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The Radboud Biobank: A Central Facility for Disease-Based Biobanks to Optimise Use and Distribution of Biomaterial for Scientific Research in the Radboud University Medical Center, Nijmegen Cover

The Radboud Biobank: A Central Facility for Disease-Based Biobanks to Optimise Use and Distribution of Biomaterial for Scientific Research in the Radboud University Medical Center, Nijmegen

Open Access
|Feb 2018

Figures & Tables

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Figure 1

The flow of biomaterial and associated clinical data of a sub-biobank for the Radboud Biobank.

Table 1

Overview of procedures on collection, processing and storage of samples defined in the Radboud Biobank biomaterial protocol.

SampleVolume/numberProcessingTime between sampling and storageAliquotingStorage
DNA (blood)6 ml EDTA bloodStandard DNA isolation from EDTA in clinical routine of the Department of Human GeneticsWithin 4 weeks (4°C) or 3 months (<–20°C)Stock solution, after first issuance: normalized fraction 100 ng/μL–20°C1
Serum10 ml, addition of a clot activator2,000 × g at room temperature for 10 minutesWithin 2–4 hoursMaximum of six aliquots (0.5 ml)–80°C2
EDTA plasma10 ml2,000 × g at room temperature for 10 minutesWithin 2–4 hoursMaximum of six aliquots (0.5 ml)–80°C2
Heparin plasma10 ml2,000 × g at room temperature for 10 minutesWithin 2–4 hoursMaximum of six aliquots (0.5 ml)–80°C2
Citrate plasma9 ml2,000 × g at room temperature for 10 minutesWithin 2–4 hoursMaximum of six aliquots (0.5 ml)–80°C2
Cerebrospinal fluid (CSF) +/– cell count (CC)3–20 ml2,000 × g or 850 × g (CC) at 4°C or at room temperature (CC) for 10 minutes or 5 minutes (CC)Within 2 hoursMaximum of six aliquots (0.5 ml)–80°C2
UrineNot specified, midstream2,000 × g at 4°C for 10 minutesWithin 4 hoursMaximum of six aliquots (0.9 ml)–80°C2
FaecesNot specifiedDirect storage or after homogenizationWithin 12 hoursMaximum of six aliquots (5 gram)–80°C2
Fresh frozen tissueSample of affected and unaffected tissueImmediately frozen after collecting the sampleImmediate0.5 cm3 samples–80°C2
FFPE tissue3Sample of affected and unaffected tissueImmediately stored in formalin after collecting the sample (0.5 cm3), afterwards embedded in paraffinImmediate fixation0.5 cm3 samplesRoom temperature

[i] 1 –20°C in a fully automated storage system.

[ii] 2 –80°C in a manual storage system.

[iii] 3 FFPE = Formalin-Fixed Paraffin-Embedded.

Table 2

Disease-based biobanks included in the Radboud Biobank.

Disease-based biobanksNumber of unique patients
July 2017 – n = 32,587 (%)
Confirmed form/increased risk of colorectal cancer1494 (1.5)
Cerebrovascular infarct/cerebral haemorrhage/venous thrombosis1733 (2.5)
Rheumatoid arthritis and arthrosis2 [2]5,274 (16.2)
Neurodegenerative disorders (e.g. Alzheimer’s)1124 (0.4)
Chronic (progressive) renal failure21,377 (4.2)
Crohn’s disease/ulcerative colitis1382 (1.2)
Leukaemia, myeloma, lymphoma1215 (0.7)
Type II diabetes1400 (1.2)
Cerebrovascular vascular accident (18–50 years)570 (1.7)
Ischaemic heart disease1162 (0.5)
Anomalies in children (e.g. malformations of the kidneys and urinary tract, intestines and anus, lip and palate, and the heart, childhood cancers; [3])4,592 (14.1)
Parkinson’s disease1,230 (3.8)
Facioscapulohumeral muscular dystrophy (FSHD)233 (0.7)
Infantile facioscapulohumeral muscular dystrophy (iFSHD)45 (0.1)
Intellectual Disability639 (2.0)
Breast Cancer170 (0.5)
Asymptomatic women invited for breast cancer screening (50–75 years; [4])5,674 (17.4)
Immune responses and microbiome [5]
– Overweight patients (BMI>27)
– Recurrent Vulvovaginal Candidiasis
– HIV-infected patients
– Type I diabetes
– Healthy controls
 
302 (0.9)
6 (<0.1)
216 (0.7)
176 (0.5)
535 (1.6)
Cancer – breast, prostate, bladder, kidney, ovarian, melanoma, lung, testis6,700 (20.7)
Autoinflammatory diseases21 (0.1)
Familial bladder cancer43 (0.1)
Myositis30 (0.1)
Endocrine diseases49 (0.2)
Urology1,312 (4.0)
Hereditary prostate cancer587 (1.8)
Congenital myopathy9 (<0.1)
Gynaecological oncology53 (0.2)
Systemic Sclerosis222 (0.7)
Rhabdomyolyse1 (<0.1)
Iron disorders [6]11 (<0.1)

[i] 1 Parelsnoer Institute participant [1].

2 Both Parelsnoer Institute participant and department based biobank.

Table 3

Criteria used by the institutional review board to review applications for the use of biobank material and the accompanying clinical data.

  1. Scientific and clinical relevance of the study.

  2. Proposal that fits the original aim (and informed consent) of the collection.

  3. Validity of the study design and proposed analyses.

  4. Relevance of the requested material (type, volume, numbers) for this study.

  5. Expertise of the applicant and the organisation for this study.

  6. Appropriate measures for privacy protection.

DOI: https://doi.org/10.5334/ojb.36 | Journal eISSN: 2056-5542
Language: English
Published on: Feb 6, 2018
Published by: Ubiquity Press
In partnership with: Paradigm Publishing Services
Publication frequency: 1 issue per year

© 2018 Peggy Manders, Jennifer E. Lutomski, Cees Smit, Dorine W. Swinkels, Gerhard A. Zielhuis, published by Ubiquity Press
This work is licensed under the Creative Commons Attribution 3.0 License.