Comparing different assessments of remnant lipoprotein cholesterol: The very large database of lipids

Remnant lipoprotein cholesterol (RLP-C) is a risk factor for atherosclerotic cardiovascular disease, but there is no standard method for measurement. Some studies have used very low-density lipoprotein cholesterol estimated by the Friedewald equation to approximate RLP-C using a basic lipid panel, w...

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Published inJournal of clinical lipidology Vol. 13; no. 4; pp. 634 - 644
Main Authors Faridi, Kamil F., Quispe, Renato, Martin, Seth S., Hendrani, Aditya D., Joshi, Parag H., Brinton, Eliot A., Cruz, Daniel E., Banach, Maciej, Toth, Peter P., Kulkarni, Krishnaji, Jones, Steven R.
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.07.2019
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Online AccessGet full text
ISSN1933-2874
1876-4789
DOI10.1016/j.jacl.2019.06.001

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Abstract Remnant lipoprotein cholesterol (RLP-C) is a risk factor for atherosclerotic cardiovascular disease, but there is no standard method for measurement. Some studies have used very low-density lipoprotein cholesterol estimated by the Friedewald equation to approximate RLP-C using a basic lipid panel, whereas others have attempted to measure RLP-C with ultracentrifugation. The aim of the study was to compare RLP-C levels estimated from basic lipid parameters to those measured by ultracentrifugation. We analyzed 1,350,908 individuals from the Very Large Database of Lipids, comparing one estimate of RLP-C using basic lipid parameters (RLP-Cestimated = non–high-density lipoprotein cholesterol − Friedewald-estimated low-density lipoprotein cholesterol for triglycerides <355 mg/dL [4 mmol/L], or non–high-density lipoprotein − directly measured low-density lipoprotein for triglycerides ≥355 mg/dL) to levels measured by vertical auto profile ultracentrifugation (RLP-Cmeasured = dense subfraction of very low-density lipoprotein cholesterol + intermediate-density lipoprotein cholesterol). We calculated correlations between RLP-Cestimated and RLP-Cmeasured along with median within-subject differences between RLP-Cestimated and RLP-Cmeasured across quintiles of RLP-Cestimated. We also assessed correlations with RLP-C estimated from basic lipid parameters using a novel method of calculating low-density lipoprotein cholesterol with a patient-specific conversion factor (RLP-Cestimated-N). Our cohort was 48% male, and median (interquartile range) age was 59 (49–69) years. Median (interquartile range) RLP-Cestimated and RLP-Cmeasured were 23 (16.4–33.2) and 24 (19–32) mg/dL, respectively. The correlation between RLP-Cestimated and RLP-Cmeasured was 0.76. Based on the specified definition of RLP-Cestimated, the correlation between RLP-Cestimated and triglyceride/5 for triglyceride < 355 mg/dL was exactly 1.0. RLP-Cestimated was lower than RLP-Cmeasured in the first and second quintiles of RLP-Cestimated but greater in the highest quintile. The correlations with RLP-Cestimated-N were 0.98 and 0.81 for RLP-Cestimated and RLP-Cmeasured, respectively. A previously used estimate of RLP-C using basic lipid parameters correlates weakly with remnants measured by ultracentrifugation. Our findings emphasize the need to standardize definitions and measurements of RLP-C. •Remnant lipoproteins are a risk factor for atherosclerotic cardiovascular disease.•A consensus method for measuring remnant lipoproteins is lacking.•Two previously studied assessments of remnant lipoproteins are weakly correlated.•Measured correlations are weaker at higher levels of remnant lipoproteins.•A standardized measurement of remnant lipoproteins is still needed.
