Exploring Variation in Known Pharmacogenetic Variants and its Association with Drug Response in Different Mexican Populations.

Abstract:

PURPOSE:Information on genetic variants that affect the pharmacokinetics and pharmacodynamics (PK/PD) of drugs in different populations from Mexico is still an ongoing endeavor. Here, we investigate allele frequencies on pharmacogenetic targets in Mexican Mestizos and Natives from three different States and its association with drug efficacy in individuals receiving either anticoagulants or antipsychotic drugs. METHODS:Natives from three different states and Mestizo patients receiving acenocoumarol or antipsychotics were genotyped using the DMET microarray (Affymetrix). RESULTS:We provide a collection of genetic variants that indicate that there are 3-times more variation than similarities between populations from Mexico and major continental groups. These differences were observed in several relevant targets including ABCB1, SLCO1A1, NAT2, UGTs, TYMS, VKORC1, and NR1I3. Moreover, Mexican Mestizos also showed allele frequency differences when compared to Natives for variants on DPYD, ADH1A, CYP3A4, SLC28A3, and SLC28A1. Significant allele differences also arose among the three Native groups here studied, mostly for transporters of the ABC-binding cassette and the solute carrier gene family. Finally, we explored genotype-drug response associations and pinpointed variants on FMOs (coumarins), and GSTM1 (haloperidol). CONCLUSIONS:These findings confirm previous results and further delve into the pharmacogenetics of Mexican populations including different Native groups.

journal_name

Pharm Res

journal_title

Pharmaceutical research

authors

Gonzalez-Covarrubias V,Martínez-Magaña JJ,Coronado-Sosa R,Villegas-Torres B,Genis-Mendoza AD,Canales-Herrerias P,Nicolini H,Soberón X

doi

10.1007/s11095-016-1990-5

subject

Has Abstract

pub_date

2016-11-01 00:00:00

pages

2644-52

issue

11

eissn

0724-8741

issn

1573-904X

pii

10.1007/s11095-016-1990-5

journal_volume

33

pub_type

杂志文章
  • Irinotecan Alters the Disposition of Morphine Via Inhibition of Organic Cation Transporter 1 (OCT1) and 2 (OCT2).

    abstract:PURPOSE:The organic cation transporters (OCTs) and multidrug and toxin extrusions (MATEs) together are regarded as an organic cation transport system critical to the disposition and response of many organic cationic drugs. Patient response to the analgesic morphine, a characterized substrate for human OCT1, is highly v...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-018-2526-y

    authors: Zhu P,Ye Z,Guo D,Xiong Z,Huang S,Guo J,Zhang W,Polli JE,Zhou H,Li Q,Shu Y

    更新日期:2018-10-25 00:00:00

  • Novel bioadhesive chitosan-EDTA conjugate protects leucine enkephalin from degradation by aminopeptidase N.

    abstract:PURPOSE:To develop a novel bioadhesive polymer that protects peptide drugs from luminal degradation by aminopeptidase N and to evaluate the system in vitro on porcine mucosa. METHODS:EDTA was covalently bound to chitosan in order to combine the bioadhesive properties of the polymer with the well known capacity of EDTA...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1012108118670

    authors: Bernkop-Schnürch A,Paikl C,Valenta C

    更新日期:1997-07-01 00:00:00

  • Nose-to-brain transport pathways of wheat germ agglutinin conjugated PEG-PLA nanoparticles.

    abstract:PURPOSE:To investigate the possible pathways for transport of wheat germ agglutinin conjugated PEG-PLA nanoparticles (WGA-NP) into the brain after nasal administration. METHODS:The nose-to-brain pathways were investigated using WGA-NP containing 6-coumarin (as a fluorescent marker) and (125)I-labeled WGA-NP. Ex vivo i...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-011-0641-0

    authors: Liu Q,Shen Y,Chen J,Gao X,Feng C,Wang L,Zhang Q,Jiang X

    更新日期:2012-02-01 00:00:00

  • Enhancement of nasal absorption of insulin using chitosan nanoparticles.

