Pakistan Study of Premature Coronary Atherosclerosis in Young Adults

Study Objectives The primary objectives of PAK-SEHAT are: 1) characterize the prevalence and severity of subclinical coronary atherosclerosis among young-to-middle aged Pakistani men and women free of clinical CVD, and 2) assess 5-year rates of ASCVD events. The secondary objectives of the study are to 1) determine the prevalence of diabetes, hypertension, dyslipidemia, and other cardiovascular risk factors among young Pakistani men and women free of clinical CVD; 2) identify the determinants of subclinical coronary atherosclerosis in this population; 3) estimate the incidence of diabetes, hypertension, dyslipidemia, and other cardiovascular risk factors at 5 years of follow-up; 4) identify independent risk factors and markers of incident clinical ASCVD among young asymptomatic Pakistanis. Study Design PAK-SEHAT is a prospective cohort study, with a target study population of 2,000 participants and a planned prospective follow-up of 5 years after study enrollment. Study Population Investigators plan to recruit 2,000 young-to-middle aged adult Pakistani men and women with no known clinical ASCVD. Because the focus of this study is to investigate the prevalence, severity, and determinants of early coronary atherosclerosis in Pakistani adults, focus will be on apparently healthy (i.e., without known clinical CVD) young-to-middle native Pakistanis. Also, because premature coronary events are more frequent and usually observed at younger ages in men than in women, the age range of male participants at enrollment will be 35-60 years, while this will be 35-65 years for female participants; and enrollment will use a 1:1 male:female ratio. Sampling Strategy: PAK-SEHAT aims to be as representative as possible of the general Pakistani population, and a multi-stage cluster sampling strategy will be used to identify candidates to participate in the study. The first stage of the sampling process occurs at the province level, which is the largest administrative division in the country, and participants will be recruited from all four Pakistani provinces and the Federal territory of Islamabad. A cluster is defined as the selected tertiary care hospital offering clinical cardiac services. The selection criteria of hospital include clinical cardiac services being provided and availability of CT coronary angiogram. Next, cities are selected, and within those, the hospitals. The distribution of the sample across the provinces was done proportionate to the size sampling method. We are collaborating with eight hospital sites across the country to achieve our sample size. Tabba Heart Institute Karachi, Safari Hospital Rawalpindi, Bahria international Hospital Lahore, Doctors Hospital and medical center Lahore, Faisalabad Institute of Cardiology, Medikay Cardiac Center Islamabad, Peshawar Institute of Cardiology and Tabba Heart Institute Quetta. Participant Enrollment The attendant of the patients admitted to the hospital will be offered to participate in the study. The volunteers for the study will be recruited through advertisement of the study using pamphlets, posters, electronic medium such as FM radio and digital platforms such as facebook, twitter, and instagram. Individuals who are deemed eligible to participate in the study will be provided with detailed information about the study, invited to ask questions, and asked to provide written informed consent for participation. All the participants will undergo study measurements that include an interview about current past clinical history, family history, lifestyle, and mental health assessment, laboratory investigations such as lipid profile, liver profile, HbA1C, CBC, CRP, Renal function tests, and Lp (a). The participants will undergo CT angio and cIMT measurement at the respective hospital sites and will be provided with their reports. The central reporting of CT angio and cIMT will be done at TabbaHeart by two readers to standardize the measurements. At 2.5 year follow-up, laboratory investigations will be repeated and 5 year CT angio along with laboratory investigations will be repeated. In between the baseline and follow-up, participants will be contacted regularly to collect data on cardiac events. Study interview and questionnaires. Participants will be interviewed by trained study personnel. Sociodemographic data, and information on past and present medical history, family history, lifestyle will be collected using structured questionnaires. Blood pressure: Systolic and diastolic blood pressure will be measured in each participant using Omron digital BP apparatus, with participants sitting in a comfortable position for 5 minutes. Anthropometry and body composition. Height (cm) will be measured through height scale. Body composition will be analyzed using the Tanita-MC-780 U body composition analyzer. Blood measurements and genetics. Trained study personnel will draw approximately 30 mL of venous blood from each participant. Approximately 10 mL of blood will be biobanked and stored at -80C to allow for future additional research studies, including genetic testing. The latter will include but not limited to testing for ApoE Genotype (information about risk of heart disease and response to amounts of dietary fat), 9p21 Genotype (risk of MI and CAD at an early age), KIF6 Genotype (risk of heart disease and reduction of MACE with statins), LPA Intron 25 (increased risk of heart disease), 4q25 A-Fib genotype (risk of atrial fibrillation and risk of stroke due to atrial fibrillation). In participants who do not consent for genetic testing, their 10 mL of biobanked blood may be used in non-genetic analyses