Nawar Dalila (Denmark)

Rigshospitalet Department of Clinical Biochemistry, Section for Molecular Genetics
Nawar Dalila is currently a staff scientist in the Department of Clinical Biochemistry, Section for Molecular Genetics at Rigshospitalet in Copenhagen, Denmark. He is a pharmacist with a master’s degree in Clinical and Hospital pharmacy from Damascus University, Syria and received his PhD in Pharmacogenetics from Göttingen University, Göttingen, Germany. His research focus is on identification new genes for LDL cholesterol and triglycerides and was awarded the Young Investigator Award 2020 in clinical research for his work on CCDC93 published in the European Heart Journal. Recent interests are on thyroid diseases and the cardiovascular system.

Presenter of 1 Presentation

O015 - Plasma TSH Concentration and Risk of Cardiovascular Disease: A Mendelian Randomization Study of 105,224 Individuals from The General Population. (ID 210)

Session Type
Genetics
Session Time
15:00 - 16:30
Date
Mon, 31.05.2021
Room
Live Streamed
Lecture Time
15:57 - 16:05

Abstract

Background and Aims

In observational studies, the association between plasma concentration of thyroid stimulating hormone (TSH) and cardiovascular disease outcomes is conflicting. Using Mendelian randomization, we tested the hypothesis that plasma TSH concentration is associated with risk of ischemic heart disease (IHD), myocardial infarction (MI), and atrial fibrillation (AF).

Methods

In a prospective cohort study of the general population, The Copenhagen General Population Study, including 105,224 individuals, we first tested whether plasma TSH concentration was associated observationally with risk of incident IHD, MI, and AF (=positive control). Subsequently, we tested the genetic association between an allele score weighted on plasma TSH concentrations and risk of the same endpoints.

Results

During a median follow-up of 7 years (0-13 years), 5,425 developed IHD, 2,148 had an incident MI, and 5,105 developed AF. Observationally, using multifactorially adjusted restricted cubic splines, low plasma TSH concentrations (<1.53mIU/L=median) were associated with an increased risk of IHD, MI, and AF. Hazard ratios (HR) increased gradually with lower TSH concentrations up to 1.11(0.99-1.23) for IHD, 1.22(1.03-1.43) for MI, and 1.22(1.10-1.35) for AF, comparing individuals with TSH concentrations in the lowest 5th (≤0.54mIU/L) versus >25th (>1.04mIU/L) percentile (=reference). In genetic analyses, comparing individuals with a gene score ≤5th percentile (who had 16% lower TSH concentrations), versus individuals with a gene score >50th percentile (=reference), HRs were 1.13(1.00-1.28) for IHD, 1.29(1.07-1.55) for MI, and 1.15(1.02-1.31) for AF.

Conclusions

Low plasma TSH concentrations are associated observationally and genetically with an increased risk of IHD, MI, and AF in the general population.

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Presenter of 1 Presentation

O015 - Plasma TSH Concentration and Risk of Cardiovascular Disease: A Mendelian Randomization Study of 105,224 Individuals from The General Population. (ID 210)

Session Type
Genetics
Session Time
15:00 - 16:30
Date
Mon, 31.05.2021
Room
Live Streamed
Lecture Time
15:57 - 16:05

Abstract

Background and Aims

In observational studies, the association between plasma concentration of thyroid stimulating hormone (TSH) and cardiovascular disease outcomes is conflicting. Using Mendelian randomization, we tested the hypothesis that plasma TSH concentration is associated with risk of ischemic heart disease (IHD), myocardial infarction (MI), and atrial fibrillation (AF).

Methods

In a prospective cohort study of the general population, The Copenhagen General Population Study, including 105,224 individuals, we first tested whether plasma TSH concentration was associated observationally with risk of incident IHD, MI, and AF (=positive control). Subsequently, we tested the genetic association between an allele score weighted on plasma TSH concentrations and risk of the same endpoints.

Results

During a median follow-up of 7 years (0-13 years), 5,425 developed IHD, 2,148 had an incident MI, and 5,105 developed AF. Observationally, using multifactorially adjusted restricted cubic splines, low plasma TSH concentrations (<1.53mIU/L=median) were associated with an increased risk of IHD, MI, and AF. Hazard ratios (HR) increased gradually with lower TSH concentrations up to 1.11(0.99-1.23) for IHD, 1.22(1.03-1.43) for MI, and 1.22(1.10-1.35) for AF, comparing individuals with TSH concentrations in the lowest 5th (≤0.54mIU/L) versus >25th (>1.04mIU/L) percentile (=reference). In genetic analyses, comparing individuals with a gene score ≤5th percentile (who had 16% lower TSH concentrations), versus individuals with a gene score >50th percentile (=reference), HRs were 1.13(1.00-1.28) for IHD, 1.29(1.07-1.55) for MI, and 1.15(1.02-1.31) for AF.

Conclusions

Low plasma TSH concentrations are associated observationally and genetically with an increased risk of IHD, MI, and AF in the general population.

Hide