Calorie Restriction Clinical Trial
Official title:
Legacy Effects of CALERIE™, a 2-year Calorie Restriction Intervention, on Hallmarks of Healthspan and Aging
The purpose of the CALERIE Legacy Study is to follow up on the health and wellness of participants from phase 2 of the Comprehensive Assessment of Long-term Effects of Reducing Intake of Energy (CALERIE) trial, which was conducted from 2007 to 2011.
Status | Recruiting |
Enrollment | 216 |
Est. completion date | January 31, 2026 |
Est. primary completion date | December 31, 2025 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 33 Years to 70 Years |
Eligibility | Inclusion Criteria: - Enrolled in the CALERIE trial and started their allocated group (CR intervention or ad libitum control condition) - Willing and able to attend one of the clinical sites for an in-person visit and provide informed consent Exclusion Criteria: - Pregnant women - Women less than 12 months postpartum - Documented note from the CALERIE trial indicating that the subject should not be contacted or requested not to be contacted for future research - Diagnosed active cancer or terminal illness |
Country | Name | City | State |
---|---|---|---|
United States | Pennington Biomedical Research Center | Baton Rouge | Louisiana |
United States | Jean Mayer USDA Human Nutrition Research Center on Aging at Tufts University | Boston | Massachusetts |
United States | Washington University School of Medicine | Saint Louis | Missouri |
Lead Sponsor | Collaborator |
---|---|
Tufts University | Duke University, National Institute on Aging (NIA), Pennington Biomedical Research Center, Washington University School of Medicine |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Biological age - Klemera-Doubal Method | Biological age will be quantified by the Klemera-Doubal Method (KDM), an algorithm-based measure. Biological age is expressed in years. | 10-15 years post CALERIE trial | |
Primary | Biological age - Homeostatic Dysregulation | Biological age will be quantified by homeostatic dysregulation, an algorithm-based measure. Biological age is expressed in years. | 10-15 years post CALERIE trial | |
Primary | Biological age - Levine Phenotypic Age | Biological age will be quantified by Levine Phenotypic Age, an algorithm-based measure. Biological age is expressed in years. | 10-15 years post CALERIE trial | |
Primary | Healthspan | Healthspan will be assessed by sex-specific metabolic syndrome score (MSS). MSS was developed using mean blood pressure (MBP; = [2 × diastolic blood pressure + systolic blood pressure]/3), high density lipoprotein cholesterol (HDL), triglycerides (TG), waist circumference (WC), and fasting blood glucose (FBG):
Women: MSS = [45-HDL]/SDHDLW+ [TG-150]/SDTG + [WC-88]/SDWCW + [FBG-100]/SDFBG + [mean BP-100]/SDMBP Men: MSS = [40-HDL]/SDHDLW+ [TG-150]/SDTG + [WC-102]/SDWCW + [FBG-100]/SDFBG + [mean BP-100]/SDMBP This score does not have a unit. |
10-15 years post CALERIE trial | |
Secondary | Height | Height will be measured in cm. | 10-15 years post CALERIE trial | |
Secondary | Weight | Weight will be measured in kg. | 10-15 years post CALERIE trial | |
Secondary | Waist circumference | Weight circumference will be measured in cm. | 10-15 years post CALERIE trial | |
Secondary | Hip circumference | Hip circumference will be measured in cm. | 10-15 years post CALERIE trial | |
Secondary | Body mass index (BMI) | BMI (kg/m2) will be calculated using height and weight measurements. | 10-15 years post CALERIE trial | |
Secondary | Blood pressure | Systolic and diastolic blood pressure will be measured in mmHg. | 10-15 years post CALERIE trial | |
Secondary | Pulse rate at rest | Pulse rate will be measured in beats/min. | 10-15 years post CALERIE trial | |
Secondary | Respiration rate at rest | Respiration rate will be measured in breaths/min. | 10-15 years post CALERIE trial | |
Secondary | Fat mass | Whole-body fat mass (%) as measured by dual-energy X-ray absorptiometry. | 10-15 years post CALERIE trial | |
Secondary | Fat-free mass | Whole-body fat-free mass (%) as measured by dual-energy X-ray absorptiometry. | 10-15 years post CALERIE trial | |
