Publications by authors named "R Geiger"

Microphysiological systems (MPS) are complex in vitro tools that incorporate cells derived from various healthy or disease-state human or animal tissues and organs. While MPS have limitations, including a lack of globally harmonized guidelines for standardization, they have already proven impactful in certain areas of drug development. Further research and regulatory acceptance of MPS will contribute to making them even more effective tools in the future.

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  • The study aimed to assess how common metabolic dysfunction-associated steatotic liver disease (MASLD) is among adolescents in Western Austria and its relationship with arterial stiffness, which indicates early vascular ageing.
  • Researchers examined liver fat content in 1,292 Austrian adolescents using advanced ultrasound technology and measured arterial stiffness through a specific pulse wave measurement, alongside assessing various cardiovascular risk factors.
  • While MASLD was identified in 4.8% of the participants, the results indicated that liver fat and MASLD were not strong independent predictors of early vascular ageing; however, knowing liver fat levels can help identify adolescents at risk for cardiovascular issues.
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  • * The revised 2022 guidelines from the European Society of Cardiology/European Respiratory Society address PH but only briefly consider the needs of adults with congenital heart defects.
  • * The article aims to enhance understanding of ACHD management by exploring various aspects such as diagnostics, specialized therapies, and unique circumstances, thereby addressing gaps in current guidelines.
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Article Synopsis
  • * The 2022 guidelines by the European Society of Cardiology and the European Respiratory Society address PH management but only briefly cover the specific needs of adults with congenital heart defects.
  • * This article reviews various aspects of ACHDs and PH, including their epidemiology, risk factors, and management challenges, aiming to enhance awareness and care strategies for this patient population.
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Although adenosine deaminase 2 (ADA2) is considered an extracellular ADA, evidence questions the physiological relevance of this activity. Our study reveals that ADA2 localizes within the lysosomes, where it is targeted through modifications of its glycan structures. We show that ADA2 interacts with DNA molecules, altering their sequences by converting deoxyadenosine (dA) to deoxyinosine (dI).

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