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Incidence and predictors of luteal phase deficiency by different ...

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Joseph B Stanford, MD<br />

Karen C Schliep, PhD<br />

Ahmad O Hammoud, MD<br />

Enrique Schisterman, PhD<br />

Sunni Mumford, PhD<br />

Christy Porucznik, PhD


Menstrual cycle ovulatory disorders range<br />

from <strong>luteal</strong> <strong>phase</strong> <strong>deficiency</strong> (LPD) to more<br />

advanced cases <strong>of</strong> anovulation.<br />

Alterations in life style (exercise, diet, <strong>and</strong><br />

stress) <strong>and</strong> abnormal endocrine dynamics are<br />

known to cause anovulation; however, their<br />

role in milder menstrual cycle phenotypes<br />

such as LPD is less known.


Clinically, LPD may be associated with:<br />

1. abnormal <strong>luteal</strong> <strong>phase</strong> progesterone <strong>and</strong> estradiol<br />

(E2) production<br />

2. shortening <strong>of</strong> the menstrual cycle (<strong>by</strong> shortening<br />

<strong>of</strong> the <strong>luteal</strong> <strong>phase</strong>)<br />

3. premenstrual spotting or bleeding<br />

4. pregnancy related disorders such as infertility (via<br />

impairment <strong>of</strong> endometrial development) <strong>and</strong><br />

early pregnancy loss.


While LPD is thought to occur in 3-20% <strong>of</strong><br />

women who are infertile <strong>and</strong> in 25-60% <strong>of</strong><br />

women with recurrent spontaneous abortion,<br />

data also suggest that 6-10% <strong>of</strong> women with<br />

normal fertility demonstrate an inadequate<br />

<strong>luteal</strong> <strong>phase</strong>.<br />

There is a need, thus, to better underst<strong>and</strong><br />

normal variations in the menstrual cycle<br />

<strong>phase</strong>s <strong>and</strong> in variations that could be<br />

pathologic.


Assess <strong>luteal</strong> <strong>phase</strong> function in the BioCycle<br />

Study <strong>by</strong> determining cycles with:<br />

1. Short <strong>luteal</strong> <strong>phase</strong>s (< 10 days in length)<br />

2. <strong>Incidence</strong> <strong>of</strong> premature luteinization (evidenced<br />

<strong>by</strong> a late follicular rise in progesterone before<br />

ovulation)<br />

3. Premenstrual spotting<br />

4. Abnormal <strong>luteal</strong> <strong>phase</strong> progesterone


1. Some normal cycling women express<br />

evidence <strong>of</strong> subtle menstrual cycle disorders<br />

manifested as LPD.<br />

2. Various demographic, lifestyle,<br />

environmental, <strong>and</strong> nutritional factors<br />

increase the incidence <strong>of</strong> LPD.


BioCycle Study (2005-2007): Followed 259 women<br />

from NY region for two menstrual cycles<br />

Inclusion:<br />

Ages 18-44<br />

Regularly menstruating<br />

Exclusion:<br />

Conditions known to affect menstrual cycle function<br />

Self-reported over- or underweight or unusual diet<br />

Strong compliance: 250 completed two cycles; 9<br />

completed one cycle


BioCycle women with cycles <strong>of</strong> known length<br />

(as determined <strong>by</strong> daily records <strong>of</strong> menstrual<br />

bleeding) who reached peak fertility via<br />

Clearplan® fertility monitor (based on E3G<br />

<strong>and</strong> LH in urine) OR who reached an LH peak<br />

serum surge > 19 ng/mL (for women not<br />

peaking via the monitor or with cycle lengths<br />

≥30 days)<br />

n=241 women, 406 cycles


Observed day <strong>of</strong> ovulation (i.e., urine or serum<br />

LH surge + 1 day) was used to classify visits into<br />

correct cycle <strong>phase</strong> categories.<br />

Cycle length was defined as number <strong>of</strong> days between<br />

menstrual bleeding.<br />

Day 1 <strong>of</strong> the cycle was defined as menstruating <strong>by</strong><br />

4pm on that day (after confirming 2 consecutive days<br />

<strong>of</strong> bleeding).<br />

Follicular length: Day 1 <strong>of</strong> bleeding through day <strong>of</strong><br />

ovulation.<br />

Luteal length: Day after ovulation through last day <strong>of</strong><br />

cycle.


