Reproductive Endocrinology · Thyroid and Metabolic Function

Preconception maternal lipoprotein levels in relation to fecundability

Pugh SJ, Schisterman EF, Browne RW, Lynch AM, Mumford SL, Perkins NJ, Silver R, Sjaarda L, Stanford JB, Wactawski-Wende J, Wilcox B, Grantz KL

Published May 2017 Human reproduction (Oxford, England), 32(5), 1055-1063
DOI 10.1093/humrep/dex052 PMID 28333301 PMC PMC6075456

RRM Academy Synopsis

High cholesterol linked to lower conception odds after pregnancy loss

In women with past pregnancy losses, high total cholesterol went with a 24% lower chance of conceiving each cycle. A trial cohort of 1,228 women with one or two earlier losses and no infertility diagnosis was tracked for up to six cycles. High LDL-C, high triglycerides and low HDL-C also went with lower chances in this cohort.

Key Findings

  • Among 1,228 women, 148 (12.3%) had elevated total cholesterol, 94 (7.9%) elevated LDL-C, 280 (23.2%) elevated triglycerides and 606 (50.7%) low HDL-C.
  • Elevated total cholesterol went with 24% reduced fecundability by hCG-detected pregnancy (fecundability odds ratio, FOR, 0.76, 95% CI 0.59, 0.97).
  • By ultrasound-confirmed pregnancy, the reduction for elevated total cholesterol was 29% (FOR 0.71, 95% CI 0.55, 0.93).
  • Further adjustment for BMI and waist-hip ratio kept the direction, but the estimates reached only borderline significance and some were null.
  • Fecundability fell with high cholesterol in overweight women (FOR 0.61, 95% CI 0.38, 0.98) and obese women (FOR 0.58, 95% CI 0.36, 0.93), with no change in lean women.

Interpretation

This cohort study followed 1,228 women with one or two past pregnancy losses and no infertility diagnosis for up to six cycles. Researchers measured blood lipid levels once before women tried to conceive. Women with high cholesterol, high LDL-C, high triglycerides or low HDL-C had lower odds of pregnancy each cycle. The pattern held whether pregnancy was confirmed by a blood test or by ultrasound. The link was strongest in women who were overweight or obese, with no drop in lean women. The authors note the results may apply mainly to women with a history of pregnancy loss. The findings support larger studies on whether treating high lipids helps women conceive.

RRM Context

Restorative reproductive medicine looks for root causes of slow conception, and metabolic health is part of that evaluation. Lipid levels are easy to screen and can be changed through diet and activity. A study the authors cite found a similar lipid link in men. This supports checking lipid levels in both partners.

Abstract

Study Question

Are maternal preconception lipid levels associated with fecundability?

Summary Answer

Fecundability was reduced for all abnormal female lipid levels including total cholesterol, low-density lipoprotein cholesterol (LDL-C), high-density lipoprotein cholesterol (HDL-C) and total triglyceride levels.

What Is Known Already

Subfecundity affects 7-15% of the population and lipid disorders are hypothesized to play a role since cholesterol acts as a substrate for the synthesis of steroid hormones. Evidence illustrating this relationship at the mechanistic level is mounting but few studies in humans have explored the role of preconception lipids in fecundity.

Study Design, Size, Duration

A secondary analysis of the Effects of Aspirin in Gestation and Reproduction (EAGeR) trial (2007-2011), a block-randomized, double-blind, placebo-controlled trial.

Participants/Materials, Setting, Methods

A total of 1228 women, with 1-2 prior pregnancy losses and without a diagnosis of infertility, attempting pregnancy for up to six menstrual cycles were recruited from clinical sites in Utah, New York, PA and Colorado. Time to pregnancy was the number of menstrual cycles to pregnancy as determined by positive hCG test or ultrasound. Individual preconception lipoproteins were measured at baseline, prior to treatment randomization and dichotomized based on clinically accepted cut-points as total cholesterol ≥200 mg/dl, LDL-C ≥130 mg/dl, HDL-C <50 mg/dl and triglycerides ≥150 mg/dl.

Main Results and the Role of Chance

There were 148 (12.3%) women with elevated total cholesterol, 94 (7.9%) with elevated LDL-C, 280 (23.2%) with elevated triglycerides and 606 (50.7%) with low HDL-C. The fecundability odds ratio (FOR) was reduced for all abnormal lipids before and after confounder adjustment, indicating reduced fecundability. Total cholesterol ≥200 mg/dl was associated with 24% (FOR: 0.76, 95% CI: 0.59, 0.97) and 29% (FOR: 0.71, 95% CI: 0.55, 0.93) reduced fecundability for hCG-detected and ultrasound-confirmed pregnancy, respectively, compared with total cholesterol <200 mg/dl. There was a 19-36% decrease in the probability of conception per cycle for women with abnormal lipoprotein levels, though additional adjustment for central adiposity and BMI attenuated observed associations.

Limitations, Reasons for Caution

Although the FOR is a measure of couple fecundability, we had only measures of female lipid levels and can therefore not confirm the findings from a previous study indicating the independent role of male lipids in fecundity. The attenuated estimates and decreased precision after adjustment for central adiposity and obesity indicate the complexity of potential causal lipid pathways, suggesting other factors related to obesity besides dyslipidemia likely contribute to reduced fecundability.

Wider Implications of the Findings

Our results are consistent with one other study relating preconception lipid concentrations to fecundity and expand these findings by adding critically important information about individual lipoproteins. As lipid levels are modifiable they may offer an inexpensive target to improve female fecundability.

STUDY FUNDING AND COMPETING INTEREST(S): This study was funded by the Intramural Research Program of the Eunice Kennedy Shriver National Institute of Child Health and Human Development. The authors have declared that no conflicts of interest exist.

Trial Registration

#NCT00467363.

Topics

By this author

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Reproductive Endocrinology › Thyroid and Metabolic Function › Insulin and Metabolism
Sarah J Pugh, Enrique F Schisterman, Richard W Browne, Anne M Lynch, Sunni L Mumford, Neil J Perkins, Robert Silver, Lindsey Sjaarda, Joseph B Stanford, Jean Wactawski-Wende, Brian Wilcox, Katherine L Grantz
S Pugh, E Schisterman, Rick Browne, Dick Browne, Rich Browne, R Browne, A Lynch, S Mumford, N Perkins, Bob Silver, Rob Silver, Bobby Silver, R Silver, L Sjaarda, Joe Stanford, Joey Stanford, J Stanford, J Wactawski-Wende, B Wilcox, Kathy Grantz, Kate Grantz, Katie Grantz, K Grantz
PMID 28333301 28333301 DOI 10.1093/humrep/dex052 10.1093/humrep/dex052 Pugh et al. 2017, Pugh 2017