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. 2022 Apr 11;12:152. doi: 10.1038/s41398-022-01919-9

Table 1.

N cases and % prevalence of lifetime evaluated somatic health outcomes (N = 10,645).

Disease area/outcome Combined Register-based Self-reported
Cardio-metabolic
Ischemic heart disease 1206 (11.3) 1104 (10.4) 231 (2.2)
Heart failure 1174 (11.0) 453 (4.3) 843 (7.9)
Cerebrovascular disease 1686 (15.8) 1431 (13.4) 760 (7.1)
Peripheral vascular disease 523 (4.9) 408 (3.8) 157 (1.5)
Hypertension 2730 (25.6) 735 (6.9) 2379 (22.4)
Obesity 1538 (14.4) 67 (0.6) 1526 (14.6)
Type 2 Diabetes 554 (5.2) 385 (3.6) 347 (3.3)
Autoimmune/inflammatory disease
Type 1 Diabetes 163 (1.5) 161 (1.5) 46 (0.4)
Rheumatoid arthritis 594 (5.6) 163 (1.5) 521 (4.9)
Psoriasis 605 (5.7) 195 (1.8) 503 (4.7)
Inflammatory bowel disease 243 (2.3) 176 (1.7) 153 (1.4)
Neurology
Migraine 2207 (20.7) 298 (2.8) 2125 (20.0)
Epilepsy 231 (2.2) 116 (1.1) 121 (1.2)
Dementia 374 (3.5)a 374 (3.5) N/A
Parkinson disease and parkinsonism 473 (4.4) 472 (4.4) 10 (0.1)
Sleep disorder 1272 (11.9)a 1272 (11.9) N/A

Register-based outcomes were treated as lifetime and defined based on a discharge diagnosis in the National Patient Register, the Cause of death register or disorder-specific drug dispensations. Self-report refers to questions answered as part of the SALT interview and were phrased as lifetime. Combined prevalence refers to the total number of cases identified via National Registers, self-report, or both. For details, see methods and Table S1.

aPrevalence based on register data only as there were no measures of dementia or sleep disorders available from self-report in the full SALT cohort.