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Hyperparathyroidism

Metabolism and Endocrine Disease · NLM MeSH · updated 2026-11-04 · version 1

Citations verified against PubMedNot yet clinician-reviewed10 referencesApproximately 5 min read

A condition of abnormally elevated output of parathyroid hormone (or PTH) triggering responses that increase blood calcium.

Table of Contents

1. Definition2. Research landscape3. Reading the evidence4. Open-access studies5. Key reviews6. References7. About this article

Definition and research guide

This page combines a MeSH definition, publication statistics and selected research abstracts. It is a starting point for reading the literature, not a medical textbook or a systematic evidence review.

Content available: 4 complete abstracts (1,052 words), 10 references. Full article text is not stored or reproduced here; follow the PMID, DOI or PMC links to read the original sources and their access terms.

Definition

A condition of abnormally elevated output of parathyroid hormone (or PTH) triggering responses that increase blood calcium. It is characterized by hypercalcemia and bone resorption, eventually leading to bone diseases. primary hyperparathyroidism is caused by parathyroid hyperplasia or parathyroid neoplasms. secondary hyperparathyroidism is increased PTH secretion in response to hypocalcemia, usually caused by chronic kidney diseases.

Definition: NLM Medical Subject Headings (MeSH) scope note (Public domain (U.S. National Library of Medicine); attribution requested). View the MeSH record.

Where it fits in the MeSH classification

Broader topics
Parathyroid Diseases
Narrower topics
Hyperparathyroidism, Primary; Hyperparathyroidism, Secondary
See also
Osteitis Fibrosa Cystica; Multiple Endocrine Neoplasia Type 1

Related concepts

  • Parathyroid Hormone
  • Calcium
  • Hypercalcemia
  • Bone Resorption
  • Primary Hyperparathyroidism
  • Hyperplasia
  • Parathyroid Neoplasms
  • Secondary Hyperparathyroidism
  • Hypocalcemia
  • Kidney Diseases

Research landscape

PubMed indexes 26,942 records tagged with the MeSH heading “Hyperparathyroidism” (counts retrieved 2026-11-04). 3,049 of them (11.3%) were published from 2020 onward, and the busiest period so far is through 1999 with 13,472 records.

Reviews account for 4,279 records (15.9%) and meta-analyses for 174. Randomized controlled trials number 448 (1.7%) as a share of all records on the topic. Randomized trials make up only a small share of this literature, so much of what is known comes from laboratory, observational or descriptive work.

PubMed records by publication periodthrough 1999: 13,472 records; 2000-2009: 5,297 records; 2010-2019: 5,124 records; 2020 onward: 3,049 records13,472through 19995,2972000-20095,1242010-20193,0492020 onward
Records in PubMed indexed with this heading, by publication period. Real counts from NCBI E-utilities; the final period covers only part of the current year. Volume reflects how much has been published, not how strong the evidence is.
Show the data
PeriodRecords
through 199913,472
2000-20095,297
2010-20195,124
2020 onward3,049
Share of records by publication typeReviews: 15.9 percent; Meta-analyses: 0.6 percent; Randomized controlled trials: 1.7 percentReviews15.9% (4,279)Meta-analyses0.6% (174)Randomized controlled trials1.7% (448)
Share of all PubMed records on this heading that carry each publication type. Types overlap with other records, so the shares do not sum to 100%.
Publication-type chart data
Publication types among 26,942 PubMed records
TypeRecordsShare
Reviews4,27915.9%
Meta-analyses1740.6%
Randomized controlled trials4481.7%

Method: PubMed query "Hyperparathyroidism"[MeSH Terms] with publication-type and date filters, retrieved 2026-11-04.

Reading the evidence in metabolism and endocrine disease

Studies of diabetes, obesity and hormone disorders often follow blood tests such as glucose, HbA1c or hormone levels, which are stand-ins for outcomes that matter more, such as complications. Lifestyle and diet research is largely observational, and weight and diabetes trials can differ in how long people were followed. Nothing on this page is advice about medicines, insulin or diet; talk to a qualified clinician about your own situation. Check whether the outcome was a lab value or a clinical event, and the type and duration of the condition studied.

