In contrast to common diseases, which are usually characterized by a complex interaction of multiple genetic and environmental factors, rare diseases can often be traced back to a single defective gene. Targeted decoding and analysis of a gene defect and its phenotypic consequences therefore provides important information for understanding underlying mechanisms in the body and helps in choosing targeted treatment strategies. However, the individual search for the cause of disease is usually lengthy and costly. A new, systematic approach to the study of rare, uncharacterized diseases using a so-called multiplex network is now presented by the research group of network scientist Jörg Menche at CeMM and the Max Perutz Labs in their latest study, published today in the journal Nature Communications.
Three times higher probability of identifying causative genetic defect
Menche's research group has been dedicated for several years to better understanding genetic interactions using molecular network analysis to improve the diagnosis and treatment of rare diseases. For their current study, first author Pisanu Buphamalai, a CeMM PhD student in Menche's research group, built a multilayer network mapping more than 20 million gene relationships with information ranging from protein interactions to phenotypic similarities. To do this, the scientist integrated a comprehensive dataset of more than 3,700 rare diseases with a known genetic basis. Study leader Menche explains, "The multiplex network integrates different network layers that map different levels of the biological organization of our body, from the genome to the transcriptome, proteome and phenotype. By mapping protein interactions and mechanisms, we can also better characterize those proteins whose roles in diseases were previously unknown and thus track down gene defects more quickly." Pisanu Buphamalai adds, "We are guided by the interactions among proteins at both physical and functional levels. This allows us to draw conclusions about the potential defective gene as well as associated effects. Our network approach increases the probability of finding the crucial gene aberration threefold compared to when these networks are considered separately."
Progress for network medicine: more accurate analysis, better prognosis
On the one hand, the multiplex network's modular design makes it possible to quantify the impact of a particular rare disease on a specific level of biological organization. This means determining whether certain cells, tissue forms, organs, etc. are particularly affected by a genetic defect. On the other hand, the importance of certain molecular processes for a disease can also be measured. "It is precisely because of its complexity, the linking of molecular sequences and processes, that our multiplex network is significantly more powerful and successful than looking at each network individually. It also makes it easier to make predictions about possible consequences of the genetic defect," Menche says. The network was successfully tested for functionality in collaboration with Vanja Nagy, Principal Investigator at the Ludwig Boltzmann Institute for Rare and Undiagnosed Diseases and CeMM Adjunct Principal Investigator, using data from patients with neurological diseases whose underlying genetic defect was already known. "Our study shows how a huge dataset can be used in the context of network medicine to address several practical and conceptual challenges in rare disease research to improve diagnosis and treatment for the benefit of patients," Menche says.
The study “Network analysis reveals rare disease signatures across multiple levels of biological organization” was published in the journal Nature Communications on November 09, 2021. DOI: 10.1038/s41467-021-26674-1
Authors: Pisanu Buphamalai, Tomislav Kokotovic, Vanja Nagy, Jörg Menche
Funding: The study was supported by the Vienna Science and Technology Fund (WWTF) through project VRG15-005.