AbstractList Remnant lipoprotein cholesterol (RLP-C) is a risk factor for atherosclerotic cardiovascular disease, but there is no standard method for measurement. Some studies have used very low-density lipoprotein cholesterol estimated by the Friedewald equation to approximate RLP-C using a basic lipid panel, whereas others have attempted to measure RLP-C with ultracentrifugation.BACKGROUNDRemnant lipoprotein cholesterol (RLP-C) is a risk factor for atherosclerotic cardiovascular disease, but there is no standard method for measurement. Some studies have used very low-density lipoprotein cholesterol estimated by the Friedewald equation to approximate RLP-C using a basic lipid panel, whereas others have attempted to measure RLP-C with ultracentrifugation.The aim of the study was to compare RLP-C levels estimated from basic lipid parameters to those measured by ultracentrifugation.OBJECTIVEThe aim of the study was to compare RLP-C levels estimated from basic lipid parameters to those measured by ultracentrifugation.We analyzed 1,350,908 individuals from the Very Large Database of Lipids, comparing one estimate of RLP-C using basic lipid parameters (RLP-Cestimated = non-high-density lipoprotein cholesterol - Friedewald-estimated low-density lipoprotein cholesterol for triglycerides <355 mg/dL [4 mmol/L], or non-high-density lipoprotein - directly measured low-density lipoprotein for triglycerides ≥355 mg/dL) to levels measured by vertical auto profile ultracentrifugation (RLP-Cmeasured = dense subfraction of very low-density lipoprotein cholesterol + intermediate-density lipoprotein cholesterol). We calculated correlations between RLP-Cestimated and RLP-Cmeasured along with median within-subject differences between RLP-Cestimated and RLP-Cmeasured across quintiles of RLP-Cestimated. We also assessed correlations with RLP-C estimated from basic lipid parameters using a novel method of calculating low-density lipoprotein cholesterol with a patient-specific conversion factor (RLP-Cestimated-N).METHODSWe analyzed 1,350,908 individuals from the Very Large Database of Lipids, comparing one estimate of RLP-C using basic lipid parameters (RLP-Cestimated = non-high-density lipoprotein cholesterol - Friedewald-estimated low-density lipoprotein cholesterol for triglycerides <355 mg/dL [4 mmol/L], or non-high-density lipoprotein - directly measured low-density lipoprotein for triglycerides ≥355 mg/dL) to levels measured by vertical auto profile ultracentrifugation (RLP-Cmeasured = dense subfraction of very low-density lipoprotein cholesterol + intermediate-density lipoprotein cholesterol). We calculated correlations between RLP-Cestimated and RLP-Cmeasured along with median within-subject differences between RLP-Cestimated and RLP-Cmeasured across quintiles of RLP-Cestimated. We also assessed correlations with RLP-C estimated from basic lipid parameters using a novel method of calculating low-density lipoprotein cholesterol with a patient-specific conversion factor (RLP-Cestimated-N).Our cohort was 48% male, and median (interquartile range) age was 59 (49-69) years. Median (interquartile range) RLP-Cestimated and RLP-Cmeasured were 23 (16.4-33.2) and 24 (19-32) mg/dL, respectively. The correlation between RLP-Cestimated and RLP-Cmeasured was 0.76. Based on the specified definition of RLP-Cestimated, the correlation between RLP-Cestimated and triglyceride/5 for triglyceride < 355 mg/dL was exactly 1.0. RLP-Cestimated was lower than RLP-Cmeasured in the first and second quintiles of RLP-Cestimated but greater in the highest quintile. The correlations with RLP-Cestimated-N were 0.98 and 0.81 for RLP-Cestimated and RLP-Cmeasured, respectively.RESULTSOur cohort was 48% male, and median (interquartile range) age was 59 (49-69) years. Median (interquartile range) RLP-Cestimated and RLP-Cmeasured were 23 (16.4-33.2) and 24 (19-32) mg/dL, respectively. The correlation between RLP-Cestimated and RLP-Cmeasured was 0.76. Based on the specified definition of RLP-Cestimated, the correlation between RLP-Cestimated and triglyceride/5 for triglyceride < 355 mg/dL was exactly 1.0. RLP-Cestimated was lower than RLP-Cmeasured in the first and second quintiles of RLP-Cestimated but greater in the highest quintile. The correlations with RLP-Cestimated-N were 0.98 and 0.81 for RLP-Cestimated and RLP-Cmeasured, respectively.A previously used estimate of RLP-C using basic lipid parameters correlates weakly with remnants measured by ultracentrifugation. Our findings emphasize the need to standardize definitions and measurements of RLP-C.CONCLUSIONSA previously used estimate of RLP-C using basic lipid parameters correlates weakly with remnants measured by ultracentrifugation. Our findings emphasize the need to standardize definitions and measurements of RLP-C.
Remnant lipoprotein cholesterol (RLP-C) is a risk factor for atherosclerotic cardiovascular disease, but there is no standard method for measurement. Some studies have used very low-density lipoprotein cholesterol estimated by the Friedewald equation to approximate RLP-C using a basic lipid panel, whereas others have attempted to measure RLP-C with ultracentrifugation. The aim of the study was to compare RLP-C levels estimated from basic lipid parameters to those measured by ultracentrifugation. We analyzed 1,350,908 individuals from the Very Large Database of Lipids, comparing one estimate of RLP-C using basic lipid parameters (RLP-Cestimated = non–high-density lipoprotein cholesterol − Friedewald-estimated low-density lipoprotein cholesterol for triglycerides <355 mg/dL [4 mmol/L], or non–high-density lipoprotein − directly measured low-density lipoprotein for triglycerides ≥355 mg/dL) to levels measured by vertical auto profile ultracentrifugation (RLP-Cmeasured = dense subfraction of very low-density lipoprotein cholesterol + intermediate-density lipoprotein cholesterol). We calculated correlations between RLP-Cestimated and RLP-Cmeasured along with median within-subject differences between RLP-Cestimated and RLP-Cmeasured across quintiles of RLP-Cestimated. We also assessed correlations with RLP-C estimated from basic lipid parameters using a novel method of calculating low-density lipoprotein cholesterol with a patient-specific conversion factor (RLP-Cestimated-N). Our cohort was 48% male, and median (interquartile range) age was 59 (49–69) years. Median (interquartile range) RLP-Cestimated and RLP-Cmeasured were 23 (16.4–33.2) and 24 (19–32) mg/dL, respectively. The correlation between RLP-Cestimated and RLP-Cmeasured was 0.76. Based on the specified definition of RLP-Cestimated, the correlation between RLP-Cestimated and triglyceride/5 for triglyceride < 355 mg/dL was exactly 1.0. RLP-Cestimated was lower than RLP-Cmeasured in the first and second quintiles of RLP-Cestimated but greater in the highest quintile. The correlations with RLP-Cestimated-N were 0.98 and 0.81 for RLP-Cestimated and RLP-Cmeasured, respectively. A previously used estimate of RLP-C using basic lipid parameters correlates weakly with remnants measured by ultracentrifugation. Our findings emphasize the need to standardize definitions and measurements of RLP-C. •Remnant lipoproteins are a risk factor for atherosclerotic cardiovascular disease.•A consensus method for measuring remnant lipoproteins is lacking.•Two previously studied assessments of remnant lipoproteins are weakly correlated.•Measured correlations are weaker at higher levels of remnant lipoproteins.•A standardized measurement of remnant lipoproteins is still needed.