    abstract:PURPOSE:To investigate the potential of chitosan nanoparticles as a system for improving the systemic absorption of insulin following nasal instillation. METHODS:Insulin-loaded chitosan nanoparticles were prepared by ionotropic gelation of chitosan with tripolyphosphate anions. They were characterized for their size a...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1018908705446

    authors: Fernández-Urrusuno R,Calvo P,Remuñán-López C,Vila-Jato JL,Alonso MJ

    更新日期:1999-10-01 00:00:00

  • Formulating weakly basic HCl salts: relative ability of common excipients to induce disproportionation and the unique deleterious effects of magnesium stearate.

    abstract:PURPOSE:Nine common excipients were examined to determine their ability to cause disproportionation of the HCl salt of a a weakly basic compound. The goal was to determine which excipients were problematic and correlate the results to known properties such as surface pH, slurry pH, or molecular structure. Such a correl...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-013-1002-y

    authors: John CT,Xu W,Lupton LK,Harmon PA

    更新日期:2013-06-01 00:00:00

  • Velocity distribution and shear rate variability resulting from changes in the impeller location in the USP dissolution testing apparatus II.

    abstract:PURPOSE:The United States Pharmacopoeia (USP) imposes strict requirements on the geometry and operating conditions of the USP Dissolution Testing Apparatus II. A previously validated Computational Fluid Dynamics (CFD) approach was used here to study the hydrodynamics of USP Apparatus II when the impeller was placed at ...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-007-9477-z

    authors: Bai G,Armenante PM

    更新日期:2008-02-01 00:00:00

  • Stabilization of lyophilized porcine pancreatic elastase.

    abstract::Porcine pancreatic elastase, a well-characterized serine protease, has been used as a model to assess the effects of excessive humidity on solid-state stability of the lyophilized protein. Elastase lyophilized without excipients retained full activity immediately after freeze-drying but became denatured upon continued...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1018979410338

    authors: Chang BS,Randall CS,Lee YS

    更新日期:1993-10-01 00:00:00

  • Heat-treated Fungizone retains amphotericin B antifungal activity without renal toxicity in rats infected with Aspergillus fumigatus.

    abstract:PURPOSE:The purpose of this study was to assess the antifungal activity and renal and hepatic toxicity of amphotericin B (AmpB) following administration of Fungizone (FZ) and a heat-treated form of FZ (HFZ) to rats infected with Aspergillus fumigatus. METHODS:Infected rats were administered FZ and HFZ at a dosing regi...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/b:pham.0000041449.46054.b4

    authors: Sivak O,Bartlett K,Wasan KM

    更新日期:2004-09-01 00:00:00

  • Systematic Investigation of the Role of Surfactant Composition and Choice of oil: Design of a Nanoemulsion-Based Adjuvant Inducing Concomitant Humoral and CD4+ T-Cell Responses.

    abstract:PURPOSE:Induction of cell-mediated immune (CMI) responses is crucial for vaccine-mediated protection against difficult vaccine targets, e.g., Chlamydia trachomatis (Ct). Adjuvants are included in subunit vaccines to potentiate immune responses, but many marketed adjuvants stimulate predominantly humoral immune response...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-017-2180-9

    authors: Schmidt ST,Neustrup MA,Harloff-Helleberg S,Korsholm KS,Rades T,Andersen P,Christensen D,Foged C

    更新日期:2017-08-01 00:00:00

  • The effect of formulation on the antimicrobial activity of cetylpyridinium chloride in candy based lozenges.

    abstract:PURPOSE:The purpose of this investigation was to determine the influence on the antimicrobial activity of cetylpyridinium chloride of the various components of the formulation of each of six candy based lozenges. METHODS:In vivo activity was investigated using six volunteers by determining the reduction in colony form...

