Search

Objectives: Recruitment strategies usually focused on a single International Classification of Diseases, Ninth Revision, Clinical Modification (ICD-9-CM) code and rarely included exclusion criteria. The purpose of this study was to validate a claims-based algorithm to identify, from Veterans Affairs administrative data, eligible participants to be recruited into a hypertension trial., Study Design: Cross-sectional., Methods: Subjects were labeled as eligible if they were 75 years or older, had a hypertension ICD-9-CM code (401.x-405.x, 437.2) and did not have a diabetes (250.xx) or stroke (430.x-436.x, 437.1, 437.9, 438.x) ICD-9-CM code. We compared the eligible subjects with the medical record-which was considered the gold standard-and we calculated the positive predictive value (PPV) of identifying a subject in the medical record., Results: The algorithm identified 3591 elderly veterans with hypertension with no diabetes or stroke, and we reviewed the medical records of 76 randomly selected patients. In the sample of medical record review, the mean age in years was 83 ± 5.3, 48% had coronary artery disease, and the mean systolic blood pressure was 134 mm Hg ± 15.5. When compared with the medical record, the PPV for any hypertension code was 93% (95% CI, 85%-98%), and for the entire algorithm, including 75 years or older and the absence of both diabetes and stroke, the PPV was 83% (95% CI, 73%-91%)., Conclusions: The use of any ICD-9-CM code for hypertension is useful to identify elderly patients with hypertension. The algorithm to identify elderly patients with hypertension and without diabetes or stroke is a useful tool to also identify eligible patients for clinical trial participation.

Rationale: Insulin resistance and low high-density lipoprotein (HDL) are associated with pulmonary morbidity, including asthma, but the underlying mechanisms are not well elucidated., Objectives: To investigate whether systemic inflammation underlies the association of metabolic abnormalities with pulmonary function among urban adolescents., Methods: Th-cell responses and monocyte subsets, and their association with serum homeostatic model assessment of insulin resistance (HOMA-IR) and HDL, and pulmonary function were quantified in 168 adolescents, including 42 obese subjects with asthma, 42 normal-weight subjects with asthma, 40 obese subjects without asthma, and 44 healthy control subjects. Th-cell responses (Th1 [CD4(+)IFNγ(+)] and Th2 [CD4(+)IL4(+)] cells) to stimulation with phytohemagglutinin, leptin, and dust mite, and classical (CD14(+)CD16(-)), resident (CD14(+)CD16(+)), and patrolling (CD14dimCD16(+)) monocytes, and their C-C chemokine receptor type-2 (CCR2) expression were quantified by flow cytometry., Measurements and Main Results: Th1/Th2 ratio to all three stimuli was higher in obese subjects with asthma than normal-weight subjects with asthma and directly correlated with HOMA-IR. Classical monocytes inversely associated with Th1/Th2 ratio to phytohemagglutinin (r = -0.43; P = 0.01) and directly with Asthma Control Test score (β = 1.09; P = 0.04), while patrolling monocytes correlated with Composite Asthma Severity Index score (β = 1.11; P = 0.04) only among obese subjects with asthma. HDL was inversely associated with patrolling monocytes and directly associated with CCR2 expression on resident monocytes. CCR2 expression on patrolling monocytes predicted residual volume (RV), RV/TLC ratio, and FRC, after adjusting for HDL, but not after adjusting for body mass index. Association of Th1/Th2 ratio with RV, FRC, and inspiratory capacity was attenuated after adjusting for HOMA-IR., Conclusions: Th1 polarization and monocyte activation among obese subjects with asthma correlates with metabolic abnormalities. Association of monocyte activation with pulmonary function is mediated by body mass index, whereas that of Th1 polarization is mediated by insulin resistance.

The frequency of chronic renal failure increases with age, especially in women after menopause. Glomerulosclerosis is a common cause of chronic renal failure in aging. We reported that pre-menopausal female C57BL6 (B6) mice are resistant to glomerulosclerosis, irrespective of the type of injury. However, we now show that B6 mice develop progressive glomerulosclerosis after menopause. Glomerular lesions, first recognized in 18-month-old mice, consisted of hypertrophy, vascular pole sclerosis, and mesangial cell proliferation. Diffuse but moderate mesangial sclerosis and more marked hypertrophy were present at 22 months. At 28 to 30 months the glomerulosclerosis was diffuse and increased levels of type I and type IV collagen and transforming growth factor-beta 1 mRNA were present. Urine albumin excretion was significantly increased in 30-month-old mice. Mesangial cells isolated from 28-month-old mice retained their sclerotic phenotype in vitro. Comparison of the effects of uninephrectomy (Nx) in 20-month-old and 2.5-month-old mice revealed a 1.7-fold increase in urine albumin excretion, accelerated glomerulosclerosis, and renal function insufficiency in 20-month-old Nx mice, but not in 2.5-month-old Nx mice. Glycemic levels, glucose, insulin tolerance, and blood pressure were normal at all ages. Thus, B6 mice model the increased frequency of chronic renal failure in postmenopausal women and provide a model for studying the mechanism(s) of glomerulosclerosis in aging women.