Biomarkers · Chemical
Cholesterol/HDL Ratio (calculated)
- Primary unit
- Ratio
- LOINC codes
- 13457-7, 2085-9, 2093-3, 2571-8, 33248-6, 43396-1, 64234-8, 79423-0, 8480-6, 95547-6, 95548-4, 95549-2, 9830-1, 2345-7, 4548-4, 10834-0, 14957-5, 1742-6, 1751-7, 1759-0, 1920-8, 1968-7, 1971-1, 1975-2, 2160-0, 2161-8, 2885-2, 6768-6, 9318-7, 98979-8, 11054-4
- Tests that measure Cholesterol/HDL Ratio (calculated)
- Quest Diagnostics 7
Ranges
Each lab publishes a reference range for the population groups it tests, usually the middle 95% of results. These intervals describe that population, not an optimal or healthy target. How ranges differ
Quest Diagnostics, ASCVD Risk Panel with Score 92053
| Total Cholesterol | Male (mg/dL) | Female (mg/dL) |
|---|---|---|
| <20 Years | <170 | <170 |
| ≥20 Years | <200 | <200 |
| HDL Cholesterol | ||
| <20 Years | >45 | >45 |
| ≥20 Years | ≥40 | ≥50 |
| Triglycerides | ||
| ≤9 Years | <75 | <75 |
| 10-19 Years | <90 | <90 |
| ≥20 Years | <150 | <150 |
| LDL-Cholesterol (Calc) | ||
| <20 Years | <110 | <110 |
| ≥20 Years | <100 | <100 |
| Cholesterol/HDL Ratio (Calc) | <5.0 | <5.0 |
| Non-HDL Cholesterol | ||
| <20 Years | <120 | <120 |
| ≥20 Years | <130 | <130 |
| ASCVD Risk Scores | See Laboratory Report |
Quest Diagnostics, Lipid Panel with Ratios 19543
| Total Cholesterol | Male (mg/dL) | Female (mg/dL) |
|---|---|---|
| <20 Years | <170 | <170 |
| ≥20 Years | <200 | <200 |
| HDL Cholesterol | ||
| <20 Years | >45 | >45 |
| ≥20 Years | ≥40 | ≥50 |
| Triglycerides | ||
| ≤9 Years | <75 | <75 |
| 10-19 Years | <90 | <90 |
| ≥20 Years | <150 | <150 |
| LDL-Cholesterol (Calc) | ||
| <20 Years | <110 | <110 |
| ≥20 Years | <100 | <100 |
| Cholesterol/HDL Ratio (Calc) | <5.0 | <5.0 |
| LDL/HDL Ratio (Calc) | ||
| Below Average Risk | <2.28 | <2.34 |
| Average Risk | 2.29-4.90 | 2.35-4.12 |
| Moderate Risk | 4.91-7.12 | 4.13-5.56 |
| High Risk | >7.13 | >5.57 |
| Non-HDL Cholesterol | ||
| <20 Years | <120 | <120 |
| ≥20 Years | <130 | <130 |
Quest Diagnostics, Lipid Panel with Reflex to Direct LDL 14852
| Total Cholesterol | Male (mg/dL) | Female (mg/dL) |
|---|---|---|
| <20 Years | <170 | <170 |
| ≥20 Years | <200 | <200 |
| HDL Cholesterol | ||
| <20 Years | >45 | >45 |
| ≥20 Years | ≥40 | ≥50 |
| Triglycerides | ||
| ≤9 Years | <75 | <75 |
| 10-19 Years | <90 | <90 |
| ≥20 Years | <150 | <150 |
| LDL-Cholesterol (Calc) | ||
| <20 Years | <110 | <110 |
| ≥20 Years | <100 | <100 |
| Cholesterol/HDL Ratio (Calc) | <5.0 | <5.0 |
| Non-HDL Cholesterol | ||
| <20 Years | <120 | <120 |
| ≥20 Years | <130 | <130 |
Quest Diagnostics, Lipid Panel, Non-Fasting without Triglycerides 91247
| Total Cholesterol | Male (mg/dL) | Female (mg/dL) |
|---|---|---|
| <20 Years | <170 | <170 |
| ≥20 Years | <200 | <200 |
| HDL Cholesterol | ||
| <20 Years | >45 | >45 |
| ≥20 Years | ≥40 | ≥50 |
| Cholesterol/HDL Ratio (calc) | <5.0 | <5.0 |
| Non-HDL Cholesterol (calc) | ||
| <20 Years | <120 | <120 |
| ≥20 Years | <130 | <130 |
Quest Diagnostics, Lipid Panel, Standard 7600
| Total Cholesterol | Male (mg/dL) | Female (mg/dL) |
|---|---|---|
| <20 Years | <170 | <170 |
| ≥20 Years | <200 | <200 |
| HDL Cholesterol | ||
| <20 Years | >45 | >45 |
| ≥20 Years | ≥40 | ≥50 |
| Triglycerides | ||
| ≤9 Years | <75 | <75 |
| 10-19 Years | <90 | <90 |
| ≥20 Years | <150 | <150 |
| LDL-Cholesterol (calc) | ||
| <20 Years | <110 | <110 |
| ≥20 Years | <100 | <100 |
| Cholesterol/HDL Ratio (calc) | <5.0 | <5.0 |
| Non-HDL Cholesterol (calc) | ||
| <20 Years | <120 | <120 |
| ≥20 Years | <130 | <130 |
Tests
