Evidence map›Paper›PMID 22235252›Full record

Trial reportPloS one2012

Clinical subtypes of depression are associated with specific metabolic parameters and circadian endocrine profiles in women: the power study.

Giovanni Cizza, Donna S Ronsaville, Hayley Kleitz, Farideh Eskandari, Sejal Mistry, Sara Torvik, Nina Sonbolian, James C Reynolds, Marc R Blackman, Philip W Gold and 2 more

Registry-linked trialAbstract readClinical Trial
In one paragraph

Trial report in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00006180 (The P.O.W.E.R. STUDY), which is not on this map. Cited by 40 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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.

NCT00006180 phase4completednot on this map

The P.O.W.E.R. STUDY (Premenopause, Osteopenia/Osteoporosis, Women, Alendronate, Depression)

TypeinterventionalSponsorNational Institute of Mental Health (NIMH)Ran2000 to 2007Enrolled220ConditionsDepression, Healthy, Osteopenia, OsteoporosisArmsAlendronate
3 · Its place in the literature

Who cites it

40 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
  3. Trial
  4. Monocyte epigenetic age acceleration is linked to non-somatic depressive symptoms in women with and without HIV.The journals of gerontology. Series A, Biological sciences and medical sciences · 2026
    Article
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  12. Peripheral Markers of Depression.Journal of clinical medicine · 2020
    Review
  13. Depression and Obesity: Analysis of Common Biomarkers.Diseases (Basel, Switzerland) · 2020
    Review
  14. 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

12 authors.

Giovanni CizzaSection on Neuroendocrinology of Obesity, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Department of Health and Human Services, Bethesda, Maryland, United States of America. cizzag@intra.niddk.nih.gov
Donna S Ronsaville
Hayley Kleitz
Farideh Eskandari
Sejal Mistry
Sara Torvik
Nina Sonbolian
James C Reynolds
Marc R Blackman
Philip W Gold
Pedro E Martinez
P.O.W.E.R. (Premenopausal, Osteopenia/Osteoporosis, Women, Alendronate, Depression) Study Group

Funding

Pathophysiological Mechanisms in Major Depression and Bipolar DisorderZIAMH002940 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI GOLD, PHILIP W · 2013 to 2014
$10k
Intramural NIH HHS
6 · The paper itself

Abstract

backgroundMajor depressive disorder (MDD) has been associated with adverse medical consequences, including cardiovascular disease and osteoporosis. Patients with MDD may be classified as having melancholic, atypical, or undifferentiated features. The goal of the present study was to assess whether these clinical subtypes of depression have different endocrine and metabolic features and consequently, varying medical outcomes.

methodsPremenopausal women, ages 21 to 45 years, with MDD (N = 89) and healthy controls (N = 44) were recruited for a prospective study of bone turnover. Women with MDD were classified as having melancholic (N = 51), atypical (N = 16), or undifferentiated (N = 22) features. Outcome measures included: metabolic parameters, body composition, bone mineral density (BMD), and 24 hourly sampling of plasma adrenocorticotropin (ACTH), cortisol, and leptin.

resultsCompared with control subjects, women with undifferentiated and atypical features of MDD exhibited greater BMI, waist/hip ratio, and whole body and abdominal fat mass. Women with undifferentiated MDD characteristics also had higher lipid and fasting glucose levels in addition to a greater prevalence of low BMD at the femoral neck compared to controls. Elevated ACTH levels were demonstrated in women with atypical features of depression, whereas higher mean 24-hour leptin levels were observed in the melancholic subgroup.

conclusionsPre-menopausal women with various features of MDD exhibit metabolic, endocrine, and BMD features that may be associated with different health consequences.

trial registrationClinicalTrials.gov NCT00006180.

Indexed as

Circadian RhythmPremenopauseAdrenocorticotropic HormoneAdultAlendronateBiomarkersBody CompositionBone DensityEndocrine SystemFemaleHumansHydrocortisoneLaboratoriesLeptinMajor Depressive DisorderMiddle AgedAdrenocorticotropic HormoneAlendronateBiomarkersHydrocortisoneLeptin

Identifiers

PMID22235252
PMCPMC3250402

What OpenQuestion holds

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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.