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DESCRIPTION (provided by applicant): The overarching purpose of this proposal is to address a set of critical questions about the etiology of interstitial cystitis (IC) using multivariate data from a large population-based classical twin study. Despite ongoing research, IC remains a controversial entity for two critical reasons. First, the validity of the case definition remains uncertain. There are few data that address a historically important validator--the degree to which IC results from genetic and/or environmental factors. Second, IC is often comorbid with one or more additional physical disorders and yet the causes of comorbidity are uncertain. Taken together, these two sets of unanswered questions contribute significantly to the controversies that continue to surround IC. Moreover, the strong female predominance of IC has been amply documented but is not well understood. To address these fundamental issues, we propose to conduct a twin study of IC in the population-based Swedish Twin Registry (STR). We propose to assess IC in the cohort of STR twins aged 18-45 years using a web-based screening instrument. Those not participating in the web-based assessment will be offered a computer assisted telephone interview. Based on previous experience, we anticipate that of the 50,011 individuals in this cohort, 75% or 37,500 will respond. These unique data will be used to address the following Specific Aims: (1) To estimate the prevalence of IC and its key co-morbidities in STR participants. To assess the phenotypic patterns of comorbidity of IC with other disorders. (2) To evaluate the genetic and environmental sources of variation for IC through concordances and structural equation modeling. To examine the effects of gender on these effects. (3) To use multivariate twin analyses to investigate the sources of covariation between IC and its frequently co-morbid conditions and (4) To use case-control designs with external controls and internal controls ("co-twin control" design) to evaluate the importance of exposures which may infer risk for disease.
期刊论文(13)
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科研奖励(0)
会议论文
DOI: 10.1016/j.fertnstert.2008.07.002
发表时间: 2009-08
期刊: Fertility and sterility
影响因子: 6.7
作者: [Iliadou A, Milsom I, Pedersen NL, Altman D]
通讯作者: Altman D
DOI: 10.1016/j.eururo.2010.10.028
发表时间: 2011-02
期刊: EUROPEAN UROLOGY
影响因子: 23.4
作者: [Altman, Daniel, Lundholm, Cecilia, Milsom, Ian, Peeker, Ralph, Fall, Magnus, Iliadou, Anastasia N., Pedersen, Nancy L.]
通讯作者: Pedersen, Nancy L.
DOI: 10.1007/s00439-013-1267-6
发表时间: 2013-05-01
期刊: HUMAN GENETICS
影响因子: 5.3
作者: [Ganna, Andrea, Rivadeneira, Fernando, Tiemeier, Henning]
通讯作者: Tiemeier, Henning
DOI: 10.1186/1471-2350-15-38
发表时间: 2014-03-28
期刊: BMC medical genetics
影响因子: --
作者: [Ran C, Graae L, Magnusson PK, Pedersen NL, Olson L, Belin AC]
通讯作者: Belin AC
8
    Archiving Additional Waves of the Swedish Adoption/Twin Study of Aging (SATSA)
    • 批准号:
      8368292
    • 项目类别:
    • 资助金额:
      $5.4万
    • 财政年份:
      2012
    • 负责人:
      NANCY L PEDERSEN
    • 依托单位:
    Gene-Environment Interplay of Social Contexts and Aging-Related Outcomes
    • 批准号:
      8142897
    • 项目类别:
    • 资助金额:
      $65.29万
    • 财政年份:
      2010
    • 负责人:
      NANCY L PEDERSEN
    • 依托单位:
    Gene-Environment Interplay of Social Contexts and Aging-Related Outcomes
    Gene-Environment Interplay of Social Contexts and Aging-Related Outcomes
    • 批准号:
      8318109
    • 项目类别:
    • 资助金额:
      $63.94万
    • 财政年份:
      2010
    • 负责人:
      NANCY L PEDERSEN
    • 依托单位:
    国内基金
    海外基金
    补阳还五汤通过AGE-RAGE通路调控脓毒症免疫失衡的机制与转化研究
    靶向递送一氧化碳调控AGE-RAGE级联反应促进糖尿病创面愈合研究
    • 批准号:
      JCZRQN202500010
    • 项目类别:
      省市级项目
    • 资助金额:
      --
    • 批准年份:
      2025
    • 负责人:
    • 依托单位:
    对香豆酸抑制AGE-RAGE-Ang-1通路改善海马血管生成障碍发挥抗阿尔兹海默病作用
    • 批准号:
      2025JJ70209
    • 项目类别:
      省市级项目
    • 资助金额:
      --
    • 批准年份:
      2025
    • 负责人:
      雷芬芳
    • 依托单位:
    AGE-RAGE通路调控慢性胰腺炎纤维化进程的作用及分子机制
    • 批准号:
      --
    • 项目类别:
      面上项目
    • 资助金额:
      --
    • 批准年份:
      2024
    • 负责人:
      万荣
    • 依托单位: