficiency. Thromb Haemost. 1997;77: An HIV-Resistant Allele Is Exceptionally Frequent in New Guinean Highlanders To the Editor. Stromal-derived factor (SDF-1) is the natural ligand for CXCR4, a coreceptor with CD4 for T-lymphocyte cell line tropic human immunodeficiency virus 1 (HIV-1). Recently, a common variant, SDF1-3 A, was identified in SDF-1, and an SDF1-3 A/3 A homozygous state was shown to delay the onset of acquired immunodeficiency syndrome (AIDS) in an association study involving 2857 patients. 1 The recessive protection of the SDF-1-3 A allele was pronounced to be twice as effective as the dominant genetic restriction of AIDS conferred by CCR5 and CCR2 chemokine receptor variants. 1-3 Using a polymerase chain reaction restriction fragment length polymorphism assay, we investigated the distribution of the SDF1-3 A allele in 16 worldwide representative populations. 1 Our results showed that the SDF1-3 A allele frequencies vary drastically among the populations surveyed, ranging from 2.9% to 71.4% (Table). African populations exhibit the lowest frequencies (2.9%-9.1%), rates that agree with the reported frequency in African Americans. 1 No SDF1-3 A homozygous individuals were found in African samples in this study. The frequency of the allele increases in American Indians, Europeans, and Asians, ranging from 12.2% to 36.6%. However, exceptionally high frequencies were found in 4 non Austronesian-speaking populations, especially in 2 New Guinean highlander populations(66.7%-71.4%). The frequency of homozygotes in those populations can be as high as 47.6%. Samples from New Guinean Aborigines were collected from 2 New Guinean highlander populations (the New Guinean 1 population sample from an unspecified region was collected by A. Kimura, PhD, and the New Guinean 2 population sample from the Kwoma, Iatmul, and Bargan areas was collected by A. Wilson, PhD, and P. Parham, PhD [oral communication, January 10, 1996]). The description of other samples appears in the Table. In addition, no significant deviation from Hardy-Weinberg equilibrium was detected in each population studied, implying the absence of detectable selection differentials between the individuals with and without the SDF1-3 A allele and population substructure in those samples. Our data indicate that the SDF1-3 A allele is distributed across all continents, which contrasts with the predominant presence of the HIV-resistant allele CCR5-32 (at the CCR5 locus) in only white populations. 4 Thus, the global presence of the SDF1-3 A allele together with its rareness in African populations (near absence of homozygotes in Africa) implies that the mutation originally occurred in Africa, and the frequency of the mutant alleles was elevated in non-african populations because of the subsequent Frequency of SDF1-3 A Allele and Homozygote in Worldwide Populations SDF1-3 A Frequency Continent Population Chromosomes Typed* Allele Homozygote Africa Biaka pygmy Africa Mbuti pygmy Africa Lissongo America Karitiana America Surui America Mayan Europe Italian Europe Northern European Asia Northern Chinese Asia Southern Chinese Asia Japanese Asia Cambodian Oceania Australian Aborigine Oceania Nasioi Melanesian Oceania New Guinean Oceania New Guinean *The number of subjects studied is half this number. bottleneck events during the migration of modern humans from Africa. 5 Bing Su, PhD Ranajit Chakraborty, PhD Li Jin, PhD University of Texas Houston School of Public Health Junhua Xiao, PhD Daru Lu, PhD Fudan University Shanghai, China 1. Winkler C, Modi W, Smith MW, et al. Genetic restriction of AIDS pathogenesis by an SDF-1 chemokine gene variant. Science. 1998;279: Dean M, Carrington M, Winkler C, et al. Genetic restriction of HIV-1 infection and progression to AIDS by a deletion allele of the CKR5 structural gene. Science. 1996; 273: Smith MW, Dean M, Carrington M, et al. Contrasting genetic influence of CCR2 and CCR5 variants on HIV-1 infection and disease progression. Science. 1997;277: Martinson JJ, Chapman NH, Rees DC, et al. Global distribution of the CCR5 gene 32-basepair deletion. Nat Genet. 1997;16: Tishkoff SA, Dietzsch E, Speed W, et al. Global patterns of linkage disequilibrium at the CD4 locus and modern human origins. Science. 1996;271: CORRECTION Incorrect Footnotes in Table. In the Original Contribution entitled Association of Inhaled Corticosteroid Use With Cataract Extraction in Elderly Patients, published in the August 12, 1998, issue of THE JOURNAL (1998;280: ), there was an incorrect unit of measure and a misspelling in the last 2 footnotes of Table 4. The third footnote read, Low to medium dose, average daily dose of up to 1gofbeclomethasone or budesnoide. It should have read, Low to medium dose, average daily dose of up to 1 mg of beclomethasone or budesonide. The fourth footnote read, High dose, average daily dose of more than 1 g of beclomethasone or budesonide. It should have read, High dose, average daily dose of more than 1 mg of beclomethasone or budesonide JAMA, December 2, 1998 Vol 280, No. 21 Letters