Secondary | Bone mineral content | Whole-body bone mineral content (g/cm2) as measured by dual-energy X-ray absorptiometry. | 10-15 years post CALERIE trial | |
Secondary | Resting metabolic rate (RMR) | RMR will be measured in kcal/d by indirect calorimetry using a ventilated hood system. | 10-15 years post CALERIE trial | |
Secondary | Respiratory quotient (RQ) | RQ will be measured by indirect calorimetry using a ventilated hood system. This is a ratio and does not have a unit. | 10-15 years post CALERIE trial | |
Secondary | Maximal aerobic capacity (V?O2max) | Maximal aerobic capacity (V?O2max) will be measured in mL/kg/min using the Cornell incremental treadmill test. | 10-15 years post CALERIE trial | |
Secondary | Interleukin-6 (IL-6) | IL-6, a blood-based biomarker of aging proposed by the Targeting Aging with MEtformin (TAME) Biomarkers Workgroup, will be measured in pg/mL. | 10-15 years post CALERIE trial | |
Secondary | Insulin - TAME panel | Insulin, a blood-based biomarker of aging proposed by the TAME Biomarkers Workgroup, will be measured in µIU/mL. | 10-15 years post CALERIE trial | |
Secondary | Insulin - 0 min (OGTT) | Insulin (µIU/mL) will be measured at 0 minutes (pre-dose) during an oral glucose tolerance test (OGTT) to evaluate glucoregulatory response. | 10-15 years post CALERIE trial | |
Secondary | Insulin - 30 min (OGTT) | Insulin (µIU/mL) will be measured at 30 minutes post dose during an OGTT to evaluate glucoregulatory response. | 10-15 years post CALERIE trial | |
Secondary | Insulin - 60 min (OGTT) | Insulin (µIU/mL) will be measured at 60 minutes post dose during an OGTT to evaluate glucoregulatory response. | 10-15 years post CALERIE trial | |
Secondary | Insulin - 90 min (OGTT) | Insulin (µIU/mL) will be measured at 90 minutes post dose during an OGTT to evaluate glucoregulatory response. | 10-15 years post CALERIE trial | |
Secondary | Insulin - 120 min (OGTT) | Insulin (µIU/mL) will be measured at 120 minutes post dose during an OGTT to evaluate glucoregulatory response. | 10-15 years post CALERIE trial | |
Secondary | Insulin-like growth factor 1 (IGF-1) | IGF-1, a blood-based biomarker of aging proposed by the TAME Biomarkers Workgroup, will be measured in ng/mL. | 10-15 years post CALERIE trial | |
Secondary | Hemoglobin A1c (HbA1c) | HbA1c, a blood-based biomarker of aging proposed by the TAME Biomarkers Workgroup, will be measured in mmol/mol. | 10-15 years post CALERIE trial | |
Secondary | Tumor necrosis factor a receptor II (TNFRII) | TNFRII, a blood-based biomarker of aging proposed by the TAME Biomarkers Workgroup, will be measured in ng/mL. | 10-15 years post CALERIE trial | |
Secondary | High-sensitivity C-reactive protein (hsCRP) | hsCRP, a blood-based biomarker of inflammation, will be measured in µg/mL. | 10-15 years post CALERIE trial | |
Secondary | Growth/differentiation factor 15 (GDF15) | GDF15, a blood-based biomarker of aging proposed by the TAME Biomarkers Workgroup, will be measured in pg/mL. | 10-15 years post CALERIE trial | |
Secondary | Cystatin C | Cystatin C, a blood-based biomarker of aging proposed by the TAME Biomarkers Workgroup, will be measured in mg/L. | 10-15 years post CALERIE trial | |
Secondary | N-terminal B-type natriuretic peptide (NT-proBNP) | NT-proBNP, a blood-based biomarker of aging proposed by the TAME Biomarkers Workgroup, will be measured in pg/mL. | 10-15 years post CALERIE trial | |
Secondary | Senescence-associated secretory phenotype (SASP) proteins | SASP proteins, blood-based biomarkers of cellular senescence, will be measured using a SASP panel. | 10-15 years post CALERIE trial | |
Secondary | Urinary Isoprostanes - iPF(2a)-III | Urinary iPF(2a)-III, a biomarker of systemic oxidative stress, will be measured in ng/mL. | 10-15 years post CALERIE trial | |
Secondary | Urinary Isoprostanes - 2,3-dinor-iPF(2a)-III | Urinary 2,3-dinor-iPF(2a)-III, a biomarker of systemic oxidative stress, will be measured in ng/mL. | 10-15 years post CALERIE trial | |
