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Association Between SYNTAX Score and Leukoglycemic Index In Patients Wiht Acute Coronary Syndrome

Association Between SYNTAX Score and Leukoglycemic Index In Patients Wiht Acute Coronary Syndrome

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07276256
Enrollment
552
Registered
2025-12-11
Start date
2025-09-24
Completion date
2025-10-21
Last updated
2026-02-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Coronary Syndromes (ACS)

Keywords

Acute coronary syndrome, Coronary artery disease, inflammation, risk stratification, SYNTAX score, leukoglycemic index

Brief summary

This study looks at people who come to the hospital with acute coronary syndrome, a serious heart condition. When these patients first arrive, doctors take routine blood tests. The investigators use these test results to calculate a value called the leukoglycemic index (LGI), which combines white blood cell count and blood sugar level. The investigators also use a heart imaging score called the SYNTAX score to see how complex their coronary artery disease is. Patients are divided into two groups based on their SYNTAX scores: one group with lower scores (22 or less), and one with higher scores (above 22). The investigators compare their health data to see if LGI is linked to the severity of their heart disease. The investigators also check if LGI can help predict how complex the disease is. Information like age, family history, and chronic illnesses is collected from patient records and medical interviews.

Detailed description

This observational study aims to evaluate the association between the SYNTAX score-a validated angiographic tool used to assess the complexity of coronary artery disease-and the leukoglycemic index (LGI), a composite biomarker calculated from white blood cell count and blood glucose level. The study population consists of patients diagnosed with acute coronary syndrome (ACS) who were admitted to the hospital and underwent coronary angiography as part of their clinical evaluation. At the time of initial hospital admission, routine laboratory parameters were obtained, including complete blood count and fasting glucose levels. These values were used to calculate the LGI. Patients were stratified into two groups based on their SYNTAX scores: Group I (SYNTAX score ≤22) and Group II (SYNTAX score \>22). Demographic characteristics, family history of cardiovascular disease, and chronic comorbidities (such as diabetes mellitus, hypertension, and hyperlipidemia) were extracted from patient medical records and clinical anamnesis. The primary objective of the study is to determine whether LGI correlates with the angiographic severity of coronary artery disease as measured by the SYNTAX score. Secondary objectives include identifying independent predictors of coronary complexity and evaluating the potential role of LGI as a non-invasive biomarker in risk stratification. Statistical analyses will be performed using SPSS software. Normality of data distribution will be assessed using the Shapiro-Wilk test. Depending on distribution characteristics, appropriate parametric (e.g., Student's t-test) or non-parametric (e.g., Mann-Whitney U test) methods will be applied for group comparisons. Pearson correlation analysis will be used to assess the relationship between LGI and SYNTAX score. Multivariate linear and logistic regression models will be constructed to identify independent predictors of high SYNTAX scores, adjusting for potential confounders. This study is expected to contribute to the understanding of LGI as a simple, cost-effective, and accessible biomarker for predicting coronary artery disease complexity in ACS patients

Interventions

OTHERleukoglycemic index calculation

leukoglycemic index calculation

Sponsors

Kırıkkale University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 88 Years
Healthy volunteers
No

Inclusion criteria

* Adult patients aged 18 years and older * Patients who underwent coronary angiography due to acute coronary syndrome

Exclusion criteria

* Patients with diabetes mellitus (Diagnosis based on current use of oral antidiabetic or insulin therapy and/or fasting glucose level ≥126 mg/dL and HbA1c ≥6.5%) * Patients with atrial fibrillation, history of pacemaker implantation, asthma, pulmonary hypertension, pregnancy, anemia, malignancy, rheumatoid arthritis, or peripheral artery disease * Obese individuals (defined as body mass index \[BMI\] \>30 kg/m²) * Patients whose medical records could not be accessed

Design outcomes

Primary

MeasureTime frameDescription
Leukoglycemic Index (LGI)First dayThe LGI is calculated as the product of blood glucose concentration (mg/dL) and leukocyte count (cells/mm³). This composite measure provides a single numerical value that reflects both metabolic status (via blood glucose) and hematological status (via white blood cell count). At baseline, LGI serves as an integrated indicator of participants' metabolic and immune activity. It is simple to compute and offers a practical way to capture two fundamental aspects of health in one measure. Higher values are considered worse outcomes because they reflect an increased metabolic and inflammatory burden

Countries

Turkey (Türkiye)

Participant flow

Pre-assignment details

Inclusion Criteria * Adults aged ≥18 years * Patients undergoing coronary angiography due to acute coronary syndrome * Non-obese patients Exclusion Criteria * Patients \<18 years of age * Patients with diabetes mellitus (diagnosed by ongoing oral or insulin therapy and/or fasting glucose ≥126 mg/dL with HbA1c ≥6.5%) * Patients with atrial fibrillation, pacemaker history, asthma, pulmonary hypertension, pregnancy, anemia, malignancy, rheumatoid arthritis, peripheral artery disease * Obese patient

Baseline characteristics

Characteristic
Age, Continuous63.6 years
STANDARD_DEVIATION 14.1
Leucoglycemic Index (LGI)1.230 mg/dL*cells per mm^3
Race and Ethnicity Not Collected0 Participants
Sex: Female, Male
Female
118 Participants
Sex: Female, Male
Male
434 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 00 / 0
other
Total, other adverse events
0 / 00 / 0
serious
Total, serious adverse events
0 / 00 / 0

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 27, 2026