이 페이지는 자동 번역되었으며 번역의 정확성을 보장하지 않습니다. 참조하십시오 영문판 원본 텍스트의 경우.

Antipsychotics and Blood Vessel Function

2019년 8월 27일 업데이트: Jess G. Fiedorowicz

Cardiovascular Complications of First-line, Second-generation Antipsychotics

Over the last decade, second generation antipsychotics have been increasingly utilized. Since their introduction, however, atypical antipsychotics have been increasingly associated with significant metabolic complications including hyperlipidemia, insulin resistance/diabetes mellitus, and obesity. These metabolic complications increase the risk for cardiovascular disease in populations with an already elevated risk.

The initial goal of the proposed study is to identify early signs of endothelial dysfunction and vascular disease in those treated with atypical antipsychotics. The identification of early signs of vascular disease may further link metabolic complications with any cardiovascular risk. Demonstration of changes in vascular function associated with atypical antipsychotics represents an important identifiable intermediate of more long-term cardiovascular risk.

The second goal of the proposed study is to identify genetic factors that may be associated with the development of cardiovascular disease, which can later serve as a guide to predict risk. Accurate prediction of risk may facilitate the future development of an empirical, risk-based, individualized selection process for antipsychotic medications.

Aim 1: To quantify the role of antipsychotic-induced metabolic complications on the development of vascular disease using measures of endothelial function.

Hypothesis 1: Atypical antipsychotics will lead to greater impairments in endothelial function, evidenced by decreased flow-mediated dilation from baseline measures and compared with changes over time in controls. Medication-induced metabolic complications will be temporally associated with these impairments in endothelial function.

Aim 2: To investigate the role of candidate pharmacogenetic polymorphisms with cardiovascular and metabolic complications of atypical antipsychotics.

Hypothesis 2: Profiles of polymorphisms at receptors targeted by atypical antipsychotics will be associated with impaired cardiovascular function and metabolic complications.

연구 개요

상태

완전한

상세 설명

Participants will have all evaluations related to metabolic complications performed in the University of Iowa Clinical Research Unit (CRU) or in the EndoPAT laboratory located in Room 269 GH. For all visits, weights will be measured without shoes, in light clothing, using an electronic scale that measures to the nearest 0.25 kg. Standing heights will be measured without shoes, to the nearest 0.1 cm using a free-standing stadiometer. These weights and heights will be utilized for the computation of body mass index (BMI). Waist circumference will be measured horizontally at the tip of the right iliac crest in the standing position using a measuring tape. Blood pressure and heart rate will be measured in the sitting position after five minutes of silent rest, using an automated sphygmomanometer. An ambulatory blood pressure will also be obtained at each visit. An EKG will be conducted during Visit 1. Dual energy X-ray absortionmetry (DEXA) will assess percentage of body fat at intake, Visit 4 and Visit 8. If a participant is unable to complete a DEXA scan, body fat will be determined using the BOD POD® Gold Standard Body Composition Tracking System. The BOD POD® is an integrated system consisting of a digital scale to measure subject mass, a large egg-shaped fiberglass air displacement plethysmography (ADP) to determine body volume (BV), and a computer that operates the equipment and calculates body composition. Body density is determined from subject mass and volume measurements and then percent fat is calculated using one of several standard formulas. CRU dieticians will perform skin fold measurements at intake and completion. Fasting measures of triglycerides, LDL-C, HDL-C, IDL, VLDL, apolipoprotein A, apolipoprotein B, Lp(a) cholesterol, C-reactive protein, IL-6, leptin levels, insulin levels, and glucose will be obtained at baseline, 2 weeks, 12 weeks, 26 weeks, 1 year, 2 years, 3 years and 4 years. Hemoglobin A1C will be collected at baseline and weeks 12 and 26, 1 year, 2 years, 3 years and 4 years. Cholesterol levels will be determined by an enzymatic calorimetric test using cholesterol esterase and cholesterol oxidase. LDL-C and HDL-C fractions will be obtained via a homogeneous enzymatic in vitro colorimetric assay. For the determination of triglyceride levels, free glycerol is eliminated prior to hydrolysis of triglycerides in a preliminary reaction where lipase and 4-aminophenazone are omitted, followed by enzymatic hydrolysis of triglycerides and determination of the liberated glycerol by a fully enzymatic colorimetric assay reaction. Apolipoproteins and other lipid parameters will be measured using beta quantification through the Mayo Medical Laboratories (unit code 83673).

