NHLBI GO-ESP: Early-Onset Myocardial Infarction (Broad EOMI)
Anthropometry (1)
- ESP_BMI - Baseline BMI in kg/m2 (phv00160324.v2.p1)
Biomarkers (2)
- ESP_LDL - Baseline calculated LDL in mg/dL (missing where trigs>400) (phv00160320.v2.p1)
- ESP_LDL_UNTREATED - Estimated untreated LDL (In HeartGO, it is currently baseline LDL divided by 0.75 for those on lipid lowering meds) (phv00160322.v2.p1)
Demographics (6)
- ESP_AGE_AT_BMI - Age at baseline BMI (phv00160325.v2.p1)
- ESP_AGE_AT_FRS - Age at FRS calculation (phv00160319.v2.p1)
- ESP_AGE_AT_LAST_FU - Age at last follow-up for MI (missing for anyone with a baseline or incident MI) (phv00160327.v2.p1)
- ESP_AGE_AT_LDL - Age in years at baseline LDL (phv00160321.v2.p1)
- ESP_AGE_AT_MI - Age at incident MI. For HeartGO, this is only filled in (i.e. non-missing) for those with adjudicated MI that occurred during the study. It is missing for those that are censored. (phv00160317.v2.p1)
- ESP_SEX - Male; Female (phv00160313.v2.p1)
Disease Events (2)
- ESP_MI_BASELINE - MI status at baseline (0/1) (phv00160316.v2.p1)
- ESP_T2DIABETES - Type 2 diabetes status at baseline (0/1) (phv00160326.v2.p1)
Geography (1)
- ESP_STUDY_SITE - Clinic or field center within cohort (phv00160314.v2.p1)
Medications (1)
- ESP_LIPID_MED - Any lipid lower med at baseline (phv00160323.v2.p1)
Race and Ethnicity (1)
- ESP_RACE - European American; African American (phv00160312.v2.p1)
Study Administration (1)
- ESP_FRS_CHDPROB - Framingham Risk Score predicted prob. (only calcultated in HeartGO for those with no baseline or incident MI) (phv00160318.v2.p1)
Other (15)
- ANALYTE_TYPE - Analyte Type (phv00174041.v1.p1)
- BODY_SITE - Body site where sample was collected (phv00174040.v1.p1)
- CONSENT - Consent group as determined by DAC (phv00098588.v2.p1)
- ESP_PHENOTYPE - EOMI_Case; EOMI_Control; LDL_High; LDL_Low; Stroke; BP_High; BP_Low; DPR (phv00160315.v2.p1)
- HISTOLOGICAL_TYPE - Cell or tissue type or subtype of sample (phv00174042.v1.p1)
- IS_TUMOR - Tumor status (phv00174043.v1.p1)
- SAMPID - De-identified Sample ID (phv00174039.v1.p1)
- SAMPID - Sample ID (phv00098590.v2.p1)
- SAMPLE_USE - Sample Use. Seq_DNA_SNP: SNP genotypes derived from sequence data; Seq_DNA_SNP_CNV: SNP and CNV genotypes derived from sequence data; Seq_DNA_WholeExome: Whole exome sequencing (phv00174044.v1.p1)
- SOURCE_SUBJID - Subject ID used in the Source Repository (phv00160310.v2.p1)
- STUDY - HeartGO cohort (ARIC, CARDIA, CHS, FHS, JHS, MESA) (phv00160311.v2.p1)
- SUBJ_SOURCE - Source repository where subjects originate (phv00160309.v2.p1)
- SUBJID - Subject ID (phv00098591.v2.p1)
- SUBJID - Subject ID (phv00098587.v2.p1)
- SUBJID - Subject ID (phv00098589.v2.p1)