Secondary | Urinary Isoprostanes - iPF(2a)-VI | Urinary iPF(2a)-VI, a biomarker of systemic oxidative stress, will be measured in ng/mL. | 10-15 years post CALERIE trial | |
Secondary | Urinary Isoprostanes - 8,12-iso-iPF(2a)-VI | Urinary 8,12-iso-iPF(2a)-VI, a biomarker of systemic oxidative stress, will be measured in ng/mL. | 10-15 years post CALERIE trial | |
Secondary | Creatinine | Creatinine, a byproduct of routine activity in the muscle, will be measured in urine in mg/mL. | 10-15 years post CALERIE trial | |
Secondary | Dehydroepiandrosterone (DHEA) | DHEA, a blood-based steroid hormone, will be measured in µg/dL. | 10-15 years post CALERIE trial | |
Secondary | Interleukin 1 beta (IL-1b) | IL-1b, a blood-based marker of inflammation, will be measured in pg/mL. | 10-15 years post CALERIE trial | |
Secondary | Interleukin 8 (IL-8) | IL-8, a blood-based marker of inflammation, will be measured in pg/mL. | 10-15 years post CALERIE trial | |
Secondary | Tumor necrosis factor a (TNF-a) | TNF-a, a blood-based marker of inflammation, will be measured in pg/mL. | 10-15 years post CALERIE trial | |
Secondary | Insulin-like growth factor-binding protein 1 (IGFBP-1) | IGFBP-1, a blood-based transport protein, will be measured in ng/mL. | 10-15 years post CALERIE trial | |
Secondary | Transforming growth factor beta 1 (TGFB1) | TGFB1, a blood-based marker of immune function, will be measured in ng/mL. | 10-15 years post CALERIE trial | |
Secondary | Insulin-like growth factor-binding protein 3 (IGFBP-3) | IGFBP-3, a blood-based transport protein, will be measured in ng/mL. | 10-15 years post CALERIE trial | |
Secondary | Platelet-derived growth factor-AB (PDGF-AB) | PDGF-AB, a blood-based marker of cellular function, will be measured in ng/mL. | 10-15 years post CALERIE trial | |
Secondary | Intercellular Adhesion Molecule 1 (ICAM-1) | ICAM-1, a blood-based marker of inflammation, will be measured in ng/mL. | 10-15 years post CALERIE trial | |
Secondary | Growth hormone | Growth hormone, a blood-based bio-marker of cellular function, will be measured in ng/mL. | 10-15 years post CALERIE trial | |
Secondary | Monocyte Chemoattractant Protein 1 (MCP1) | MCP1, a blood-based marker of inflammation, will be measured in pg/mL. | 10-15 years post CALERIE trial | |
Secondary | Leptin | Leptin, a hormonal regulator of energy balance, will be measured in pg/mL. | 10-15 years post CALERIE trial | |
Secondary | Total adiponectin | Total adiponectin, a protein hormone that regulates several metabolic processes, including glucose regulation and fatty acid oxidation, will be measured in µg/mL. | 10-15 years post CALERIE trial | |
Secondary | High molecular weight adiponectin | High molecular weight adiponectin, a protein hormone that regulates several metabolic processes, including glucose regulation and fatty acid oxidation, will be measured in µg/mL. | 10-15 years post CALERIE trial | |
Secondary | Muscle strength - Knee extension (60°) | Knee extension at 60 degrees per second will be expressed in Nm. | 10-15 years post CALERIE trial | |
Secondary | Muscle strength - Knee extension (180°) | Knee extension at 180 degrees per second will be expressed in Nm. | 10-15 years post CALERIE trial | |
Secondary | Muscle strength - Knee flexion (60°) | Knee flexion at 60 degrees per second will be expressed in Nm. | 10-15 years post CALERIE trial | |
Secondary | Muscle strength - Knee flexion (180°) | Knee flexion at 180 degrees per second will be expressed in Nm. | 10-15 years post CALERIE trial | |
Secondary | Handgrip Strength | Handgrip strength will be measured via a hand dynamometer and expressed in kg. | 10-15 years post CALERIE trial | |
Secondary | Physical functioning | Physical functioning as measured by a physical performance battery. This physical performance battery provides a composite score ranging from 0 to 12 and includes results from the balance, gait and chair stand tests. | 10-15 years post CALERIE trial | |