Check the catalog code, specimen, method and preparation for every test that measures Cholesterol/HDL Ratio (calculated). Select up to five tests to compare them side by side.
Quest Diagnostics 7 tests
Panels that include this biomarker
Lipid Panel, Non-Fasting without Triglycerides 91247
4 analytes · Serum · Fasting not stated
Quest Diagnostics catalog pageMethod and collection
- Method
- Spectrophotometry (SP)
- Preparation
- If a cholesterol measurement is to be performed along with triglycerides, but not part of a lipid panel, then the patient should be fasting 9-12 hours prior to collection. If the cholesterol is ordered as part of a lipid panel, then a fasting sample is not required. The assay manufacturer Beckman Coulter advises: N-Acetyl Cysteine (NAC), when administered in therapeutic concentrations (for the treatment of acetaminophen overdose), has been determined to interfere with assays for cholesterol and uric acid where "NAC interference may lead to falsely low results." According to Beckman Coulter, the NAC interference should be insignificant by 12 hours after completion of the initial loading dose of an IV infusion treatment regimen consisting of an initial loading dose of 150 mg/kg administered over 1 hour, a second dose of 50 mg/kg administered over 4 hours and a third dose of 100 mg/kg administered over 16 hours.
Lipid Panel with Reflex to Direct LDL 14852
6 analytes · Serum · Fasting not stated
Quest Diagnostics catalog pageMethod and collection
- Method
- Spectrophotometry (SP)
- Preparation
- If a cholesterol measurement is to be performed along with triglycerides, but not part of a lipid panel, then the patient should be fasting 9-12 hours prior to collection. If the cholesterol is ordered as part of a lipid panel, then a fasting sample is not required. The assay manufacturer Beckman Coulter advises: N-Acetyl Cysteine (NAC), when administered in therapeutic concentrations (for the treatment of acetaminophen overdose), has been determined to interfere with assays for cholesterol and uric acid where "NAC interference may lead to falsely low results." According to Beckman Coulter, the NAC interference should be insignificant by 12 hours after completion of the initial loading dose of an IV infusion treatment regimen consisting of an initial loading dose of 150 mg/kg administered over 1 hour, a second dose of 50 mg/kg administered over 4 hours and a third dose of 100 mg/kg administered over 16 hours.
- Collection
- Centrifuge within 30-60 minutes following collection
Lipid Panel, Standard 7600
6 analytes · Serum · Fasting not stated
Quest Diagnostics catalog pageMethod and collection
- Method
- Spectrophotometry (SP)
- Preparation
- If a cholesterol measurement is to be performed along with triglycerides, but not part of a lipid panel, then the patient should be fasting 9-12 hours prior to collection. If the cholesterol is ordered as part of a lipid panel, then a fasting sample is not required. The assay manufacturer Beckman Coulter advises: N-Acetyl Cysteine (NAC), when administered in therapeutic concentrations (for the treatment of acetaminophen overdose), has been determined to interfere with assays for cholesterol and uric acid where "NAC interference may lead to falsely low results." According to Beckman Coulter, the NAC interference should be insignificant by 12 hours after completion of the initial loading dose of an IV infusion treatment regimen consisting of an initial loading dose of 150 mg/kg administered over 1 hour, a second dose of 50 mg/kg administered over 4 hours and a third dose of 100 mg/kg administered over 16 hours.