Endothelial and Cardiovascular Function: Participants will have endothelial function measured at baseline, and each subsequent visit. To maximize completion rates, participants planning to discontinue their antipsychotic between weeks 16 and 26 will have their final measures taken at the time of discontinuation. Prior to these appointments, participants will be instructed to not eat or drink anything (including caffeinated products such as coffee, tea, soda, etc.) except water for at least 12 hours prior to the appointment. They will also be instructed to not drink any alcohol for 24 hours prior to each study. They will be asked not to smoke for the two hours prior to the study. Administration of blood pressure and lipid lowering medications for that day will be delayed until after the procedures. Measures of endothelial function will be obtained in the Clinical Research Unit (CRU).

CONDUIT VESSEL FUNCTION: Conduit vessel endothelial function will be assessed non-invasively via ultrasound measurement of brachial artery diameter during changes in brachial artery flow. The technique uses a 10-13 MHz linear array transducer ultrasound system (Biosound ESAOTE, Indianapolis, IN). A 5 cm length of the brachial artery is imaged in longitudinal section above the antecubital fossa and the optimal probe site on the skin marked. Baseline images of brachial artery diameter and Doppler velocities from the center of the vessel are recorded on videotape. While images for brachial artery diameter are being continuously recorded, an occluding forearm cuff placed just below the antecubital fossa is inflated for 5 minutes. The brachial artery diameter and Doppler velocities are continuously recorded before, during and after cuff deflation. After approximately 5 minutes, once basal diameter and flow have been restored, nitroglycerin (300 mcg) will be administered sublingually and measurements made for an additional 6 minutes.

HEART RATE AND BLOOD PRESSURE VARIABILITY: We will also assess blood pressure and heart rate variability using recordings of indirect arterial pressure with a beat-to-beat finger systolic and diastolic blood pressure recording in conjunction with the electrocardiogram tracing during the conduit vessel function procedures. Data from this measurement will allow us to assess blood pressure and heart rate variability. Cardiovascular variability (HRV) is a marker for cardiovascular risk whereby lower variability indicates greater risk for myocardial infarct and stroke. This procedure can be performed during assessment of conduit vessel function so requires no additional time.

ARTERIAL TONOMETRY: We will utilize arterial tonometry through measurement of pulse wave analysis (PWA) and pulse wave velocity (PWV) using a SphygmorCor machine. This machine uses a noninvasive probe, pressed lightly on the skin over the carotid, radial and femoral arteries for about five minutes each. These measurements will provide a measure of arterial compliance, stiffness, and other hemodynamic information. The PWA system is a computerized diagnostic tool for the assessment of central blood pressure. The peripheral pressure pulse waveform contains information in addition to the maximum and minimal values (systolic and diastolic pressures). The PWA system can derive the central aortic pressure waveform from the peripheral pressure waveform recorded at the radial or carotid arteries. The system uses mathematical transforms to derive the central aortic pressure pulse waveform and then calculates a range of central indices of ventricular-vascular interaction, which are displayed both graphically and numerically. The PWV system measures the velocity of the blood pressure waveform between any two superficial artery sites. A pressure tonometer is used to transcutaneously record the pressure pulse waveforms in the underlying artery. The pressure pulse waveform is recorded simultaneously with an electrocardiogram (ECG) signal, which provides an R-wave timing reference. Pressure pulse recordings are performed consecutively at the two superficial artery sites over the carotid and femoral artery. The software processes each set of pressure pulse and ECG waveform data to calculate the mean time difference between the R-wave and the pressure wave- on a beat-by-beat basis. The PWV is then calculated using the mean time difference and the arterial path length between the two recording sites. The velocity of the blood pressure pulse waveform is dependent on the stiffness of the artery along which the pulse is traveling. Serial measurement of pulse wave velocity in a section of artery will indicate the magnitude of change in arterial stiffness in that section of the artery.