Secondary | Cognition | Cognition as measured by the Cambridge Neuropsychological Test Automated Battery (CANTAB). The CANTAB evaluates six main areas of cognitive function: reaction time; verbal recognition memory; intra-extra dimensional set shift; rapid visual information processing; delayed matching to sample; and spatial working memory. | 10-15 years post CALERIE trial | |
Secondary | Dietary intake- calories | Dietary intake in calories (kcals/day), as measured by multiple-pass 24-hour dietary recalls and Nutrition Data System for Research (NDSR) software. | 10-15 years post CALERIE trial | |
Secondary | Dietary intake - carbohydrates | Dietary carbohydrate as % of energy or grams will be measured by multiple-pass 24-hour dietary recalls and Nutrition Data System for Research (NDSR) software. | 10-15 years post CALERIE trial | |
Secondary | Dietary intake - proteins | Dietary proteins as % of energy or grams will be measured by multiple-pass 24-hour dietary recalls and Nutrition Data System for Research (NDSR) software. | 10-15 years post CALERIE trial | |
Secondary | Health-related quality of life | Quality of life as measured by the RAND 36-Item Short Form Survey (SF-36). The RAND SF-36 measures eight aspects of health: physical functioning, role limitations due to physical health problems, role limitations due to personal or emotional problems, energy/fatigue, emotional well-being, social functioning, bodily pain, and general health perceptions. It also includes a single item that provides an indication of perceived change in health. Each item is on a 3- or 5-point Likert scale (1-3 or 1-5). Each response is transformed to a recoded value of 0-100, and the transformed scores of the 9 subscales are averaged to derive a composite score. Higher scores indicate more favorable health states. | 10-15 years post CALERIE trial | |
Secondary | Depression status | Depression status as measured by the Beck Depression Inventory II (BDI-II). The 21-item BDI-II measures depression severity. The score range is 0-63, with higher scores indicating greater depression severity. Nineteen items are on a 4-point Likert scale (0-3). Two items are on a 7-point Likert scale, and responses are scaled to 0-3. The values are summed to calculate the total score. | 10-15 years post CALERIE trial | |
Secondary | Mood | Mood as measured by the Profile of Mood States Second Edition (POMS 2). The POMS 2 assesses six mood subscales using 65 items, each on a 5-point Likert scale (0-4): tension-anxiety (9 items, score range 0-36), depression-dejection (15 items, range 0-60), anger-hostility (12 items, range 0-48), vigor-activity (8 items, range 0-32), fatigue-inertia (7 items, range 0-28), and confusion-bewilderment (7 items, range 0-28). High vigor-activity scores reflect a good mood or emotion, and low scores in the other subscales reflect a good mood or emotion. Total mood disturbance, which is calculated by subtracting the vigor subscale score from the total subscale score (range 0-200), also will be assessed. | 10-15 years post CALERIE trial | |
Secondary | Sleep | Sleep as measured by the Pittsburgh Sleep Quality Index (PSQI). The PSQI measures sleep quality and disturbance over the course of one month using seven subscales: subjective sleep quality; sleep latency; sleep duration; habitual sleep efficiency; sleep disturbances; use of sleeping medication; and daytime dysfunction. The scoring range of each subscale is 0-3. The scoring range of the Global PSQI (the composite score of the seven subscales) is 0-21. For both the subscales and Global PSQI, higher scores indicate greater difficulties with sleeping. | 10-15 years post CALERIE trial | |
Secondary | Sexual function | Sexual function as measured by the Derogatis Interview for Sexual Functioning - Self Report (DISF-SR). Both versions of the DISF-SR (male and female) are scored from 20 to 75, with higher scores indicating higher sexual functioning. | 10-15 years post CALERIE trial | |
Secondary | Food cravings | Food cravings as measured by the Food Cravings Questionnaire-Trait (FCQ-T). The FCQ-T measures frequency and intensity of food cravings. It has 39 items on a 6-point Likert scale (1-6) and a score range of 39-234. Higher scores indicate more frequent and intense food cravings. Scores on all items are summed for a total score. | 10-15 years post CALERIE trial | |