Evidence from open-access studies

These open-access studies come from PubMed’s best-match results for this heading (papers whose main topic it is), ranked here by citation count, with one recent addition. Each abstract is reproduced in full under its recorded open licence so that you can read the authors’ own words. They illustrate the literature; they are not a systematic summary of it. Citation counts measure attention, not reliability or clinical benefit.

Study comparison — selected abstracts, not a systematic review
Study / authorsYearSource label / designEurope PMC citationsLicence / source
The role of nutritional vitamin D in chronic kidney disease-mineral and bone disorder in children and adults with chronic kidney disease, on dialysis, and after kidney transplantation-a European consensus statement
Jørgensen HS, Vervloet M, Cavalier E, Bacchetta J, de Borst MH, Bover J, et al.
2025Research article
Design not recorded in structured metadata
45cc by
PMID 39875204 · DOI · PMC11960744
Secondary hyperparathyroidism in chronic kidney disease: A narrative review focus on therapeutic strategy
Tsai SH, Kan WC, Jhen RN, Chang YM, Kao JL, Lai HY, et al.
2024Review article
Design not recorded in structured metadata
31cc by
PMID 39208984 · DOI · PMC11414656
F18-Choline PET/CT or MIBI SPECT/CT in the Surgical Management of Primary Hyperparathyroidism: A Diagnostic Randomized Clinical Trial
Quak E, Lasne-Cardon A, Cavarec M, Lireux B, Bastit V, Roudaut N, et al.
2024Randomized controlled trial
Design not recorded in structured metadata
26cc by
PMID 38900416 · DOI · PMC11190825
Hyperparathyroidism: historical milestones and modern therapeutic strategies
Niederle B, Niederle MB
2026Review article
Design not recorded in structured metadata
1cc by
PMID 41874647 · DOI · PMC13099686

The role of nutritional vitamin D in chronic kidney disease-mineral and bone disorder in children and adults with chronic kidney disease, on dialysis, and after kidney transplantation-a European consensus statement [1]

Research article Jørgensen HS, Vervloet M, Cavalier E, Bacchetta J, de Borst MH, Bover J, et al. · · 2025 · cited 45 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
Vitamin D deficiency is common in patients with chronic kidney disease (CKD) and associates with poor outcomes.
Closing excerpt
Future clinical trials should investigate the benefit of vitamin D supplementation on patient-relevant outcomes in the setting of vitamin D deficiency across different stages of CKD.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (237 words)

Vitamin D deficiency is common in patients with chronic kidney disease (CKD) and associates with poor outcomes. Current clinical practice guidelines recommend supplementation with nutritional vitamin D as for the general population. However, recent large-scale clinical trials in the general population failed to demonstrate a benefit of vitamin D supplementation on skeletal or non-skeletal outcomes, fueling a debate on the rationale for screening for and correcting vitamin D deficiency, both in non-CKD and CKD populations. In a collaboration between the European Renal Osteodystrophy initiative of the European Renal Association (ERA) and the European Society for Paediatric Nephrology (ESPN), an expert panel performed an extensive literature review and formulated clinical practice points on vitamin D supplementation in children and adults with CKD and after kidney transplantation. These were reviewed by a Delphi panel of members from relevant working groups of the ERA and ESPN. Key clinical practice points include recommendations to monitor for, and correct, vitamin D deficiency in children and adults with CKD and after kidney transplantation, targeting 25-hydroxyvitamin D levels >75 nmol/l (>30 ng/ml). Although vitamin D supplementation appears well-tolerated and safe, it is recommended to avoid mega-doses (≥100 000 IU) and very high levels of 25 hydroxyvitamin D (>150-200 nmol/l, or 60-80 ng/ml) to reduce the risk of toxicity. Future clinical trials should investigate the benefit of vitamin D supplementation on patient-relevant outcomes in the setting of vitamin D deficiency across different stages of CKD.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 39875204 · DOI · PMC11960744

Secondary hyperparathyroidism in chronic kidney disease: A narrative review focus on therapeutic strategy [2]

Review article Tsai SH, Kan WC, Jhen RN, Chang YM, Kao JL, Lai HY, et al. · · 2024 · cited 31 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
Chronic kidney disease (CKD) affects over 10% of the global population.
Closing excerpt
Future research should explore the molecular mechanisms of parathyroid gland hyperplasia and evaluate various treatments' impacts.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (138 words)

