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variances in DBS observed for neonatal screening

An article published by SK Hall et al at three hospitals in the United Kingdom in the June 2015 issue of Journal of Medical Screening, reported on an investigation into biases seen with dried blood spot (DBS) sampling in newborn screening laboratories. The paper is entitled “Newborn screening blood spot analysis in the UK: influence of spot size, punch location and haematocrit.” It describes how the location of the punch on a DBS card, spot size and hematocrit all affect analytical data from biomarkers of inborn errors of metabolism and related conditions.

The research team was able to conclude that differences in blood spot size, hematocrit and punch location substantially affected measured concentrations for analytes used in the UK newborn screening program. They reported in their article that this could affect false positive and negative rates. The researchers proposed that to minimize analytical bias, “these variables should be controlled or adjusted for where possible.”

The Importance of Neonatal Screening

heel-infant-finger-prick-capillaryNeonatal screening programs are vital to help identify metabolic disorders at birth so that treatment interventions can be initiated early to prevent progression of a disease or to manage the symptoms.

There is currently a wide range of genetic and metabolic conditions that are screened for at birth, including congenital hypothyroidism, phenylketonuria, cystic fibrosis, Medium-chain acyl-CoA dehydrogenase deficiency (MCADD), and maple syrup urine disease (MSUD).

Since the early 1960s, early newborn screening has involved the collection of capillary blood, usually from a heel-prick, onto a DBS filter paper or card where the blood is dried and sent to a laboratory for tests.

The tests vary dependent on the condition being screened, but often they measure the build-up of a metabolite such as phenylalanine as observed in phenylketonuria patients. The DBS technique of collecting samples from newborns has eradicated the use of the more invasive and complicated venipuncture technique to collect blood.

Biases Seen with Dried Blood Samples     

DBS CardDBS cards have stayed the test of time in the microsampling industry, but there are several fundamental drawbacks of DBS technology that make it difficult to obtain high precision in analytical data. The primary reason for this is due to the way DBS cards are processed in the laboratory.

To attempt to obtain a volumetrically precise sample, DBS cards are ‘hole punched’ to obtain fixed diameter sub-punches. In neonatal screening for example, 3.2 mm punches are popular, which yields about 3 µL of blood at 45% hematocrit (HCT). However, HCT can vary in newborns (from ~30 -65%) and this can have deleterious effect on results. This is because the actual volume of blood collected from the sub-punch can be very misleading due to the following analytical biases:

  • Spot spread bias – The higher the % of HCT, the more viscous the sample, which leads to smaller spot diameters for the same volume applied. The more enriched the fixed volume sub-punch is, the more often this leads to +ve biases.

  • Punch location bias – This is where different values are seen for some analytes dependent on where the punch was taken.

  • Extraction bias – This describes how the % HCT affects the extraction efficiency. Without method optimization, negative biases are often observed at higher % HCT levels. This can also be observed with volumetrically collected samples.

  • Matrix bias – The greater the HCT level the greater the chance of matrix effects.

Another bias that can be observed, even if a fixed % HCT is applied, is spot area bias. This is because it is difficult to meter the volume of blood collected from a finger or heel directly to a DBS card so the actual diameter of the spot can vary the concentration of the analytes in the spot which, in turn, can bias the results.

To test the extent to which biases are observed in neonatal screening, SK Hall and co-authors of the study paper summarized here investigated to evaluate the following biases: spot spread bias, punch location bias, and spot area bias.

DBS Study Methods and Findings

  • L-phenylalanine, L-methionine, L-tyrosine, L-leucine, Octanoylcarnitine (C8), human thyroid stimulating hormone (TSH), and immunoreactive trypsinogen (IRT) were measured from blood spots at different concentrations and at different HCT levels.

  • To measure punch location bias and spot area bias, cards with increasing spot sizes were created by applying 10, 20, 50 and 75 µL for all spot sizes 30.2 µL sub-punches were taken in the middle of each spot. For 50 and 75 µL spots peripheral samples were also taken.

