NIH, National Cancer Institute, Division of Cancer Treatment and Diagnosis (DCTD) NIH - National Institutes of Health National Cancer Institute DCTD - Division of Cancer Treatment and Diagnosis

Comparison of methods for collection of DNA samples by mail in the Black Women's Health Study.

Author(s): Cozier YC, Palmer JR, Rosenberg L

Publication: Ann Epidemiol, 2004, Vol. 14, Page 117-22

PubMed ID: 15018884 PubMed Review Paper? No

Purpose of Paper

The purpose of this paper was to compare buccal cell collection by mouth swab or mouthwash with respect to DNA yield and PCR success rate.

Conclusion of Paper

Buccal cell DNA extracted from mouth swab specimens was slightly less contaminated with protein than that obtained from mouthwash specimens (p<0.001), as determined by OD 260/280 ratio. However, the average yield and concentration of DNA as determined by spectrophotometry from mouthwash specimens (30,179 ng/uL specimen and 509 ng/uL, respectively) were much greater than those from mouth swab specimens (4,344 ng/uL specimen and 66 ng/uL, respectively, p<0.001). PCR amplification of the NAT2-341 gene polymorphism was successful for 93% of mouth swab specimens and 94% of mouthwash specimens on the first try.

Studies

  1. Study Purpose

    The purpose of this study was to compare buccal cell collection by mouth swab or mouthwash with respect to DNA yield and PCR-based SNP analysis success rate. All specimens were collected by mail. Once received, mouth swabs were stored at -20 degrees C and mouthwash specimens were stored at 4 degrees C until DNA was extracted.

    Summary of Findings:

    Buccal cell DNA extracted from mouth swab specimens was slightly less contaminated with protein than that obtained from mouthwash specimens (p<0.001), as determined by OD 260/280 ratio. However, the average yield and concentration of DNA as determined by spectrophotometry from mouthwash specimens (30,179 ng/uL specimen and 509 ng/uL, respectively) were much greater than those from mouth swab specimens (4,344 ng/uL specimen and 66 ng/uL, respectively, p<0.001). PCR amplification of the NAT2-341 gene polymorphism was successful for 93% of mouth swab specimens and 94% of mouthwash specimens on the first try. A second attempt at PCR allowed for a 98% success rate from mouthwash specimens and 94% from mouth swab specimens.

    Biospecimens
    Preservative Types
    • Frozen
    • Other Preservative
    Diagnoses:
    • Neoplastic - Carcinoma
    Platform:
    AnalyteTechnology Platform
    DNA Spectrophotometry
    DNA SNP assay
    Pre-analytical Factors:
    ClassificationPre-analytical FactorValue(s)
    Biospecimen Acquisition Method of fluid acquisition Mouth swab
    Swishing
    Biospecimen Preservation Type of fixation/preservation Frozen
    Refrigeration
    Biospecimen Acquisition Method of cell acquisition Mouth swab
    Swishing

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