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Conditions/Immune and joints

Sjögren's syndrome

What research knows about Sjögren's syndrome comes from people who live with it. Here is how many do, what records they usually have, and what sharing yours is worth.

Living with it

60.82 cases per 100 000 inhabitants

Pooled prevalence of primary Sjögren's syndrome

source

New diagnoses

6.92 per 100 000 person-years

Pooled incidence of primary Sjögren's syndrome

source

How rare

Common

about 6.1 in 10,000 people

sourcesource

What patients usually have

The records behind Sjögren's syndrome

  • Baseline blood tests for associated conditions (thyroid, liver, TTG, immunoglobulins, vitamin D and others)

    Lab results

    at baseline, and repeated as clinically indicated

    guideline
  • Hydroxychloroquine prescription

    Medication history

    a trial of 6 to 12 months

    guideline
  • Minor labial salivary gland biopsy

    Pathology reports

    at diagnosis, when clinical and serological features are not enough

    guideline
  • Salivary gland ultrasound

    Scan reports

    at diagnosis

    guideline

What sharing it is worth

$96

per licence for a complete story and one year of these records, $96 to $1,224

Value your own data
  • Your health story$23how
  • Lab resultsx1$0.24how
  • Medication historyx1$2.33how
  • Pathology reportsx1$3.49how
  • Scan reportsx1$2.79how
  • Richness premium (5 kinds of data linked)x3how

A benchmark from published prices, not a promise: contributors earn a share each time a licence includes their data. How the benchmark works · What health data sells for

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