Abstract
Objective: To better understand the characteristics associated with a participant's willingness to consent to the Mayo Clinic Biobank (MCB) and examine factors associated with willingness to participate in follow-up studies embedded within MCB that require re-contact and participant approval.Participants and Methods: Consent rates were compared across patient demographics to the MCB. Rates of participation to follow-up studies were also compared across demographics and request types.Results: Among 272,102 Mayo Clinic patients invited to the MCB, 48,314 (19%) consented across the three recruitment sites within 90 days of initial invitation. A significant age by gender interaction was identified, showing young males consent at a lower rate than young females and older males consent at a higher rate than older females. Over the recruitment time frame of 2009–2015, there was a significant decrease in consent rates (decline of 2.5%/year). Of the 57,041 consented MCB participants, 33,487 participants (59%) have been invited to participate in follow-up studies via re-contact. Follow-up studies of the MCB may require participants to provide additional samples, complete questionnaires, and/or release their identity to a research team. MCB participants have been invited to enroll in a median of two studies (IQR: 1–3). Seventy-one percent of participants consented to at least one follow-up study, with individual follow-up study consent rates ranging from 14 to 87% depending on study type, with a median consent rate of 61% (IQR: 47–70%). Studies requesting return of a questionnaire had the highest participation rates. White participants, older participants, and participants with some college or a degree were significantly more likely to participate to follow-up studies, while there was no association with gender.Conclusion: Consent rates among younger and non-white patients were lower than in older, white patients. However, we also found that participation rates among those already enrolled in the biobank were much higher than those seen in new recruitment efforts, external to an existing biobank. We thus demonstrate an important way that biobanks can advance precision medicine goals: through provision of populations from which studies can draw participants for future studies.
Highlights
Biobanks are a key element in the advancement of precision medicine by facilitating research
We found that consent rates to the Mayo Clinic Biobank were associated with year of consent, declining from 32% in 2009 to 17% in 2015 with an overall consent rate of 19%
We found that consent rates to follow-up studies followed the same downward trends over time noted in the rates of consent to the Mayo Clinic Biobank (MCB)
Summary
Biobanks are a key element in the advancement of precision medicine by facilitating research. The majority of biobanks accomplish this through the use of stored samples, but some enable efficient re-contact and enrollment of subjects into new research projects. The Mayo Clinic Biobank (1) is one such collection that allows additional contacts for embedded follow-up studies. Understanding the factors related to participation in existing biobanks can aid in identifying patterns that predict recruitment to future collections. Current biobanking literature has limited data on the rate at which subjects are willing to participate in additional embedded follow-up studies within biobanks to which they had consented. This study sought to investigate the factors associated with consent to the Mayo Clinic Biobank (MCB) as well as willingness to participate in additional follow-up research projects embedded in the MCB
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