Health disparities among adult patients with a phenotypic diagnosis of familial hypercholesterolemia in the CASCADE-FH™ patient registry

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. We analyzed data from 3167 adults enrolled in the...

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Published in:Atherosclerosis Vol. 267; pp. 19 - 26
Main Authors: 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.
Format: Journal Article
Language:English
Published: Ireland Elsevier B.V 01-12-2017
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Abstract 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. 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. 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). 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. •Disparities by sex and race/ethnicity were noted in US lipid clinics.•Women were less likely than men to achieve LDL-C goals and to receive statins.•Asians and blacks were 40–50% less likely to achieve LDL-C goals than whites.
AbstractList 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. 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. 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). 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. •Disparities by sex and race/ethnicity were noted in US lipid clinics.•Women were less likely than men to achieve LDL-C goals and to receive statins.•Asians and blacks were 40–50% less likely to achieve LDL-C goals than whites.
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. 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. 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). 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.
BACKGROUND AND AIMSMost 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.METHODSWe 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.RESULTSIn 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).CONCLUSIONSIn 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.
Author Ballantyne, Christie M.
Linton, MacRae F.
Baum, Seth J.
Shrader, Peter
Wilemon, Katherine
Mitri, Joanna
Roe, Matthew T.
O'Brien, Emily C.
Duffy, Dannielle
Larry, John A.
Murray, Michael F.
Moriarty, Patrick M.
Ahmad, Zahid S.
Guyton, John R.
Knowles, Joshua W.
Knickelbine, Thomas
Thompson, Paul
Rader, Daniel J.
Kindt, Iris
Fishberg, Robert
Hemphill, Linda C.
Duell, P. Barton
Martin, Seth S.
McCann, Dervilla
Shapiro, Michael D.
Underberg, James A.
Amrock, Stephen M.
Watson, Karol E.
Andersen, Rolf L.
Ahmed, Catherine D.
Kullo, Iftikhar J.
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  organization: Minneapolis Heart Institute Foundation, Minnaepolis, MN, USA
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  organization: Division of Cardiology, Department of Medicine, Johns Hopkins University, Baltimore, MD, USA
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  organization: UCLA Center for Cholesterol and Lipid Management, Los Angeles, CA, USA
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  fullname: Mitri, Joanna
  organization: Joslin Diabetes Center, Harvard Medical School Boston, MA, USA
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  organization: The FH Foundation, Pasadena, CA, USA
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  organization: Duke Clinical Research Institute, Durham, NC, USA
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  fullname: Baum, Seth J.
  organization: Seth J. Baum, MD. Preventive Cardiology Inc., Boca Raton, FL, USA
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  surname: Hemphill
  fullname: Hemphill, Linda C.
  organization: Massachusetts General Hospital, Boston, MA, USA
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  organization: The FH Foundation, South Pasadena, CA, USA
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  organization: Lancaster General Health/Penn Medicine, Lancaster, PA, USA
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  organization: Department of Cardiovascular Diseases, Mayo Clinic, Rochester, MN, USA
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  organization: Central Maine Heart and Vascular Institute/Central Maine Medical Center (CMMC), Lewiston ME, USA
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  givenname: John A.
  surname: Larry
  fullname: Larry, John A.
  organization: The Ohio State University Medical Center, Columbus, OH, USA
– sequence: 17
  givenname: Michael F.
  surname: Murray
  fullname: Murray, Michael F.
  organization: Geisinger Health System, Forty Fort, PA, USA
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  organization: Atlantic Health System, Springfield, NJ, USA
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  orcidid: 0000-0003-0224-7923
  surname: Guyton
  fullname: Guyton, John R.
  organization: Duke University Medical Center, Durham, NC, USA
– sequence: 20
  givenname: Katherine
  orcidid: 0000-0003-4629-6866
  surname: Wilemon
  fullname: Wilemon, Katherine
  organization: The FH Foundation, South Pasadena, CA, USA
– sequence: 21
  givenname: Matthew T.
