Evidence map›Paper›PMID 28875423›Full record

ArticleEndocrine2018

Glucose homeostasis in GHD children during long-term replacement therapy: a case-control study.

Donatella Capalbo, Andrea Esposito, Nicola Improda, Malgorzata Gabriela Wasniewska, Raffaella Di Mase, Filippo De Luca, Dario Bruzzese, Mariacarolina Salerno

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In one paragraph

Article in Endocrine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 17% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

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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

8 authors at 2 institutions in 1 country.

Donatella CapalboDepartment of Pediatrics, University "Federico II" of Naples, Naples, Italy.
Andrea EspositoDepartment of Translational Medical Sciences Pediatric Endocrinology Section, University "Federico II" of Naples, Naples, Italy.
Nicola ImprodaDepartment of Pediatrics, University "Federico II" of Naples, Naples, Italy.
Malgorzata Gabriela WasniewskaDepartment of Pediatric Gynecological, Microbiological and Biomedical Sciences, University of Messina, Messina, Italy.
Raffaella Di MaseDepartment of Pediatrics, University "Federico II" of Naples, Naples, Italy.
Filippo De LucaDepartment of Pediatric Gynecological, Microbiological and Biomedical Sciences, University of Messina, Messina, Italy.
Dario BruzzeseDepartment of Public Health, University "Federico II" of Naples, Naples, Italy.
Mariacarolina SalernoDepartment of Translational Medical Sciences Pediatric Endocrinology Section, University "Federico II" of Naples, Naples, Italy. salerno@unina.it.ORCID http://orcid.org/0000-0003-1310-3300
Federico II University Hospital · ITUniversity of Messina · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo evaluate glucose homeostasis in children with growth hormone (GH) deficiency (GHD) receiving long-term replacement therapy.

methodsWe evaluated glucose, insulin, HOmeostasis Model Assessment (HOMA-IR), and HbA1c in 100 GHD children at diagnosis and during 5 years of therapy. One hundred healthy children comparable to patients were evaluated at baseline and after 1 and 5 years.

resultsNo difference was detected at baseline between GHD patients and controls in glucose (79.58 ± 9.96 vs. 77.18 ± 8.20 mg/dl), insulin (4.50 ± 3.24 vs. 4.30 ± 2.60 µU/ml), HbA1c (5.20 ± 0.31 vs. 5.25 ± 0.33%) levels, and HOMA-IR (0.93 ± 0.72 vs. 0.86 ± 0.61). One year of GH was associated with a significant increase in insulin (7.21 ± 4.84, p < 0.001) and HOMA-IR (1.32 ± 0.98, p < 0.001) in GHD children, which became different from controls (p < 0.001 and p = 0.004). These parameters did not change further during the following years of treatment in GHD subjects. In contrast, controls did not show significant changes in insulin (4.40 ± 2.60) and HOMA-IR (0.82 ± 0.60) during the first year; however, at the fifth year of the study a significant increase in insulin (6.50 ± 3.50, p = 0.004) and HOMA-IR (1.29 ± 0.54, p < 0.001) was documented, making these parameters comparable between patients and controls.

conclusionsOur results suggest that growth hormone (GH) treatment is not associated with significant impairment of insulin sensitivity in GHD children. The slight impairment observed in GHD adolescents after long-term GH is comparable to that physiologically occurring in healthy pubertal subjects.

Indexed as

Hormone Replacement TherapyAdolescentBlood GlucoseCase-Control StudiesChildChild, PreschoolDwarfism, PituitaryHomeostasisHuman Growth HormoneHumansMaleBlood GlucoseHuman Growth HormoneGH replacement therapyGlucose homeostasisGrowth hormone deficiencyInsulin sensitivity

Identifiers

PMID28875423
OpenAlexW2753814118

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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.