Evidence map›Paper›PMID 27154872›Full record

ArticleEndocrine2017

Vitamin D status in primary hyperparathyroidism: effect of genetic background.

Claudia Battista, Vito Guarnieri, Vincenzo Carnevale, Filomena Baorda, Mauro Pileri, Maria Garrubba, Antonio S Salcuni, Iacopo Chiodini, Salvatore Minisola, Elisabetta Romagnoli and 9 more

Abstract read
PubMed Publisher
In one paragraph

Article in Endocrine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.9field-weighted citation impact, top 10% 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Primary Hyperparathyroidism.The Journal of clinical endocrinology and metabolism · 2018
    Review
  13. Article
  14. VITAMIN D BINDING PROTEIN AND 25-HYDROXYVITAMIN D LEVELS: EMERGING CLINICAL APPLICATIONS.Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists · 2017
    Review
  15. Article
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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

19 authors at 7 institutions in 2 countries.

Claudia BattistaUnit of Endocrinology, Medical Genetics, Internal Medicine, Clinical Pathology, Radiotherapy, Nuclear Medicine, Biostatistics, IRCCS "Casa Sollievo della Sofferenza", 71013, San Giovanni Rotondo, Foggia, Italy.
Vito GuarnieriUnit of Endocrinology, Medical Genetics, Internal Medicine, Clinical Pathology, Radiotherapy, Nuclear Medicine, Biostatistics, IRCCS "Casa Sollievo della Sofferenza", 71013, San Giovanni Rotondo, Foggia, Italy.
Vincenzo CarnevaleUnit of Endocrinology, Medical Genetics, Internal Medicine, Clinical Pathology, Radiotherapy, Nuclear Medicine, Biostatistics, IRCCS "Casa Sollievo della Sofferenza", 71013, San Giovanni Rotondo, Foggia, Italy.
Filomena BaordaUnit of Endocrinology, Medical Genetics, Internal Medicine, Clinical Pathology, Radiotherapy, Nuclear Medicine, Biostatistics, IRCCS "Casa Sollievo della Sofferenza", 71013, San Giovanni Rotondo, Foggia, Italy.
Mauro PileriUnit of Endocrinology, Medical Genetics, Internal Medicine, Clinical Pathology, Radiotherapy, Nuclear Medicine, Biostatistics, IRCCS "Casa Sollievo della Sofferenza", 71013, San Giovanni Rotondo, Foggia, Italy.
Maria GarrubbaUnit of Endocrinology, Medical Genetics, Internal Medicine, Clinical Pathology, Radiotherapy, Nuclear Medicine, Biostatistics, IRCCS "Casa Sollievo della Sofferenza", 71013, San Giovanni Rotondo, Foggia, Italy.
Antonio S SalcuniUnit of Endocrinology, Medical Genetics, Internal Medicine, Clinical Pathology, Radiotherapy, Nuclear Medicine, Biostatistics, IRCCS "Casa Sollievo della Sofferenza", 71013, San Giovanni Rotondo, Foggia, Italy.
Iacopo ChiodiniUnit of Endocrinology and Metabolic Diseases, Fondazione IRCCS Cà Granda, Department of Clinical Sciences and Community Health, University of Milan, 20122, Milan, Italy.
Salvatore MinisolaDepartment of Internal Medicine and Medical Discipline, "Sapienza" Rome University, 00185, Rome, Italy.
Elisabetta RomagnoliDepartment of Experimental Medicine, "Sapienza" Rome University, 00185, Rome, Italy.
Cristina Eller-VainicherUnit of Endocrinology and Metabolic Diseases, Fondazione IRCCS Cà Granda, Department of Clinical Sciences and Community Health, University of Milan, 20122, Milan, Italy.
Stefano A SantiniUnit of Endocrinology, Medical Genetics, Internal Medicine, Clinical Pathology, Radiotherapy, Nuclear Medicine, Biostatistics, IRCCS "Casa Sollievo della Sofferenza", 71013, San Giovanni Rotondo, Foggia, Italy.
Salvatore ParisiUnit of Endocrinology, Medical Genetics, Internal Medicine, Clinical Pathology, Radiotherapy, Nuclear Medicine, Biostatistics, IRCCS "Casa Sollievo della Sofferenza", 71013, San Giovanni Rotondo, Foggia, Italy.