    journal_title:Pharmaceutical research

    pub_type: 临床试验,杂志文章

    doi:10.1023/a:1016002322692

    authors: Richards RM,Xing JZ,Weir LF

    更新日期:1996-04-01 00:00:00

  • Access to the CNS: Biomarker Strategies for Dopaminergic Treatments.

    abstract::Despite substantial research carried out over the last decades, it remains difficult to understand the wide range of pharmacological effects of dopaminergic agents. The dopaminergic system is involved in several neurological disorders, such as Parkinson's disease and schizophrenia. This complex system features multipl...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章,评审

    doi:10.1007/s11095-017-2333-x

    authors: van den Brink WJ,Palic S,Köhler I,de Lange ECM

    更新日期:2018-02-15 00:00:00

  • Vaginal absorption of insulin in the rat: effect of penetration enhancers on insulin uptake and mucosal histology.

    abstract::The absorption of insulin across the vaginal mucosa into the systemic circulation was studied in ovariectomized rats given subsequent estrogen treatment. Blood glucose levels were determined as an indirect measure of insulin absorption, and the effect of various enhancers on the hypoglycemic response was investigated....

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1015892630637

    authors: Richardson JL,Illum L,Thomas NW

    更新日期:1992-07-01 00:00:00

  • Measurement of rapid release kinetics for drug delivery.

    abstract::A fluorescence measurement system and methods of data analysis were developed to measure rapid kinetics of transdermal transport in vitro. Three variations on the technique were demonstrated, where the receptor compartment concentration was determined by: 1) fluorescence measurements of aliquots removed at discrete ti...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1016254013374

    authors: Pliquett U,Prausnitz MR,Chizmadzhev YA,Weaver JC

    更新日期:1995-04-01 00:00:00

  • Estimation of the relative contribution of the transcellular and paracellular pathway to the transport of passively absorbed drugs in the Caco-2 cell culture model.

    abstract:PURPOSE:The objective of this investigation was to determine, using the Caco-2 cell culture model, the extent to which the paracellular and transcellular routes contributed to the transport of passively absorbed drugs. An effort was also made to determine the controlling factors in this process. METHODS:We selected a ...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1012111008617

    authors: Pade V,Stavchansky S

    更新日期:1997-09-01 00:00:00

  • Synthetic glycopeptide-based delivery systems for systemic gene targeting to hepatocytes.

    abstract:PURPOSE:To design, synthesize, and test synthetic glycopeptide-based delivery systems for gene targeting to hepatocytes by systemic administration. METHODS:All peptides were synthesized by the solid phase method developed using Fmoc chemistry on a peptide synthesizer. The binding of galactosylated peptides to HepG2 ce...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1007533121682

    authors: Anwer K,Logan M,Tagliaferri F,Wadhwa M,Monera O,Tung CH,Chen W,Leonard P,French M,Proctor B,Wilson E,Singhal A,Rolland A

    更新日期:2000-04-01 00:00:00

  • Swelling and dissolution kinetics during peptide release from erodible anionic gel beads.

    abstract::The transient dynamic swelling and dissolution behavior during the release of a growth hormone releasing peptide, [D-Trp2-D-Phe5]GHRP, from erodible, non-cross-linked poly(methyl methacrylate-co-methacrylic acid) (PMMA/MAA) beads has been investigated at pH 7.4 as a function of buffer concentration. Although the swell...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1018902404036

    authors: Lee PI

    更新日期:1993-07-01 00:00:00

  • Enhancement of insulin transport across primary rat alveolar epithelial cell monolayers by endogenous cellular factor(s).