Chronic kidney disease (CKD) affects over 10% of the global population. One crucial complication of CKD is secondary hyperparathyroidism (SHPT), marked by elevated parathyroid hormone levels due to hyperphosphataemia, hypocalcaemia, and low active vitamin D from impaired renal function. SHPT increases risks of bone deformities, vascular calcification, cardiovascular events and mortality. This review examines SHPT treatment strategies in patients with CKD. First-line treatments include phosphate binders, vitamin D receptor activators and calcimimetics. When these fail, invasive options like parathyroidectomy (PTX) and thermal ablation are considered. PTX effectively reduces symptoms and improves radiological outcomes, outperforming medical treatment alone in reducing cardiovascular risk and mortality. Thermal ablation techniques, such as microwave, radiofrequency, laser or high-intensity focused ultrasound, offer less invasive alternatives with promising results. Future research should explore the molecular mechanisms of parathyroid gland hyperplasia and evaluate various treatments' impacts.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 39208984 · DOI · PMC11414656

F18-Choline PET/CT or MIBI SPECT/CT in the Surgical Management of Primary Hyperparathyroidism: A Diagnostic Randomized Clinical Trial [3]

Randomized controlled trial Quak E, Lasne-Cardon A, Cavarec M, Lireux B, Bastit V, Roudaut N, et al. · · 2024 · cited 26 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
ImportanceWhether F18-choline (FCH) positron emission tomographic (PET)/computed tomographic (CT) scan can replace Tc99m-sestaMIBI (MIBI) single-photon emission (SPE)CT/CT as a first-line imaging technique for preoperative localization of parathyroid adenomas (PTA) in patients with primary hyperparathyroidism (PHPT) is unclear.
Closing excerpt
gov Identifier: NCT04040946.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (413 words)

ImportanceWhether F18-choline (FCH) positron emission tomographic (PET)/computed tomographic (CT) scan can replace Tc99m-sestaMIBI (MIBI) single-photon emission (SPE)CT/CT as a first-line imaging technique for preoperative localization of parathyroid adenomas (PTA) in patients with primary hyperparathyroidism (PHPT) is unclear.ObjectiveTo compare first-line FCH PET/CT vs MIBI SPECT/CT for optimal care in patients with PHPT needing parathyroidectomy and to compare the proportions of patients in whom the first-line imaging method resulted in successful minimally invasive parathyroidectomy (MIP) and normalization of calcemia 1 month after surgery.Design, setting, and participantsA French multicenter randomized open diagnostic intervention phase 3 trial was conducted. Patients were enrolled from November 2019 to May 2022 and participated up to 6 months after surgery. The study included adults with PHPT and an indication for surgical treatment. Patients with previous parathyroid surgery or multiple endocrine neoplasia type 1 (MEN1) were ineligible.InterventionsPatients were assigned in a 1:1 ratio to receive first-line FCH PET/CT (FCH1) or MIBI SPECT/CT (MIBI1). In the event of negative or inconclusive first-line imaging, they received second-line FCH PET/CT (FCH2) after MIBI1 or MIBI SPECT/CT (MIBI2) after FCH1. All patients underwent surgery under general anesthesia within 12 weeks following the last imaging. Clinical and biologic (serum calcemia and parathyroid hormone levels) assessments were performed 1 and 6 months after surgery.Main outcomes and measuresThe primary outcome was a true-positive first-line imaging-guided MIP combined with uncorrected serum calcium levels of 2.55 mmol/l or less 1 month after surgery, corresponding to the local upper limit of normality.ResultsOverall, 57 patients received FCH1 (n = 29) or MIBI1 (n = 28). The mean (SD) age of patients was 62.8 (12.5) years with 15 male (26%) and 42 female (74%) patients. Baseline patient characteristics were similar between groups. Normocalcemia at 1 month after positive first-line imaging-guided MIP was observed in 23 of 27 patients (85%) in the FCH1 group and 14 of 25 patients (56%) in the MIBI1 group. Sensitivity was 82% (95% CI, 62%-93%) and 63% (95% CI, 42%-80%) for FCH1 and MIBI1, respectively. Follow-up at 6 months with biochemical measures was available in 43 patients, confirming that all patients with normocalcemia at 1 month after surgery still had it at 6 months. No adverse events related to imaging and 4 adverse events related to surgery were reported.ConclusionsThis randomized clinical trial found that first-line FCH PET/CT is a suitable and safe replacement for MIBI SPECT/CT. FCH PET/CT leads more patients with PHPT to correct imaging-guided MIP and normocalcemia than MIBI SPECT/CT thanks to its superior sensitivity.Trial registrationClinicalTrials.gov Identifier: NCT04040946.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 38900416 · DOI · PMC11190825