Secondary | Dietary restraint, disinhibition, and hunger | Dietary restraint, disinhibition, and hunger as measured by the Three-Factor Eating Questionnaire (TFEQ). The 51-item TFEQ will be used to measure dietary restraint (21 items), disinhibition (16 items), and hunger (14 items). Item responses are scored as 0 or 1 and summed. Higher scores indicate higher levels of restrained eating (range 0-21), disinhibited eating (range 0-16), and predisposition to hunger (range 0-14). | 10-15 years post CALERIE trial | |
Secondary | Disordered eating | Disordered eating as measured by the Multiaxial Assessment of Eating Disorder Symptoms (MAEDS). MAEDS will be used to assess six domains of disordered eating: binge eating (range 8-56), restrictive eating (range 9-63), purgative behavior (range 7-49), fear of fatness (range 11-77), avoidance of forbidden foods (range 10-70), and depression (range 11-77). | 10-15 years post CALERIE trial | |
Secondary | Body shape perceptions | Body shapes perceptions as measured by the Body Shape Questionnaire (BSQ). Items on the BSQ are rated on a 6-point Likert-type scale. The score ranges from 34-204 points. Higher scores indicate increased concern regarding body shape. | 10-15 years post CALERIE trial | |
Secondary | Physical activity | Physical activity as measured by the 7-Day Stanford Physical Activity Recall (PAR). The PAR estimates an individual's time spent in sleep and physical activity for the 7 days prior to the interview. Energy expenditure based on time spent in sleep and physical activities can be estimated. Sub-scores of energy expenditure for each of the following activities are calculated, summed, and averaged to estimate energy expenditure as kilocalories per day: sleep, moderate physical activity, hard physical activity, and very hard physical activity. Higher scores indicate greater physical activity per day. Metabolic equivalent (MET) value for each activity is provided: 1 MET for sleep, 4 METs for moderate activity, 6 METs for hard activity, and 10 METs for very hard activity. Time spent in each activity over 7 days is multiplied by the appropriate MET value. The minimum value for each activity is zero; there is no maximum value. | 10-15 years post CALERIE trial | |
Secondary | Resilience | Resilience as measured by the 25-item Connor-Davidson Resilience Scale (CD-RISC-25). CD-RISC-25 is scored from 0 to 100, with higher scores indicating higher resilience. | 10-15 years post CALERIE trial | |
Secondary | Total cholesterol | Total cholesterol will be measured in mg/dL using a standard lipid panel. | 10-15 years post CALERIE trial | |
Secondary | High-density lipoprotein cholesterol (HDL-C) | HDL-C will be measured in mg/dL using a standard lipid panel. | 10-15 years post CALERIE trial | |
Secondary | Triglycerides | Triglycerides will be measured in mg/dL using a standard lipid panel. | 10-15 years post CALERIE trial | |
Secondary | Low-density lipoprotein cholesterol (LDL-C) | LDL-C will be calculated in mg/dL using measured values of total cholesterol, HDL-C, and triglycerides. | 10-15 years post CALERIE trial | |
Secondary | Glucose - 0 min (OGTT) | Glucose (mg/dL) will be measured at 0 minutes (pre-dose) during an OGTT to evaluate glucoregulatory response. | 10-15 years post CALERIE trial | |
Secondary | Glucose - 30 min (OGTT) | Glucose (mg/dL) will be measured at 30 minutes post dose during an OGTT to evaluate glucoregulatory response. | 10-15 years post CALERIE trial | |
Secondary | Glucose - 60 min (OGTT) | Glucose (mg/dL) will be measured at 60 minutes post dose during an OGTT to evaluate glucoregulatory response. | 10-15 years post CALERIE trial | |
Secondary | Glucose - 90 min (OGTT) | Glucose (mg/dL) will be measured at 90 minutes post dose during an OGTT to evaluate glucoregulatory response. | 10-15 years post CALERIE trial | |
Secondary | Glucose - 120 min (OGTT) | Glucose (mg/dL) will be measured at 120 minutes post dose during an OGTT to evaluate glucoregulatory response. | 10-15 years post CALERIE trial | |
