Evidence map›Paper›PMID 27194212›Full record

ReviewNature reviews. Disease primers2016

Primary hyperparathyroidism.

John P Bilezikian, Natalie E Cusano, Aliya A Khan, Jian-Min Liu, Claudio Marcocci, Francisco Bandeira

Registry-linked trialOpen access · greenAbstract readReview
In one paragraph

Review in Nature reviews. Disease primers, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06288490 (A Single Arm Study Comparing Amorphous Calcium Carbonate), which is not on this map. Cited by 124 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
124citing papers in PubMed, 3 pooled it
11.5field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT06288490 naterminatednot on this map

A Single Arm Study Comparing Amorphous Calcium Carbonate (ACC) Supplement Versus Commercially Available Crystalline Calcium Supplements (CCS) in the Management of Hypoparathyroidism

TypeinterventionalSponsorAmorphical Ltd.Ran2013 to 2014Enrolled10ConditionsHypoparathyroidismArmsamorphous calcium carbonate
3 · Its place in the literature

Who cites it

124 citing papers in PubMed, 3 syntheses or guidelines pooled it, 251 citations in OpenAlex.

  1. Pooled it
  2. Guideline
  3. Risk of fractures in primary hyperparathyroidism: a systematic review and meta-analysis.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2021
    Pooled it
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  5. Review
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64 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 5 institutions in 5 countries.

John P BilezikianDivision of Endocrinology, College of Physicians and Surgeons, Columbia University Medical Center, 630 W. 168th Street, New York, New York 10032, USA.
Natalie E CusanoDivision of Endocrinology, College of Physicians and Surgeons, Columbia University Medical Center, 630 W. 168th Street, New York, New York 10032, USA.
Aliya A KhanDivision of Endocrinology and Metabolism and Geriatrics, McMaster University, Hamilton, Canada.
Jian-Min LiuDepartment of Endocrine and Metabolic Diseases, Rui-jin Hospital, Shanghai Jiao-tong University School of Medicine, Shanghai, China.
Claudio MarcocciDepartment of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.
Francisco BandeiraDivision of Endocrinology and Diabetes, Agamenon Magalhães Hospital, Brazilian Ministry of Health, University of Pernambuco, Medical School, Recife, Brazil.
Columbia University Irving Medical Center · USMcMaster University · CAMinistério da Saúde · BRRuijin Hospital · CNUniversity of Pisa · IT

Funding

PRIMARY HYPERPARATHYROIDISMR01DK032333 · NIDDK · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI BILEZIKIAN, JOHN P · 1986 to 2018
$9.6M
NIDDK NIH HHS R01 DK032333
6 · The paper itself

Abstract

Primary hyperparathyroidism (PHPT) is a common disorder in which parathyroid hormone (PTH) is excessively secreted from one or more of the four parathyroid glands. A single benign parathyroid adenoma is the cause in most people. However, multiglandular disease is not rare and is typically seen in familial PHPT syndromes. The genetics of PHPT is usually monoclonal when a single gland is involved and polyclonal when multiglandular disease is present. The genes that have been implicated in PHPT include proto-oncogenes and tumour-suppressor genes. Hypercalcaemia is the biochemical hallmark of PHPT. Usually, the concentration of PTH is frankly increased but can remain within the normal range, which is abnormal in the setting of hypercalcaemia. Normocalcaemic PHPT, a variant in which the serum calcium level is persistently normal but PTH levels are increased in the absence of an obvious inciting stimulus, is now recognized. The clinical presentation of PHPT varies from asymptomatic disease (seen in countries where biochemical screening is routine) to classic symptomatic disease in which renal and/or skeletal complications are observed. Management guidelines have recently been revised to help the clinician to decide on the merits of a parathyroidectomy or a non-surgical course. This Primer covers these areas with particular attention to the epidemiology, clinical presentations, genetics, evaluation and guidelines for the management of PHPT.

Indexed as

AnxietyAsymptomatic DiseasesBlack PeopleFatigueHumansHypercalcemiaHyperparathyroidism, PrimaryIrritable MoodMagnetic Resonance ImagingMuscle WeaknessParathyroidectomyParathyroid HormoneParathyroid NeoplasmsSleep Wake DisordersSomatoform DisordersParathyroid Hormone

Identifiers

PMID27194212
PMCPMC5385896
OpenAlexW4211092031

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.