Hyperparathyroidism: historical milestones and modern therapeutic strategies [4]

Review article Niederle B, Niederle MB · · 2026 · cited 1 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
The Viennese Medical School was at the forefront of the clinical understanding of the relationship between parathyroid and bone metabolism.
Closing excerpt
Therefore, the direct open (mini-incision) technique with short neck incision seems to be the new gold standard.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (264 words)

The Viennese Medical School was at the forefront of the clinical understanding of the relationship between parathyroid and bone metabolism. A century ago, F. Mandl (1925) and E. Gold (1927) described two patients clinically (osteitis fibrosa cystica) and biochemically (hypercalcemia, hypercalciuria) with a disease which Gold had already termed (primary) hyperparathyroidism (PHPT) in 1928. The two patients were successfully treated by removing one enlarged parathyroid gland each. After the clinical and biochemical diagnosis was confirmed, surgery was recommended. In 1933, Mandl summarized his rules postulating bilateral cervical exploration, i.e. the macroscopic assessment of all four glands. Only enlarged glands should be removed. Until the beginning of the 1990s, in the hands of highly experienced endocrine surgeons, bilateral neck exploration was the undisputed method of choice (gold standard) with a high postoperative success rate (normocalcemia: 98-99%). Sporadic PHPT is predominantly caused by one hyperactive parathyroid gland. The development of reliable imaging techniques in combination with intraoperative parathyroid hormone (PTH) monitoring to verify the completeness of parathyroid tissue resection led to a change in surgical strategy from extended to limited explorations. The targeted (focused) exposure of the prelocated enlarged gland with the aim to reduce surgical trauma, yet resulting in the same high cure rates, was introduced. For targeted exploration, various endoscopic techniques, cervical or remote access (i.e. skin incision outside the neck), have become available. The more direct the access, the less invasive is the dissection. Surgical techniques minimizing trauma and followed by less pain should be favored. Therefore, the direct open (mini-incision) technique with short neck incision seems to be the new gold standard.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 41874647 · DOI · PMC13099686

Key reviews and meta-analyses

The most cited review-type papers among PubMed’s best-match results for this heading, listed with bibliographic details only. Follow the links for the full text and access terms.

  • Research article Evaluation and Management of Primary Hyperparathyroidism: Summary Statement and Guidelines from the Fifth International Workshop [5]
    Bilezikian JP, Khan AA, Silverberg SJ, Fuleihan GE, Marcocci C, Minisola S, et al. · J Bone Miner Res · 2022 · cited 353 times (Europe PMC)
  • Research article Overview of the 2022 WHO Classification of Parathyroid Tumors [6]
    Erickson LA, Mete O, Juhlin CC, Perren A, Gill AJ · Endocr Pathol · 2022 · cited 231 times (Europe PMC)
  • Research article Hypercalcemia: A Review [7]
    Walker MD, Shane E · JAMA · 2022 · cited 170 times (Europe PMC)
  • Research article Chronic kidney disease-mineral and bone disorder: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference [8]
    Ketteler M, Evenepoel P, Holden RM, Isakova T, Jørgensen HS, Komaba H, et al. · Kidney Int · 2025 · cited 152 times (Europe PMC)
  • Research article Epidemiology, Pathophysiology, and Genetics of Primary Hyperparathyroidism [9]
    Minisola S, Arnold A, Belaya Z, Brandi ML, Clarke BL, Hannan FM, et al. · J Bone Miner Res · 2022 · cited 152 times (Europe PMC)
  • Research article European Expert Consensus on Practical Management of Specific Aspects of Parathyroid Disorders in Adults and in Pregnancy: Recommendations of the ESE Educational Program of Parathyroid Disorders [10]
    Bollerslev J, Rejnmark L, Zahn A, Heck A, Appelman-Dijkstra NM, Cardoso L, et al. · Eur J Endocrinol · 2022 · cited 149 times (Europe PMC)

