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Validation of Differential Serum Levels for Five Minerals in South American Gallstone Patients With and Without Gallbladder Cancer (METALS)

8. juni 2026 oppdatert av: Centre Paul Strauss

Validation of the Association Between the Abundance of Three Bacterial Genera in Stool Samples and the Risk of Gallbladder Cancer in South American Patients With Gallstones

We have previously observed that serum concentrations of five minerals - aluminium, copper, sulphur, zinc, and bromine - differ between South American patients with gallbladder cancer and those with gallstones. The aim of this study is to confirm these differences using an independent set of serum samples from South American patients

Studieoversikt

Status

Fullført

Intervensjon / Behandling

Detaljert beskrivelse

Gallbladder cancer (GBC) is a highly lethal malignant tumour characterised by a low global incidence, but with a disproportionately high prevalence among indigenous populations in the Americas. The absence of specific symptoms and validated early detection tools often leads to late diagnosis and poor prognosis. To date, no biomarkers have been established for the early detection of GBC.

Minerals and metals play a fundamental role in a wide range of biological processes, and both their excess and deficiency - in the wrong compartment or at the wrong time - can disrupt internal homeostatic balance. It has been proposed that such dysregulation is a relevant factor in carcinogenesis, operating through mechanisms including oxidative stress, DNA damage, and immune dysregulation. Although altered mineral profiles have been described in GBC, and several elements have been proposed as potential risk biomarkers, these findings remain largely exploratory and lack consistent validation in independent cohorts, particularly in populations with a high incidence of GBC.

In our previous research, we quantified the serum concentrations of more than 50 metals and minerals in 240 South American patients (120 with GBC and 120 with gallstones) from the EULAT Eradicate GBC study, of whom more than 30 met strict quality control criteria (e.g., concentrations above the lower limit of detection in at least 95% of samples). We observed that serum concentrations of aluminium (Al) and copper (Cu) were elevated, whilst those of sulphur (S), zinc (Zn) and bromine (Br) were reduced, in serum samples from patients with GBC compared with patients with gallstones.

The aim of this study is to validate the differences in the concentrations of these five minerals using an independent set of South American serum samples (n=115 patients with GBC and n=115 patients with gallstones).

Serum samples will be digested and analysed by inductively coupled plasma mass spectrometry (ICP-MS) on an Agilent 7850 instrument, using indium (In) as an internal standard for signal normalization. More than 50 minerals and metals will be quantified per sample. Based on preliminary data, it is expected that approximately 30 analytes will pass all quality filters and be retained for statistical analysis.

Metal concentration data will be analysed using R. Overall mineral/metal profiles will be assessed through principal component analysis to identify samples with atypical concentration patterns. Analytes with concentrations below the lower limit of detection in more than 5% of samples, or with a median absolute deviation not exceeding the detection threshold, will be excluded from further analyses. To validate the five previously identified associations, metal concentrations will be compared between patients with GBC and patients with gallstone disease using univariate and multiple robust logistic regression, adjusting for potential confounding factors and correcting probability values for multiple comparisons using the Bonferroni method.

Studietype

Observasjonsmessig

Registrering (Faktiske)

230

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

      • Cochabamba, Bolivia
        • Complejo Hospitalario Viedma
      • Cochabamba, Bolivia
        • Hospital del Norte
      • Cochabamba, Bolivia
        • Hospital Obrero No. 2 (Caja Nacional del Seguro Social)
      • Cochabamba, Bolivia
        • Instituto Gastroenterológico
      • Cochabamba, Bolivia
        • Instituto Oncológico Nacional
      • Arica, Chile
        • Hospital Clínico de Magallanes
      • Arica, Chile
        • Hospital Regional de Arica
      • Concepción, Chile
        • Hospital Regional de Concepcion
      • Port Montt, Chile
        • Hospital De Puerto Montt
      • Rancagua, Chile
        • Hospital Regional de Rancagua
      • Santiago, Chile
        • Hospital San Juan de Dios
      • Santiago, Chile
        • Hospital Sotero Del Rio
      • Santiago, Chile
        • Hospital Clinico Universidad de Chile
      • Santiago, Chile
        • Clinica Alemana de Santiago
      • Santiago, Chile
        • Hospital Padre Hurtado
      • Santiago, Chile
        • Hospital Barros Luco
      • Santiago, Chile
        • Hospital del Salvador
      • Santiago, Chile
        • Fundación Arturo López Pérez (FALP)
      • Santiago, Chile
        • Hospital El Pino
      • Santiago, Chile
        • Hospital San Borja
      • Talca, Chile
        • Hospital Regional de Talca
      • Temuco, Chile
        • Clínica Alemana de Temuco
      • Temuco, Chile
        • Hospital Regional de Temuco
      • Temuco, Chile
        • Complejo Asistencial Padre Las Casas
      • Arequipa, Peru
        • Hospital Goyoneche
      • Arequipa, Peru
        • Hospital Honorio Delgado
      • Arequipa, Peru
        • Instituto Regional de Enfermedades Neoplásicas del Sur (IREN Sur)
      • Juliaca, Peru
        • Clínica Monte Sinaí
      • Juliaca, Peru
        • Hospital Base III- La Capilla ESSALUD
      • Lima, Peru
        • Instituto Nacional de Enfermedades Neoplásicas (INEN)
      • Puno, Peru
        • Hospital Regional Manuel Nuñez Butrón
      • Trujillo, Peru
        • Instituto Regional de Enfermedades Neoplásicas del Norte (IREN Norte)
      • Heidelberg, Tyskland
        • Statistical Genetics Research Group, Institute of Medical Biometry, University of Heidelberg

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Voksen
  • Eldre voksen

Tar imot friske frivillige

Nei

Prøvetakingsmetode

Sannsynlighetsprøve

Studiepopulasjon

Patients with gallstones and cancer-free OR - Patients with gallbladder cancer

Beskrivelse

Inclusion Criteria:

  • Patients with gallstones and cancer-free OR - Patients with gallbladder cancer

Exclusion Criteria:

  • Patients younger than 18 years

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

Kohorter og intervensjoner

Gruppe / Kohort
Intervensjon / Behandling
South American patients with gallbladder cancer
Pathological examination of the gallbladder after cholecystectomy
South American patients with gallstones
with no evidence of gallbladder cancer upon pathological examination of the gallbladder after cholecistectomy
Pathological examination of the gallbladder after cholecystectomy

Hva måler studien?

Primære resultatmål

Resultatmål
Tidsramme
Serum concentrations of five minerals among South American gallstone patients with and without gallbladder cancer
Tidsramme: Baseline
Baseline

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Publikasjoner og nyttige lenker

Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.

Hjelpsomme linker

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Faktiske)

1. desember 2019

Primær fullføring (Faktiske)

31. januar 2026

Studiet fullført (Faktiske)

31. januar 2026

Datoer for studieregistrering

Først innsendt

8. juni 2026

Først innsendt som oppfylte QC-kriteriene

8. juni 2026

Først lagt ut (Faktiske)

11. juni 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

11. juni 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

8. juni 2026

Sist bekreftet

1. juni 2026

Mer informasjon

Begreper knyttet til denne studien

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

JA

IPD-planbeskrivelse

Unidentifiable patient data will be deposited in a public data repository after publication, data accession numbers will be provided in the article and upon request.

Tilgangskriterier for IPD-deling

Upon request

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

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