Remnant lipoprotein cholesterol (RLP-C) is a risk factor for atherosclerotic cardiovascular disease, but there is no standard method for measurement. Some studies have used very low-density lipoprotein cholesterol estimated by the Friedewald equation to approximate RLP-C using a basic lipid panel, whereas others have attempted to measure RLP-C with ultracentrifugation. The aim of the study was to compare RLP-C levels estimated from basic lipid parameters to those measured by ultracentrifugation. We analyzed 1,350,908 individuals from the Very Large Database of Lipids, comparing one estimate of RLP-C using basic lipid parameters (RLP-C  = non-high-density lipoprotein cholesterol - Friedewald-estimated low-density lipoprotein cholesterol for triglycerides <355 mg/dL [4 mmol/L], or non-high-density lipoprotein - directly measured low-density lipoprotein for triglycerides ≥355 mg/dL) to levels measured by vertical auto profile ultracentrifugation (RLP-C  = dense subfraction of very low-density lipoprotein cholesterol + intermediate-density lipoprotein cholesterol). We calculated correlations between RLP-C and RLP-C along with median within-subject differences between RLP-C and RLP-C across quintiles of RLP-C . We also assessed correlations with RLP-C estimated from basic lipid parameters using a novel method of calculating low-density lipoprotein cholesterol with a patient-specific conversion factor (RLP-C ). Our cohort was 48% male, and median (interquartile range) age was 59 (49-69) years. Median (interquartile range) RLP-C and RLP-C were 23 (16.4-33.2) and 24 (19-32) mg/dL, respectively. The correlation between RLP-C and RLP-C was 0.76. Based on the specified definition of RLP-C , the correlation between RLP-C and triglyceride/5 for triglyceride < 355 mg/dL was exactly 1.0. RLP-C was lower than RLP-C in the first and second quintiles of RLP-C but greater in the highest quintile. The correlations with RLP-C were 0.98 and 0.81 for RLP-C and RLP-C , respectively. A previously used estimate of RLP-C using basic lipid parameters correlates weakly with remnants measured by ultracentrifugation. Our findings emphasize the need to standardize definitions and measurements of RLP-C.
Author Joshi, Parag H.
Cruz, Daniel E.
Hendrani, Aditya D.
Toth, Peter P.
Kulkarni, Krishnaji
Martin, Seth S.
Banach, Maciej
Jones, Steven R.
Brinton, Eliot A.
Quispe, Renato
Faridi, Kamil F.
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  fullname: Brinton, Eliot A.
  organization: Utah Lipid Center, Salt Lake City, UT, USA
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  organization: Division of Cardiovascular Disease, Department of Internal Medicine, Beth Israel Deaconess Medical Center, Boston, MA, USA
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  givenname: Maciej
  surname: Banach
  fullname: Banach, Maciej
  organization: Department of Hypertension, Chair of Nephrology and Hypertension, Medical University of Lodz, Lodz, Poland
– sequence: 9
  givenname: Peter P.
  surname: Toth
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  givenname: Steven R.
  surname: Jones
  fullname: Jones, Steven R.
  organization: Ciccarone Center for Prevention of Heart Disease, Division of Cardiology, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA
BackLink https://www.ncbi.nlm.nih.gov/pubmed/31320236$$D View this record in MEDLINE/PubMed
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Issue 4
Keywords Lipids
Remnant lipoprotein
Triglycerides
Cholesterol
Dyslipidemia
Language English
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Snippet Remnant lipoprotein cholesterol (RLP-C) is a risk factor for atherosclerotic cardiovascular disease, but there is no standard method for measurement. Some...
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SubjectTerms Cholesterol
Dyslipidemia
Lipids
Remnant lipoprotein
Triglycerides
Title Comparing different assessments of remnant lipoprotein cholesterol: The very large database of lipids
URI https://www.clinicalkey.com/#!/content/1-s2.0-S1933287419302132
https://dx.doi.org/10.1016/j.jacl.2019.06.001
https://www.ncbi.nlm.nih.gov/pubmed/31320236
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