Showing posts with label inflammation. Show all posts
Showing posts with label inflammation. Show all posts

Monday, April 11, 2011

LabEvoEndo Journal Club: Dana Ahern presents on PMDD

This is the third guest post of the LabEvoEndo Journal Club, a new series for the LabEvoEndo blog meant to highlight student contributions to the lab (first post here, second post here). The author is Honors Anthropology Junior Dana Ahern. Dana has been in my lab since her sophomore year.


* * *

I’d like to start this blog post with a little background on progesterone. Progesterone is fascinating and it affects a lot more than just the menstrual cycle. We are starting to understand just how big of an impact progesterone has, and the research project I am working on is beginning to show some of the potential applications of progesterone in medicine. These applications include improving recovery time after traumatic brain injury and strokes, as well as helping us understand postpartum depression (PPD) and premenstrual dysphoric disorder (PMDD).

PMDD is similar in mechanism with postpartum depression, although the exact mechanism is still being researched. Some research suggests a hormonal influence, as allopregnanolone, an offshoot neuroregulator of progesterone, modulates GABA, which is a neurotransmitter related to mood and anxiety. Too much GABA results in increased anxiety and mood related issues, so it is a logical conclusion that the drop in progesterone during the late luteal phase of the menstrual cycle would result in excess GABA and therefore symptoms of PMDD.

The article we discussed looked at PET scans of 12 women with and 12 women without a diagnosis of PMDD, taking scans during the follicular phase and the late luteal phase of their menstrual cycles. The women in the study were screened for two months with mood surveys and then taken in for a day of PET scans and blood/urine samples, once during the follicular phase and once during the late luteal phase, when the symptoms of PMDD would have begun. PMDD can affect certain brain functions, so they were using the PET scan to detect brain dysfunction, such as one study the article looked at that showed frontal lobe dysfunction associated with PMDD.

The hormone measurements didn’t show anything significant and PET scans showed increased cerebellum activity from follicular to late luteal phase in PMDD women only. The cerebellum has many GABA receptors, which is a possible explanation of this, but in journal club, we wondered if it is the lack of modulation after a drop in the progesterone, or if there is something going on with the number of receptors, such as perhaps some sort of diminished sensitivity to allopregnanolone.

In journal club, we discussed some of the problems we had with this study. Someone brought up the small sample size and too few collection times for samples and scan. The fact that only one cycle was measured impacted the study. Kate also mentioned that blood hormones are a less useful measure than salivary hormone measurements. Finally, while the article states that the cause of PMDD is an overactive cerebellum in women suffering from PMDD, they never really reach a definite reason for what is causing the increased action. Ultimately, the article would have benefitted from examining the hormones more closely and more often.

Reference

Rapkin AJ, Berman SM, Mandelkern MA, Silverman DH, Morgan M, & London ED (2011). Neuroimaging evidence of cerebellar involvement in premenstrual dysphoric disorder. Biological psychiatry, 69 (4), 374-80 PMID: 21092938

Monday, April 4, 2011

LabEvoEndo Journal Club: Sophia Bodnar presents on cervical cancer

This is the second guest post of the LabEvoEndo Journal Club, a new series for the LabEvoEndo blog meant to highlight student contributions to the lab (first post here). The author is Anthropology Junior Sophia Bodnar. Sophia has been in my lab since her sophomore year.

* * *

In light of recent acceptance to a summer program where I will be working in immunology, I wanted to choose an article relevant to reproductive health and immunology. The first place I turned to was the Journal of Reproductive Immunology. This seems like a copout, but I found a very interesting and recent article for the lab meeting entitled "Higher levels of cervicovaginal inflammatory and regulatory cytokines and chemokines in healthy young women with immature cervical epithelium" by Hwang et al in 2011.

It would be wonderful if human variation was always taken into account, particularly when discussing reproductive health. This is exactly what the researchers from UCSF aimed to do and why this article was a refreshing read. It is known that women aged 15-24 have the highest rates of Sexually Transmitted Infections (STIs) and is commonplace in the medical community to associate STIs with risky sexual behavior. The study looked at cervical epithelium, tissue that lines the cervix, and accompanying levels of cytokines and chemokines in order to show basic biological differences in immune function of the cervix between adults and adolescents to account for the predominance of STIs in younger women.