Vincenzo FruscianteUnit of Endocrinology, Medical Genetics, Internal Medicine, Clinical Pathology, Radiotherapy, Nuclear Medicine, Biostatistics, IRCCS "Casa Sollievo della Sofferenza", 71013, San Giovanni Rotondo, Foggia, Italy.
Andrea FontanaUnit of Endocrinology, Medical Genetics, Internal Medicine, Clinical Pathology, Radiotherapy, Nuclear Medicine, Biostatistics, IRCCS "Casa Sollievo della Sofferenza", 71013, San Giovanni Rotondo, Foggia, Italy.
Massimiliano CopettiUnit of Endocrinology, Medical Genetics, Internal Medicine, Clinical Pathology, Radiotherapy, Nuclear Medicine, Biostatistics, IRCCS "Casa Sollievo della Sofferenza", 71013, San Giovanni Rotondo, Foggia, Italy.
Geoffrey N HendyExperimental Therapeutics and Metabolism, McGill University Health Centre-Research Institute, and Departments of Medicine, Physiology and Human Genetics, McGill University, Montreal, QC, H4A 3J1, Canada.
Alfredo ScillitaniUnit of Endocrinology, Medical Genetics, Internal Medicine, Clinical Pathology, Radiotherapy, Nuclear Medicine, Biostatistics, IRCCS "Casa Sollievo della Sofferenza", 71013, San Giovanni Rotondo, Foggia, Italy. alscill@tin.it.
David E C ColeDepartments of Laboratory Medicine and Pathobiology, Medicine and Genetics, University of Toronto, Toronto, ON, M4N 3M5, Canada.
Istituti di Ricovero e Cura a Carattere Scientifico · ITCasa Sollievo della Sofferenza · ITSapienza University of Rome · ITFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico · ITMcGill University Health Centre · CAUniversity of Milan · ITUniversity of Toronto · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Primary hyperparathyroidism (PHPT) is associated with hypovitaminosis D as assessed by serum total 25-hydroxyvitamin D (TotalD) levels. The aim of this study is to evaluate whether this is also the case for the calculated bioavailable 25-hydroxyvitamin D (BioD) or free 25-hydroxyvitamin D (FreeD), and whether the vitamin D status is influenced by genetic background. We compared vitamin D status of 88 PHPT patients each with a matched healthy family member sharing genetic background, i.e., first-degree relative (FDR), or not, namely an in-law relative (ILR). We compared TotalD and vitamin D-binding protein (DBP), using the latter to calculate BioD and FreeD. We also genotyped two common DBP polymorphisms (rs7041 and rs4588) likely to affect the affinity for and levels of vitamin D metabolites. TotalD was lower (p < 0.001) in PHPT (12.3 ± 6.6 ng/mL) than either family member group (FDR: 19.4 ± 12.1 and ILR: 23.2 ± 14.1), whether adjusted for DBP or not. DBP levels were also significantly lower (p < 0.001) in PHPT (323 ± 73 mg/L) versus FDR (377 ± 98) or ILR (382 ± 101). The differences between PHPT and control groups for TotalD, BioD, and FreeD were maintained after adjustment for season, gender, and serum creatinine. 25-hydroxyvitamin D, evaluated as total, free, or bioavailable fractions, is decreased in PHPT. No difference was seen between first-degree relative and in-law controls, suggesting that neither genetic nor non-genetic background greatly influences the genesis of the hypovitaminosis D seen in PHPT.

Indexed as

FamilyPolymorphism, Single NucleotideAdultAgedFemaleHumansHyperparathyroidism, PrimaryMaleMiddle AgedSeasonsSex FactorsVitamin DVitamin D-Binding ProteinVitamin D Deficiency25-hydroxyvitamin DVitamin DVitamin D-Binding ProteinBioavailable 25-hydroxyvitamin DFree 25-hydroxyvitamin DPrimary hyperparathyroidismVitamin D-binding protein

Identifiers

PMID27154872
OpenAlexW2345926778

What OpenQuestion holds

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Registered trials

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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.