but not for studies involving genetic testing. Cardiac CT scans. Participants will first undergo a non-contrast-enhanced cardiac CT for coronary artery calcium (CAC) scoring, followed by a contrast-enhanced CCTA. Toshiba Aquilion Multislice CT scanners and prospective ECG triggering will be used. Participants will be evaluated before the CT scan by study personnel and if the heart rate is above 65 bpm will be pre-treated with a β-blocker (or ivabradine if contraindicated) to achieve a target heart rate of \~60 bpm. Sublingual nitroglycerin will be administered as per standard protocols approximately 3 minutes before the CCTA scan, and intravenous contrast will be injected at a rate of 5.5-7 ml/s depending on the body habitus of the participant; for an average patient, the dose of contrast is expected to be approximately 60-80 mL. The non-contrast-enhanced images will be transferred to the Cardiology CT core lab at Tabba Heart Institute and evaluated by trained radiologists who will quantify CAC according to Agatston's method. Carotid ultrasound imaging . All participants will undergo carotid ultrasound imaging for assessment of presence of carotid plaque and for carotid intima-media thickness (CIMT) evaluation. This will be assessed with automated measurement over bilateral carotid arteries using a Toshiba Aplio 500 ultrasound system (Otawara, Japan), using B-mode ultrasound examination with a 10-MHz multi-frequency linear array transducer. Participants will be examined in the supine position, and standard measurements will be performed. Baseline Data Management and Quality Study data will be collected in tablets and other digital platforms and will be transferred to a central server. The centralized study database will be stored at the Tabba Heart Institute using a secure server, and data privacy and confidentiality will be secured at all times. For quality control purposes, the data collection application in the tablets will have built-in features to limit erroneous data entry and inconsistency in recording participants' responses. Also, a field coordinator will monitor data collection and spot-check 5-10% of the interviews. At the centralized study database, data error reports will be generated on a monthly basis to monitor completeness, invalid values, and inconsistencies in responses. In addition, a live dashboard will be developed for pre-identified key variables to monitor and evaluate the project's progress. Follow-Up and Event Ascertainment: Besides repeat blood tests and imaging testing at 30 and 60 months (Table 2), in each of the three follow-up visits a questionnaire will be used to collect information on ASCVD outcomes. In case of an affirmative answer, participants will be asked to provide additional evidence (e.g. hospital admission records) so that the event can be confirmed. ASCVD events will include myocardial infarction, unstable angina, stable angina, stroke, transient ischemic attack, coronary revascularization, and cardiovascular death. Published definitions will be used to define each of these incident events. Independent two cardiologists from the centralized PAK-SEHAT adjudication committee and blinded to the results of the study tests will classify events as definite, probable, or absent, based primarily on available hospital documentation. They will also classify CHD-, CVD- or stroke- related deaths based on hospital records (if available) and verbal autopsy interviews with families. If there is disagreement in event adjudication between the 2 assigned experts, a third independent physician adjudicator will review the evidence to break the tie. The repeat CCTA at 60 months of follow-up will be used to evaluate the progression/regression of coronary plaque burden. Statistical Analyses For analyses using baseline data, the frequency and distribution of cardiovascular risk factors (known, unknown), coronary plaque burden, and other key baseline variables using number and frequency (%) for categorical variables and mean (standard deviation) or median (interquartile range) for normally and not normally distributed continuous variables will be described. Specifically for coronary plaque characteristics, the CAC score will be categorized as 0, \>0-\<100, ≥100, and the distribution of CAC scores and proportion of each stratum will be reported. With regards to CCTA findings, the proportion of participants with any coronary plaque and the distribution of plaque subtypes will be reported with 95% CI. Investigators will also report the frequency of having maximal coronary stenosis ≥50% and ≥70%, respectively, and the proportion of participants with high-risk plaque features. The distributions of the number of coronary vessels with plaque, the number of coronary segments affected per participant, and the location of coronary plaques (left main, anterior descending, circumflex, and right coronary artery) will also be described. In analyses of incident events during follow-up, investigators will use standard survival analysis and time-to-event techniques. Cumulative incidence at 5 years (in %) and incidence rates per 1,000 person-years (with 95% CI) will be computed for the primary and secondary study outcomes. The ASCVD event rates in the PAK-SEHAT population will be compared with those of Pakistanis of the same age and sex free of clinical ASCVD and not included in the study. Analyses of the incidence of cardiovascular risk factors during follow-up will be restricted to individuals at-risk of each of those risk factors. Investigators will use Cox Proportional Hazards regression models to evaluate the association between important baseline characteristics and incident ASCVD events during follow-up.