  • To measure HCT bias, DBS were spotted with 50 µL samples of increasing %HCT concentrations (30, 40, 45, 50 and 60%) for all analytes except for IRT where the range was 25, 50 and 65%.

  • To measure the heterogeneity of the blood samples based on size, light transmission was measured using a Cardscan™ system. The purpose of this was to see if there were differences in transmissibility levels dependent on the spot size and also on the location of the DBS paper, as well as impact of HCT level.

  • In terms of spot size, a significant reduction (sometimes up to 20%) in measured analyte levels (except for IRT where only the lower concentration showed the effect) were observed when smaller volumes of blood were deployed (10 to 20 µL) compared to 50 and 75 uL.

  • In terms of punch locations, measured analyte concentrations where significantly higher at the periphery of the blood spot (up to 35%) for all analytes tested.

  • For the HCT measurement, increasing HCT values showed a reduction of TSH and C8 levels. However, for leucine, methionine, phenylalanine and tyrosine, the levels increased with increasing HCT. IRT showed a significant reduction (10-15%) at 65% HCT.

  • In terms of light transmission, there was a reduced transmissibility with increasing spot size. Furthermore, transmission was significantly greater at the edge of the spots.

Study Authors’ Discussion and Conclusions

  • Punch location can significantly affect the measured analyte concentration, which aligns with previous published studies. As a number of these analytes have greater fractions in plasma compared to intracellular fluid, this aligned with the edge data where transmissibility is higher.

  • Analysis of spot diameter showed a decrease in analyte levels with decreasing spot size, suggesting that the smaller the volume of blood added to the filter card, the further the blood spreads.

  • Observed increase in concentrations of leucine, methionine, phenylalanine, and tyrosine with increasing hematocrit may be due to HCT spread bias or changes in plasma volume.

  • It may be more difficult to explain why some analytes decreased in concentration with increasing HCT, but it may be due to the way blood migrated in the card matrix.

  • The results from spot size, punch location and differing HCT could lead to false positives and false negatives in the data. This occurs despite the fact that instructions are given to neonatal nurses and midwives to apply appropriate blood volumes to DBS cards from a heel prick. To a certain extent, labs can QC the spots and control punch locations to help mitigate these concerns.

  • The authors proposed that the Cardscan™ could be used as a surrogate marker for punch location and HCT levels.

Comments from Neoteryx

The impact that DBS has had on early detection of genetic diseases and errors in metabolism in newborn babies cannot be underestimated. However, the fundamental issues associated with attempting to quantitate from DBS filter paper or cards, especially in a cohort where HCT can vary wildly, demanded some improvements in the field of blood microsampling.

The need to overcome the limitations of DBS cards created an opportunity in the microsampling industry for new sample-collection devices that offered a more precise volumetric approach to blood sampling. Indeed, the volumetric nature of newer sample collection tools such as hemaPEN® and Mitra® devices based on VAMS® technology have the potential to overcome many of the issues (spot size, punch location and HCT spread biases) observed in the work cited here.

HP Illustration_DBScart_12x10-1These new fixed-volume microsampling devices may offer a solution for current and next-generation newborn screening assays.

For example, the hemaPEN device offers end-users who are accustomed to using DBS cards with an easy transition to a next-generation precision DBS device. With a single heel-stick or finger-stick, the hemaPEN simultaneously collects 4 volumetrically identical (2.74 µL) blood samples via rapid capillary action.

Once the end-user has collected the samples and clicks the lid back onto the hemaPEN to shut it, those 4 samples are transferred onto 4 pre-cut DBS disks inside the device’s tamper-resistant housing. The hemaPEN now contains 4 blood spots of equal size with no HCT spread and is ready for delivery to the lab for DBS processing and analysis that eliminates the hole-punching step.

This article was summarized for our readers by James Rudge, PhD, Neoteryx Technical Director. This is curated content. To learn more about the important research outlined in this blog, visit the original article in the Journal of Medical Screening.

Image Credits: iStock, Neoteryx, Trajan

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