    abstract:PURPOSE:To characterize factor(s) contained in apical medium of primary cultured rat alveolar epithelial type II cell-like monolayers (RAECM-II) that enhance insulin absorption across alveolar epithelial cells. MATERIALS AND METHODS:Primary rat alveolar epithelial cell monolayers cultured on Transwells in the presence...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-007-9301-9

    authors: Bahhady R,Kim KJ,Borok Z,Crandall ED,Shen WC

    更新日期:2007-09-01 00:00:00

  • Effects of solute characteristics and concentration on a lyotropic liquid crystal: solute-induced phase change.

    abstract::We investigated the effects of increased concentrations of the solutes, salicylic acid, benzoic acid, and o-, m-, and p-methoxy benzoic acids, on the anisotropic properties of a liquid crystal solvent. The lamellar liquid crystal was composed of 37% polyoxyethylene (20) isohexadecyl ether in aqueous buffer of pH 1. Ph...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1018920118631

    authors: Ibrahim HG,Sallam ES,Takieddin M,Habboub M

    更新日期:1993-05-01 00:00:00

  • Novel Approach for the Bioequivalence Assessment of Topical Cream Formulations: Model-Based Analysis of Tape Stripping Data Correctly Concludes BE and BIE.

    abstract:PURPOSE:The purpose of this study was (a) to suggest a novel dermatopharmacokinetic (DPK) approach from which pharmacokinetic parameters relevant to the bioequivalence (BE) assessment of a topical formulation can be deduced while circumventing the need for numerous measurements and assumptions, and (b) to investigate w...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-019-2724-2

    authors: Ozdin D,Kanfer I,Ducharme MP

    更新日期:2020-01-02 00:00:00

  • Influence of molecular size on the retention of polymeric nanocarrier diagnostic agents in breast ducts.

    abstract:PURPOSE:To investigate the influence of nanocarrier molecular size and shape on breast duct retention in normal rats using a non-invasive optical imaging method. METHODS:Fluorescein-labeled PEG nanocarriers of different molecular weights and shapes (linear, two-arm, four-arm, and eight-arm) were intraductally administ...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-012-0763-z

    authors: Singh Y,Gao D,Gu Z,Li S,Rivera KA,Stein S,Love S,Sinko PJ

    更新日期:2012-09-01 00:00:00

  • The use of multiple doses and pharmacodynamic system analysis to distinguish between dispositional delays and time-variant pharmacodynamics.

    abstract::Pharmacokinetic-pharmacodynamic modeling algorithms, in general, rely on hysteresis minimization techniques that assume time-invariant pharmacodynamics (constant biophase concentration-effect relationships). When time-variant pharmacodynamics are observed, a specific model for tolerance or sensitization is required. H...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1018940122382

    authors: Gastonguay MR,Schwartz SL

    更新日期:1994-12-01 00:00:00

  • Predicting effect of food on extent of drug absorption based on physicochemical properties.

    abstract:PURPOSE:To develop a statistical model for predicting effect of food on the extent of absorption (area under the curve of time-plasma concentration profile, AUC) of drugs based on physicochemical properties. MATERIALS AND METHODS:Logistic regression was applied to establish the relationship between the effect of food ...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-007-9236-1

    authors: Gu CH,Li H,Levons J,Lentz K,Gandhi RB,Raghavan K,Smith RL

    更新日期:2007-06-01 00:00:00

  • Studies on the excretion of diazepam and nordazepam into milk for the prediction of milk-to-plasma drug concentration ratios.

    abstract::The influence of varying protein and fat content in milk of New Zealand White rabbits on the milk-to-plasma drug concentration (M/P) ratio of diazepam was studied. At various time points after littering, a bolus dose (1.5 mg/kg) followed by a 26-hr infusion (1.8 mg/h) of diazepam was administered to freely moving rabb...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1015809418284

    authors: Stebler T,Guentert TW

    更新日期:1992-10-01 00:00:00

  • Prinomide tromethamine pharmacokinetics: mutually dependent saturable and competitive protein binding between prinomide and its own metabolite.

