Evidence map›Paper›PMID 35898448›Full record

Trial reportFrontiers in endocrinology2022

Baseline Testosterone Predicts Body Composition and Metabolic Response to Testosterone Therapy.

Fnu Deepika, Elliot Ballato, Georgia Colleluori, Lina Aguirre, Rui Chen, Clifford Qualls, Dennis T Villareal, Reina Armamento-Villareal

2 registry-linked trialsOpen access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Frontiers in endocrinology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.1field-weighted citation impact, top 11% 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.

NCT01378299 phase1completednot on this map

CYP19A1 Gene and Pharmacogenetics of Response

TypeinterventionalSponsorVA Office of Research and DevelopmentRan2011 to 2017Enrolled105ConditionsHypogonadismArmsTestosterone Cypionate
NCT03887936 phase4completednot on this map

Testosterone Therapy and Bone Quality in Men With Diabetes and Hypogonadism

TypeinterventionalSponsorVA Office of Research and DevelopmentRan2019 to 2025Enrolled92ConditionsType 2 Diabetes Mellitus, HypogonadismArmsTestosterone gel 1.62%, Placebo
3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 15 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Rethinking Osteoporosis Drugs: Can We Simultaneously Address Sarcopenia?International journal of molecular sciences · 2025
    Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
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 4 institutions in 1 country.

Fnu DeepikaDivision of Endocrinology Diabetes and Metabolism at Baylor College of Medicine, Houston, TX, United States.
Elliot BallatoDivision of Endocrinology Diabetes and Metabolism at Baylor College of Medicine, Houston, TX, United States.
Georgia ColleluoriDivision of Endocrinology Diabetes and Metabolism at Baylor College of Medicine, Houston, TX, United States.
Lina AguirreDivision of Endocrinology, University of New Mexico School of Medicine, Albuquerque, NM, United States.
Rui ChenDivision of Endocrinology Diabetes and Metabolism at Baylor College of Medicine, Houston, TX, United States.
Clifford QuallsDivision of Endocrinology, University of New Mexico School of Medicine, Albuquerque, NM, United States.
Dennis T VillarealDivision of Endocrinology Diabetes and Metabolism at Baylor College of Medicine, Houston, TX, United States.
Reina Armamento-VillarealDivision of Endocrinology Diabetes and Metabolism at Baylor College of Medicine, Houston, TX, United States.
Baylor College of Medicine · USMichael E. DeBakey VA Medical Center · USBiomedical Research Institute of New Mexico · USUniversity of New Mexico · US

Funding

Aromatase Inhibitors and Weight Loss in Severely Obese Men with HypogonadismR01HD093047 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI VILLAREAL, REINA C · 2017 to 2022
$1.9M
CSRD VA I01 CX000424CSRD VA I01 CX001665NICHD NIH HHS R01 HD093047
6 · The paper itself

Abstract

Context: Male hypogonadism adversely affects body composition, bone mineral density (BMD), and metabolic health. A previous report showed that pre-treatment testosterone (T) levels of <200 ng/dl is associated with greater improvement in spine BMD with T therapy. However, to date, there is no study that investigates whether baseline T levels also influence body composition and metabolic response to T therapy. Objective: The aim of this study is to determine if there are differences in the changes in body composition, metabolic profile, and bone turnover markers, in addition to BMD, in response to T therapy in men with a baseline T level of <264 ng/dl compared to those with levels ≥264 ng/dl. Methods: This is a secondary analysis of a single-arm, open-label clinical trial (NCT01378299) on pharmacogenetics of response to T therapy conducted between 2011 and 2016 involving 105 men (40-74 years old), with average morning T < 300 ng/dl, given intramuscular T cypionate 200 mg every 2 weeks for 18 months. Subjects were divided into those with baseline T levels of <264 ng/dl ( Results: Men with T < 264 ng/dl showed greater increases in total fat-free mass (FFM) at 18 months compared to those with T ≥ 264 ng/dl (4.2 ± 4.1 vs. 2.7 ± 3.8%; Conclusion: T therapy results in improvement in body composition irrespective of baseline T levels but T < 264 ng/dl is associated with greater improvement in FFM, whereas a T level of ≥264 ng/dl favors improvement in metabolic profile.

Indexed as

HypogonadismTestosteroneAdultAgedBody CompositionGlycated HemoglobinHumansLeptinMaleMiddle AgedGlycated HemoglobinLeptinTestosteronebody compositionbone turn over markers (BTM)HbA1chypogonadismtestosterone

Identifiers

PMID35898448
PMCPMC9309506
OpenAlexW4285005839

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.