References

  1. Jørgensen HS, Vervloet M, Cavalier E, Bacchetta J, de Borst MH, Bover J, et al.. The role of nutritional vitamin D in chronic kidney disease-mineral and bone disorder in children and adults with chronic kidney disease, on dialysis, and after kidney transplantation-a European consensus statement. . 2025. PMID 39875204 · DOI · PMC11960744
  2. Tsai SH, Kan WC, Jhen RN, Chang YM, Kao JL, Lai HY, et al.. Secondary hyperparathyroidism in chronic kidney disease: A narrative review focus on therapeutic strategy. . 2024. PMID 39208984 · DOI · PMC11414656
  3. Quak E, Lasne-Cardon A, Cavarec M, Lireux B, Bastit V, Roudaut N, et al.. F18-Choline PET/CT or MIBI SPECT/CT in the Surgical Management of Primary Hyperparathyroidism: A Diagnostic Randomized Clinical Trial. . 2024. PMID 38900416 · DOI · PMC11190825
  4. Niederle B, Niederle MB. Hyperparathyroidism: historical milestones and modern therapeutic strategies. . 2026. PMID 41874647 · DOI · PMC13099686
  5. Bilezikian JP, Khan AA, Silverberg SJ, Fuleihan GE, Marcocci C, Minisola S, et al.. Evaluation and Management of Primary Hyperparathyroidism: Summary Statement and Guidelines from the Fifth International Workshop. J Bone Miner Res. 2022. PMID 36245251 · DOI
  6. Erickson LA, Mete O, Juhlin CC, Perren A, Gill AJ. Overview of the 2022 WHO Classification of Parathyroid Tumors. Endocr Pathol. 2022. PMID 35175514 · DOI
  7. Walker MD, Shane E. Hypercalcemia: A Review. JAMA. 2022. PMID 36282253 · DOI
  8. Ketteler M, Evenepoel P, Holden RM, Isakova T, Jørgensen HS, Komaba H, et al.. Chronic kidney disease-mineral and bone disorder: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference. Kidney Int. 2025. PMID 39864017 · DOI
  9. Minisola S, Arnold A, Belaya Z, Brandi ML, Clarke BL, Hannan FM, et al.. Epidemiology, Pathophysiology, and Genetics of Primary Hyperparathyroidism. J Bone Miner Res. 2022. PMID 36245271 · DOI · PMC10092691
  10. Bollerslev J, Rejnmark L, Zahn A, Heck A, Appelman-Dijkstra NM, Cardoso L, et al.. European Expert Consensus on Practical Management of Specific Aspects of Parathyroid Disorders in Adults and in Pregnancy: Recommendations of the ESE Educational Program of Parathyroid Disorders. Eur J Endocrinol. 2022. PMID 34863037 · DOI · PMC8789028

About this article

Sources
NLM Medical Subject Headings (definition, synonyms); NCBI PubMed (counts, identifiers); Europe PMC (open-access abstracts and citation counts).
Verification
Every reference was resolved against PubMed on 2026-11-04; title, year and DOI matched.
Review state
automated source verified; no human expert review has been recorded yet.
Version
1, last updated 2026-11-04.

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Related research topics

  • Chronic Kidney Disease-Mineral and Bone DisorderMetabolism and Endocrine Disease
  • HypoparathyroidismMetabolism and Endocrine Disease
  • HypocalcemiaMetabolism and Endocrine Disease
  • RicketsMetabolism and Endocrine Disease
  • Parathyroid GlandsAnatomy and Physiology
  • ThyrotoxicosisMetabolism and Endocrine Disease

All 77 articles in Metabolism and Endocrine Disease →

At a glance

26,942
PubMed records on this heading
11%
published since 2020
4,279
review articles
448
randomized trials
10
verified references below

Counts come from PubMed on 2026-11-04; they show how much has been written, not how strong the evidence is.

Related topics See all →

  • Chronic Kidney Disease-Mineral and Bone DisorderMetabolism and Endocrine Disease
  • HypoparathyroidismMetabolism and Endocrine Disease
  • HypocalcemiaMetabolism and Endocrine Disease
  • RicketsMetabolism and Endocrine Disease
  • Parathyroid GlandsAnatomy and Physiology

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