Increasing incidence and prevalence of biochemically confirmed primary hyperparathyroidism in Stockholm, 2006-2020.
retrospective_cohort · Level III
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- Record sourced from PubMed, PMID 41972345.
- Also identified by DOI 10.1210/clinem/dgag162.
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Abstract
Primary hyperparathyroidism (PHPT) prevalence appears to be rising, but substantial underdiagnosis persist. Accurate epidemiological data are needed, requiring population-based studies using strict biochemical criteria. To determine incidence and prevalence of biochemically confirmed PHPT in Stockholm and characterize clinical recognition and surgical management. Population-based healthcare cohort study using prespecified biochemical diagnostic algorithms. Stockholm Region, Sweden, 2006-2020, using the Stockholm CREAtinine Measurements database covering two-thirds of the adult population, including ≥90% of individuals ≥65 years. Adults aged ≥20 years with paired calcium and parathyroid hormone (PTH) measurements meeting biochemical criteria for PHPT. Individuals with eGFR ≤30 mL/min/1.73 m2, secondary hyperparathyroidism, or prior parathyroid surgery were excluded. Annual incidence rate and point prevalence of biochemically confirmed PHPT. Among 176,780 individuals contributing 578,227 PTH measurements, 10,190 patients fulfilling biochemical PHPT criteria were identified. Age- and sex-adjusted incidence rate increased from 2.81 (95% CI, 2.55-3.09) to 4.28 (95% CI, 3.98-4.59) per 10,000 person-years between 2009 and 2020, with the steepest increase among women aged ≥70 years. Prevalence increased from 0.35 to 4.76 per 1,000 individuals. Median ionized calcium was 1.39 mmol/L. Clinical diagnosis of PHPT was documented in 5,346 (52%) patients of which, 2,800 (52%) underwent parathyroidectomy, with surgery-rates stabilizing after 2013 at 4-5% annually. Using a large healthcare database, we observed substantially increasing PHPT incidence and prevalence, predominantly in older individuals. Only 52% received clinical diagnosis, underscoring the need for studies evaluating the long-term clinical burden of undiagnosed PHPT.