PSYCHIATRIC ASSESSMENT: Detailed historical information will be gathered including age, occupation, education, race, height, weight, medical history, treatment history, family history of medical illness with focus on risk factors for metabolic syndrome, and substance use history including tobacco. Basic clinical information will be obtained to verify psychiatric diagnosis and assess cardiac risk by the Framingham Heart Study formula. It is estimated that this history will take 45 minutes to complete. Affective and psychotic symptomatology will be cross-sectionally assessed using the Montgomery Asberg Depression Rating Scale, the Young Mania Scale, and the Brief Psychotic Rating Scale.

연구 유형

관찰

등록 (실제)

44

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 장소

    • Iowa
      • Iowa City, Iowa, 미국, 52242
        • University of Iowa Hospitals and Clinics

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

18년 (성인)

건강한 자원 봉사자를 받아들입니다

아니

연구 대상 성별

모두

샘플링 방법

비확률 샘플

연구 인구

Thirty patients, 18 - 50 years of age, who are being started on a first-line, second-generation, antipsychotic associated with weight gain (risperidone, olanzapine, or quetiapine) for the treatment of an affective or psychotic disorder, will be invited to participate. Participants must not have taken any of these antipsychotics or clozapine in the preceding three months. Another twenty psychiatric controls not taking antipsychotic medications will also be enrolled. Statistically, controls will serve primarily to compare changes in flow-mediated dilation over time rather than for direct comparison of variables between groups. Participation will be voluntary and initiated upon clinician or self-referral.

설명

Inclusion Criteria:

  • 18-50 years of age
  • Being started on a first-line, second-generation, antipsychotic associated with weight gain (risperidone, olanzapine, or quetiapine) for the treatment of an affective or psychotic disorder -OR- psychiatric controls not taking antipsychotic medications will also be enrolled

Exclusion Criteria:

  • Exclusion criteria will include the presence of any of the following: neoplasm, active thyroid disease (i.e. not euthyroid), pregnancy or planned pregnancy, diabetes mellitus, Raynaud's disease, anticoagulant therapy, or inability to provide informed consent. We will exclude participants who have started valproic acid derivatives in the preceding 6 months, given its association with insulin resistance and weight gain. Participants with active substance abuse or dependence will also be excluded.

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

코호트 및 개입

그룹/코호트
1
Incident users of antipsychotics.
2
Non-users of antipsychotics

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Flow-mediated dilation
기간: 6 months
% dilation of the brachial artery in response to 5 minutes of ischemia
6 months
Forearm vascular resistance
기간: 6 months
% dilation of forearm blood vessels in response to pharmacological challenge measured using plethysmography
6 months

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

수사관

  • 수석 연구원: Jess G Fiedorowicz, M.D., Ph.D., University of Iowa

간행물 및 유용한 링크

연구에 대한 정보 입력을 담당하는 사람이 자발적으로 이러한 간행물을 제공합니다. 이것은 연구와 관련된 모든 것에 관한 것일 수 있습니다.

유용한 링크

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작

2007년 9월 1일

기본 완료 (실제)

2014년 11월 1일

연구 완료 (실제)

2014년 12월 1일

연구 등록 날짜

최초 제출

2007년 12월 19일

QC 기준을 충족하는 최초 제출

2007년 12월 29일

처음 게시됨 (추정)

2008년 1월 3일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2019년 8월 29일

QC 기준을 충족하는 마지막 업데이트 제출

2019년 8월 27일

마지막으로 확인됨

2019년 8월 1일

추가 정보

이 연구와 관련된 용어

기타 연구 ID 번호

  • 200703764
  • University of Iowa GCRC #0740

개별 참가자 데이터(IPD) 계획

개별 참가자 데이터(IPD)를 공유할 계획입니까?

IPD 계획 설명

Requests for de-identified data may be presented to the principal investigator with a statistical analysis plan.

IPD 공유 기간

Data will be made available on 8/27/2019 for a period of at least three years.

IPD 공유 액세스 기준

Requests for data will be reviewed by Principal Investigator Jess Fiedorowicz for additional analyses provided a statistical analysis plan.

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

3
구독하다