Multi-omics analysis from archival neonatal dried blood spots: limitations and opportunities

Clin Chem Lab Med. 2022 Jun 8;60(9):1318-1341. doi: 10.1515/cclm-2022-0311. Print 2022 Aug 26.

Abstract

Newborn screening (NBS) programs operate in many countries, processing millions of dried bloodspot (DBS) samples annually. In addition to early identification of various adverse health outcomes, these samples have considerable potential as a resource for population-based research that could address key questions related to child health. The feasibility of archival DBS samples for emerging targeted and untargeted multi-omics analysis has not been previously explored in the literature. This review aims to critically evaluate the latest advances to identify opportunities and challenges of applying omics analyses to NBS cards in a research setting. Medline, Embase and PubMed databases were searched to identify studies utilizing DBS for genomic, proteomic and metabolomic assays. A total of 800 records were identified after removing duplicates, of which 23 records were included in this review. These papers consisted of one combined genomic/metabolomic, four genomic, three epigenomic, four proteomic and 11 metabolomic studies. Together they demonstrate that the increasing sensitivity of multi-omic analytical techniques makes the broad use of NBS samples achievable for large cohort studies. Maintaining the pre-analytical integrity of the DBS sample through storage at temperatures below -20 °C will enable this important resource to be fully realized in a research capacity.

Keywords: GenV; biobank; dried blood spot(s); emerging technologies; epigenomics; genomics; metabolomics; newborn screening; omics; proteomics.

Publication types

  • Review

MeSH terms

  • Child
  • Dried Blood Spot Testing / methods
  • Epigenomics
  • Genomics
  • Humans
  • Infant, Newborn
  • Metabolomics
  • Neonatal Screening* / methods
  • Proteomics*