Wife and husband DNA cohort

This study is part of the collection Scania Metadatabase for Epidemiology (SME)

Overview Description Data

Creator/Principal investigator(s):

Håkan Olsson - Lund University, Faculty of Medicine, The Division of Oncology and Pathology

Description:

The cohort was recruited among accompanying spouses of cancer patients at the Oncology Clinic at Lund University Hospital. The study will be used as a reference population in genetic studies and in studies on biomarkers. The individuals filled in a questionnaire about their health status and donated a blood sample.

Purpose:

The study will be used as a reference population in genetic studies and in studies on biomarkers.

Subject area:

HEALTH (CESSDA Topic Classification)
Medical Genetics, Clinical Medicine, Cancer and Oncology (The Swedish standard of fields of research 2011)

Keywords:

Blood Specimen Collection, Body Weights and Measures, Neoplasms, Biological Markers, DNA, Reproduction, Smoking, blood plasma, Serum, Scania, EpiHealth, EpiHealth_Skåne, genetic studies, reference population

Principal organisation:

Lund University

Accessibility status:

Access to data through an external actor
Access to data is restricted

Responsible department/unit:

Lund University, Faculty of Medicine

Creator/Principal investigator(s):

Håkan Olsson - Lund University, Faculty of Medicine, The Division of Oncology and Pathology

Identifiers:

SND-ID: EXT 0101

Description:

Time period(s) investigated:

2007-01-01 — ongoing

Unit of analysis:

Individual

Population:

The population is based on spouses of cancer patients at the Oncology Clinic at Lund University Hospital.

Time Method:

Longitudinal: Cohort

Sampling procedure:

Non-probability: Purposive

Ethics Review:

Lund

Biobank is connected to the study:

Yes

Subject area:

HEALTH (CESSDA Topic Classification)
Medical Genetics, Clinical Medicine, Cancer and Oncology (The Swedish standard of fields of research 2011)

Keywords:

Contact for questions about the data:

Håkan Olsson

Is part of collection at SND:

Scania Metadatabase for Epidemiology (SME)

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Publications

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Broberg K, Höglund M, Gustafsson C, Björk J, Ingvar C, Albin M, Olsson H. Genetic variant of the human homologous recombination-associated gene RMI1 (S455N) impacts the risk of AML/MDS and malignant melanoma. Cancer Lett. 2007 Dec 8;258(1):38-44.

Broberg K, Huynh E, Schläwicke Engström K, Björk J, Albin M, Ingvar C, Olsson H, Höglund M. Association between polymorphisms in RMI1, TOP3A, and BLM and risk of cancer, a case-control study. BMC Cancer. 2009 May 11;9:140.
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