This page last changed on 05.02.2015 by ttuv.

Link to MORGAM cohort description


PRIME Belfast participates in the MORGAM Project, and the PRIME Belfast data which have been harmonized to the MORGAM database is specified in the cohort description of MORGAM (as RUA UNK-BEL). This page describes the parts of PRIME Belfast which are not included in MORGAM but may be relevant to CHANCES.

Contact person(s) for this cohort description

Mark O'Doherty

Institute

The Queen's University of Belfast, Belfast, Northern Ireland

Key personnel for CHANCES

Principal Investigator - Prof Frank Kee (f.kee@qub.ac.uk)
Former Principal Investigator: Alun Evans

Definition of the cohort

see MORGAM

Target population

see MORGAM

Recruitment

see MORGAM

Years of recruitment

see MORGAM

Size of the cohort

see MORGAM

Recontacts

Recontact 1 -

~10 year follow-up re-examination performed

Period

2001-2006

Approach

similar to baseline (questionnaires and blood samples)

- 2010 participants in this round

- follow-up of endpoints extended to ~18 years

Measurements at baseline and recontacts

see MORGAM for baseline measurements that have been harmonized to the MORGAM database from PRIME Belfast.

Below are measurements that have not been harmonized to the MORGAM database, but are available within PRIME Belfast and may be relevant to CHANCES (the recontact data and updated follow-up is currently being harmonized to the MORGAM database and will be reported by MORGAM soon).

Socioeconomic Baseline Recontact1
Education   No
Income   No
Marital status   Yes
Occupation   No
Employment status   No
History of Baseline Recontact1
Diabetes   Yes
High cholesterol   Yes
Coronary heart disease   Yes
Stroke   Yes
Cancer   No
Benign neoplasms   No
Fracture   No
  - Which site(s)?    
Osteoporosis   No
Family history of Baseline Recontact1
Coronary heart disease   No
Stroke   No
Diabetes   No
Cancer   No
Hypertension   No
Lifestyle Baseline Recontact1
Current smoking   Yes
Past smoking   Yes
Alcohol use   No
Physical activity Yes No
Nutrition (yes/no) Yes No
  - Number of food items available (approximately) <20 only food group level  
  - Method(s) of dietary assessment (e.g. 24h-recall, food frequency questionnaire, dietary records) FFQ
 
  - Supplement use Yes
Yes
Anthropometry Baseline Recontact1
Weight and height   Yes
  - Measured or self-reported   Measured
Unintended weight loss   No
Waist circumference   Yes
  - Measured or self-reported   Measured
Hip circumference   Yes
Measured or self-reported   Measured
Blood pressure Baseline Recontact1
Measured blood pressure   Yes
History of hypertension   Yes
Blood tests Baseline Recontact1
Total cholesterol   Yes
HDL cholesterol   Yes
Triglycerides   Yes
  - Fasting period   ?
ApoA1   No
ApoB   No
Glucose Yes
No
  - Fasting period    
Glucose tolerance test   No
HbA1c   No
GGT Yes No
CRP   No
25-Hydroxy-Vitamin D Yes
No
Other tests (specify) Others available on request
No
Availability of frozen sera for further analysis Possible
Possible
  - Storage temperature (°C) of sera    
Availability of frozen plasma for further analysis Possible Possible
  - Storage temperature (°C) of plasma    
Genetics Baseline Recontact1
Genotypic data Yes
Yes
GWAS (specify)    
Other high-throughput array data (specify)    
Availability of DNA for further genotyping    
Plated DNA    
Otherwise stored DNA    
Other measurements Baseline Recontact1
Perceived health   No
Cognitive decline/dementia   Yes - MMSE
Depression   Yes
Grip Strength   No
Lung function   Yes
Audiometry   No
Measurement of bone density (DEXA)   No
Quality of life instruments (such as SF-12, EUROQoL)   No
Limitations in ADL/IADL (i.e. Activities of daily living/Instrumental activities of daily living)   No
Multimorbidity instruments (such as CIRS-G)   No
Frailty scales   No
Reproductive history (for women)   N/A
Menstruation and menopausal status   N/A
Fertility problems   N/A
Pregnancies   N/A
Breast feeding   N/A
Hysterectomy and ovariectomy   N/A
History of oral contraceptive use   N/A
History of menopausal hormones use   N/A
Current use of exogenous hormones   N/A
Use of drugs Yes Yes
Availability of classification of drugs, specify (e.g. Anatomical Therapeutic Chemical(ATC) classification system) No No
Additional Topics Baseline Recontact1
  Attitude Survey
Social support questions
Dental questionnaire

Future recontacts

Other follow-up

New follow-up currently ongoing (started Autumn 2014)

Follow-up period

In year 2012 the follow-up was extended to 18yrs from baseline for each person for fatal and nonfatal events

Sources of data

  • Person himself
  • Relatives
  • GP, specialist or occupational medicine department
  • Registrar's General's data: The responsibilities of the General Registrar's Office, lead by the Registrar General, includes the administration of registration of deaths through the 26 District Registration Offices of Northern Ireland. Death certificates of deaths in Northern Ireland were obtained from the General Register Office
  • Business Services Organisation (BSO)

Follow-up procedure

BSO informed the PRIME Belfast co-ordinators when any of the PRIME subjects died, moved to a health authority in Great Britain or moved outside Northern Ireland.

Each year, on the anniversary of the initial examination, each subject was followed-up by means of a questionnaire sent to his home. Some of the answers to this questionnaire lead to further enquiry.

The procedure for contacting the subjects was:

  1. Mail an Annual Follow-up Questionnaire, the letter of introduction and a stamped pre-addressed envelope, on the anniversary of the initial PRIME examination.
  2. If there is no answer try to make contact by telephone.
  3. If all this fails, contact:
    • his doctor(s) (general practitioner and/or specialist)
    • his Occupational Medicine Department
  4. If this is unsuccessful make a home visit and, if necessary, talk to neighbours.
  5. If no answer is obtained, search the Registrar General's data to verify that he is still alive.
  6. If the person is alive, classify him as "lost to follow-up".
  7. After 10 years try to establish if the subject is alive or dead by:
    • searching the Registrar General's data
    • reviewing the BSO reports

Whenever there was suspicion of an event, clinical information was sought directly from the hospital or general practitioner notes. All details of electrocardiograms, hospital admissions, enzymes, surgical operations, angioplasty, treatment etc. were collected. Death certificates were checked for supporting clinical and post-mortem information on cause of death. Whenever necessary, the circumstances of death were obtained from the practitioner or the family.

End-points covered through the follow-up

  • All deaths:Yes
    • Specification of the cause: Yes
  • Non-fatal cancers:Yes
    • Cancer survival: ?
  • Non-fatal acute coronary events: Yes
  • Non-fatal stroke: Yes
  • Non-fatal diabetes: Yes
  • Fractures: No
  • Cognitive impairment/dementia: No
  • Nursing home admission: No

ICD-version used for classification of diseases in the data

see MORGAM

References

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