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Health disparities among adult patients with a phenotypic diagnosis of familial hypercholesterolemia in the CASCADE-FH™ patient registry.
Amrock, Stephen M; Duell, P Barton; Knickelbine, Thomas; Martin, Seth S; O'Brien, Emily C; Watson, Karol E; Mitri, Joanna; Kindt, Iris; Shrader, Peter; Baum, Seth J; Hemphill, Linda C; Ahmed, Catherine D; Andersen, Rolf L; Kullo, Iftikhar J; McCann, Dervilla; Larry, John A; Murray, Michael F; Fishberg, Robert; Guyton, John R; Wilemon, Katherine; Roe, Matthew T; Rader, Daniel J; Ballantyne, Christie M; Underberg, James A; Thompson, Paul; Duffy, Dannielle; Linton, MacRae F; Shapiro, Michael D; Moriarty, Patrick M; Knowles, Joshua W; Ahmad, Zahid S.
Afiliação
  • Amrock SM; Department of Medicine, Oregon Health & Science University, Portland, OR, USA.
  • Duell PB; Knight Cardiovascular Institute, Oregon Health & Science University, Portland, OR, USA.
  • Knickelbine T; Minneapolis Heart Institute Foundation, Minnaepolis, MN, USA.
  • Martin SS; Division of Cardiology, Department of Medicine, Johns Hopkins University, Baltimore, MD, USA.
  • O'Brien EC; Duke Clinical Research Institute, Durham, NC, USA.
  • Watson KE; UCLA Center for Cholesterol and Lipid Management, Los Angeles, CA, USA.
  • Mitri J; Joslin Diabetes Center, Harvard Medical School Boston, MA, USA.
  • Kindt I; The FH Foundation, Pasadena, CA, USA.
  • Shrader P; Duke Clinical Research Institute, Durham, NC, USA.
  • Baum SJ; Seth J. Baum, MD. Preventive Cardiology Inc., Boca Raton, FL, USA.
  • Hemphill LC; Massachusetts General Hospital, Boston, MA, USA.
  • Ahmed CD; The FH Foundation, South Pasadena, CA, USA.
  • Andersen RL; Lancaster General Health/Penn Medicine, Lancaster, PA, USA.
  • Kullo IJ; Department of Cardiovascular Diseases, Mayo Clinic, Rochester, MN, USA.
  • McCann D; Central Maine Heart and Vascular Institute/Central Maine Medical Center (CMMC), Lewiston ME, USA.
  • Larry JA; The Ohio State University Medical Center, Columbus, OH, USA.
  • Murray MF; Geisinger Health System, Forty Fort, PA, USA.
  • Fishberg R; Atlantic Health System, Springfield, NJ, USA.
  • Guyton JR; Duke University Medical Center, Durham, NC, USA.
  • Wilemon K; The FH Foundation, South Pasadena, CA, USA.
  • Roe MT; Duke Clinical Research Institute, Durham, NC, USA.
  • Rader DJ; University of Pennsylvania, Philadelphia, PA, USA.
  • Ballantyne CM; Baylor College of Medicine, Houston, TX, USA.
  • Underberg JA; New York University School of Medicine, New York, NY, USA.
  • Thompson P; Hartford Hospital, Hartford CT, USA.
  • Duffy D; Thomas Jefferson University, Philadelphia, PA, USA.
  • Linton MF; Vanderbilt University School of Medicine, Nashville, TN, USA.
  • Shapiro MD; Knight Cardiovascular Institute, Oregon Health & Science University, Portland, OR, USA.
  • Moriarty PM; University of Kansas Medical Center, Kansas City, KS, USA.
  • Knowles JW; The FH Foundation, South Pasadena, CA, USA; Division of Cardiovascular Medicine and Cardiovascular Institute, Department of Medicine, Stanford University, Stanford, CA, USA.
  • Ahmad ZS; Division of Nutrition and Metabolic Diseases, Department of Internal Medicine, University of Texas Southwestern, Dallas, TX, USA. Electronic address: zahid.ahmad@utsouthwestern.edu.
Atherosclerosis ; 267: 19-26, 2017 Dec.
Article em En | MEDLINE | ID: mdl-29080546
ABSTRACT
BACKGROUND AND

AIMS:

Most familial hypercholesterolemia (FH) patients remain undertreated, and it is unclear what role health disparities may play for FH patients in the US. We sought to describe sex and racial/ethnic disparities in a national registry of US FH patients.

METHODS:

We analyzed data from 3167 adults enrolled in the CAscade SCreening for Awareness and DEtection of Familial Hypercholesterolemia (CASCADE-FH) registry. Logistic regression was used to evaluate for disparities in LDL-C goals and statin use, with adjustments for covariates including age, cardiovascular risk factors, and statin intolerance.

RESULTS:

In adjusted analyses, women were less likely than men to achieve treated LDL-C of <100 mg/dL (OR 0.68, 95% CI, 0.57-0.82) or ≥50% reduction from pretreatment LDL-C (OR 0.79, 95% CI, 0.65-0.96). Women were less likely than men to receive statin therapy (OR, 0.60, 95% CI, 0.50-0.73) and less likely to receive a high-intensity statin (OR, 0.60, 95% CI, 0.49-0.72). LDL-C goal achievement also varied by race/ethnicity compared with whites, Asians and blacks were less likely to achieve LDL-C levels <100 mg/dL (Asians, OR, 0.47, 95% CI, 0.24-0.94; blacks, OR, 0.49, 95% CI, 0.32-0.74) or ≥50% reduction from pretreatment LDL-C (Asians, OR 0.56, 95% CI, 0.32-0.98; blacks, OR 0.62, 95% CI, 0.43-0.90).

CONCLUSIONS:

In a contemporary US population of FH patients, we identified differences in LDL-C goal attainment and statin usage after stratifying the population by either sex or race/ethnicity. Our findings suggest that health disparities contribute to the undertreatment of US FH patients. Increased efforts are warranted to raise awareness of these disparities.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Inibidores de Hidroximetilglutaril-CoA Redutases / Disparidades nos Níveis de Saúde / Hiperlipoproteinemia Tipo II / LDL-Colesterol Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Inibidores de Hidroximetilglutaril-CoA Redutases / Disparidades nos Níveis de Saúde / Hiperlipoproteinemia Tipo II / LDL-Colesterol Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2017 Tipo de documento: Article