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Heavy Metal Index

Adults and Potential Modification by Prenatal Methylmercury Exposure

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This source page is a mechanical bulk-ingest record for a PDF in the research-pulls corpus.

Page snapshot
Cited by7 pages
Metals measured4
Evidence tierB
Year1986

Overview

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Key numbers

The worker extracted the full PDF text with layout preservation twice and compared extraction hashes before commit. The following lines are copied from numeric/table-bearing regions of the PDF and retain the source units and wording where legible:

  • short-term memory and cognitive processing speed by 0.21 SD (95% CI: –0.04, 0.46) and 0.28 SD provided written, informed consent.
  • (95% CI: 0.02, 0.54), respectively. In the group with lower prenatal methylmercury exposure, a
  • studies have demonstrated a detrimental A Faroese birth cohort study (n = 1,022) was Material published in EHP articles may not conform to
  • of seconds of the last step. Maximal oxygen (Debes et al. 2006, 2016), we also consid- for physical activity (n = 1), smoking status
  • uptake (VO 2Max) in L/min was estimated ered predictors of neurocognitive outcomes: (n = 2), maternal and paternal employ-
  • using the formula: VO2Max (L/min) = 0.16 + maternal and paternal employment, maternal ment (n = 17), maternal education/training
  • (0.0117 × MPO), and then divided by weight and paternal education/training, and mother’s (n = 18), paternal education/training (n = 17),
  • and expressed in mL/kg/min. intelligence (Raven score). maternal Raven score (n = 21), and single
  • Prenatal Methylmercury Exposure final models using a combined approach. First, except for block designs (n = 48)). We imputed
  • ical cord blood samples collected at birth confounders. Second, plausible variables that number of iterations (n = 10) according to
  • (CB-Hg in μg/L). Briefly, blood samples changed the effect estimates by ≥ 10% were the proportion of missing information (White
  • from the umbilical cord were taken in 10-mL also retained. et al. 2011). Mean estimates and variances
  • (Gaithersburg, MD, USA) as previously regressions adjusting only for sex. Furthermore, (23.5 μg/L), whereas in the second analysis
  • to assess the relationship between VO2Max (35 μg/L) and ran the analysis across two
  • Neurocognitive Functions and groups of neurocognitive outcomes. In groups of low (< 35 μg/L; lower two tertiles)
  • A battery of neuropsychological tests was this approach, we considered test scores from and high (≥ 35 μg/L; highest tertile) prenatal
  • to test whether participants with better and 0.93 (Table 2). cognitive processing speed by 0.28 SD (95%
  • age 22 years (Debes et al. 2006), we consid- Final models included VO2Max, sex, physical scores by 0.21 SD (95% CI: –0.04, 0.46;
  • variable. Finally, we considered the three for cognitive processing speed (Table 3). We motor function for which the standardized
  • VO 2Max at age 22 years, adjusting for the Table 1. Levels of maximal oxygen uptake in relation to important covariates.
  • modeling” in the Supplemental Material. Low (< 23.5 μg/L) 99 (50) 34.7 ± 6.4
  • Table S1). Adjusting for sex, higher VO2Max Yes 152 (84) 35.3 ± 7.6
  • neurocognitive g score of 0.24 SD (95% CI: increased short-term memory and cogni- function (g), the associations were similar
  • –0.02, 0.50; z = 1.81, p = 0.07). In the final tive processing speed by 0.28 SD (95% CI: in the two groups of exposure, although
  • tions, aerobic fitness was significantly associ- (95% CI: 0.19, 0.74; z = 3.22, p = 0.001). lower exposure group (0.27 SD; 95% CI:
  • ated with cognitive efficiency. Here, a 1-SD No significant association was observed for –0.02, 0.55; z = 1.89, p = 0.06) (Table 5).
  • increase of 0.32 SD (95% CI: 0.01, 0.62; the group with higher prenatal methylmercury comparing results in the tertile groups of
  • general thinking abilities (Table 3). with a median cut-off, the associations differed efficiency and general thinking abilities. Thus,
  • In multiple group SEMs comparing the the other neurocognitive outcomes (Table 5). in VO2Max associated with increased cognitive
  • high (≥ 23.5 μg/L) prenatal methylmercury Table 2. Factor loadings and estimated correlation of measured test scores to the neurocognitive latent
  • by 0.45 SD (95% CI: 0.08, 0.81; z = 2.45, Spatial span forward 0.25 0.08 0.002 0.28
  • (Table 4). In the group with higher prenatal Boston Naming Test, correct with cues 0.86 0.03 < 0.001 0.79
  • functions (Table 4). Although the associa- Verbal analogies 0.32 0.05 < 0.001 0.67
  • group (0.27 SD: 95% CI: –0.05, 0.59; CVLT, long delay, recognition, correct 0.45 0.11 < 0.001 0.42
  • z = 1.65, p = 0.10) (Table 4). However, Incidental Memory 0.83 0.24 0.001 0.25
  • increases by 0.43 SD (95% CI: 0.07, 0.80; standard error.
  • tion was found in the group of higher prenatal Table 3. Adjusted associations between VO2Max and neurocognitive functions.
  • exposure (0.24 SD; 95% CI: –0.20, 0.68; Neurocognitive domain B (95% CI)a p-Value
  • and higher prenatal exposures (Table 4). Visual processing 0.07 (–0.24, 0.38) 0.64
  • of 35 μg/L (67% percentile), we observed Cognitive efficiency 0.32 (0.01, 0.62)** 0.04
  • mates were slightly attenuated (see Tables S3, ­domain-­representation differs between tests, neuronal stem cells.
  • with VO2Max at age 22 years (standardized Table 4. Adjusted associations between VO2Max and neurocognitive functions in regard to prenatal

Methods (brief)

  • A subsample of 262 cohort members under-
  • Chan School of Public Health, Landmark Center 3E,
  • ical cord blood samples collected at birth confounders. Second, plausible variables that number of iterations (n = 10) according to
  • (CB-Hg in μg/L). Briefly, blood samples changed the effect estimates by ≥ 10% were the proportion of missing information (White
  • reference material samples from the National We explored associations between VO2Max ences in associations using two cut-offs. In the
  • campus (Tyler and Allan 2013). It also induced VO2Max in an American sample was 43.9 specific performances.

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Update history

The five most recent substantive edits to this page, classified major (evidence or structure moved), correction (a published value or statement was wrong and has been fixed), or minor (narrative rewritten without changing the underlying evidence). Each description is derived from what the edit did to this page; the linked commit is the authoritative record, routine regeneration passes are excluded, and the full version history lives in git. When DOI minting comes online (see schema docs), each entry below will also link to a version-pinned DataCite DOI.

CommitDateChangeDescription
b01ec52c2026-08-04major2 sections added
d49e450f2026-08-03major5 sections added; narrative text revised