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Association Between Phthalates Exposure and Renal Function Impairment in TYpe 2 Diabetes

Exploring the Association Between Phthalates Exposure, Measured Through Their Urinary Metabolites, and Renal Function Impairment in Individuals With TYpe 2 Diabetes - Protocol 2

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03622957
Acronym
PURITY-2
Enrollment
200
Registered
2018-08-09
Start date
2018-08-10
Completion date
2018-09-03
Last updated
2018-08-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Albuminuria, Cardiovascular Risk Factor, Diabetes Mellitus, Type 2

Brief summary

The global incidence of diabetic nephropathy (DN) is increasing, with no appreciable reduction in the percent of patients progressing toward end stage renal disease (ESRD) and dialysis (Tuttle et al, 2014, Winocour et al, 2018). Therefore, identification of modifiable risk factors and early biomarkers of progressive decline in kidney function is an urgent clinical need. Phthalates are environmental and dietary contaminants with a various array of use that are identified in many consumer and industrial products; among them, di-(2-ethylhexyl) phthalate (DEHP) and its metabolites (mono 2-ethylhexyl phthalate (MEHP), 5OH-MEHP (MEHHP) and 5oxo-MEHP (MEOHP)) are widely used (Kato et al 2004, Braun et al, 2013). They partially distribute to the human tissues and their urinary and serum levels are directly related; therefore, urinary concentration of phthalates is commonly used as proxy of their exposure in humans (Kato et al 2004). While the association between phthalates exposure and development of T2D is currently being explored (Dong et al 2017, Dales et al, 2018), little is known about their role in DN. Recent observations show that DEHP and its metabolites are associated with a higher prevalence of low-grade albuminuria and in children exposed to higher phthalates concentrations (Trasande et al, 2014, Wu et al, 2018), however such association has yet to be verified in adults. The environmental ubiquity of the phthalates enhances the importance of investigating the potential relation between their exposure and different degrees of renal function. (Kato et al 2004, Kataria et al, 2015). Given this premise, the investigators will explore this potential association in a population of subjects with T2D consecutively referring to the outpatient diabetes clinic in Santa Chiara Hospital, Pisa, enrolled on a volunteer basis. During their routine visit at Santa Chiara Hospital outpatient diabetes clinic participants will provide the results of blood tests prescribed as per standard clinical practice along with a first morning, overnight fasting, urine sample collected in a phthalates-free container. The investigators will record the participants' clinical history, physical examination and anthropometric measurements, will measure their renal function, evaluated by eGFR (calculated with the CDK-EPI formula), albumin excretion, fasting glucose, HbA1c%, and the exposure to phthalates, assessed by total concentrations of MEHP, MEOHP, MEHHP and adjusted for urinary creatinine. In this way, the investigators aim to point out the relationship of urinary phthalates with higher degrees of albuminuria and/or lower eGFR after adjustment for all potential confounders, including therapies.

Interventions

None listed

Sponsors

Istituto di Fisiologia Clinica CNR
CollaboratorOTHER
University of Pisa
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

Age 18-85 years, T2D diagnosis, T2D duration \>6 months,

Exclusion criteria

occurring acute clinical conditions, eGFR \<15 ml/min/1.73m2, BMI \> 40 Kg/m2.

Design outcomes

Primary

MeasureTime frameDescription
Phthalates exposure [ug/g]Single routine clinical visitConcentrations of metabolites of DEHP \[ug/ml\] in a first morning spot urine sample (obtained during clinical visit) measured by ultra-HPLC coupled with electrospray ionization/quadrupole time-of-flight MS and then normalized for urinary creatinine \[g/ml\].
Albuminuria [mg/g]Single routine clinical visitGrade of albuminuria measured by albuminuria/creatininuria ratio \[mg/g\] in a first morning spot urine sample (obtained during clinical visit).
Glomerular Filtration Rate [ml/min/1.73m2]Single routine clinical visitGFR measured by eGFR (calculated with CDK-EPI formula). Creatinine \[mg/dL\] is measured in a serum sample (obtained during clinical visit). Physiological parameters (age, sex, race) are obtained during clinical visit.

Secondary

MeasureTime frameDescription
CV Events (Yes/No)Single routine clinical visitHistory of cardiovascular events (Non fatal: Acute Myocardial infarction, Unstable Angina, Stroke), evaluated by clinical interview during routine clinical visit.

Countries

Italy

Contacts

Primary ContactAnna Solini, Associate Professor, MD, PhD
anna.solini@med.unipi+39 050993482
Backup ContactAlessandro Mengozzi, MD
alessandro.mengozzi@medmcs.unipi.it+ 39050993640

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026