Based on previous research, we defined LPD in 5<br />

unique ways:<br />

1. Luteal <strong>phase</strong> duration < 10 days in length.<br />

2. Deficient <strong>luteal</strong> <strong>phase</strong> progesterone production via<br />

AUC analysis (i.e., lowest quintile).<br />

3. Deficient <strong>luteal</strong> <strong>phase</strong> progesterone production via<br />

cutpoint (i.e., ≤ 5 ng/mL for all 3 <strong>luteal</strong> visits).<br />

4. Progesterone ≥ 2ng/mL before ovulation.<br />

5. Premenstrual spotting (defined as ≤ 2 consecutive<br />

days <strong>of</strong> menstrual bleeding).


Data on potential<br />

confounders were<br />

collected <strong>by</strong><br />

anthropometric<br />

measurement (height<br />

<strong>and</strong> weight),<br />

questionnaires (lifestyle,<br />

physical activity, <strong>and</strong><br />

reproductive history), or<br />

interview (demographic<br />

<strong>and</strong> dietary information).


Descriptive statistics <strong>by</strong> LPD for all 3<br />

definitions were computed for potential<br />

confounding variables <strong>and</strong> menstrual cycle<br />

characteristics (i.e., overall cycle length,<br />

premenstrual spotting, <strong>and</strong> geometric mean<br />

hormone levels) taking into account multiple<br />

cycles from the same women.


Nonlinear harmonic models were used to<br />

assess the association between LPD <strong>and</strong><br />

hormonal patterns.<br />

All models were adjusted for age, BMI, race.<br />

We used centered models for mean <strong>and</strong><br />

amplitude <strong>and</strong> non-centered models for<br />

<strong>phase</strong> shift assessment.


Luteal <strong>phase</strong><br />

< 10 days<br />

Luteal<br />

progesterone<br />


n=328 cycles<br />

Luteal<br />

<strong>phase</strong><br />

length


Luteal <strong>phase</strong> < 10 days<br />

Significantly (P


Estradiol<br />

Luteal <strong>phase</strong> < 10 days Luteal AUC progesterone < 54.5 ng/mL<br />

Luteal progesterone < 5 ng/mL<br />

Mean<br />

P=0.008


LH<br />

Luteal <strong>phase</strong> < 10 days Luteal AUC progesterone < 54.5<br />

Luteal progesterone < 5 ng/mL<br />

Amplitude<br />

P=0.12


FSH<br />

Luteal <strong>phase</strong> < 10 days Luteal AUC progesterone < 54.5<br />

Luteal progesterone < 5 ng/mL<br />

Mean<br />

P


Progesterone<br />

Mean<br />

P=0.02<br />

Amplitude<br />

P=0.03<br />

Luteal <strong>phase</strong> < 10 days


Findings suggest that normal cycling women<br />

do express evidence <strong>of</strong> subtle menstrual cycle<br />

disorders manifested as LPD.<br />

Age, race, sleep, <strong>and</strong> dietary factors (e.g.,<br />

fiber intake) may be associated with LPD in<br />

normal cycling women.<br />

LPD may express itself in <strong>different</strong> ways,<br />

potentially through <strong>different</strong> mechanisms.


Decreased E2 across the cycle significantly<br />

associated with deficient <strong>luteal</strong> progesterone<br />

production.<br />

Increased FSH significantly associated with<br />

short <strong>luteal</strong> <strong>phase</strong> duration <strong>and</strong> deficient<br />

<strong>luteal</strong> progesterone production.<br />

Decreased progesterone significantly<br />

associated with short <strong>luteal</strong> <strong>phase</strong> duration.


Need for a better diagnostic test to assess<br />

<strong>luteal</strong> <strong>phase</strong> insufficiency.<br />

LPD, an independent entity causing<br />

infertility, has not been proven.<br />

While we show here that LPD is present in<br />

normal cycling women, we cannot infer if it is<br />

pathological in regards to fertility.


Further research is needed to assess what<br />

factors influence LPD, so that preventive<br />

strategies via lifestyle modifications or<br />

minimally invasive therapeutic treatments<br />

might be implemented for women suffering<br />

from reproductive disorders due to LPD.

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