  surname: Roe
  fullname: Roe, Matthew T.
  organization: Duke Clinical Research Institute, Durham, NC, USA
– sequence: 22
  givenname: Daniel J.
  surname: Rader
  fullname: Rader, Daniel J.
  organization: University of Pennsylvania, Philadelphia, PA, USA
– sequence: 23
  givenname: Christie M.
  surname: Ballantyne
  fullname: Ballantyne, Christie M.
  organization: Baylor College of Medicine, Houston, TX, USA
– sequence: 24
  givenname: James A.
  surname: Underberg
  fullname: Underberg, James A.
  organization: New York University School of Medicine, New York, NY, USA
– sequence: 25
  givenname: Paul
  surname: Thompson
  fullname: Thompson, Paul
  organization: Hartford Hospital, Hartford CT, USA
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  fullname: Duffy, Dannielle
  organization: Thomas Jefferson University, Philadelphia, PA, USA
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  givenname: MacRae F.
  surname: Linton
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  organization: Vanderbilt University School of Medicine, Nashville, TN, USA
– sequence: 28
  givenname: Michael D.
  surname: Shapiro
  fullname: Shapiro, Michael D.
  organization: Knight Cardiovascular Institute, Oregon Health & Science University, Portland, OR, USA
– sequence: 29
  givenname: Patrick M.
  surname: Moriarty
  fullname: Moriarty, Patrick M.
  organization: University of Kansas Medical Center, Kansas City, KS, USA
– sequence: 30
  givenname: Joshua W.
  surname: Knowles
  fullname: Knowles, Joshua W.
  organization: The FH Foundation, South Pasadena, CA, USA
– sequence: 31
  givenname: Zahid S.
  surname: Ahmad
  fullname: Ahmad, Zahid S.
  email: zahid.ahmad@utsouthwestern.edu
  organization: Division of Nutrition and Metabolic Diseases, Department of Internal Medicine, University of Texas Southwestern, Dallas, TX, USA
BackLink https://www.ncbi.nlm.nih.gov/pubmed/29080546$$D View this record in MEDLINE/PubMed
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ContentType Journal Article
Copyright 2017 Elsevier B.V.
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Keywords Ethnicity
FH
Hyperlipidemia
ASCVD
LDL-C
Race
Sex
PCSK9
Disparities
Familial hypercholesterolemia
Language English
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PublicationTitle Atherosclerosis
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Snippet Most familial hypercholesterolemia (FH) patients remain undertreated, and it is unclear what role health disparities may play for FH patients in the US. We...
BACKGROUND AND AIMSMost familial hypercholesterolemia (FH) patients remain undertreated, and it is unclear what role health disparities may play for FH...
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SubjectTerms Adult
African Americans
Aged
Asian Americans
Cardiovascular Diseases - metabolism
Cholesterol, HDL - metabolism
Cholesterol, LDL - blood
Disparities
Ethnic Groups
Ethnicity
Familial hypercholesterolemia
Female
Health Status Disparities
Healthcare Disparities
Humans
Hydroxymethylglutaryl-CoA Reductase Inhibitors - therapeutic use
Hyperlipidemia
Hyperlipoproteinemia Type II - blood
Hyperlipoproteinemia Type II - diagnosis
Hyperlipoproteinemia Type II - ethnology
Male
Middle Aged
Multicenter Studies as Topic
Odds Ratio
Phenotype
Prospective Studies
Race
Registries
Retrospective Studies
Risk Factors
Sex
Sex Factors
Title Health disparities among adult patients with a phenotypic diagnosis of familial hypercholesterolemia in the CASCADE-FH™ patient registry
URI https://dx.doi.org/10.1016/j.atherosclerosis.2017.10.006
https://www.ncbi.nlm.nih.gov/pubmed/29080546
https://search.proquest.com/docview/1957491197
Volume 267
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