Secondary | Insulin resistance | Insulin resistance will be calculated using the Homeostatic Model Assessment (HOMA) and measured values of fasting glucose (mmol/L) and fasting insulin (µ/L): (fasting glucose × fasting insulin) / 22.5 | 10-15 years post CALERIE trial | |
Secondary | Beta-cell function | Beta-cell function will be calculated using HOMA-ß and measures of fasting insulin (µ/L) and fasting glucose (mg/dL): HOMA-ß (%) = (360 × fasting insulin) / (fasting glucose - 63) | 10-15 years post CALERIE trial | |
Secondary | Triiodothyronine (T3) | T3, a blood-based marker of thyroid function, will be measured in ng/dL. | 10-15 years post CALERIE trial | |
Secondary | Thyroxine (T4) | T4, a blood-based marker of thyroid function, will be measured in ng/dL. | 10-15 years post CALERIE trial | |
Secondary | Thyroid stimulating hormone (TSH) | TSH, a blood-based marker of thyroid function, will be measured in µIU/mL. | 10-15 years post CALERIE trial | |
Secondary | Alkaline phosphatase (ALKP) | ALKP, a blood-based marker of liver function, will be measured in IU/L. | 10-15 years post CALERIE trial | |
Secondary | Alanine transaminase (ALT) | ALT, a blood-based marker of liver function, will be measured in U/L. | 10-15 years post CALERIE trial | |
Secondary | Aspartate aminotransferase (AST) | AST, a blood-based marker of liver function, will be measured in U/L. | 10-15 years post CALERIE trial | |
Secondary | Albumin | Albumin, a blood-based marker of liver and kidney function, will be measured in g/dL. | 10-15 years post CALERIE trial | |
Secondary | Blood Urea Nitrogen (BUN) | BUN, a blood-based marker of kidney function, will be measured in mg/dL. | 10-15 years post CALERIE trial | |
Secondary | Total Proteins | Total proteins is a measurement sum of albumin and globulin. Total proteins is indicative of blood vessel and immune system function. It will be measured in g/dL. | 10-15 years post CALERIE trial | |
Secondary | Bilirubin | Bilirubin, a blood-based marker of liver function, will be measured in mg/dL. | 10-15 years post CALERIE trial | |
Secondary | Creatine Phosphokinase (CPK) | CPK, an enzyme marker of energy homeostasis, will be measured in U/L. | 10-15 years post CALERIE trial | |
Secondary | Lactate Dehydrogenase (LDH) | LDH, an enzyme marker of liver function, will be measured in U/L. | 10-15 years post CALERIE trial | |
Secondary | Globulin | Globulin, a blood-based marker of liver function, will be measured in g/dL. | 10-15 years post CALERIE trial | |
Secondary | Albumin/Globulin (A/G) ratio | A/G ratio is a blood-based marker used to monitor nutritional status and immune system, kidney, and liver function. This marker is a ratio, and therefore does not have units. | 10-15 years post CALERIE trial | |
Secondary | Uric Acid | Uric acid, a blood-based marker of purine metabolism, will be measured in mg/dL. | 10-15 years post CALERIE trial | |
Secondary | Calcium (Ca) | Calcium, a blood-based mineral, will be measured in mg/dL. | 10-15 years post CALERIE trial | |
Secondary | Phosphorus (P) | Phosphorus, a blood-based mineral, will be measured in mg/dL. | 10-15 years post CALERIE trial | |
Secondary | Magnesium (Mg) | Magnesium, a blood-based mineral, will be measured in meq/L. | 10-15 years post CALERIE trial | |
Secondary | Sodium (Na+) | Sodium, an electrolyte that reflects the body's fluid balance, will be measured in meq/L. | 10-15 years post CALERIE trial | |
Secondary | Potassium (K+) | Potassium, an electrolyte that reflects the body's fluid balance, will be measured in meq/L. | 10-15 years post CALERIE trial | |
Secondary | Chloride (Cl-) | Chloride, an electrolyte that reflects the body's fluid balance, will be measured in meq/L. | 10-15 years post CALERIE trial | |
Secondary | Apoprotein A1 | Apoprotein A1, a blood-based marker of lipid metabolism, will be measured in mg/dL. | 10-15 years post CALERIE trial | |
Secondary | Apoprotein B | Apoprotein B, a blood-based marker of lipid metabolism, will be measured in mg/dL. | 10-15 years post CALERIE trial |
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