    abstract::Prinomide tromethamine, a nonsteroidal antiinflammatory drug, was orally administered at doses of 250, 500, and 1000 mg every 12 hr for 28 days to healthy male volunteers. The pharmacokinetic behavior of prinomide and its primary plasma metabolite displayed nonlinear characteristics, while those of free prinomide and ...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1018916811904

    authors: Kochak GM,Pai S,Iannucci R,Honc F,Kachmar D,Perrino P,Egger H

    更新日期:1993-01-01 00:00:00

  • Role of phosphatidylserine in the cellular and subcellular lung distribution of quinidine in rats.

    abstract::The role of phosphatidylserine in the cellular and subcellular lung distribution of quinidine was investigated in rats, since quinidine was found to bind preferentially to phosphatidylserine. The concentration of phosphatidylserine in the cellular and subcellular fractions was determined after separation by two-dimens...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1015985511653

    authors: Nishiura A,Murakami T,Higashi Y,Yata N

    更新日期:1988-04-01 00:00:00

  • Sequence alignments of the H(+)-dependent oligopeptide transporter family PTR: inferences on structure and function of the intestinal PET1 transporter.

    abstract:PURPOSE:To study the structure and function of the intestinal H+/ peptide transporter PET1, we compared its amino acid sequence with those of related transporters belonging to the oligopeptide transporter family PTR, and with more distant transporter families. METHODS:We have developed a new approach to the sequence a...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1012070726480

    authors: Graul RC,Sadée W

    更新日期:1997-04-01 00:00:00

  • N-terminal site-specific mono-PEGylation of epidermal growth factor.

    abstract:PURPOSE:N-terminal site-specific mono-PEGylation of recombinant human epidermal growth factor (EGF) was accomplished using polyethyleneglycol (PEG) derivatives (Mw = 2000 and 5000) through a reactive terminal aldehyde group. METHODS:The site-specific PEG conjugation was conducted ata slightly acidic pH condition (pH 5...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1023402123119

    authors: Lee H,Jang IH,Ryu SH,Park TG

    更新日期:2003-05-01 00:00:00

  • Blocking effect of an immuno-suppressive agent, cynarin, on CD28 of T-cell receptor.

    abstract:PURPOSE:Cynarin, a potential immunosuppressant that blocks the interaction between the CD28 of T-cell receptor and CD80 of antigen presenting cells, was found in Echinacea purpurea by a new pharmaceutical screening method: After Flowing Through Immobilized Receptor (AFTIR; Dong et al., J Med Chem, 49: 1845-1854, 2006)....

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-008-9754-5

    authors: Dong GC,Chuang PH,Chang KC,Jan PS,Hwang PI,Wu HB,Yi M,Zhou HX,Chen HM

    更新日期:2009-02-01 00:00:00

  • Mechanisms involved in iontophoretic transport of angiotensin.

    abstract:PURPOSE:The feasibility of using iontophoresis to enhance the permeation rate of a model peptide was investigated in vitro using hairless mouse skin. METHODS:Angiotensin 2 (AT 2) was employed as a permeant probe, using optimum iontophoresis conditions. A number of physicochemical parameters (donor ionic strength; vale...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1023/a:1016254230155

    authors: Clemessy M,Couarraze G,Bevan B,Puisieux F

    更新日期:1995-07-01 00:00:00

  • An improved nonlinear model describing the hepatic pharmacokinetics of digoxin: evidence for two functionally different uptake systems and saturable binding.

    abstract:PURPOSE:To develop a semi-distributed liver model for the evaluation of saturable sinusoidal uptake and binding kinetics of the Oatp1a4 substrate digoxin. METHODS:In the perfused rat liver, two successive digoxin doses of 42 and 125 microg were administered, and the outflow concentration was determined by LC/MS/MS. [1...

    journal_title:Pharmaceutical research

    pub_type: 杂志文章

    doi:10.1007/s11095-010-0204-9

    authors: Weiss M,Li P,Roberts MS

    更新日期:2010-09-01 00:00:00