Thirty-two women aged 13-21 were selected. The women were placed in the immature group (>50% columnar epithelium) or mature cervical group (<5% columnar epithelium). In order to help you envision these epithelial cells, think of a single line of figure skaters (fragile, columnar cells) versus a stack of sumo wrestlers (strong, squamous cells). Younger women have more columnar cells and throughout development the columnar cells become squamous cells. This is why it is extremely important to take variation into account, because at any given point in a woman’s development the ratio of squamous to columnar cells varies.

Participants were excluded for pregnancy, surgery on the cervix, cervical dysplasia (grades above 1), taking immunosuppressive agents, or being symptomatic for genital complaints such as yeast. However, women were not excluded for having HPV because the researchers consider it a very common infection. The women filled out surveys detailing sexual and nonsexual behavior (number of partners, contraception, substance abuse, etc) and reproductive health history (previous pregnancies, menarche, etc). Colpophotagraphs were taken of the cervical epithelium and the researchers measured and rated maturity by counting pixels from the photograph. Women were evaluated only once, a strong drawback to this study as they are interested in the variation of the epithelium.

They found that ten of the cytokines and chemokine levels were higher in the immature group (one cytokine was excluded). Although other studies have previously looked at cervical levels of cytokines and chemokines, this study looked at levels of these cell-signaling protein molecules in relation to type of cervical epithelium. The authors note that having more columnar cells may be considered beneficial for young women as these cells are more easily damaged and likely to initiate an immune response, but this would mean that younger women are less prone toward infection. The researchers then go on to conclude that because these columnar cells are more prone to damage and thus immune response, chronic inflammation is more likely which could lead to greater rates of infection. This study only looked at the epithelium of healthy women, so it is important to examine women with various infections in the future. The epithelium and levels of cytokines/chemokines in women with STIs could lead to a better understanding or correlation between type of epithelium and its subsequent immune response and risk rate.

In our discussion of the article, it was mentioned that there are no “normal” levels of cytokine and chemokine levels with which to compare the researcher’s values. In the study this was referred to as a challenge. Perhaps there will never be established normative levels of these protein molecules, but so what? Our lab group concluded that this should not be considered a challenge and may be beneficial as we will simply have to take variation into account which is strongly lacking in the medical realm of reproductive health! We all agreed that this study should have been conducted over a longer period of time, and that the women should have had their epithelium photographed and correlating levels of cytokines/chemokines measured far more often. Because this study’s main focus was variation of the epithilium, it would make sense for these women to contribute visits over the course of their entire menstrual cycle whereas this study simply adjusted for days since last menstrual cycle. We also discussed that this study may be perceived as far more qualitative than quantitative. However, we acknowledged that the clarity of the cervical photos was great so quantitative measurements of the pixels could be taken seriously. It was also noted that these findings were not all that surprising. It seems commonsense that younger women have cells that are more easily damaged and that this could lead to chronic inflammation that poses negative risks. Although this may be true, I think that we should still applaud these authors for acknowledging variation throughout their research.

I also find it interesting that the most common cervical cancer is squamous cell carcinoma. Columnar cells may be damaged more easily, but it seems that squamous cells are more prone towards division and supporting abnormal growth. Most cases of cervical cancer are due in part to HPV infection, which in going along with the findings of this article, is more common in younger women with immature columnar cells. It would be interesting to see how the squamous cells in women with cervical cancer compare to the columnar cells of women with HPV. Perhaps cervical cancer, as a result of HPV, is more common in women who have more columnar cells than squamous cells, but the cancer arises in and prefers the squamous cells because they are less likely to initiate a strong immune response. In general, I appreciate how easy and enjoyable this article is to read. Hopefully more articles acknowledging variation, particularly when it comes to reproductive health, will be published as a result of this interesting finding.

Reference

Hwang LY, Scott ME, Ma Y, & Moscicki AB (2011). Higher levels of cervicovaginal inflammatory and regulatory cytokines and chemokines in healthy young women with immature cervical epithelium. Journal of reproductive immunology, 88 (1), 66-71 PMID: 21051089