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Anergia-anhedonia by Lithium-induced Phosphorus Diabetes

Anergia-anhedonia by Lithium-induced Phosphorus Diabetes

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06111664
Acronym
ALIPo-D
Enrollment
60
Registered
2023-11-01
Start date
2023-05-01
Completion date
2024-04-24
Last updated
2023-11-01

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

Conditions

Mood Disorders

Keywords

Diabetes, Phosphate, Anergia-anhedonia, Lithium (Li+), Mood Disorders

Brief summary

Lithium (Li+) is prescribed to 1‰ of the French population (\ 60,000 patients). More than half of patients describe subjective symptoms linked to Li+ (SSL) similar to those of chronic fatigue syndrome: muscle weakness, fatigability, cognitive disorders, emotional blunting. SSL are the 2nd cause of stopping Li+ (28%), just behind kidney problems (30%). In animals, the administration of lithium (Li+) increases the urinary excretion of phosphate (Pi) by 6, inducing phosphate diabetes (DPi). However, idiopathic forms of DPi explain up to 10-15% of chronic fatigue syndromes and these disappear when supplementing with Pi (± vitamin D). In humans, the introduction of Li+ leads to a reduction in serum phosphate but we have not found any publication on the possible induction of DPi or on a possible link between DPi and SSL. However, the dosages necessary to detect a DPi are carried out during the annual follow-up assessment of patients on Li+. All you have to do is calculate the standardized maximum reabsorption rate of Pi (TmPi) to make the diagnosis! Finally, if the patients presenting with DPi turn out to be the same as those who complain of SSL, we can imagine that correcting the first by simple supplementation with Pi (± vitamin D) could provide relief.

Detailed description

The aim of the study is to determine the prevalence of hypophosphatemia, DPi and SSL in a population of ambulatory patients controlled on Li+ (\> 6 months).

Interventions

None listed

Sponsors

University Hospital, Strasbourg, France
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

* Major subject (≥ 18 years old) * Man or woman * Subject balanced on Li+ (\> 6 months, regardless of the underlying pathology). * Outpatient monitoring by one of the members of CEDRA (Alsace expert center for resistant depression). * Subject not opposing, after information, the reuse of their data for the purposes of this research

Exclusion criteria

* Subject having expressed opposition to participating in the study * Subject under judicial protection * Subject under guardianship or curatorship

Design outcomes

Primary

MeasureTime frameDescription
Prevalence of hypophosphatemia, DPi and SSL at the population level.from 6 months after lithium treatment (Li+)The prevalence is determined retrospectively on a population balanced on lithium (Li+) for more than 6 months.

Countries

France

Contacts

Primary ContactJack FOUCHER, MD, PhD
jack.foucher@chru-strasbourg.fr33 3 88 11 69 21

Outcome results

None listed

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