ASCVD Risk Panel with Score 92053
7 analytes · Serum · Fasting not stated
Quest Diagnostics catalog pageMethod and collection
- Method
- Enzymatic • Spectrophotometry (SP)
- Preparation
- If a cholesterol measurement is to be performed along with triglycerides, but not part of a lipid panel, then the patient should be fasting 9-12 hours prior to collection. If the cholesterol is ordered as part of a lipid panel, then a fasting sample is not required. The assay manufacturer Beckman Coulter advises: N-Acetyl Cysteine (NAC), when administered in therapeutic concentrations (for the treatment of acetaminophen overdose), has been determined to interfere with assays for cholesterol and uric acid where "NAC interference may lead to falsely low results." According to Beckman Coulter, the NAC interference should be insignificant by 12 hours after completion of the initial loading dose of an IV infusion treatment regimen consisting of an initial loading dose of 150 mg/kg administered over 1 hour, a second dose of 50 mg/kg administered over 4 hours and a third dose of 100 mg/kg administered over 16 hours.
- Collection
- For risk calculations to be performed, the following patient specific information have to be provided at time of order: Age: Years Gender: M (for male) or F (for female) Race-African American: Y (for yes) or N (for no) Systolic Blood Pressure: mmHg Treatment for High Blood Pressure: Y (for yes) or N (for no) Diabetes Status: Y (for yes) or N (for no) Smoking Status: Y (for Yes) or N (for no)
Lipid Panel with Ratios 19543
7 analytes · Serum · Fasting not stated
Quest Diagnostics catalog pageMethod and collection
- Method
- Spectrophotometry (SP)
- Preparation
- If a cholesterol measurement is to be performed along with triglycerides, but not part of a lipid panel, then the patient should be fasting 9-12 hours prior to collection. If the cholesterol is ordered as part of a lipid panel, then a fasting sample is not required. The assay manufacturer Beckman Coulter advises: N-Acetyl Cysteine (NAC), when administered in therapeutic concentrations (for the treatment of acetaminophen overdose), has been determined to interfere with assays for cholesterol and uric acid where "NAC interference may lead to falsely low results." According to Beckman Coulter, the NAC interference should be insignificant by 12 hours after completion of the initial loading dose of an IV infusion treatment regimen consisting of an initial loading dose of 150 mg/kg administered over 1 hour, a second dose of 50 mg/kg administered over 4 hours and a third dose of 100 mg/kg administered over 16 hours.
- Collection
- Centrifuge within 30-60 minutes following collection
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Quest Diagnostics test catalog
7 tests: codes, specimens, methods, preparation and reference intervals.
LOINC 13457-7, 2085-9, 2093-3, 2571-8, 33248-6, 43396-1, 64234-8, 79423-0, 8480-6, 95547-6, 95548-4, 95549-2, 9830-1, 2345-7, 4548-4, 10834-0, 14957-5, 1742-6, 1751-7, 1759-0, 1920-8, 1968-7, 1971-1, 1975-2, 2160-0, 2161-8, 2885-2, 6768-6, 9318-7, 98979-8, 11054-4
Regenstrief Institute codes that identify the same result across labs.
Search ClinicalTrials.gov for Cholesterol/HDL Ratio (calculated)
Registered studies that measure Cholesterol/HDL Ratio (calculated), on the U.S. National Library of Medicine registry.
Verify these ranges and sources
We compile this page from named laboratory catalogs, guidelines and studies. Labs calculate reference intervals from the people they test, for one assay method and one population group, so an interval describes that population rather than an optimal target.
Interpret your own results with a licensed clinician, or track your lab history and health goals in Aumnivida.
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