Evidence mapPaperPMID 39367145Full record

ArticleScientific reports2024

Opposing impact of hypertension/diabetes following hormone therapy initiation and preexisting statins on castration resistant progression of nonmetastatic prostate cancer: a multicenter study.

Tomonori Hayashi, Tomoyoshi Miyamoto, Shiori Iwane, Masanori Fujitani, Kazuki Uchitani, Yuichi Koizumi, Atsushi Hirata, Hidefumi Kinoshita, Atsufumi Kawabata

Abstract readMulticenter Study
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
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.

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

1 citing paper in PubMed.

  1. Review
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

9 authors.

Tomonori HayashiDepartment of Pharmacy, Kindai University Nara Hospital, 1248-1 Otodacho, Ikoma, Nara, 630-0293, Japan.
Tomoyoshi MiyamotoSchool of Pharmacy, Hyogo Medical University, 1-3-6 Minatojima, Chuo-ku, Hyogo, 663- 8530, Japan.
Shiori IwaneDepartment of Hospital Pharmacy, Kansai Medical University, 2-3-1 Shinmachi, Hirakata, Osaka, 573-1191, Japan.
Masanori FujitaniDepartment of Pharmacy, Seichokai Fuchu Hospital, 1-10-1, Hiko-Town, Izumi, Osaka, 594-0076, Japan.
Kazuki UchitaniDepartment of Hospital Pharmacy, Kansai Medical University, 2-3-1 Shinmachi, Hirakata, Osaka, 573-1191, Japan.
Yuichi KoizumiDepartment of Pharmacy, Seichokai Fuchu Hospital, 1-10-1, Hiko-Town, Izumi, Osaka, 594-0076, Japan.
Atsushi HirataDepartment of Pharmacy, Kindai University Nara Hospital, 1248-1 Otodacho, Ikoma, Nara, 630-0293, Japan.
Hidefumi KinoshitaDepartment of Urology and Andrology, Kansai Medical University, 2-3-1 Shinmachi, Hirakata, Osaka, 573-1191, Japan.
Atsufumi KawabataLaboratory of Pharmacology and Pathophysiology, Faculty of Pharmacy, Kindai University, 3- 4-1 Kowakae, Higashi-Osaka, Osaka, 577-8502, Japan. kawabata@phar.kindai.ac.jp.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hormone therapy, especially androgen deprivation therapy (ADT), is effective against prostate cancer (PC), whereas long-term ADT is a risk for metabolic/cardiovascular disorders including diabetes (DM), hypertension (HT) and dyslipidemia (DL), and might result in progression to castration-resistant prostate cancer (CRPC). We thus conducted a multicenter retrospective cohort study to ask whether CRPC progression would be associated positively with HT, DM or DL and negatively with statins prescribed for treatment of DL. In this study, 1,112 nonmetastatic PC patients undergoing ADT were enrolled. Univariate statistical analyses clearly showed significant association of HT or DM developing after ADT onset, though not preexisting HT or DM, with early CRPC progression. On the other hand, preexisting DL or statin use, but not newly developed DL or started statin prescriptions following ADT, was negatively associated with CRPC progression. Multivariate analysis revealed significant independent association of the newly developed DM or HT, or preexisting statin use with CRPC progression [adjusted hazard ratios (95% confidence intervals): 3.85 (1.65-8.98), p = 0.002; 2.75 (1.36-5.59), p = 0.005; 0.25 (0.09-0.72), p = 0.010, respectively]. Together, ADT-related development of HT or DM and preexisting statin use are considered to have positive and negative impact on CRPC progression, respectively.

Indexed as

Androgen AntagonistsDisease ProgressionHydroxymethylglutaryl-CoA Reductase InhibitorsHypertensionProstatic Neoplasms, Castration-ResistantAgedAged, 80 and overDiabetes MellitusHumansMaleMiddle AgedRetrospective StudiesAndrogen AntagonistsHydroxymethylglutaryl-CoA Reductase InhibitorsAndrogen deprivation therapyCastration-resistant prostate cancerDiabetesHormone therapyHypertensionStatin

Identifiers

PMID39367145
PMCPMC11452672

What Socratic holds

Texttitle and abstract
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.