Evidence map›Paper›PMID 16041916›Full record

ReviewEssential psychopharmacology2005

Genetics and psychopharmacology: prospects for individualized treatment.

Charles U Nnadi, Joseph F Goldberg, Anil K Malhotra

Abstract readReview
In one paragraph

Review in Essential psychopharmacology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Article
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

3 authors.

Charles U NnadiDepartment of Psychiatry Research, Zucker Hillside Hospital, Glen Oaks, New York, USA.
Joseph F Goldberg
Anil K Malhotra

Funding

CLINICAL TRIALS IN SCHIZOPHRENIA--MOLECULAR APPROACHESK23MH001760 · NIMH · LONG ISLAND JEWISH MEDICAL CENTER · PI MALHOTRA, ANIL K · 1999 to 2003
$621k
NIMH NIH HHS K23 MH001760
6 · The paper itself

Abstract

This article provides a clear and succinct description of the components of inheritance, such as trait transmission, genetic variability, and gene interaction. Genetic sequences constitute the prime focus of pharmacogenetic studies. Variations in drug-metabolizing enzyme systems tend to be monogenic, whereas the pharmacologic effects of medications appear to be polygenic, i.e., complex phenotypes shaped by the interaction of genes and environment. Translated into clinical terms, a history of a good response to a drug in a close relative of a patient is presumed to predict a good response to the same medication by the patient. This seems to hold for antidepressants, antipsychotics, and lithium, but the evidential studies generally have meaningful limitations. Bit by bit, information about the relationship between particular genetic formations and the effectiveness of these medications as well as their side effects, is appearing. The authors cite a number of examples, one such being an association between impaired antidepressant activity and the short allele of SLC6A4. This research promises to strengthen the accuracy, effectiveness, safety, and cost of our psychopharmacological practices.

Indexed as

PharmacogeneticsAffectAntidepressive AgentsGenomic InstabilityGenotypeHumansPolymorphism, GeneticPsychotropic DrugsAntidepressive AgentsPsychotropic Drugs

Identifiers

PMID16041916
PMCPMC2268899

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.